Saved From The Frankenvax

How a Psycho Vaccine Marrying the Infamous COVID Spike Protein to HIV’s Neurotoxic gp41 Was [Allegedly] Canned by a Mere Testing SNAFU

How Australia Dodged The First Mad Vax Bullet of the WEF Scamdemic / Plannedemic

Darwin Award Vaccine Featured Insane Merger of HIV and COVID But Failed Due to Buggering of AIDS Tests, NOT Because of the Obvious Risks

Was It Ever Really For COVID? The gp41 HIV Protein is a TOP Target For AIDS Vaccines

How Science Monetization and Corruption Has Broken All Vaccine Safety Mechanisms and Made Sneaky Liars Out of Scientists

Mood Music

Intro – Prepare To Be Shocked

This is one of the craziest stories your either never heard, or barely heard. I am certain of the following. Nobody ever spelled out to you how NUTS this failed vaccine really was. This absolutely bonkers vaccine, that was almost used on all Australians.

AND MAY STILL BE.

The fact that nobody even followed this story, shows that the captured corporate media is absolutely not doing its job. Either THAT, or their job is to help deceive us.

And you know where my money is on that.

Surely, in the past, both journalists and scientists might have said something to the effect of “Hey – marrying a cardiovascular pathogenic bat virus spike protein and a neurotoxic AIDS protein in a vaccine to prevent a cold seems a little weird.”

BUT NO. NOT NOW.

And yet, some of us, few as we might be, might still have some questions.

We assume – ASSUME – as in ASS / U / ME – that all people in all of science are acting in all of our best interests all the time.

I have been completely broken of this spell, and I can tell you – what I can see now is not pretty.

I need to prepare you for what I’m about to tell you.

State of Corruption of Vaccine Science

First, a fantastic interview of Dr. Robert Malone by Tucker Carlson. It’s very folksy and long – a bit over an hour – but it will absolutely cure you of any idea that science in 2022 has not been almost totally corrupted by money, power, and SECRET AGENDAS.

This guy Malone is as close to a Moderna insider / honest outsider as you’re gonna get, and he clearly sees the dirty play from the Moderna point of view.

Hat tips to FG&C and GA/FL for keeping this video in play. Gail has been pumping this video, too. EVERYBODY need to watch this.

LINK: https://rumble.com/vuo2uu-dr.-robert-malone-on-tucker-carlson-today-feb-10-2022.html

In fact, I suspect that there is some relationship between this interview dropping that the following “factoid”.

Probably nothing https://t.co/vyKLfNHxCq
— Jack Posobiec (@JackPosobiec) February 12, 2022

Indeed, let’s just save that tweet as an image, in case Twitter decides Jack is becoming too much of a liability.

One of the biggest BOOMS dropped in the video, IMO, is the fact that Robert Malone WARNED the FDA about the toxicity of the spike protein, and they SHRUGGED IT OFF.

Yes. Malone gave them documentation, as asked, and they came back to him and said everything was OK. And THAT is when he started to think something was very wrong.

We’re about to do it AGAIN – only I’m not the first – I’m just rediscovering an obvious “why the heck are they doing THAT” point.

But we’ll get to that in a minute. We need to broaden our list of corrupt suspects.

You see, corporate “science” isn’t the only bad actor here. What about governments that conspire with the corporations to “mandate” their products for a mutual PAYOFF?

It turns out that both Justin Trudeau and the Canadian government have a very large incentive in mandating the broken, dubious, and just plain BAD Moderna and Pfizer “vaccines”.

LINK: https://rumble.com/vupkuv-breaking-criminal-canadian-monopoly-dr.-david-martin-exposes-why-trudeau-wo.html

When you realize that Justin Trudeau is not only following his mandate madness for WEFfian ideological reasons, and for Papa Fidel power, but also for CASTRO CASH, you understand what’s REALLY going on.

SO – now that you realize THESE PEOPLE care more about other things, than they care about us, the following will make more sense.

The Frankenvax That Almost Was

So just today, FG&C posted THIS TWEET which made me go WTF…..

"False positives" https://t.co/cwr0PLRoPI
— Catturd ™ (@catturd2) February 12, 2022

Basically, an Australian COVID vaccine that falsely triggers AIDS / HIV tests was recalled. The vaccine was NOT sent out for use by the public, because it gave people positive AIDS tests.

GREAT, but…..

WHY did the vaccine do this? And by the way….
Didn’t this happen BEFORE – like over a year ago?
I could have SWORN this happened before.
Is this OLD NEWS or a DIFFERENT VACCINE?
Or did they bring the SAME vaccine BACK?
Or even worse….. AND logic…..

You see, I remember something just like this bit of news, over a year ago. It was some vaccine from an Australian university that accidentally triggered AIDS tests.

Well, when I looked closer at this, it turned out to be THE SAME NEWS. Meaning that this recent tweet was just OLD NEWS.

HOWEVER – I happen to know a lot more now, a year later, so I dug DEEPER and FOUND MORE.

And now I want to explain to you, exactly what is going on.

Because this monster AIN’T DEAD.

VolksWackcine 451

Let’s begin by looking at the actual announcement that all this news came from. The paragraph in BOLD is the critical one. If you’re going to TL;DR past all the rest, read THAT paragraph.

Update on The University of Queensland COVID-19 vaccine

11 Dec 2020

Friday, 11th December, 2020: The University of Queensland (UQ) and CSL today announce that the Phase 1 trial of the UQ-CSL v451 COVID-19 vaccine has shown that it elicits a robust response towards the virus and has a strong safety profile. There were no serious adverse events or safety concerns reported in the 216 trial participants. However, following consultation with the Australian Government, CSL will not progress the vaccine candidate to Phase 2/3 clinical trials.

The University of Queensland commenced a Phase 1 trial of their COVID-19 vaccine candidate – v451 – in July 2020, to assess safety and immunogenicity in healthy volunteers. CSL was working towards taking responsibility for the Phase 2/3 clinical trial and large-scale manufacture of the vaccine, upon completion of successful trials.

The Phase 1 data also showed the generation of antibodies directed towards fragments of a protein (gp41), which is a component used to stabilise the vaccine. Trial participants were fully informed of the possibility of a partial immune response to this component, but it was unexpected that the levels induced would interfere with certain HIV tests.

There is no possibility the vaccine causes infection, and routine follow up tests confirmed there is no HIV virus present.

With advice from experts, CSL and UQ have worked through the implications that this issue presents to rolling out the vaccine into broad populations. It is generally agreed that significant changes would need to be made to well-established HIV testing procedures in the healthcare setting to accommodate rollout of this vaccine. Therefore, CSL and the Australian Government have agreed vaccine development will not proceed to Phase 2/3 trials.

The Phase 1 trial will continue, where further analysis of the data will show how long the antibodies persist, with studies so far showing that levels are already falling. The University of Queensland plans to submit the full data for peer review publication.

UQ Vice-Chancellor, Professor Deborah Terry, said while the outcome was disappointing, she was immensely proud of the UQ team who had shouldered a heavy burden of responsibility while the world watched on. “I also want to thank our many partners, our donors – including the Federal and Queensland Government – and of course the 216 Queenslanders who so willingly volunteered for the Phase 1 trials.”

UQ vaccine co-lead, Professor Paul Young, said that although it was possible to re-engineer the vaccine, the team did not have the luxury of time needed. “Doing so would set back development by another 12 or so months, and while this is a tough decision to take, the urgent need for a vaccine has to be everyone’s priority.”

“I said at the start of vaccine development that there were no guarantees, but what is really encouraging is that the core technology approach we used has passed the major clinical test. It is a safe and well-tolerated vaccine, producing the strong virus-neutralising effect that we were hoping to see.

So we will continue to push forward and we are confident that with further work the Molecular Clamp technology will be a robust platform for future vaccine development here in Australia and to meet future biosecurity needs.

Dr Andrew Nash, Chief Scientific Officer for CSL said “This outcome highlights the risk of failure associated with early vaccine development, and the rigorous assessment involved in making decisions as to what discoveries advance.”

“This project has only been made possible by the innovative science developed by world-class scientists at The University of Queensland and the strong collaboration between our organisations, and many others, over the last 10 months. CSL and Seqirus are committed to continuing our work to protect the Australian population against COVID-19. Manufacture of approximately 30 million doses of the Oxford/AstraZeneca vaccine candidate is underway, with first doses planned for release to Australia early next year. In addition, CSL has agreed at the request of the Australian Government to manufacture an additional 20 million doses.”

UQ and CSL acknowledge the support of the Coalition for Epidemic Preparedness Innovations (CEPI) in partnering to enable the rapid development of the vaccine candidate through clinical trials.

– ENDS –

LINK: https://www.csl.com/news/2020/20201211-update-on-the-university-of-queensland-covid-19-vaccine

WOLF AGAIN.

So what they’re saying is that this vaccine – which uses the HIV protein gp41 – sets off HIV tests. And THAT made the test unacceptable to move forward. The remaining phase II and phase III trials were cancelled, while the phase I trials continued to finish collecting data.

And WHILE they say that the phase I testing showed that the vaccine was safe and effective, if you look more closely, they only tested it on 216 people.

We KNOW from the Moderna and Pfizer tests, that even after HUGE phase II and phase III trials, using thousands or tens of thousands of participants, there are serious side effects that are STILL not discovered until actual roll-out to the public, when millions receive the shot.

And that does NOT include long-term effects. We know NOW that this determination can be critical in many cases.

And one more point for the record. As you can see by the statement at the end of the press release, this vaccine was supported by the Bill Gates organization CEPI.

Yeah, that CEPI, and THAT Bill Gates.

Like I say, CEPI is how Gates gets TWO VOTES, and GAVI is how he gets THREE.

So the bottom line – this vaccine was killed because it set off AIDS tests.

But let’s dig a little deeper into that.

So What’s With HIV and the COVID Vaccines?

When I first heard about this particular Australian vaccine (UQ-CSL v451, or v451 hereafter) triggering HIV tests, my immediate thought was that this might be proof that the Indian researchers were CORRECT – that the spike protein really contained those four inserts from HIV, and that THIS was setting off tests for HIV.

Later, I heard that – no – there was actually some segment of HIV protein being used in the v451 vaccine INTENTIONALLY. Thus, the whole problem seemed stupid, the use of the HIV protein seemed short-sighted, and I promptly forgot about it. No smoking gun – just a stink bomb.

However, a year’s time changed all that.

Think how different the perspective is now.

virus almost certainly came out of a biowarfare lab in China with PLA/NIH ties
Fauci, Dazsak and minions now known to have LIED about origins
Fauci gang also lied when pooh-poohing the Indian HIV insert hypothesis
mRNA vaccines seem to be producing immune deficiency, a.k.a. “VAIDS”
there are working hypotheses now which explain immune deficiency
Fauci’s history with HIV mirrors current history with COVID – lies and hidden agenda
Fauci seems to be obsessed with immunodeficiency and vaccines
Fauci promoted bad killer drugs as treatments in both cases (AZT, remdesivir)
Fauci seems to have an agenda clearly counter to truth as we know it, and is likely serving something beyond the increasing “fake” science which the public believes is operant in the world, but which is very likely a “reduced set” intended to deceive us

Thus, with all that WEIRD background, it NOW seems a bit “par for the course” that somebody in that world would want to bring HIV into the COVID equation.

But is that a good idea?

Now – before I go talking about why this might be a BAD idea, I want to give you plenty of references as to why they SAY it was a good idea.

Let’s start with a good explanation of why the false positives occurred. This article includes a lot of information on the v451 vaccine itself.

LINK: https://theconversation.com/how-did-the-university-of-queensland-csl-vaccine-fail-due-to-false-positive-hiv-tests-a-vaccine-expert-explains-151911

ARCHIVE: https://archive.fo/duxjK

The article mentions, without too much detail, that the HIV protein is part of a “molecular clamp” – a trimeric molecular “holder” of spike protein molecules. This holder allows three molecules of any attached spike-type protein to stay locked into a rigid, parallel conformation, which will remain in the desirable pre-fusion (with a cell) configuration, and not change into the useless post-fusion configuration.

The article also links to a scientific paper on the technology:

LINK: https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7672035/

Front Immunol. 2020; 11: 592370. Published online 2020 Nov 4. doi: 10.3389/fimmu.2020.592370 PMCID: PMC7672035 PMID: 33250897

Rapid Response Subunit Vaccine Design in the Absence of Structural Information

Danushka K. Wijesundara,^{1 , 2}Michael S. Avumegah,^{1 , 2}Julia Lackenby,^{1 , 2}Naphak Modhiran,^{1 , 3}Ariel Isaacs,¹Paul R. Young,^{1 , 2 , 3}Daniel Watterson,^{1 , 2 , 3 , *}and Keith J. Chappell^{1 , 2 , 3 , *}

ABSTRACT

Prior to 2020, the threat of a novel viral pandemic was omnipresent but largely ignored. Just 12 months prior to the Coronavirus disease 2019 (COVID-19) pandemic our team received funding from the Coalition for Epidemic Preparedness Innovations (CEPI) to establish and validate a rapid response pipeline for subunit vaccine development based on our proprietary Molecular Clamp platform. Throughout the course of 2019 we conducted two mock tests of our system for rapid antigen production against two potential, emerging viral pathogens, Achimota paramyxovirus and Wenzhou mammarenavirus. For each virus we expressed a small panel of recombinant variants of the membrane fusion protein and screened for expression level, product homogeneity, and the presence of the expected trimeric pre-fusion conformation. Lessons learned from this exercise paved the way for our response to COVID-19, for which our candidate antigen is currently in phase I clinical trial.

Here is part of a really good graphic from the paper.

You can see how it’s possible to produce a spike protein with the “molecular clamp” attached, and then simply let this recombinant construction TRIMERIZE (form a triple, side to side) around the three molecular clamps, and thereby stabilize the three spike protein molecules next to each other.

This is a bit like a “motif” within an actual virus, where spike proteins, sticking out next to each other, protect each other’s sides. THAT is the basic idea of this thing.

Remember how Novavax assembles a bunch of spikes via modified ass ends into a kind of antigenic cloved apple, to create a kind of fake virus? Same very basic principle.

Indeed, the molecular clamp is even a bit like TWO motifs, since gp41 serves a somewhat similar purpose in the HIV virus, being the root of a stalk to an attack mechanism.

HIV-1 fusion process. It involves both subunits of the envelope spike complex. Notably, gp41 is shown in green with its transmembrane region buried in the virion membrane, both segments of heptad repeats (CHR closer to the virus and NHR closer to the host cell) before and after conformational changes, and the N-terminal end of the ectodomain in gray. In the last two panels pointed out by the red arrows, gp41 is observed following penetration of the host cell and following a conformational change resulting in the six-helix bundle which brings the viral and cell membranes into close proximity.

So – in a very real sense – this whole “vaccine” thingie is a literal marriage of HIV and coronavirus – the simplest possible one.

And they didn’t tell you ANY of this shit – did they?

So all of that WORKS, but the problem is that antibodies don’t just form to the attached spike protein – they ALSO form to the “molecular clamp”, meaning to the gp41 protein.

And what does that mean?

An AIDS Vaccine in Disguise?

The people who made the v451 vaccine say they didn’t expect there to be so much antibody response to the gp41 parts of the vaccine, thus triggering HIV tests.

You know what?

I don’t believe them.

I think they were gaslighting us all along.

Part of this is due to the fact that I’ve seen gp41 named numerous times as a potential basis for subunit vaccines against HIV. In fact, in one reference, I saw it named as THE BEST HOPE for an AIDS vaccine.

They didn’t mention that? LOL. OH, REALLY.

So WHY would anybody be using gp41 as part of an antigen, and not expect it to generate antibodies?

In fact, one might almost look at this v451 vaccine and regard it as an HIV vaccine, with spike proteins tacked onto gp41 as a kind of “nasty adjuvant” to initiate the immune response to the HIV protein.

Seriously – which is the real target here – COVID or HIV? Or BOTH?

This looks to me like a perfect example of…..

WAIT FOR IT….

“REVERSO”.

But let’s just set that aside for now, and pretend that the thing which COULD be a vaccine for EITHER ONE of the two things they stuck in it, is REALLY a vaccine for the fakey-fake cold that we don’t need a vaccine for, and NOT a vaccine for the sexual disease that stands in the way of Luciferian scum creating their polyamorous sexual paradise of literal epic random phuckery.

OMG, these people have just lied, and lied, and lied again. And they will KEEP lying.

But we’ll pretend they’re not lying, for just a little while longer.

So if we have an actual COVID vaccine here…..

…..is it a good idea to include the HIV gp41 protein subunit?

Well, after what we’ve seen with the spike protein, I was thinking maybe it wouldn’t be.

And it turns out, I wasn’t the first person who thought of this.

Doorless Carp’s Suspicious Cat In A Box

When I went looking for the toxicity of the gp41 protein, one of the first things that came up was some guy or gal who appears to have been actively suppressed on Twitter, eventually banned to Gab, and whose substack article on the topic has only two likes – ONE OF THEM MINE.

Doesn’t mean the article’s not important. And I think it’s about to get a few more hits.

LINK: https://doorlesscarp953.substack.com/p/update-on-the-university-of-queensland

Update on The University of Queensland COVID-19 vaccine. “..trial did not give trial participants HIV”, just a neurotoxic glycoprotein

11 Dec 2020

DoorlessCarp Feb 11

This is a wonderful article that is simply SKEPTICAL of the entire “it was pulled because of triggering AIDS tests” reasoning.

DoorlessCarp read the same press release I cited above, and pokes and prods it from the point of view of somebody who knows a heck of a lot about HIV and AIDS, and doesn’t buy what (s)he’s reading in that press release. Something doesn’t sniff right to “them”, and “they” spell out the issues.

I will attempt to summarize DoorlessCarp’s concerns (noted as “DLC” hereafter).

First, DLC admits to actually being led to the problem by one of those Fake News “straw man fact checks”, which attempt to either “debunk” facts or mislead scandals by setting up an adjacent strawman and knocking it down. OBSERVE.

“Fact check: An Australian vaccine trial did not give trial participants HIV”

https://www.reuters.com/article/uk-factcheck-hiv-idUSKBN28R2WT

LOL. No. The truth they’re protecting is that the “COVID vaccine” gave them HIV antibodies, and it was very likely the whole point.

To quote DLC about the Aussie vaccine researchers: “I wouldn’t let these clowns dispense aspirin, let alone design fast tracked vaccines.“

DLC then makes this statement, noting that there is a curious skew between the reality of HIV testing and the idea that there is some kind of a problem here.

Interesting rapid response to the effect that antibody only HIV tests have long since been debunked as a diagnostic tool on their own due to cross reactivity from other antibodies. They don’t tell you anything useful.

DLC then quotes extensively from this letter which explains why HIV testing via antibodies is actually a rather horrible mishmash of false positives and negatives, ultimately requiring a clinical diagnosis and “validation by lifestyle facts”.

Which leads to the next section, which I quote:

So what was the real reason for pulling the Australian trial, was it the gp41 toxicity?
The antibody problem raises more questions than it answers as spike S2 has homology to P24, GP41 and GP120.
This is dark stuff, P24 has been ported straight across from HIVs capsid to the spike protein. Here’s the proof, at least as far as what specific antibodies are telling us, which don’t lie:
What is p24 antigen?
“One distinctive HIV antigen is a viral protein called p24, a structural protein that makes up most of the HIV viral core, or ‘capsid’. High levels of p24 are present in the blood serum of newly infected individuals during the short period between infection and seroconversion, making p24 antigen assays useful in diagnosing primary HIV infection.”
https://www.aidsmap.com/about-hiv/faq/what-p24-antigen

This section makes the following points:

suspects the real reason for pulling the vaccine was the toxicity of gp41
notes that the spike protein already has potentially dangerous homologies to three HIV proteins, p24, gp41 and gp120
p24 is basically the nucleocapsid protein of HIV
p24 tends to be detected early in the AIDS process, before antibodies to it form

DLC then cites several papers demonstrating that there is already a lot of understanding of antibody cross-talk between the SARS-CoV-2 spike protein and either (1) original SARS-CoV proteins, and (2) HIV-1 proteins.

In the latter case, there is specific interaction with gp41.

References given:

The SARS CoV-2 spike directed non-neutralizing polyclonal antibodies cross-react with Human immunodeficiency virus (HIV-1) gp41 (Dec. 2021)
https://www.sciencedirect.com/science/article/pii/S1567576921008237?via%3Dihub
Cros-reactivity of SARS-CoV-2 with HIV chemiluminescent assay leading to false-positive results (2020)
https://jcp.bmj.com/content/74/9/614#request-permissions

DLC then lays the hammer down on the fact that gp41 is responsible for the dementia of AIDS.

I’m including the whole thing here.

Pathology:
Accumulation of β-Amyloid Precursor Protein in Axons Correlates with CNS Expression of SIV gp41 (2002)
“In this study, a strong association (p = 0.005) was identified between elevated axonal β-APP levels and the amount of SIV gp41 present in white matter, implicating HIV/SIV gp41 as a mediator of axonal damage.“
https://academic.oup.com/jnen/article/61/1/85/2916415
For those who don’t know, beta amyloid is associated with several degenerative neurological disorders:
Amyloid-β and Parkinson’s disease (2018)
https://pubmed.ncbi.nlm.nih.gov/30377818/
Beta-amyloid 42 accumulation in the lumbar spinal cord motor neurons of amyotrophic lateral sclerosis patients (2004)
https://www.sciencedirect.com/science/article/abs/pii/S0969996105000276?via%3Dihub
Alzheimer’s Disease and the β-Amyloid Peptide (2010)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813509/
They knew this way back in 1999:
Mechanisms and Structural Determinants of HIV-1 Coat Protein, gp41-Induced Neurotoxicity (1999)
Abstract
Of the individuals with human immunodeficiency virus type 1 (HIV-1) infection, 20–30% will develop the neurological complication of HIV-associated dementia (HAD). The mechanisms underlying HAD are unknown; however, indirect immunologically mediated mechanisms are theorized to play a role. Recently, the HIV-1 coat protein gp41 has been implicated as a major mediator of HAD through induction of neurocytokines and subsequent neuronal cell death. Using primary mixed cortical cultures from neuronal nitric oxide synthase (NOS) null (nNOS−/−) mice and immunological NOS null (iNOS−/−) mice, we establish iNOS-derived NO as a major mediator of gp41 neurotoxicity. Neurotoxicity elicited by gp41 is markedly attenuated in iNOS−/− cultures compared with wild-type and nNOS−/− cultures. The NOS inhibitor l-nitroarginine methyl ester is neuroprotective in wild-type and nNOS−/− cultures, confirming the role of iNOS-derived NO in gp41 neurotoxicity. Confirming that iNOS−/− cultures lack iNOS, gp41 did not induce iNOS in iNOS−/− cultures, but it markedly induced iNOS in wild-type and nNOS−/− cultures. We elucidate the region of gp41 that is critical for iNOS induction and neuronal cell death by monitoring iNOS induction with overlapping peptides spanning gp41. We show that the N-terminal region of gp41, which we designate as the neurotoxic domain, induces iNOS protein activity and iNOS-dependent neurotoxicity at picomolar concentrations in a manner similar to recombinant gp41 protein. Our experiments suggest that gp41 is eliciting the induction of iNOS through potential cell surface receptors or binding sites because the induction of iNOS is dose dependent and saturable and occurs at physiologically relevant concentrations. These data confirm that the induction of iNOS by gp41 and the production of NO are primary mediators of neuronal damage and identify a neurotoxic domain of gp41 that may play an important role in HAD.
Keywords: HIV-1, HIV-associated dementia, neurotoxicity, gp41, immunological nitric oxide synthase, nitric oxide
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782354/

DLC’s concluding remark:

“Off to Moderna we go”

Insist that love drive the clown car – Pam Grout

Yeah, I kinda get this sentiment.

And I quote again:

“I wouldn’t let these clowns dispense aspirin, let alone design fast tracked vaccines.“

Is gp41 a danger? It may well be. And nobody is asking the question, because (IMO) the neural pathogenic initiator that gp41 is, was passed off as a “molecular clamp” instead of the REAL ANTIGEN.

If they’re going to resurrect this weirdo COVID-HIV vaccine – and YES, they’re thinking about it – then there needs to be some examination FIRST of what the HELL is going on.

So What The Heck Is Going On Here?

When I was a young lad in the old days of science, there was lying, misrepresentation, and thievery, but it was on a much smaller scale.

We used to joke very cynically, back in the ’70’s, that every natural product being synthesized in a laboratory cured cancer, because we all knew that was not true.

We knew that these substances were really being synthesized merely because the molecules were a synthetic challenge, and a way for professors to make a name for themselves in synthetic chemistry. Almost NONE of these substances would EVER be used to treat cancer, and most would wash out very soon upon investigation. Almost none of them would ever even LEAD to a useful cancer drug. But LYING about their importance was how people got money for their labs. Every structurally interesting new molecule was always the next savior – until it wasn’t.

I used to think that the people giving out the money were fools about this, but not any more. I am beginning to think that the “givers” have always been just as corrupt as the “takers” – they’re just the “insiders” who turn on the spigots for their fellow “outsiders”.

I have no reason to think that vaccines are any different.

I think that a false crisis was used as a massive MONEY-BOMB – a global pile-on of the giddiest and most corrupt kind.

Probably the biggest one in 20 years.

I think that an AIDS vaccine was passed off as a COVID vaccine, by plausibly passing off the natural function of the HIV subunit as a new tool for other things, because – well – it IS such a new tool – just like every new interesting molecule MIGHT actually be some amazing new drug that cures cancer.

They lie skillfully, and they lie with truth, and it’s almost impossible to PROVE that the secondary “oh by the way” was actually the primary motivation.

We have changed from white lies that everybody understood WERE lies, to much more devious lies where scientists engage in fooling not just the public, but even other scientists.

I do think we have to wake up now. We can no longer afford the luxury of pretending not to know.

If I have to thank Joe Biden and his puppetmasters, including his “handler” Obama, for anything, it is for WAKING ME UP with these stupid mandates.

Nothing worked so well, to show us that the NEW WORLD ORDER is a direct threat to humanity, and needs to be stopped.

Science can be good again. But it must never, ever, abandon TRUTH.

And here we are.

W

DEAR KAG: 20220211 – The Pub is OPEN / G-Bay (Gab Marketplace) Is Here / Fake Science Normalized by Fake News and Fake Entertainment / Malone and Bhakdi Validated by “Pro-Vax” Paper

The Pub is STILL OPEN!

We are doing our best under the circumstances!

While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.

Christmas Spirit

We still have lights up all over the area. LOL!

Hey – how about we just keep believing?

And now, the rules of the pub.

HOUSE RULES

God bless us, every one! Tiny Tim had such a beautiful soul. He hadn’t a mean bone in his body…unlike most of us. But in keeping with Christmas, we promise to honor Wolf’s rules and keep Scrooge at bay. The Utree is where the Ghost of Christmas Present will conduct you should you need to rattle some chains. Another option, should all hell break loose is here.

Now, back to business.

AMEN!

Free the January Brothers

(no matter what the SHANGHAI SLIDER says)

Current Art On The Wall

We ordered a crate of ivermectin from Mexico, and instead got a box of counterfeit paintings marked “L.A.”.

We’re selling the paintings to make enough back for a new order of ivermectin.

Colorful!

https://thegallerist.art/leonid-afremov-2/

LINK: https://thegallerist.art/leonid-afremov-2/

Hey! Maybe we can sell them on G-bay!

G-Bay (Gab Marketplace) Is Here

As a Gab Pro member, I just got an email about the opening of the Gab Marketplace, which is now best described as a rudimentary “Gbay” precursor, using Gab Chat (the integrated version, not the end-to-end encrypted one) as the negotiating mechanism.

Here are some exemplary screenshots. Click on them to enlarge.

The landing page…..

Electronics…..

Beauty…..

There are no bells and whistles now, but the goal is to soon integrate GabPay, their PayPal substitute that has been under development for some time now.

Here is the text of the email.

Introducing the Gab Marketplace, a giant leap forward for the Parallel Economy on Gab!
GabPRO members can create listings for a variety of categories including books, electronics, tools, home goods, and more.
Anyone can view Gab Marketplace listings, ask about its availability, and chat with sellers to buy their items.
The Gab Marketplace can also be explored without having a Gab account and listings can be shared anywhere.
Gab does not handle transactions for Marketplace listings yet, but we will be integrating GabPay, our Paypal alternative, once it is live.
Sellers and buyers must converse amongst themselves regarding purchasing listings.
We have many different categories and listings are filling up quickly, be sure to check back often to see new listings added.
We’ve also created a Job Board and Classifieds section in the Gab Marketplace.
Sell those electronics you haven’t used in forever, sell that Christmas gift you never opened, or anything in-between!
Upgrade to GabPRO to start posting Marketplace listings.
There are no additional listing fees and you can create up to 15 listings per day.
Join the Parallel Economy
Advertise Your Business on Gab
Reach 20 million+ people who share your values

It’s not that full of items yet, but there is some intriguing stuff already.

Check it out!!!

Fake Science Normalized by Fake News and Fake Entertainment

Thanks to Sadie for showing me these truly egregious, horror-show examples of the absolute worst of FAKE SCIENCE.

ICYMI, it’s not the pokes, it’s CLOCKS! 🤡 pic.twitter.com/46qwwaDgkY
— Dr. Lynn Fynn (Fan Account)🐭 (@fynn_fan) February 7, 2022

BUT WAIT – THERE’S MOAR!

Or could it be your electric bill? 🤡🤡🤡 pic.twitter.com/AHxSTQcaFM
— Dr. Lynn Fynn (Fan Account)🐭 (@fynn_fan) February 7, 2022

We have seen some of these already, alleging things like “pandemic stress” being responsible for clot-shot cardiac consequences. Those were bad, but now it’s just becoming ludicrous.

It’s very clear to me that the “Fake News” has been tasked with trying to GET PEOPLE TO INNOCENTLY RATIONALIZE the downstream effects of the FAILED plandemic and clot shot plot, whatever those might eventually be proven to have involved.

Trump really tried to get people to see the MEDIA ROLE in regard to “climate change” – that CLIMATE ALARMISM was basically a SIMULTANEOUS media hoax on both scientists and non-scientists.

As long as the media will defend the LIE that science itself, individual scientists, and scientists as a group, are ALL in full, 100% control of what they themselves think, then the TRUTH that the media controls what science thinks and says can be hidden from the public.

It is only NOW – at a moment when many scientists are WAKING UP to what the media has done TO THEM, and are actively TURNING IT OFF, that they realize the media was LEADING THEM.

Let me state this clearly.

FAKE SCIENCE – controlled by the media – is one of the greatest dangers to humanity EVER.

FAKE NEWS is used to lead Fake Science – to hint subconsciously to science and scientists where it’s “going”.

FAKE ENTERTAINMENT is used to normalize Fake Science – to raise the barriers to questioning it.

IT IS YOUR DUTY TO PERCEIVE AND REJECT FAKE SCIENCE.

Being moderately scientifically literate is now a SURVIVAL SKILL, just like being politically literate, or even being just plain literate.

We will continue to bash fake science here, and I personally will continue to appreciate all examples of it that you may find and bring here, because dissecting and analyzing fake science is one of the best ways to fight it.

REAL SCIENCE is making a comeback, and YOU, DEAR AND PATRIOTIC CITIZEN, are part of that GREAT AWAKENING.

Malone and Bhakdi Validated by “Pro-Vax” Paper

On Monday, I covered a recent paper coauthored by Dr. Peter McCullough, which hypothesizes that documented failure of the mRNA vaccines to activate the interferon system, in combination with documented migration of both vaccine-induced spike protein and specific interferon-suppressing microRNAs via exosomes, is behind a variety of health problems associated with the current COVID vaccines.

Dear KMAG: 20220207 Joe Biden Didn’t Win ❀ Open Topic / Pandemic of the Vaccine – Are mRNA Vaccines Fundamentally Flawed?

The hypothesis of this paper is based on rough but obvious signals from VAERS, existing mRNA vaccine data in the literature (interferons and related species, microRNAs, exosomes), and known mechanisms which would explain the VAERS signals if connected to the vaccine data.

I was only partway through that paper, when I was saying to myself “Good grief – why are we even USING these vaccines, much less mandating them?”

Now, as a kind of second strike, Malone has found a paper which not only confirms his suspicions and fears of mRNA vaccine problems, but which also perfectly confirms Dr. Sucharit Bhakdi’s contention that the mRNA vaccines are producing too much of the WRONG antibody type and none of the two more desirable types.

. @JikkyKjj
Look what Malone dug up. This is basically what #Bhakdi postulated, but worse. Much worse.https://t.co/35BjSecPRD
— Straker (@EnjoyTheDecline) February 8, 2022

You can go directly to Malone’s Substack post here:

https://rwmalonemd.substack.com/p/a-health-public-policy-nightmare

Let me cite the beginning of this post – up to where Malone poses the big question.

A Health Public Policy Nightmare

Vaccine spike antigen and mRNA persist for two months in lymph node germinal centers… protein production of spike is higher than those of severely ill COVID-19 patients!

Robert W Malone MD, MS

Feb 8

1,119 243

Immune imprinting, breadth of variant recognition and germinal center response in human SARS-CoV-2 infection and vaccination

Cell. Published: January 24, 2022

DOI: https://doi.org/10.1016/j.cell.2022.01.018

Highlights (per the journal)

Vaccination confers broader IgG binding of variant RBDs than SARS-CoV-2 infection
Imprinting from initial antigen exposures alters IgG responses to viral variants
Histology of mRNA vaccinee lymph nodes shows abundant germinal centers
Vaccine spike antigen and mRNA persist for weeks in lymph node germinal centers

The hidden highlight (lede) buried in this peer reviewed paper is that protein production of spike in people vaccinated with the Moderna or Pfizer vaccine is higher than those of severely ill COVID-19 patients! A person might ask, “How could that be?” In order to understand this, we must carefully analyze what the study shows.

I urge you to finish reading Malone’s post about this paper.

LINK: https://rwmalonemd.substack.com/p/a-health-public-policy-nightmare

I ALSO urge you to read the paper itself (PDF is public), which looks at the same data, and cheer-leads vaccines, stating but otherwise ignoring EVERYTHING that Malone and Bhakdi are concerned about. Ignore the parts you can’t read – there’s plenty that you CAN read, and it is very instructive.

I will attempt to explain the difference between the two views of the same results, but let me give you the Bottom Line Up Front (BLUF).

The original paper was researched and written while the participants were fully under “Gates Vaccine Mind Control” and “Fauci Antibody Hypnosis”, both of which cause scientists to rather blindly follow the laser-pointers which control their outlook on vaccine science.

Gates: Vaccines are the only legitimate way to fight viral disease.

Fauci: Antibodies which I designate determine if a vaccine is safe and effective.

These are the lies of SMART SCIENCE LIARS, because they’re difficult to prove untrue in a way that normies can understand.

As Robert Malone notes, one of the most important facts in the paper [that the vaccines produce more spike protein than even severe cases of COVID-19] is a “buried lede”, although I would go further and state that it was never buried, because it’s not even a concern to the authors.

Once one accepts a priori that:

vaccines are good
vaccine side effects are obvious, immediate, and allergic in nature
spike makes antibodies, and antibodies are good
concerns about the spike protein are misinformation

…..then it is pretty much impossible for these COVID vaccines to do any wrong.

Just ask a scientist, who believes all these things BECAUSE OF THE MEDIA.

More spike protein means more antibodies, and more antibodies is good – RIIIIIGHT?

And if there are problems, it’s the vaccine working! Just ask Jabcinda Ardour!

ANTIBODY HYPNOSIS WILL DO THAT. Under antibody hypnosis, anything which contributes to antibodies which Fauci highlights, is “good” – all other antibodies or other responses are either bad or irrelevant.

The authors of the paper make sure to say all sorts of good things about vaccines, and never say anything critical, despite the fact that they’re sitting on all kinds of evidence that something is very wrong with these mRNA vaccines.

Example:

The appearance of virus variants, waning antibody levels after infection or vaccination (Falsey et al., 2021; Levin et al., 2021), and breakthrough infections in previously immunized individuals (Keehner et al., 2021) indicate that periodic vaccine boosting of immunity to SARS-CoV-2 is warranted.

REALLY? Some of us scientists believe the exact opposite – that these diverse FAILURES indicate that a vaccination strategy is dubious if not highly UNWARRANTED – but OUR view is called “misinformation”.

Seriously – it’s like hypnosis. The authors of the paper CANNOT SEE the things that Malone points out, or that Bhakdi pointed out.

Likewise, the problems which WE can see were clearly NOT found in “peer review”, precisely because the PEERS are for the most part just as much under vaccine hypnosis and antibody hypnosis as the authors, so real and deep questions about the jabs are simply never going to get asked. And if any peers DO recognize the problems, they will keep their mouths shut, or “test the waters” gently, to see if any concerns are allowed.

Those who CAN see the problems, know enough to keep their mouths shut, if they want to remain players in the Science Game.

I go back to what I said earlier about the media – including the science media – including journals – literally CONTROLLING what scientists think – and that scientists have no clue. Sad.

Anyway, now that I’ve provided background of what is going on here – a “pro-vax” paper in which Malone finds shocker evidence of problems, let’s discuss the specifics that Malone found, and that Bhakdi also predicted.

One of the first things that Malone catches is the persistence of both the mRNA and the spike protein in lymph node germinal centers – lasting for WEEKS instead of a few days. Note that this perfectly matches a clinical case that we featured here on these pages!

Interview With A Victim of Jab-Haul COVID

I have here an absolutely fascinating video (end of article) from Gab TV that fits right into everything I know about COVID-19 and the spike protein vaccines, like the last piece of a puzzle. The video is just under 1/2 hour in length, but it is FILLED with little AHA moments. An extremely articulate, healthy, …

Basically, this woman (on the left) got “long haul COVID” symptoms from a JAB – including massively swollen lymph nodes that lasted for WEEKS. That led to a lot of permanent damage. What she experienced is now explained PERFECTLY by what Dr. Malone postulates.

AND I NOTE THIS AS WELL. What Dr. Malone postulates (below), is exactly what The Ethical Skeptic noted as a CONCERN on Twitter in 2020, before the vaccines ever arrived! Yes, I have not gone looking for his tweet, but TES specifically noted that these vaccines are not “actual” mRNA vaccines – they are PSEUDO-mRNA vaccines.

WHUUUUUUUUT?????!!!!!

Yes. To evade immune protection from foreign mRNA, the vaccine mRNA uses a “pseudo” base to trick the human immune system into thinking it’s not mRNA, even though it works the same way. It’s something of a beautiful hack, but it’s a hack.

Malone:

One very real hypothesis is that the substitution of pseudouridine for uridine to avoid the immune response is working so well that the mRNA is completely evading the normal clearance/degradation pathways. Hence, mRNA that is not being incorporated into cells at the injection site, is migrating to the lymph nodes (and throughout the body as the non-clinical Pfizer data suggest?) and continuing to express protein there. In this case, the cytotoxic protein antigen is spike. Spike protein can be detected for at least 60 days after administration of dose. Note that the duration of the protein expression was only tested for 60 days.

But it gets worse. After reminding us of the pathogenicity of the spike protein (merely citing others), Malone reminds us that the use of pseudouridine to evade immune cleanup is not actually necessary in mRNA vaccines – but it IS (and this is rather horrible) PATENTABLE as an “improvement”.

Again, Malone.

To note: The use of pseudouridine in these mRNA vaccines is not the only option. It has often been hypothesized that the reason Dr. Kariko added pseudouridine to the mRNA vaccine was to make an improvement to the original mRNA patents that I was an inventor on. An improvement to an existing patent allows commercialization of that patent. It is an old trick. Remember, that Curevac does not use pseudouridine in its formulation and it is not required or necessary for a significant immune response. In the next generation of mRNA vaccine experiments (hopefully done in an animal model), it is clear that the issues of adding pseudouridine need to be addressed prior to any more of these vaccines going into humans.

So how much spike protein does this stuff produce? Again, Malone.

Knowing what we know about the spike protein in these vaccines, the study quantitatively measured spike protein levels in plasma after vaccination. Which, it turns out, are higher than the levels observed in a person with a severe COVID-19 infection. Just to write it, the fact that this only now being discovered or it it was known, released to the public is criminal in my opinion. This should have been characterized long ago, including prior to beginning human clinical trials.
That this has not been published or investigated more demonstrates the gross regulatory dereliction of duty by Pfizer, Biointech, Moderna, NIAID VRC and that whole crew. Using these vaccines, which include pseudouridine without fully understanding the implications and without the FDA requiring a complete pre-clinical toxicology regulatory package, including long-term follow-up, as is done with any other unique chemical or adjuvant additive is shocking. Then there is the novel use of the unique nano particles being used in these vaccines, which also were only marginally assessed, as shown by the Japanese Pfizer data.
Protein expression is not being turned off, because the immune response against the mRNA/pseudouridine complex is either not happening or is ineffective. It may also be that the mRNA/pseudouridine complex has a longer half-life than normal mRNA. The In either case, this is regulatory nightmare.
I do not know how to write this more strongly. This technology is immature. The WHO has approved six, more traditional vaccines, all of which the US government could license. These genetic vaccines are not the only option.

And just to make sure you get it, Malone quotes the relevant parts of the paper, and says it again.

Read that again: Protein production of spike is higher than those of severely ill COVID-19 patients!

As an understated closer, without mentioning him by name, Malone adds how THIS paper confirms a concern that Dr. Sucharit Bhakdi had about THE WRONG ANTIBODY TYPES being produced by the vaccines.

The paper also notes that the antibody response is IgG, not IgA or IgM. IgA and IgM antibodies produce a strong mucosal immune response needed for respiratory diseases, unlike IgG.

Finally, Malone makes this statement.

This Substack article has only skimmed the surface of the implications of this paper in terms of both the science and the malfeasance on the part of our government and pharmaceutical corporations. There is more to come on this issue.

You will note that, by implication, the AUTHORS of this paper clearly said nothing indicative of malfeasance. Now it may be entirely possible that they were “getting out truth” while keeping their heads out from under any funding guillotines, but they clearly evidenced no overt concerns for any problems.

And THAT is how FAKE SCIENCE works, my friends.

Lastly, let me add one of my own “concerns”.

Allow me to repeat the authors’ own highlights of the paper, for commentary.

Vaccination confers broader IgG binding of variant RBDs than SARS-CoV-2 infection
Imprinting from initial antigen exposures alters IgG responses to viral variants
Histology of mRNA vaccinee lymph nodes shows abundant germinal centers
Vaccine spike antigen and mRNA persist for weeks in lymph node germinal centers

To these FOUR items, I have FOUR responses, all of which I know Karl Denninger will get.

Leaving aside IgG being the wrong antibodies (see above), BINDING antibodies can still, also, be “wrong” (or more accurately “inappropriate”) antibodies, depending on what happens next, including enhanced variants and ADE. NEUTRALIZING antibodies are the “most appropriate” kind. BINDING antibodies may or may not help. So DO NOT take this point as an automatic score for the vaccines. In my humble opinion, NATURE is likely smarter than Pfizer and Rochelle Alinsky on what to do here.
Original antigen sin. They’re calling it. “Imprinting.” It means that every exposure to an antigen can potentially MISLEAD the immune system for the purposes of the next exposure. Great. SO – how confident are you folks that these vaccines are giving a superior “imprinting” to natural infection? I am NOT confident, and in fact, I believe that the “pseudouridine error” is proof that NIH, Pfizer, Moderna, CDC, CEPI, and all the rest are not even remotely competent to choose the best “imprinting” for children. They are choosing the one that gives themselves the most power, control, and money. SHAME!
The vaccines are going to the lymph nodes. Well, well, well. Not only does this destroy the establishment TROLL talking point about vaccine localization in the deltoid muscle – it provides a nice explanation of the exosome-based spread of the spike protein and interferon-suppressing microRNAs.
Persistence of vaccine and thus-produced spike in the lymph nodes lasts for weeks. Add to this the liberation of spike protein in LIPID-BASED EXOSOMES into the bloodstream. What’s that going to do? Why, it’s going to SPREAD SPIKE IN LIPIDS to other places where lipids collect. Which means spike ends up in other organs. Which can potentially include organs (like skin and other glands) which SHED LIPIDS. Which includes breast milk (dead infants in VAERS) and skin oils (see prior posts on this blog, where my incredulity about “shedding” was overcome). AND don’t forget the ovaries. Etc.

So – that is where we are.

And where is Fake News on this? Totally absent.

We’re not only the news now.

We’re the science now.

ENJOY THE SHOW.

Thank you all for being here. Have a great weekend.

W

Dear KMAG: 20220207 Joe Biden Didn’t Win ❀ Open Topic / Pandemic of the Vaccine – Are mRNA Vaccines Fundamentally Flawed?

Joe Biden didn’t win. This is our Real President:

AND our beautiful REALFLOTUS.

Get your rest, Trumpy Bear! You’re going back to the White House!!!

We need to restore sanity in the White House, and it’s time to get Winnie the Pooh OUT.

The Business At Hand

This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).

And indeed, it’s Monday…again.

But it doesn’t matter, because with God, every day is glorious!

And if you need that in a song…… ONE MORE TIME…..

The Rules

Boilerplate, more or less, but worth reading again and again, if only for the minor changes, and to stay out of moderation.

The bottom line is Free Speech. Theories and ideas you don’t agree with must be WELCOME here, and you must be part of that welcoming. But you do NOT need to be part of any agreement.

Thus we are assembled here to peacefully address our grievances to whom they may concern, even each other, using both our freedom of speech and of press, as well as our freedom of religion.

SO….. [ENGAGE BOILERPLATE…..]

We must endeavor to persevere to love our frenemies – even here.

Those who cannot deal with this easy requirement will be forced to jump the hoops of moderation, so that specific comments impugning other posters and violating the minimal rules can be sorted out and tossed in the trash.

In Wheatie’s words, “We’re on the same side here so let’s not engage in friendly fire.”

That includes the life skill of just ignoring certain other posters.

We do have a site – The U Tree – where civility is not a requirement. Interestingly, people don’t really go there much. Nevertheless, if you find yourself in an “argument” that can’t really stay civil, please feel free to “take it to the U Tree”. The U Tree is also a good place to report any technical difficulties, if you’re unable to report them here. Please post your comment there on one of Wolf’s posts, or in reply to one of Wolf’s comments, to make sure he sees it (though it may take a few hours).

We also have a backup site, called The Q Tree as well, which is really The Q Tree 579486807. You might call it “Second Tree”. The URL for that site is https://theqtree579486807.wordpress.com/. If this site (theqtree.com) ever goes down, please reassemble at the Second Tree.

If the Second Tree goes down, please go to The U Tree, or to our Gab Group, which is located at https://gab.com/groups/4178.

We also have some “old rules” and important guidelines, outlined here, in a very early post, on our first New Year’s Day, in 2019. The main point is not to make violent threats against people, which then have to be taken seriously by law enforcement, and which can be used as a PRETEXT by enemies of this site.

In the words of Wheatie, “Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”

A Moment of Prayer

Our policy on extreme religious freedom on this site is discussed HERE. Please feel free to pray and praise God anytime and anywhere.

Thus, please pray for our real President, the one who actually won the election.

Republican presidential nominee Donald Trump prays with pastors during a campaign visit to the International Church of Las Vegas and the International Christian Academy in Las Vegas, Nevada, U.S., October 5, 2016. REUTERS/Mike Segar

MUSICAL INTERLUDE

For your listening enjoyment, and general encouragement, we continue Wheatie’s tradition of fine music videos, shipped fresh from the seas of information by our intrepid authors.

YouTube is absolutely bombarding me with videos of that Japanese art-pop girl-band “Perfume” that I showed on Friday. The YouTube Wocommie Mensheviks must have some foul intention, so I think I’ll go looking for something else, but just ONE video is a good lead-in, so here you go.

Thankfully, YouTube isn’t just recommending girl groups to me, as long as I get OFF a girl group video page, in which case girl groups are THE ONLY THINGS they recommend.

On a “blank” YouTube page, I also get “epic music” now!

This is a nice one. Don’t mind the “furries” and assorted anime characters.

https://youtu.be/XrisCsNzOlo

This is a long one, too – you can come back for it while reading the features below.

Next, we have one of Wheatie’s favorite artists – Two Steps From Hell – celebrating our lady warriors!

Yes – beware those who would go after our kids…….

They might not be expecting WHO exactly it is, who will DELIVER THE MILLSTONES.

So let’s close out with a REAL girl group – complete with a fiddle!

Now THAT’S what I’m talkin’ about!

Call To Battle

Our beloved country is under Occupation by hostile forces.

Daily outrage and epic phuckery abound.

We can give in to despair…or we can be defiant and fight back in any way that we can.

Joe Biden didn’t win.

And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.

Pandemic of the Vaccine

Are mRNA Vaccines Fundamentally Flawed?

As promised in Friday’s post…..

DEAR KAG: 20220204 – … The End of the mRNA Vaccines …

…..I want to discuss a research paper that was brought to my attention by Gail Combs.

BUT FIRST, let me freshen you up with where things were as of February 3, when Robert Malone had THIS to say about the military data showing that the mandated mRNA jabs were definitively causing harm.

LINK: https://rumble.com/vtztbk-the-covid-vaccine-side-effects-are-worse-than-expected.html

That’s just a quick overview of the problem. Here’s the latest, and in more detail. H/T TradeBait2 for this one. This addresses the jaw-dropping and eye-rolling defense by NIH and their Pentagram buddies, which just dropped military credibility by another factor of two.

Is woke mil causing damage? COMMUNISM always causes damage!

LINK: https://rwmalonemd.substack.com/p/regarding-the-defense-medical-epidemiological

As Malone points out in the latter article, in a beautifully understated way, the “defenders of the jab” are now offering excuses that strain credibility to the breaking point. It is very easy to see that the other side is committed to any deception, of other or of self, to keep the jab train rolling.

They are NOT willing to honestly look at the striking relative dangers of these BAD VACCINES.

Something is very wrong, we can plainly see, but let’s just play along and pretend that this whole ridiculous scenario still deserves debate.

We have plenty of observations at this point, but the “old theory of harmless jabs” is able to play “what about” and temporarily evade many if not most of those explanations, lacking an obviously more compelling theory of WHY THE JABS CAUSE HARM, which would make “whataboutisms” unpalatable, even to those who want to believe them.

Well, is there such a compelling theory?

We have advanced certain key principles which explain things, and those are important.

We know about the pathogenic spike protein.

We know about vaccine migration and persistence.

But something is different, now.

NOW we have a theory which includes both of those things, PLUS a principle of IMMUNOLOGICAL ERROR.

In my opinion, we’re there.

The title of this work is:

Innate Immune Suppression by SARS-CoV-2 mRNA Vaccinations: The role of G-quadruplexes, exosomes and microRNAs

January 2022

DOI:10.22541/au.164276411.10570847/v1

Project: COVID 19

Authors:

Stephanie Seneff

Massachusetts Institute of Technology

Greg Nigh

Immersion Health

Anthony Kyriakopoulos

Nasco AD Biotech Lab

Peter A Mccullough

(Could have said Baylor College of Medicine, but Baylor is historically inept, IMO)

LINK: https://www.researchgate.net/publication/357994624_Innate_Immune_Suppression_by_SARS-CoV-2_mRNA_Vaccinations_The_role_of_G-quadruplexes_exosomes_and_microRNAs

PDF: https://www.researchgate.net/profile/Stephanie-Seneff/publication/357994624_Innate_Immune_Suppression_by_SARS-CoV-2_mRNA_Vaccinations_The_role_of_G-quadruplexes_exosomes_and_microRNAs/links/61f0b7838d338833e395e22f/Innate-Immune-Suppression-by-SARS-CoV-2-mRNA-Vaccinations-The-role-of-G-quadruplexes-exosomes-and-microRNAs.pdf

The Abstract

The abstract is instructive, and if you want to “TL;DR” past the rest of things, at least give that a read. Better yet, stick around for my interpretation of the abstract.

ABSTRACT

The mRNA SARS-CoV-2 vaccines were brought to market in response to the widely perceived public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease had no precedent, but desperate times seemed to call for desperate measures. The mRNA vaccines utilize genetically modified mRNA encoding spike proteins. These alterations hide the mRNA from cellular defenses, promote a longer biological half-life for the proteins, and provoke higher overall spike protein production. However, both experimental and observational evidence reveals a very different immune response to the vaccines compared to the response to infection with SARS-CoV-2. As we will show, the genetic modifications introduced by the vaccine are likely the source of these differential responses. In this paper, we present the evidence that vaccination, unlike natural infection, induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. We explain the mechanism by which immune cells release into the circulation large quantities of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances are shown to have a potentially direct causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, increased tumorigenesis, and DNA damage. We show evidence from adverse event reports in the VAERS database supporting our hypothesis. We believe a comprehensive risk/benefit assessment of the mRNA vaccines excludes them as positive contributors to public health, even in the context of the Covid-19 pandemic.

What I absolutely LOVE, LOVE, LOVE about this abstract, is that it takes some of the most key points of what the Fake News calls “conspiracy theories” and restates them in fact-bolstered scientific jargon that absolutely cannot be disputed. It’s just beautiful.

Because this abstract is important for understanding as we go into the paper, I’m going to take it “line by line” and explain, so that when we get to the paper itself, you can understand what is being talked about and get the gist of it, even if the scientific nuances are not entirely clear to you.

There are TWELVE sentences, each worthy of consideration.

HANG ON FOR A QUICK WARM-UP RIDE.

Analyzing the Abstract

(1) The mRNA SARS-CoV-2 vaccines were brought to market in response to the widely perceived public health crises of Covid-19.

“Widely perceived”.

This is an unarguable fact. It’s a great way to start the argument. State a truth without leaning on the “real crisis” narrative cheese in the center of the trap.

It does NOT say that the mRNA vaccines were brought to market unreasonably, which is open to debate, and which will be a contested question. Remember – many people (including me) HOPED that new technologies – which we were led to believe were needed – would free us from the virus.

Are you starting to see how they USED Trump? In my opinion, we still don’t understand the full extent of the deception and counter-deception. But none of that is said here – it is just ALLOWED under the statement of fact without narrative.

(2) The utilization of mRNA vaccines in the context of infectious disease had no precedent, but desperate times seemed to call for desperate measures.

“Seemed to”.

This is also factual, if we’re honest. The Jab Justifiers will quibble about veterinary vaccines, and experimental vaccines, and all that, as precedents, but those are quibbles. The truth is, you and I never got one of these genetic vaccines before, and that’s because they had never been approved before.

The beauty of this phrasing – “but desperate times seemed to call for desperate measures” – is that it forces us to admit the context of the phony crisis created by the Fake News and Democrats, by only saying “seemed to call for” instead of “called for”.

What the authors are doing here is dropping out the “fake normal” created by the media.

And THAT is an ongoing lesson for science itself to return to control by science and TRUTH.

(3) The mRNA vaccines utilize genetically modified mRNA encoding spike proteins.

This is absolutely true, and absolutely key. The mRNA of the vaccines encodes a FULL “half” of a very particular version of the SARS-CoV-2 spike protein. However, in order to accomplish several goals, the mRNA which WOULD code for that half of the spike protein is substantially altered in several different ways to make the whole process work.

And that leads to the next sentence.

(4) These alterations hide the mRNA from cellular defenses, promote a longer biological half-life for the proteins, and provoke higher overall spike protein production.

There is a lot of nuance here, so I will take some time to explain the 3 items.

(a) These alterations hide the mRNA from cellular defenses

There are multiple reasons that the “mRNA” of the vaccines is not actually normal mRNA, but a kind of “pseudo” mRNA.

Cells have to be careful not to “execute the instructions” of what is essentially WRONG RNA. Cells are a lot like soldiers who have been trained to NOT carry out unconstitutional orders.

The fact that mRNA vaccines and related forms of mRNA-based gene therapy actually work AROUND cellular defenses is a hint RIGHT THERE that they might do something bad. Our bodies are designed to FIGHT OFF foreign mRNA.

Be careful how you interpret what I’m saying there. It’s not an indictment of the mRNA method per se, because MANY if not ALL drugs have to “work around cellular and bodily defenses”. That is a huge part of the science of drug delivery.

HOWEVER, it is always cautionary to admit THAT one is working around defenses, because this will inform one as to the RISKS which are being taken BY working around those defenses.

What if you aren’t actually working around the risks?

So, one truth is that the mRNA has certain bases changed to avoid “tipping off” those defenses. It’s a SNEAKY and LUCKY break that we actually CAN work around those defenses.

But are we doing so CLEANLY and to good outcome?

(b) promote a longer biological half-life for the proteins

This is a HUGE double-edged sword.

Remember – the SARS-CoV-2 spike protein CHANGES SHAPE as it breaks into the cell. When it’s all done, it looks like a different protein – even to antibodies.

The drug designers have (literally, but synthetically) mutated the original reported Wuhan spike protein sequence. The primary reason to do this, is to make the protein “LOCK IN” the original, highly infectious, three-dimensional shape of the “fresh” protein, so that antibodies will form PROPERLY against that, instead of forming against depleted, spent, “used” spike protein. This reduces the chances of ADE (antibody-dependent disease enhancement), which comes from “inappropriate antibodies” that evolved to the WRONG TARGET.

The problem with stabilizing the highly pathogenic spike protein for triggering more desirable antibody formation, is that it also stabilizes the highly pathogenic spike protein for pathogenesis, too.

“WHOOPS!”

So – spike-protein-based “long haul” symptoms from the vaccine can be very long – even compared to long haul from the disease. The synthetic spike protein is really good at sticking around in its mutated, long-lasting, highly pathogenic form.

And THAT might not be a good thing.

Ask this question – why doesn’t the VIRUS do that? Maybe a more stable protein is not only bad for the virus, but also bad for the host, and THAT is in turn bad for the virus AGAIN.

Nature is smart – especially when it cuts a deal with multiple organisms to INCREASE LIFE.

This is a DIRECT call-out of a problem that will almost certainly lead to arguments with “peer reviewers” who want to defend the vaccines. Note that the wording very intentionally does not say “These alterations are intended to…..[three things]” – it simply says “These alterations….. [three things].”

The alterations are INTENDED to provoke higher overall spike protein antibody production. But the fact is, unless the increase in antibodies comes from better and stronger adjuvants, which act as immunity multipliers, then it’s coming from higher (or otherwise more antigenic and pathogenic) overall spike protein production.

Thus, peer reviewers who want to cover up spike protein malfeasance will likely insist on dragging the wording back to being about the antibodies. This follows the lead of Tony Fauci and his “antibody hypnosis” act, designed to keep attention OFF all of the things that are WRONG with the vaccines.

As you can see, we’re only 4 sentences in, and there is a lot of “battle prep” already going on.

(5) However, both experimental and observational evidence reveals a very different immune response to the vaccines compared to the response to infection with SARS-CoV-2.

This is a very general but very powerful FACTUAL statement, which DEFIES the Fauci / Fake News narrative – a narrative which can’t even bring itself to ADMIT that disease-conferred immunity is a reality.

This is a point about which – if you have read even SOME of the COVID-19 scientific literature – there is literally no debate. Only in the Fake News media and on controlled social media is this twisted. Scientists now marvel ALL THE TIME at the differences between vaccine-conferred immunity and disease-conferred immunity.

And, almost ALWAYS, practically speaking (but ignoring any risks of acquiring immunity), disease-conferred immunity is superior.

You will note that Fauci NEVER talks about this stuff.

But there is more – much more. ANY adverse effects which happen due to the vaccines and not the disease, or happen MORE with the vaccines, rightly count as differences.

The paper is not saying this out loud – but you can understand that it is implied.

This right here – the point about a difference between vaccine immunity and disease immunity – is the HAMMER of the gun going back and making a “clicking” noise.

(6) As we will show, the genetic modifications introduced by the vaccine are likely the source of these differential responses.

THIS HERE IS THE BIGGIE.

There are SO MANY potential implications here, I don’t want to steal their thunder from the analysis of the paper.

However, without knowing ANYTHING FURTHER, this is a profoundly common-sense scientific statement. It is simply saying that different molecules from the virus RNA may lead to different outcomes. That’s almost a no-brainer.

This could happen in multiple different ways.

differences in how the “changed mRNA” is handled by the body
differences in how it is interpreted
differences in the protein product

All of this makes wonderful sense.

(7) In this paper, we present the evidence that vaccination, unlike natural infection, induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health.

Oh, wait – THIS is the biggie.

This is saying that there is an important cellular communication screw-up with mRNA vaccination – a screw-up which does not occur with natural infection. Stated in reverse, there IS an important cellular communication channel opened during natural infection, which is MISSED by the mRNA vaccines.

IN OTHER WORDS, A PROGRAMMING ERROR.

This is all too believable to me, because I’ve seen this before. And NOT just when I “learned to code”.

This is LITERALLY a sibling programming error of what happens when too many vaccines are given at the same time, and interferon signals STEP ON EACH OTHER.

Now the Fake News media “fact checkers” absolutely will not admit that there is a problem with multiple simultaneous vaccines, but once the standard mechanism of vaccine-acquired immunity was explained to me, it became OBVIOUS AS HELL that signal interference was behind the observed but somewhat unpredictable problems with tight vaccine schedules.

You are allowed to have a different scientific opinion from these biased and forked-tongued “fact checkers” with agenda.

But let’s save the details for later.

For now, just remember that humans are evolutionarily adapted for disease, not hacky pseudo-mRNA vaccines. Our PROGRAMMING MODEL – our DESIGN – our API – is different from what the hackers thought they could get away with, and they got caught.

(8) We explain the mechanism by which immune cells release into the circulation large quantities of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites.

More specifics.

This is fascinating, because AND LOGIC is now telling me that it’s not just the vaccine migrating, but spike protein as well.

And THAT explains a LOT.

Do you see how everything is tying together nicely around the pathogenic spike protein that is NOT being degraded soon enough or fast enough, like the VIRUS DOES FOR US?

Think about our little human biome friends next time, science. They may have a BETTER PLAN.

(9) We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance.

OK, this is bad stuff. But it’s also bad stuff that is right up the alley of FAKE SCIENCE to now “discover” and get big bucks to study. It’s DETAILS that cannot be dismissed.

This is the GRENADE thrown into the narrative machine gun bunker with half a second left on the fuse.

KABOOM.

This is where every “me too!” funding whore is going to jump on the bandwagon with justification.

(10) These disturbances are shown to have a potentially direct causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, increased tumorigenesis, and DNA damage.

Oh, wait! Isn’t this the stuff that Robert Malone warned us about?

Isn’t this the stuff that Ryan Cole spotted?

Isn’t this the stuff that FAKE NEWS ignored and “debunked”, but is now appearing in every possible mainstream source of data?

Common sense is going to win here.

INVESTORS had better TAKE NOTE. The landscape is going to change, IMO.

(11) We show evidence from adverse event reports in the VAERS database supporting our hypothesis.

The beauty of VAERS is that it’s flawed, but we know HOW it’s flawed.

Thus, if you see something that can only be MAGNIFIED by correcting for the known flaws, then you have something you can use.

Just stroll past those Fake News fact checkers and Fake Social Media “con-TROLLS” who spew their talking point about “VAERS IS A FLAWED SYSTEM”. SORRY. Not good enough, trolls.

Everything is a flawed system. Knowing the DIRECTION of the flaws is what turns all systems into useful logical tools.

We will use common sense here, long after these people who deny it are OUT OF POWER.

(12) We believe a comprehensive risk/benefit assessment of the mRNA vaccines excludes them as positive contributors to public health, even in the context of the Covid-19 pandemic.

This is where they land when all is said and done.

They’re saying that they believe the risks outweigh the benefits with THESE vaccines.

This does NOT say that vaccination per se is a bad strategy for COVID-19.

It says that mRNA vaccination as it currently exists is not a good strategy for COVID-19.

It doesn’t say that viral vector cDNA, “full” spike protein subunit antigen, or RBD subunit antigen vaccines are doubtful in any way. They may be, but the authors don’t say that (although some of the specifics DO have implications for the other vaccines).

The authors only say that THESE particular, current, mRNA vaccines are “not positive contributors to public health”.

And you can do the math from there.

Can the current mRNA vaccines be fixed?

Good question. This paper is likely a roadmap to any such fixes. But until then…..

Mandating these vaccines is WRONG, if not INSANE.

Analyzing the Paper

Now we get to the meat of the paper.

I am just going to drop my impressions, placing them in context as needed. On some of these, I blab on and on. On others, I just make a short point. I do a lot of quoting where the authors say it nicely. This is very seat-of-the-pants.

Introduction

The FIRST paragraph is a generous summary of the basics of vaccination, FULLY in compliance with the CDC definitions. Please take note of that. There is no quibbling about the mRNA vaccines not being vaccines.

The SECOND paragraph summarizes and exemplifies the presence in the literature of a viewpoint that the mRNA vaccines are very similar to natural immunity. There is a point made that is basically my contention of Fauci’s “antibody hypnosis”, but it is phrased very politiely.

The U.S. Centers for Disease Control and Prevention (CDC) makes the case based upon antibody titers generated by prior infection vs. vaccination, in addition to production of memory B cells, to argue that the immune response to vaccination is analogous to the response to natural infection [4]. It is this similarity in the humoral immune response to vaccination vs natural infection, paired with both trial and observational data demonstrating reduced risk of infection following vaccination, that stands as the justiﬁcation for the mass vaccination campaign.

The THIRD paragraph is long, but absolutely key.

It is the summary of the guts of the paper.

You will note that the authors are pointing out EXISTING MAINSTREAM SCIENCE which is contradicting the media-trumpeted, but “CDC-silent” narrative that vaccination is superior to “natural immunity”, by pointing out (without saying it bluntly) that it’s not even AS GOOD as disease-conferred immunity, because known “good” responses to the natural antigen are completely missing.

And worse than that, the mRNA vaccines seem to do WRONG THINGS to the immune system as well.

In this paper we explore the scientiﬁc literature suggesting that vaccination with an mRNA vaccine initiates a set of biological events that are not only diﬀerent from that induced by vaccination but are in several ways demonstrably counterproductive to both short- and long-term immune competence and normal cellular function. These vaccinations have now been shown to downregulate critical pathways related to cancer surveillance, infection control, and cellular homeostasis. They introduce into the body highly modiﬁed genetic material. A medRxiv preprint has revealed a remarkable diﬀerence between the characteristics of the immune response to an infection with SARS-CoV-2 as compared with the immune response to an mRNA vaccine against COVID-19 [5]. Diﬀerential gene expression analysis of peripheral dendritic cells revealed a dramatic upregulation of both type I and type II interferons (IFNs) in COVID-19 patients, but not in vaccinees. One remarkable observation they made was that there was an expansion of circulating hematopoietic stem and progenitor cells (HSPCs) in COVID-19 patients, but this expansion was notably absent following vaccination. A striking expansion in circulating plasmablasts observed in COVID-19 patients was also not seen in the vaccinees. All of these observations are consistent with the idea that the vaccines actively suppress type I IFN signaling, as we will discuss below. In this paper we will be focusing extensively, though not exclusively,on vaccination-induced type I IFN suppression and the myriad downstream eﬀects this has on the related signaling cascade.

Again, I point out that this is being pulled out of the “mainstream” literature.

Does this immune suppression that researchers found remind you of anything?

LINK: https://www.bitchute.com/video/NmhFesU2aPue/

Note that this is on BitChute because YouTube deleted it as “misinformation”.

If you’re thinking “Wow, the media and social media has really screwed up science!”, well, all I can say is “They won’t be able to walk the streets.”

The FOURTH paragraph then begins dropping bombs on the Pfizer clinical trial shenanigans, which basically covered up the placebo group to obfuscate vaccine problems.

The message is roughly “Because Pfizer covered things up by vaccinating their placebo group, as well as other tricks, we were forced to look at VAERS and the scientific literature to find out what the vaccines are doing – AND BOY, DID WE FIND A TON OF PROBLEMS.”

But done much more politely.

The next two paragraphs are a WITHERING ATTACK on the vaccines, simply using the scientific literature. OMG – the spatter on the walls – there are quite a few easy targets that the Fake News Media has been protecting by ignoring, but it’s very hard to “memory hole” the scientific literature to those who can “pay to play”, so the authors just mention a string of scientific findings that Fauci hoped the public would never see.

Thus, the FIFTH paragraph is a summary of VACCINE FAILURE, with references.

The SIXTH paragraph then brings up the wonderful idea that if benefits are as low as we now understand them to be, maybe RISKS need a closer look.

You may want to read the whole introduction, because that is the last easily readable section of the paper for a while.

NOW it gets really technical.

Interferons: An Overview with Attention to Cancer Surveillance

This section is extremely complex and hard to read, even if you’re familiar with most or all of the various biochemical and biological acronyms that are thrown into the melange.

It starts off with a review of what is known about INTERFERONS (IFNs), as well as substances which regulate them, known as INTERFERON REGULATING FACTORS (IRFs).

This is what you need to know:

Type I IFNs play a powerful role in the immune response to multiple stressors. In fact, they have enjoyed clinical therapeutic value as a treatment option for a variety of diseases and conditions, including viral infections, solid tumors, myeloproliferative disorders, hematopoietic neoplasms and autoimmune diseases such as multiple sclerosis [16].
As a group, IFNs play exceedingly complicated and pleiotropic roles that are coordinated and regulated through the activity of the family of IFN regulatory factors, or IRFs [17]. IRF9 is most directly involved in anti-viral as well as anti-tumor immunity and genetic regulation [18-20].

Basically, interferons are critical players in the CLEANUP OF GENETIC BAD GUYS CAUSING TROUBLE. Those genetic bad guys can be EXTERNAL WRONG-GENES (viruses) or they can be ROGUE CELLS (cancer and the like).

This section then summarizes the complex interactions and feedback loops which characterize anything involving interferons, but particularly related to their anti-cancer role. It is made exceedingly clear that improper interferon levels and disruptions of the complex interferon systems are known to lead very directly to clinical appearance of cancers of various kinds.

Near the end, COVID-19 is brought into the mix. A recent Chinese paper is cited, the work having shown interference with IRF signaling by a non-mRNA, inactivated virus, COVID-19 vaccine. The changes are EXPECTED to reduce resistance to cancers, and the mechanisms are discussed in detail. ELEGANTLY, those same mechanisms are found in Alzheimer’s patients, and appear related to development of dementia symptoms that sound remarkably like COVID brain fog.

Finally, a documented case of a rare lymphoma being accelerated by the Pfizer vaccine is described, and a summary statement is given:

Given the universally recognized importance of optimally functioning BRCA1/2 for cancer prevention and given the central role of the TRAIL signal transduction pathway for additional cancer surveillance, the suppression of IRF7 and IRF9 through vaccination and subsequent spike protein production is extremely concerning for long-term cancer control in injected populations.

Considerations in the Design of mRNA Vaccines

This section basically describes the long list of HACKS – many of them very ELEGANT HACKS – that were needed to get all the way from Robert Malone’s initial discovery which enabled mRNA gene therapy, to where mRNA vaccines are today.

The implications of all these hacks for relevant IMMUNOLOGICAL and GENETIC biochemistry, including INTERFERONS and CANCER, are described.

This section SETS UP the long list of concerns which are going to necessarily follow.

Quite a bit of attention is paid to the components of the lipid nanoparticles, their roles, and their potential risks and side-effects.

This section is fairly readable, and if you’re curious about the various hacks, and particularly the purpose and mechanism of the lipid nanoparticles, then you may enjoy reading past the jargon.

GC enrichment and potential G4 (pG4) structures in vaccine mRNAs

This is a difficult section to understand, if you’re not familiar with DNA and RNA “beyond the double helix”. It’s a bit like Morse code. Everybody knows what Morse code is, and maybe how to do an “SOS”, but not many people remember Morse code well enough to compose and send long signals at will, let alone send a telegram. OTOH, if you’re in genetic medicine or biology, you may be familiar with more than just 4 bases and the double helix.

The bottom line is that, among the various hacks that have gone into the mRNA vaccines, some of them are basically “genetic tricks” to increase production of spike protein. The PROBLEM with that, is that the FINAL implications of some of these tricks are not fully known.

Because there is redundancy in the genetic language, and the efficiency of different spellings is not the same (nite vs. night, thru vs. through, etc.), certain things can be re-encoded using the most efficient letters to create MOAR SPIKE PROTEIN. And MOAR is always BETTER. RIIIIIIIIGHT?

Well, it turns out that spellings have implications for how mRNA behaves. How mRNA behaves has implications for things like CANCER.

Going back to the title of this section, “G” and “C” are the efficient bases that are switched to, to make proteins with higher efficiency. The problem THERE is that “G” can do something every interesting – it can bind with itself in a square, to form a quadruple helix called a “G quadruplex”, which is abbreviated G4. See the image above for cross-sections of such a structure, at the point of binding.

There are ways to predict if a G quadruplex will form – these cases are called “pG4” for “potential G quadruplex”.

Midway through the section, this quote:

Summarizing the topic to this point, the enrichment of GC content in vaccine mRNA will inevitably lead to an increase in the pG4 content of the vaccines. This, in turn, will lead to dysregulation of the G4-RNA-protein binding system and a wide range of potential disease-associated cellular pathologies including suppression of innate immunity, neurodegeneration, and malignant transformation [83].

There are further implications. The more mRNA can form these self-shielding quadruplexes, the less that “micro RNAs” – miRNAs – can bind to the mRNA and control the expression. And THAT leads to another cascade of potentially unintended consequences.

The multitude of pG4s in the mRNA of the vaccine would predictably act as decoys, distracting miRNAs from their normal function in regulating human protein expression. The increase in G4 targets due to the vaccine would decrease the availability of miRNAs to target human-expressed G4s for regulation of gene expression. This can result in downregulation of miRNA expression which is implicated in cardiovascular pathology [96], onset of neurodegeneration [97], and/or cancer progression [98].

Type I IFNs and COVID-19

This is a very interesting section on the relationship of interferons to COVID-19. It appears that:

lower levels of interferons lead to more severe COVID-19 outcomes
IFNs can be used for treatment early, but make things worse if given late
interferons seem to prevent infection by COVID-19
this would explain enhanced susceptibility to COVID-19 after vaccination
COVID patients with antibodies against interferons are common in severe cases

Interferons are clearly key, and look to be one of the most significant differences between the disease and the vaccine.

Are the methylation strategies for cellular housekeeping generally omitted by vaccine mRNAs?

This is a rhetorical question about one of the hacks used by the mRNA vaccines.

To put it a bit too simply, the synthetic mRNA is “capped” both to evade detection AND to generate more spike protein, and most likely without regard for downstream unintended consequences, due to the fact that capping is normally supposed to be both a signaling and a regulating mechanism. The “hack” abuses this feature to make more spike protein.

Rather than simply making an accusation, the question is asked, whether the hack accounted for some of the more likely consequences.

E.g., …..

Furthermore, this also means that eIF4E, which is a powerful oncogene regulator and cell proliferation modulator, will sustain its activities by this competition, for an unnaturally prolonged period of time, trying to counterbalance the competition between robustly-capped mRNAs in vaccines and IRES-containing mRNAs[113,65]. This type of condition results in dysregulation of co-transcriptional m6A mRNA modiﬁcations and seriously links to molecular progressions of various cancers [114], as well as creating predisposing conditions for subsequent viral infections [113].

My money is on the idea that nobody in the management chain at Pfizer or Moderna gave a flying F, because Fauci and Walensky are all about the antibodies. This is a CLASSIC downstream effect of antibody hypnosis.

Exosomes and MicroRNAs

This is an interesting grab-bag of stuff, and it’s not that hard to follow, for the most part, so you may want to read it.

Exosomes are basically little bubbles of cell that break off and carry crap, a lot like “virus-like particles” or even “lipid nanoparticles”. It turns out that much of the spike protein which is produced in vaccine-infected cells LEAVES THE SCENE inside exosomes, or studded into their surface. This was in fact discovered by a group in India.

Also, under conditions of overwhelming production of spike protein due to SARS-CoV-2 molecular vaccination, it would of course be expected that a signiﬁcant proportion of over-abundant intra-cellular spikeproteins would also be exported via exosome cargoes [128]. A seminal paper by a research team in India investigated the role of exosomes in the cellular response to internally synthesized SARS-CoV-2 spike protein [50]. They wrote in the abstract:“We propose that SARS-CoV-2 gene product, Spike, is able to modify the host exosomal cargo, which gets transported to distant uninfected tissues and organs and can initiate a catastrophic immune cascade within Central Nervous System (CNS).”

Things get even worse. It turns out that these exosomes also carry micro-RNAs that turn off interferons in the distant places to which they carry the spike protein.

Thus, the available evidence strongly suggests that endogenously produced spike protein creates a diﬀerent microRNA proﬁle than does natural infection with SARS-CoV-2, and those diﬀerences entail a potentially wide range of deleterious eﬀects.
A central point of our analysis below is the important distinction between the impact of vaccination versus natural infection on type I IFN. While vaccination actively suppresses its production, natural infection promotes type I IFN production very early in the disease cycle. Those with preexisting conditions often exhibit impaired type I IFN signaling, which leads to more severe, critical, and even fatal COVID-19. If the impairment induced by the vaccine is maintained as antibody levels wane over time, this could lead to a situation where the vaccine causes a more severe disease expression than would have been the case in the absence of the vaccine.
Another expected consequence of suppressing type I IFN would be reactivation of preexisting, chronic viral infections, as described in the next section.

SO – this would explain “vaccine-induced disease enhancement” – not antibody-dependent (ADE), but rather interferon-dependent (IDE). And in this case, it could be significantly different diseases that are being enhanced, because of the generality of the interferon network.

Speaking of which…..

Reactivation of Varicella-zoster

Fully consistent with the proposed vaccine-induced negative effects on interferon signaling, would be the significant number of cases of shingles appearing post-vaccination with the mRNA vaccines.

There is also a documented case of viral hepatitis flaring up because of the vaccine.

An additional case of viral reactivation is noteworthy as well. It involved an 82-year-old woman who had acquired a hepatitis C viral (HCV) infection in 2007. A strong increase in HCV load occurred a few days after vaccination with an mRNA Pﬁzer/BioNTech vaccine, along with an appearance of jaundice. She died three weeks after vaccination from liver failure [142].

Personally, I have no desire to get shingles again.

Impaired DNA Repair and Adaptive Immunity

As stated – more examples from the literature.

We have to speed up here. This is a long paper.

Immune Thrombocytopenia

This is your “clot shot” mechanism, explained.

This quote is interesting.

It has been shown that the mRNA vaccines elicit primarily an immunoglobulin G (IgG) immune response, with lesser amounts of IgA induced [155], and even less IgM production [156]. The amount of IgG antibodies produced is comparable to the response seen in severe cases of COVID-19. It is IgG antibodies in complex with heparin that induce HIT. One can hypothesize that IgG complexed with the spike protein and PF4 is the complex that induces VITT in response to mRNA vaccines. It has in fact been shown experimentally that the receptor binding domain (RBD) of the spike protein binds to PF4 [157].

PPAR-α, Sulfatide and Liver Disease

Two paragraphs are worthy of your attention.

As we have already stated, an experiment by Mishra and Banerjea (2021) demonstrated that the spike protein induces the release of exosomes containing microRNAs that speciﬁcally interfere with IRF9 synthesis[50]. In this section we will show that one of the consequences of suppression of IRF9 would be reduced synthesis of sulfatide in the liver, mediated by the nuclear receptor peroxisome proliferator-activated receptor α (PPAR-α).
…
Multiple case reports in the research literature describe liver damage following mRNA vaccines [165-167]. A plausible factor leading to these outcomes is the suppression of PPAR-α through downregulation of IRF9,and subsequently decreased sulfatide synthesis in the liver.

As you can see, there is a prediction here, and plenty of room to investigate.

Guillain Barre Syndrome and Other Neurological Conditions

This is worth reading. There is a laundry list of neurological conditions clearly attributed to the vaccine, and a clear mechanism by which they happen.

Bell’s Palsy

A known problem which appeared during the clinical trials of the mRNA vaccines.

Placebo 1, Treatment 7. Do the math.

Myocarditis

Signals and mechanisms are discussed. Particularly compelling is the proposed role of exosomes in carrying the toxic spike to cardiac tissue.

My money is still on migrating vaccine, but AND LOGIC will do for now.

Considerations Regarding the Vaccine Adverse Event Reporting System (VAERS)

The underreporting of the system is discussed, with some doubt about the commonly cited figure of “100X” underreporting, as well as mention of a more sophisticated figure of 31X obtained by Rose.

VAERS Signal for Immune Suppression, Thrombocytopenia and Neurodegeneration

A comparison of the data from COVID vaccines to ALL OTHER VACCINES COMBINED is made, and the results are impressive.

Many different things are listed. It’s worth looking at.

VAERS Signal for Cancer

After detailing the numbers for cancer (nice table), where the mRNA vaccines have HUGE numbers compared to all other vaccines combined, this statement:

This cannot be explained by reference to a disproportionately large number of people receiving an mRNA vaccination in the past year compared to all other vaccinations. The total number of people receiving a non-COVID-19 vaccination is unknown, but over the 31 years history of reports VAERS contains it is unquestionably many orders of magnitude larger than the number receiving an mRNA vaccination in the past year. Overall, in the above table, twice as many cancer reports to VAERS are related to a COVID-19 vaccination compared to those related to all other vaccines. That, in our opinion, constitutes a signal in urgent need of investigation.

To me, this is enough to say that the mRNA vaccines are related to cancer. Period.

Discussion

This is worth reading:

There has been an unwavering message about the safety and eﬃcacy of mRNA vaccinations against SARS-CoV-2 from the public health apparatus in the US and around the globe. The eﬃcacy is increasingly in doubt, as shown in a recent letter to the Lancet Regional Health by G¨unter Kampf [215]. Kampf provided data showing that the vaccinated are now as likely as the unvaccinated to spread disease. He concluded:“It appears to be grossly negligent to ignore the vaccinated population as a possible and relevant source of transmission when deciding about public health control measures.”
In this paper we call attention to three very important aspects of the safety proﬁle of these vaccinations. First is the extensively documented subversion of innate immunity, primarily via suppression of IFN-α and its associated signaling cascade. This suppression will have a wide range of consequences, not the least of which include the reactivation of latent viral infections and the reduced ability to eﬀectively combat future infections. Second is the dysregulation of the system for both preventing and detecting genetically driven malignant transformation within cells and the consequent potential for vaccination to promote those transformations. Third, mRNA vaccination potentially disrupts intracellular communication carried out by exosomes, and induces cells taking up spike mRNA to produce high levels of spike-carrying exosomes, with potentially serious inﬂammatory consequences. Should any of these potentials be fully realized, the impact on billions of people around the world could be enormous and could contribute to both the short-term and long-term disease burden our health care system faces.
Given the current rapidly expanding awareness of the multiple roles of G4s in regulation of mRNA translation and clearance through stress granules, the increase in pG4s due to enrichment of GC content as a consequence of codon optimization has unknown but likely far-reaching consequences. Speciﬁc analytical evaluation of the safety of these constructs in vaccines is urgently needed, including mass spectrometry for identiﬁcation of cryptic expression and immunoprecipitation studies to evaluate the potential for disturbance of or interference with the essential activities of RNA and DNA binding proteins.

This is what I was talking about at the beginning. There is enough here for an enormous amount of productive research on the downside of these vaccines. It’s EASY RESULTS. Maybe not easy grant money, but plenty of easy CLOUT when it’s all over.

This does NOT go back in the toothpaste tube.

Conclusions

Presented in whole:

It is imperative that worldwide administration of the mRNA vaccinations be stopped immediately until further studies are conducted to determine the extent of the potential pathological consequences outlined in this paper. It is not possible for these vaccinations to be considered part of a public health campaign without a detailed analysis of the human impact of the potential collateral damage. It is also imperative that VAERS and other monitoring system be optimized to detect signals related to the health consequences of mRNA vaccination we have outlined. We believe the upgraded VAERS monitoring system described in the Harvard Pilgrim Health Care, Inc. study, but unfortunately not supported by the CDC, would be a valuable start in this regard [208].
In the end, we are not exaggerating to say that billions of lives are at stake. We call on the public health institutions to demonstrate, with evidence, why the issues discussed in this paper are not relevant to public health, or to acknowledge that they are and to act accordingly. Until our public health institutions do what is right in this regard, we encourage all individuals to make their own health care decisions with this information as a contributing factor in those decisions.

That’s where I’m at. Do not take the clot shot. Do not give it to your kids. Tell people how you honestly feel.

I am OK with people having the freedom to take a bad vaccine, but I personally think that coercing anybody in the slightest to take it, is a CRIME.

If you’re scared of getting or giving COVID, there are far better ways to deal with it, than a bad vaccine that does a lot of damage.

Can the mRNA Vaccines Be Fixed?

That’s MY question.

I suspect that they CAN be fixed, but not for at least several years – maybe 5-10, if we’re lucky.

Until then, they should be taken off the market, IMO.

Hopefully antigen vaccines will do better, but if they don’t, we can fall back to treatment and “real” immunity.

Wolfie’s Wheatie’s Word of the Day:

wolven

noun

Of or pertaining to wolves; wolflike; wolfish.

Used in a sentence:

Adjectives for wolf include wolfish, wolfless, wolflike, wolfly, wolfy, wolven, wolvish, wolfed, wolfing, wolved and wolving.

(If you can find a better one, please add it to the comments!)

ENJOY THE SHOW

W

DEAR KAG: 20220204 – The Pub is OPEN / The End of the mRNA Vaccines / Bad Medicine as a Weapon of War / Mayor Gramsci III’s War On Freedom of Movement

The Pub is OPEN!

We may serve “off-label” drinks here, including hydroxychloroquine, ivermectin, and truck diesel, but we don’t serve spike protein, remdesivir, or anything made in Wuhan, Chinazia.

While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.

Christmas Spirit

Feel free to celebrate the birth of Christ any time. We’re dragging it out this year! One MORE month of Christmas begins!

Hey – where’s Santa? We need his famous line about his VP!

And now, the rules of the pub.

HOUSE RULES

Now, back to business.

AMEN!

#FJB – Free the January Brothers

Current Art On The Wall

This is another off-beat shipment. “Spice” is all it said on the box. Let’s take a look.

I am informed that this one has something to do with the “Spice Islands”.

This one is related to Morocco. I think I see some kind of actually trustworthy pharmaceuticals, although it also looks a bit like that “pot-poury” stuff.

Not sure what this one is, other than what’s on the label – “Moroccan Spice”.

This one is also labeled “Moroccan Spice”, with a reference URL. I am informed by an expert that this genre of art is something known as “purse porn”.

**https://www.mynewsdesk.com/sg/tanandbrown/images/ava-martin-moroccan-spice-editorial-chaise-photo-87783**

OK – now it’s starting to look like actual art. This one even had a reasonable price tag.

**https://amywhitehousepaintings.blogspot.com/2012/01/lets-cook-6×8-oil-painting-of-cooking.html**

This one is even cheaper. $9.99 at Walmart. Well, it’s FREE here!

**Still Life with Spices and Olive Oil Food Still Life Kitchen Photo Print Wall Art By Andrii Gorulko**

More in the same genre, but with a nod to local astronomers and others like me who enjoy looking at the sky at night and going WTF.

**Baking For Stargazers by Dina Belenko**

This is a trick to flush out any kids on this site.

If you ever saw one of these in real life, you’re a kid, or you had some. Or both!

And then somebody decided to get cute with the jukebox…..

On The Jukebox

This is from the early days, when the “talent” was just getting started, and it shows.

Here’s where the “spice” started flowing to the cabal coffers, and the recruits were now famous for being famous. Different fan-exciting material was possible…..

I was going to queue up some of their reunion material, but I absolutely cannot take any more of it.

SO ENJOY.

There – that’s better!

OK, I cannot leave you with that earworm, so I’m going to perform a really neat trick.

The following performance is by a similar “girl group” in Japan, doing a number called “Spice“. Because it’s designed to infect the brains of Japanese and not Westerners, it’s essentially white noise MK to gai-jin, and will erase the Spice Girls stuff.

WE HOPE.

You can turn on English captions to see what they’re saying.

Because this group “Perfume” rides on a more techno/electronica carrier wave, and comes in at a more “artistic” level than the Spice Girls, it actually gets MUCH more respect than the Spice Girls, in both the East and the West. Many people regard it as techno art-pop rather than J-pop. But don’t kid yourself. Down deep, it’s still a “girl band”. These ladies are huge cultural celebrities in Japan, just like the Spice Girls remain in England, even disbanded.

And thus we return to reality.

Or do we?

THE SPICE MUST FLOW

And now for our feature presentation…..

The End of the mRNA Vaccines

This topic right here is just a WARM-UP for my Monday post, which will explain WHY these particular mRNA vaccines are OVER. GONE. KAPUT. DONE.

You want to know why Joe Rogan / Spotify happened?

Pfizer-CNN-DNC-BlackRock-[CB]-Mr.Global can’t attack Drs. Malone and McCullough directly, at this CRITICAL MOMENT, so they FAKED IT, and attacked Joe Rogan to indirectly “prove” that Malone and McCullough are providing “misinformation”.

That is how desperate they are.

Sorry.

As China said to the Biden administration, “You are dealing from a position of weakness.”

The TRUTH is a SOLID FORTRESS.

“They” are in so much trouble.

And Malone and McCullough are in the CATBIRD SEAT.

There are tens of billions – hundreds of billions – maybe trillions of dollars on the line, and those dollars are not just on a rickety foundation – they are on QUICKSAND.

Couldn’t happen to a nicer guy – 😂https://t.co/OdHXdATzTo
— Catturd ™ (@catturd2) February 3, 2022

(H/T FG&C)

You can understand the panic. And it will only get worse.

First, I want you to watch this video, and understand that every word you hear is 100 times truer than even those people realized when they said those things.

The truth 🔥🔥 pic.twitter.com/OxFO7bOnxI
— Frontline Freedom (@FrontlineFree) January 31, 2022

Now I want you to understand WHY.

Hat tip to Gail Combs for cluing me in to this very recent paper, which I expect to come under merciless attack, but it won’t do any good.

This paper may NEVER reach or pass “peer review”, but it doesn’t matter. Even if it NEVER passes peer review, the payload has been delivered.

The paper has DETONATED in information space.

More “cautious” scientists will BET THEIR CAREERS on the truth therein, and “discover” everything discussed here, but in slower, politically correct, and damage-controlling ways.

Limited damage control remains possible if “they” are extremely lucky and drop mandates world-wide NOW. But as long as their side keeps forcing mandates, the WOODEN STAKE OF TRUTH will be driven into the VAMPIRE HEARTS OF PFIZER, MODERNA, AND ALL WHO BACKED THE CLOT SHOT.

GOVERNMENTS are going to FALL.

I think that SOMEBODY knew this paper was coming.

Once you see WHY the mRNA vaccines are fundamentally flawed, you can’t unsee it.

Innate Immune Suppression by SARS-CoV-2 mRNA Vaccinations: The role of G-quadruplexes, exosomes and microRNAs

January 2022

DOI:10.22541/au.164276411.10570847/v1

Project: COVID 19

Authors:

Stephanie Seneff

Massachusetts Institute of Technology

Greg Nigh

Immersion Health

Anthony Kyriakopoulos

Nasco AD Biotech Lab

Peter A McCullough

[Could have said “Baylor College of Medicine”, but they were FOOLS!]

ABSTRACT

LINK: https://www.researchgate.net/publication/357994624_Innate_Immune_Suppression_by_SARS-CoV-2_mRNA_Vaccinations_The_role_of_G-quadruplexes_exosomes_and_microRNAs

I will go through this in more detail on Monday.

I was only part-way through the body of the paper, when I realized that if even a fraction of it is correct, the mRNA vaccines are as good as over.

Worse than that, other non-mRNA vaccines are likely subject to many of the same concerns.

It may very well be that vaccination is a poor strategy for this virus, SARS-CoV-2.

BUT ONE THING IS CERTAIN.

Now that there is a clean, elegant, and intellectually appealing explanation of the adversity of the mRNA clot shot, which happens to align perfectly with common sense, mandates are murder.

Do not back down. Do not give up. We are on the right side of this.

I will explain.

SOON.

Bad Medicine as a Weapon of War

If you ever find yourself weakening on NOT GETTING THE CLOT SHOT – (and I’ve actually run into some of these failure-of-will cases in real life, so it’s not impossible) – try to remember just ONE of the items discussed below.

Don’t let Chinazia and the Globonazis inject you with their Slow-Motion Koolaid designed to assassinate America.

What follows are several items (or groups of items), many of which have been sitting around in my tabs, which have been bothering me. I have been TRYING to fit them into a pure and simple negligence scheme, and I simply can’t.

There is a highly destructive and very intentional aspect to all that has happened, that defies letting us categorize “Obamacare and what came after it” as mere stupidity.

insurance data showing manifold increased deaths of military-aged people, mostly men
- https://www.thecentersquare.com/indiana/indiana-life-insurance-ceo-says-deaths-are-up-40-among-people-ages-18-64/article_71473b12-6b1e-11ec-8641-5b2c06725e2c.html
- https://archive.fo/9p1TP
British ONS data showing increased deaths among children AFTER vaccination began
- https://dailyexpose.uk/2021/11/24/child-deaths-increasing-since-offered-covid-vaccine/
vaccine failure to reduce all-cause mortality AFTER excess deaths due to COVID-19
- https://beckernews.com/exclusive-its-game-over-for-the-cdc-if-these-death-rates-hold-true-43385/
lack of association between vaccination and new cases of COVID-19
- https://pjmedia.com/columns/stacey-lennox/2021/10/28/a-shocking-study-on-vaccine-rates-and-covid-19-you-may-have-missed-n1527669
funeral home director with validating mortality data
- https://www.kla.tv/21382
pathologist Ryan Cole with validating mortality and morbidity data
- https://stuartbramhall.wordpress.com/2022/01/30/dr-ryan-cole-explains-how-the-covid-vaccines-compromise-the-immune-system/
- https://www.brighteon.com/898419ab-e36f-43a5-8700-e0e35b126273
cardiac deaths of athletes, students, normies, and children under stress
- https://www.americanthinker.com/blog/2021/12/japan_warns_of_cardiac_health_risks_from_covid_vaccines.html
Pfizer hiding vaccine migration, while misleading toward spike migration per se
- https://www.theqtree.com/2021/05/31/the-spike-proteins-purpose-betrayed-by-its-own-superiority/
Hoffe’s data on post-vaccination D-dimer testing and pulmonary insufficiency
- https://www.theqtree.com/2021/10/13/dr-charles-hoffes-observation-of-spike-protein-mrna-vaccine-induced-pulmonary-hypertension/
the toxic batch phenomenon, IMO, likely due to mRNA vaccine overdoses
- https://www.theqtree.com/2022/01/21/dear-kag-20220121-the-pub-is-open-the-anti-saline-theory-and-the-toxic-batch-problem/
clearly duplicitous mischaracterization of post-vaccination deaths as COVID-19
- a.k.a. “14 days to hide the data”
- https://joannenova.com.au/2021/12/blockbuster-paper-covid-vaccines-may-not-improve-your-chances-of-staying-alive-at-all-even-in-a-pandemic/
- https://www.researchgate.net/publication/356756711_Latest_statistics_on_England_mortality_data_suggest_systematic_mis-categorisation_of_vaccine_status_and_uncertain_effectiveness_of_Covid-19_vaccination
- https://notrickszone.com/2022/01/21/analysis-by-german-prof-thousands-of-hidden-deaths-daily-may-be-greatest-medical-debacle-in-human-history/
- https://www.thegatewaypundit.com/2022/01/alberta-canada-inadvertently-published-quickly-deleted-health-data-exposing-half-vaccinated-deaths-counted-unvaccinated/
- https://twitter.com/mdccclxx/status/1482322142041673734
- https://metatron.substack.com/p/alberta-just-inadvertently-confessed
- https://archive.fo/R6w2z
promotion of toxic loser drug remdesivir to treat SARS-CoV-2 infection
- https://www.theqtree.com/2021/09/20/the-murder-of-veronica-wolski-by-fauci-and-gileads-zyklon-d/
“programming” the remdesivir treatment at a point in the disease when there is no virus
- https://www.theqtree.com/2021/09/20/the-murder-of-veronica-wolski-by-fauci-and-gileads-zyklon-d/
“programming” hospitals with cash incentives to kill using vents and remdesivir
- https://rense.com/general96/hospitals-are-being-bribed.php
Joe Biden and SecDef “Idi Amin” Austen mandating bad vaccines for the military
- https://clarion.causeaction.com/2022/01/27/whistleblower-bombshell-dod-medical-data-reveals-surges-in-oft-cited-vaxx-adverse-events-in-2021/
WEF and Klaus Schwab turning up like bad pennies at every juncture in COVID-19
- https://www.globalresearch.ca/klaus-schwabs-wefs-school-for-covid-dictators-a-plan-for-the-great-reset/5764929

And now the final straw that breaks the camel’s back

the “Trusted News Initiative” which was ready to tamp down knowledge of bad vaccines
- https://www.theqtree.com/2022/01/31/covid-and-beyond-fake-news-the-trusted-news-initiative/

I know you have limited time, but of all those links, I would suggest the following article and the following video.

https://www.globalresearch.ca/klaus-schwabs-wefs-school-for-covid-dictators-a-plan-for-the-great-reset/5764929

LINK: https://www.globalresearch.ca/klaus-schwabs-wefs-school-for-covid-dictators-a-plan-for-the-great-reset/5764929

LINK: https://www.kla.tv/21382

LINK: https://www.thegatewaypundit.com/2022/01/never-seen-many-deaths-around-500-600-increase-funeral-director-uk-reveals-increasing-number-death-vaccinated-young-adults/

Hat tips to RAC, Aubergine and Linda, for bringing the full extent of this one to my attention.

Further hat tips to those who brought all the other “tabbed” items above.

To me, this is only explained by what amounts to a secret “war” against the United States. Not everybody fighting on “their” side knows everything. In fact, almost all of them know nothing. But I think that Tony Fauci, Hillary Clinton, and a few others either know the entirety of the plot, or are following orders without question.

Their mission is based on ideas that America is bad and responsible for every bad thing, and that America and Americans need to be disempowered and punished for it.

Thus, like the general idea that Obama wasn’t as much “for Russia” or “for China” as he was “against America”, we can see that the modern Democrat party is now an embodiment of skepticism about, if not antipathy toward, America and Americans themselves.

Here’s the video and the URL, which long ago disappeared from YouTube.

LINK: https://www.bitchute.com/video/XqreFRHoXTFX/

In my opinion, this all goes back to the Soviet-supported MAOIST Weather Underground types of the late 60s and early 70s, who were actively planning a revolution in which 25 million Americans would need to be killed. This is around the same time that Klaus Schwab got his start. INTERESTINGLY ENOUGH.

There are basically two sides – individual freedom and state control. In the past we’ve tended to have wars which were not cleanly on that boundary, such as Hitler vs. Stalin, but I think THIS ONE is fairly clean. “They” try to make “free forces” fight each other, which is very smart, but I think we’re wising up.

They HAD to have known that, without getting the guns, they could never defeat us ON AMERICAN SOIL.

It HAD to be gradual. It HAD to be Sun Tzu. It HAD to be carried out by Americans, on American soil.

I am really thinking now that SOMEBODY on the radical left realized that they could not set up CAMPS unless we were fully under the grip of socialism, like China or North Korea, BUT that until such a time, there WERE ways to trick us into allowing ourselves to be killed.

Disease used as a weapon of war can be efficient, but it’s obvious. But using the medicine allegedly meant to TREAT a disease as a weapon of war is NOT obvious.

Turning our own medical system against us is a cruel and cynical method of war, but I have to admit that it’s rather brilliant.

It’s a sobering thought.

Something is very wrong here. Stay frosty. I think that they’re trying to get as much as they can WITHOUT WAR, before they actually go TO WAR.

And speaking of WAR……

Mayor Gramsci III’s War On Freedom of Movement

The son of the torch-bearer of Antonin Gramsci, a founding father of cultural Marxism, is not exactly undamaged goods. As you can see above, Pothole Pete was (assuming this bit of news is not completely phony) a PRETTY SICK KID.

People like that are PSYCHOPATHS. Pet murderers rarely turn into saints. There is usually something VERY wrong with them – something that does NOT go away without a lot of GOD in the process.

Personally, I don’t care to push a campaign against “Mayor Pete” over his alleged juvenile criminality. There is a reason that juvenile records are sealed. Many if not most people “get serious” at the point of LEGAL RESPONSIBILITY. They grow up. Bad kids can turn out good. However, I still think Kid Pete’s history is relevant to Secretary Pete’s personality.

We’ve gotta KEEP OUR EYE on this boy.

I suspect that many people are glad “Possible Pet-Killer Pete” is “only” Secretary of Transportation. Still, he could do a LOT of damage there. For example, that office could be a real problem for an American truckers’ strike.

Trust me, Pete Buttigieg is not here to fix the roads. He is a typical communist control freak who is going to take our freedoms away if we don’t take him seriously.

And taking Pothole Pete seriously is hard. Because on the surface, the guy is SUCH a DOUFUS.

He wouldn’t hurt a fly – right?

So when this infuriating poser bicyclist idiot does something like this…..

“Our Goal is Zero Traffic Deaths” – Buttigieg Announces New Federal Strategy to Combat Traffic Fatalities (VIDEO)

LINK: https://www.thegatewaypundit.com/2022/01/goal-zero-traffic-deaths-buttigieg-announces-new-federal-strategy-combat-traffic-fatalities-video/

…..one is tempted to view this as merely stupid and impossible.

DO NOT make that mistake.

“Zero traffic deaths” is not only a fundamentally and intentionally MISDIRECTED GOAL that has a “feel-good” appearance of self-justification – which leverages our wish to “do the impossible” – it is CODE for all of the following:

personal transportation for the elite only
Mercedes for the elite – Chinese Trabants for luckier serfs
where you live becomes determined by your job
Soviet-level, corrupt, inefficient public transit for plebes
no freedom of movement – internal passporting
omnipresent cameras and surveillance, just like China
TSA internal control, “papers, please”, and all the rest

This is how these ASSHOES bring CHINA to AMERICA.

Zero traffic deaths is just like MOAR ANTIBODIES.

A PHONY and MISLEADING GOAL.

Now, before we get to the fact that we simply have to stop this crazy commie twerp, you need to know him better.

A great AUDIO will help.

Notice how PRESCIENT this talk is, right at the beginning.

You will ALSO love the end, when you realize that TRUMP is headed straight into confrontation with this joker.

LINK: https://sovereignnations.com/2021/10/22/buttigieg-and-gramsci-public-occurrences-ep-39/

I invite you to resolve to NEVER accept what Pet-Killer Pete has in store for us.

NEVER. EVER. Accept it.

All that is left is HOW you choose to resist this guy.

Have a great weekend, and don’t forget to…..

ENJOY THE SHOW.

Because frustrating evil and stopping future sorrow is rewarding for a reason.

W

THE SALT MUST FLOW

COVID and BEYOND FAKE NEWS: The “Trusted News Initiative”

A Gail Combs deep dive into a curious item revealed by Robert Malone on Joe Rogan.

https://www.mediainfoline.com/wp-content/uploads/2018/11/Beyond-Fake-News-logo.jpg

Preface by Wolf Moon

Follow along as Gail Combs digs down a snake-infested rabbit hole from something that Dr. Robert Malone mentioned on Joe Rogan.

Once you understand how much preparation went into what is going on RIGHT NOW, you’ll realize that all the usual suspects had a plan, and it’s exactly what we’re seeing now, except they weren’t banking on us understanding their criminal conspiracy.

2:40:50 “We are in an environment where truth and consequences are fungible. This is Modern media management and warfare. The Truth is what those that are managing ‘The Trusted News Initiative’ say it is. “
Dr Robert Malone

From video Dr Robert Malone on Joe Rogan

https://rumble.com/vrv7k1-dr.-robert-malone-on-joe-rogans-podcast.html

CRITICAL TIMELINE

JULY 2019

BBC: Beyond Fake News

Trusted News Initiative
How news organisations can rebuild trust and tackle the next disinformation challenges.
Trust In News
The BBC’s Trusted News Initiative is a partnership that includes organisations such as Facebook, Twitter, Reuters and The Washington Post. It is the only forum in the world of its kind designed to take on disinformation in real time. Now we and our partners are going to share what we’ve all learned about how to tackle disinformation, and you are invited.

Trusted News Initiative or Corrupted News Initiative? Mission: Systematic censorship of the world’s top public health experts

In this August 13, 2021 article for Global Research, Elizabeth Woodworth explains how the Trusted News Initiative (TNI) was formed and what it means to our modern society.
According to Woodsworth, even before the pandemic, there has been a continued increase in public distrust to mainstream media. The TNI began in July 2019 when BBC Director-General Tony Hall convened various media companies and Big Tech companies to “arrive at a practical set of actions we can take together, right now, to tackle the rise of misinformation and bias…[by creating a] global alliance for integrity in news…to promote freedom and democracy worldwide”.
From the beginning, the goal of TNI was to counter “anti-vaxxers [who] were gaining traction on social media as a part of a “fake news” movement spreading “misleading and dangerous information”….
TNI has become an instrumental tool for the suppression of life-saving information….

Trump-Ukraine impeachment scandal: timeline of key events

YEAR 2019

18 July Trump issues instructions to withhold $392m in military aid from Ukraine

25 July Trump and Zelenskiy speak on the phone.

12 August A whistleblower complaint is filed.

24 September The House speaker, Nancy Pelosi, announces a formal impeachment inquiry into Trump’s actions.

6 October Lawyers for the first whistleblower say they are now representing a second.

8 October The state department prevents Gordon Sondland, US ambassador to the EU and a Trump donor, from testifying to a congressional impeachment hearing.

October 18 Event 201

https://i.ytimg.com/vi/YxxNZ5u6JXo/maxresdefault.jpg

Event 201

The Johns Hopkins Center for Health Security in partnership with the World Economic Forum and the Bill and Melinda Gates Foundation hosted Event 201, a high-level pandemic exercise on October 18, 2019, in New York, NY. The exercise illustrated areas where public/private partnerships will be necessary during the response to a severe pandemic in order to diminish large-scale economic and societal consequences.

….

October 18 – 28, 2019

https://obj.shine.cn/files/2019/10/18/b9afeeca-61e9-4c63-b79d-44a28dd12340_0.jpg

CISM Military World Games – U.S. Department of Defense

Top U.S. military athletes are competing against their counterparts from more than 100 nations during the 2019 Military World Games in Wuhan, China, Oct. 18-28.

Did the Military World Games Spread COVID-19?

The 2019 Military World Games, branded the “Peace Games,” was the largest military sports event ever held in China. More than 9,000 athletes representing the militaries of more than 100 countries competed in 27 sports…

Whistleblower: 2019 Wuhan Military Games Were China’s First Intentional COVID Super-Spreader Event

On July 21, 2021, Lawrence Sellin, Ph.D. broke the news on The Gateway Pundit from a China source that the release of COVID-19 at the 2019 Military World Games in Wuhan was a test of the longer-term effects of that type of bioweapon because foreign visitors to the Games would carry it back to their own countries and the consequences could be observed. . .

Letter to Congress:

https://gallagher.house.gov/sites/gallagher.house.gov/files/Letter_World%20Military%20Games_6.21.pdf

December 11, 2019 The Hill

Scientist claims first known COVID-19 case was Wuhan market vendor

Michael Worobey, head of the Department of Ecology and Evolutionary Biology at the University of Arizona, wrote in a piece published in the journal Science that a female seafood vendor who worked at the live animal market in Wuhan and became ill on Dec. 11, 2019, was likely the first known case of COVID-19.

December 18 – House voted to impeach Trump

CDC Museum COVID-19 Timeline

December 31, 2019 The World Health Organization China Country Office is informed of a number cases of pneumonia of unknown etiology…

January 2, 2020 The World Health Organization activates its incident management system…

January 5, 2020 CDC’s National Center for Immunization and Respiratory Diseases (NCIRD) activates a Center Level Response…

January 7, 2020 Chinese authorities identify and isolate a novel coronavirus….

January 7, 2020
CDC establishes a 2019-nCoV Incident Management Structure to guide the response….

[January 16, 2020 – Articles delivered & Impeachment Trial began in the Senate]
January 17, 2020 CDC begins screening passengers on direct and connecting flights from Wuhan, China

January 17, 2020 CDC deploys a team to Washington state to assist with contact tracing efforts in response to the first reported case

January 20, 2020 CDC confirms the first U.S. laboratory-confirmed case of COVID-19 in the U.S.

January 21, 2020 CDC transitions from a Center-led Incident Management Structure to an Agency-wide Structure and activates its Emergency Response System

[January 25, 2021, House impeachment managers delivered the article of impeachment to the U.S. Senate.]

February 5, 2020 Senate voted to acquit

March 27 2020 CARES act passed It pays hospitals to kill elderly covid patients. See Sec. 3710….. Assoc of American Physicians & Surgeons : Biden’s Bounty on your Life

The Timeline seems to indicate that President Trump was kept distracted while the Democrats and Mr Global put the pieces in place to unleash the Plandemic and force the world to take the clot shot.

…………….

The NUREMBERG CODE is worth rereading before we go down into the snake pit.

https://pbs.twimg.com/media/FIQ9KIsVIAAeZ17.jpg

While Collins, Fauci, hospitals and medical boards moved to silence and censor ALL opinions by dissenting experts, the Trusted News Initiative also muzzled anyone else not advocating for the Clot Shot. However Mr Global went even further than censorship and threatening jobs and medical licenses.

TEN NIH STUDIES ON ‘VACCINE REFUSAL’

‘Vaccine Refusal’ is considered a ‘condition or disease’ that needs ‘treatment’ The following are trials to determine how to ~~convince~~ brainwash people into consenting to taking an experimental drug WITHOUT giving them full disclosure.

NEW TRIAL!!! COVID-19 Messaging for Vaccination

MIT Cambridge, MA ; Behavioral: Doctor Videos

Behavioral: Sharing Videos
Behavioral: Sharing Videos (Influencers)
(and 3 more…)

Collaborators:

Facebook, Inc. aka Mark Zuckerberg who was Caught Stealing Election With Ballot Drop Boxes

And his CHINESE WIFE (Red Diaper Baby from China?)

She was mostly raised by her Chinese grandmother, who spoke no English. She was a very dignified woman who clearly was a huge influence in Priscilla’s life…. But the precise details of how the family arrived in America are unclear. Reports in China say they came originally from the city of Xuzhou in eastern Chandong province, also the home city of Rupert Murdoch’s wife Wendi Deng. Others say that the family lived in Nanjing, an industrial town 150 miles west of Shanghai, before leaving to live first in Hong Kong and later in the US.
A source at the Asian-American Civic Association in Boston said it was ‘highly likely’ the family spent time in a refugee camp, either in Hong Kong or on arrival in the US.
Priscilla’s father said he was a refugee who had lived in Vietnam, according to Thai-born Napat
Records show Dennis,[Her father] who now owns a small wholesale fish business, was given a social security number as an ‘Asian Refugee’ between April 1975 and November 1979.

Code3

Stanford University

Harvard University

Yale University

Johns Hopkins University

Massachusetts General Hospital

Ludwig-Maximilians – University of Munich

National Institutes of Health (NIH)

Study Description

Brief Summary:

This study will distribute videos of health professionals encouraging Covid-19 vaccination to a large sample of Facebook users, and will test the most effective ways to maximize diffusion of this vaccine-related content to increase vaccination rates. The study sample will be U.S. states where vaccination rates remained low in fall 2021. The experimental design is an RCT with 4 groups, randomized at the county level: 1) a control group which receives no intervention, 2) a treatment group in which Facebook users receive ads which include videos of health professionals telling them to get vaccinated, 3) a treatment group in which Facebook users receive ads which include videos of health professionals encouraging them to help their friends to get vaccinated, and 4) a treatment group in which Facebook users receive ads which include videos of health professionals encouraging them to get their most influential friends to help their friends get vaccinated. In treatments 3 and 4, participants will have the option to sign up to be a “vaccine ambassador,” in which case they will get notifications when the study team posts new vaccine-related content, and will receive reminders about encouraging their friends to be vaccinated. The vaccine ambassadors will also be entered into a lottery to win prizes. The study team is building a website to host the videos of health professionals which answer common questions about Covid-19 vaccination. The investigators will measure engagement with the vaccine-related content as well as assess effects on vaccination rates at the county level.

Interventional (Clinical Trial)
Estimated Enrollment :	40,000,000 participants
Allocation:	Randomized
Intervention Model:	Parallel Assignment
Intervention Model Description:	There are four arms in the study which geographic areas are assigned to in parallel. The geographic areas in the three treatment arms will receive a Facebook ad campaign over the same time period to one another.
Masking:	None (Open Label)
Primary Purpose:	Treatment
Official Title:	Increasing the Effectiveness and Diffusion of COVID-19 Messaging for Vaccination
Actual Study Start Date :	December 22, 2021
Estimated Primary Completion Date :	January 2022
Estimated Study Completion Date :	June 2022

THAT IS 40 MILLION PEOPLE!!!

……….

A Tailored, Health Communication Intervention for HPV Vaccine Hesitant Families – Meharry Medical College, Nashville TN

……….

COVID-19 Vaccine Hesitancy and Dental Faculty Staff Members

– Ain Shams University Cairo, Egypt

………..

Development and Testing of ADEPT: A Parent Decision Support for Childhood Vaccinations

— Duke University Health System, Durham, NC ( Childhood vaccination decision support tool) Principal Investigator Lavanya Vasudevan, Ph.D.

Collaborator: National Institutes of Health (NIH) 1KL2TR002554 ( U.S. NIH Grant/Contract )

………..

Clinic-based HPV and COVID-19 Vaccine Promoting Intervention for AfAm Adolescents in Alabama

– University of Alabama at Birmingham (Behavioral: Intervention)

Contact: Henna Budhwani, PhD, MPH

……….

– Annenberg School Philadelphia, PA

Behavioral: Online Social Network and Collective Intelligence Intervention :

Behavioral: Independent Control

Collaborators: University of California, Davis, University of California, San Francisco, University of California, Berkeley

Brief Summary:

Social technologies for health have already become essential means for providing underserved populations greater social connectedness and increased access to novel health information. However, these technologies have also had negative unintended consequences. The resulting digital divide in social technology takes many forms – from explicit racism that excludes African American and Latinx populations from the resources enjoyed by White and Asian members of online communities, to self-segregation for the purposes of identity preservation and community-building that unintentionally results in limited informational diversity in underserved communities. The result is an often unnoticed, but highly consequential compounding of inequities.
This research seeks to use an online social network approach to address these challenges, in which the investigators demonstrate how reducing the online levels of network centralization and network homophily among African American community members directly increases their productive engagement with health-promoting information.

………..

Project 2VIDA! COVID-19 Vaccine Intervention Delivery for Adults in Southern California –

San Ysidro Health Chula Vista CA;
Care View Health Center San Diego, CA;
San Ysidro Health Care View Health Center, San Diego, CA; and 3 more…
Principal Investigator: Argentina Servin, MD, MPH, Asst Prof,
Sponsors/Collaborators National Institute on Minority Health and Health Disparities (NIMHD)
Behavioral: COVID-19 Individual Awareness and Education;
Behavioral: COVID-19 Community Outreach & Health Promotion;
Behavioral: COVID-19 Individual Health Education & Linkages to Medical and Supportive Services;
Biological: Pop-up community vaccination sites

-GC

Conclusion by Wolf Moon

Do you see it now? They knew exactly what they were doing. Schiff’s kabuki with Zuckerberg was like a GO signal to start the censorship.

That creepy pedophile loser, the compromised Dem Rep on the committee that’s SUPPOSED to control the IC, but is in fact CONTROLLED BY IT, signals to the IC social media that’s SUPPOSED to serve us, but in fact SERVES THE IC, that they need to start censoring us by removing InfoWars and Natural News.

It ALL makes sense now.

CHICOMS. These people are no better than CHICOMS. Allies of the enemies of America. Traitors of the worst kind.

W

Who Approved and Upheld These Vaccines? The Covid Second Opinion Forum Held by Ron Johnson vs. the FDA Vaccines & Related Biological Products Advisory Committee (VRBPAC)

A background research post by Gail Combs

PREFACE

by Wolf Moon

It is useful for me to explain Gail’s post – to help you understand the importance of it.

People in government regulation of science and medicine do not make decisions in a vacuum – but they may make their decisions in an artificial atmosphere which is created, composed, and altered by those with the extreme power and ability to CONTROL INFORMATION.

LancetGate was very demonstrative of this ability to control science and medicine.

After watching a variety of FDA decisions under the Trump and Biden administrations, it has become very clear to me that FDA resides in a political and economic crosswinds, highly influenced by many parties with strong expectations and abilities to influence. And yet, the shocking (but welcome) advisory recommendation AGAINST COVID vaccine boosters – then overridden by the political operative Rochelle ~~Alinsky~~ Walensky in CDC – shows how a coordinated injection of honest medicine and common sense into FDA decision-making (THANK YOU, Steve Kirsch!) can sometimes make its case heard – even if only momentarily.

Sadly, it seems to me that Pfizer is back in the driver’s seat again. We thus have to ask WHY.

What Gail has done is to look at one endpoint of the argument (frontline doctors and publishing scientists who have run into the problems), which leads to the other, where we begin to find the reasons why FDA generally decides things in favor of big industry and big government, and not to the benefit of individual patients and doctors.

By looking at the doctors and scientists who supported logical and ethical TREATMENT of COVID-19, and who were wrongly and unethically BLOCKED and DENIED PERMISSION at every point – we can see that undue industry and political influence in NIH, CDC, and FDA are most likely responsible for decisions that make absolutely no sense to truly independent scientists and doctors. The video Gail includes is rather astounding in terms of showing us how much went wrong. What we are now seeing reminds me of science and medicine in the Soviet Union. Absolutely incredible.

What Gail has done here is to “follow the influence” – to show that FDA decision-making has NOT been in a vacuum, precisely because the members of the FDA advisory committee are not truly independent, but are in fact actors for the very same powerful forces that benefit from FDA decisions which are now inscrutable at the doctor-patient frontline.

Perhaps even more astoundingly, the very SYSTEM of NIH, FDA, and CDC seems to be designed, at this point, to leave NOBODY ACCOUNTABLE. Advisory groups and even department responsibilities are created, rearranged, and dismissed, so that NOBODY takes responsibility for mandates that defy logic and even violate the common medical sense of the past.

If something goes wrong in this chaotic system of responsibilities in the wrong places, you either blame everybody or nobody at all. This is why, in my opinion, the entire federal governent had to get rid of Trump.

DIG ALONG WITH GAIL, as she finds the CLUES – first in the testimony of Ron Johnson’s witnesses – then in the backgrounds of members of an important FDA advisory panel.

With that, here’s Gail.

The Covid Second Opinion Forum

It would be nice to let Senator Johnson know we saw this:

CONTACT: https://www.ronjohnson.senate.gov/contact

Offices – Mail address and Phone: https://www.ronjohnson.senate.gov/office_locations

MANY THANKS TO GA/FL and Wolf M00n for alerting us to the Covid 2nd opinion Forum

Here’s a must watch – A SECOND OPINION – SENATOR RON JOHNSON FORUM.
Begins at 40:19 – https://rumble.com/vt62y6-covid-19-a-second-opinion.html
“Discussion begins around 40 minute mark. Sen. Ron Johnson moderates a panel discussion, COVID-19: A Second Opinion. A group of world renowned doctors and medical experts provide a different perspective on the global pandemic response, the current state of knowledge of early and hospital treatment, vaccine efficacy and safety, what went right, what went wrong, what should be done now, and what needs to be addressed long term.”
More at https://www.ronjohnson.senate.gov
GA/FL

It is five hours long and I went through the whole video. I recommend listening to it as you work on other things since there is not much to watch. It is much better than the speeches at the March Against Mandates.

My, comments posted 1/25/2020:
1:41:50 – 1:50:00 Dr Paul Marik on Remdesivir:
4 million hospitalized 850,000 million died. He says cheap approved drugs could have save 500,000 lives (That is the 1/2 million again that I figured out by a different method.)
He eviscerated NIH/FAUCI.

Fauci Told POTUS Remdesivir was good 10 days in. Researchers Changed the study END POINT to HIDE DEATHS. The OTHER study SHOWING the deaths/toxicity of Remdesivir in Ebola trial was released at 11:00 am JUST before the Afternoon presentation of the corrupted Remdesivir-Covid study that was presented by Fauci to POTUS. (More on this below) He also mentioned U.S. Centers for Medicare & Medicaid Services gives bonuses to hospital to treat MEDICARE (the old and ‘useless’) patients with this toxic drug.

Steve Kirsch made it clear he thought it was corruption and worse several times.

Incriminating evidence – Steve Kirsch’s newsletter
New VAERS analysis reveals hundreds of serious adverse Events that the CDC and EDA Never Told Us About

3:12:00 MyFreeDoctor (dot)com:
This group treated 150,000 and only lost four.

3:35:00 Dr Peter McCollough talks about vaccines:
Originally there were three different advisory boards during the trials but when it came to the EUA those boards were gotten rid of AND THAT IS WHY CLOT SHOT WAS NOT PULLED IN JANUARY 2021!
Steven Kirsch says right after that there is HARD evidence at least 4 in the CDC/FDA were getting royalties…

4:02:00
The risk increases with each shot. mRna was ENGINEERED to TAMP DOWN RESPONSE to evade ADE BUT it looks like it ALSO tamps down response to viruses, bacteria, and cancer.
New Study Dr Voss out of the Netherlands.
There are too many Dr Voss in the netherlands for me to hunt down the correct one.
https://pubmed.ncbi.nlm.nih.gov/?term=voss%20netherlands&sort=date
(Could be KL Koss since she has papers about the heart and colon and cancer. papers: https://pubmed.ncbi.nlm.nih.gov/?term=Koss+KL&cauthor_id=8943944

4:43:00 Attorney Tom Renz:

He has Dept of Defense Whistleblowers with the data from the D-Med data base. They have taken data ‘snapshots’ over time and it shows THE DATA BASE WAS TAMPERED WITH TO HIDE THE INJURIES TO OUR SOLDIERS!
Senator Johnson Ordered PRESERVE YOUR RECORDS….

January 25, 2022 14:52
Apparently Daniel Horowitz chased down Attorney after the Ron Johonson Senate Hearing for some additional clarifications.
https://thelibertydaily.com/bombshell-cover-up-cancer-diagnoses-in-the-military-rose-over-three-fold-since-jabs-were-introduced/
para59r

5:05:00
Myocarditis and heart Hits 18 to 24 yr old males the worst. up to 50 years 21,000 cases so far.
A lot more good info.

Dr. Christina Parks made comments through out the presentation.

January 25, 2022 20:09
Yes – Dr. Christina Parks has made some excellent points about how differently people with African genetic background react to CV19 AND THE VACCINES.
Ethnicity does matter in medicine – my sister had concurrent dengue fever and malaria and her response was severe and peculiar to a certain ethnicity so….we learned may have some middle eastern/african blood somewhere previously unknown to us.
GA/FL

The Timeline of FDA Decisions

Heading down the Rabbit Hole on Vaccines that Dr Peter McCollough opened.

Emergency Use Authorization — FDA
As background, this gives the laws, who has the authority and the timeline.

TIME LINE:

October 13, 1976 – New York Times:
Swine Flu Program Is Halted in 9 States As 3 Die After Shots
“After the deaths, swine flu vaccinations were halted throughout Allegheny County, which includes Pittsburgh, and the Federal Center for Disease Control sent doctors to investigate….“

September 1, 2020 CNN
Past vaccine disasters show why rushing a Covid-19 vaccine now would be ‘colossally stupid’
This is actually a very good article on BAD vaccines and what it can do to the public’s trust.

And then we come to the FDA, the meetings and WHO is on the board.

October 22, 2020
Discussing, in general, the development, authorization and/or licensure of vaccines to prevent COVID-19

On October 22, 2020, the Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session, to discuss, in general, the development, authorization and/or licensure of vaccines to prevent COVID-19.
FDA

Those are probably the three boards Dr Peter McCollough talks about. The third was the FDA Vaccines and Related Biological Products Advisory Committee that hold these meetings. Note they are meeting just before the election and it contains ALL three boards.
….

These meetings are AFTER the STOLEN ELECTION but again all three advisory boards are present.

December 10, 2020
Discussing First Emergency Use Authorization Request for a COVID-19 Vaccine

On December 10, 2020, the Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session to discuss Emergency Use Authorization (EUA) of the Pfizer-BioNTech COVID-19 Vaccine for the prevention of COVID-19 in individuals 16 years of age and older.
FDA

December 17,2020

Discussing Second Emergency Use Authorization Request for a COVID-19 Vaccine

Agenda
The meeting presentations will be heard, viewed, captioned, and recorded through an online teleconferencing platform. On December 17, 2020, the Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) will meet in open session to discuss Emergency Use Authorization (EUA) of the Moderna, Inc., COVID-19 Vaccine for the prevention of COVID-19 in individuals 18 years and older.
FDA

December 15, 2020 updated December 18

The ACIP met last week to review the Pfizer-BioNTech vaccine and recommended moving forward with its distribution to anyone over age 16. The FDA issued an EUA on Saturday following the meeting and notified the CDC and Operation Warp Speed to coordinate distribution plans. Initial doses were shipped over the weekend. The first round of deliveries will be completed in all 50 states this week…
Pfizer’s initial distribution of vaccines will be given to 21 million health care workers and 3 million mostly elderly people living in long-term care facilities.
As vaccines are deployed, data on potential or delayed side effects will be collected to answer questions that would have been addressed in long-term trials with millions of participants under nonemergency circumstances….
Nat’l Conf. of State Legislators

December 14, 2020, 8:33 PM – Black nurse in New York, Sandra Lindsay, gets the first vaccine.

A month later we get the first Adverse Reaction Reports.
January 18, 2021 – Coronavirus: California calls for pause, investigation after Allergic Reactions to Moderna Vaccine

Biden is installed in the White House and the FDA/CDC does no real investigation. Instead NOTE THE CHANGE IN MEETING MINUTES.

February 26, 2021
Discussing Third Emergency Use Authorization Request for a COVID-19 Vaccine

Agenda
The meeting presentations will be heard, viewed, captioned, and recorded through an online teleconferencing platform. The committee will meet in open session to discuss EUA of the Janssen Biotech Inc. COVID-19 Vaccine for active immunization to prevent COVID-19 caused by SARS-CoV-2 in individuals 18 years and older. <== NO ADDITIONAL ADVISORY BOARDS!
Meeting Materials
FDA intends to make background material available to the public no later than 2 business days before the meeting. <== THIS IS THE INFORMATION people are having to SUE FOR!
FDA

Note there are NO MEETINGS TO DISCUSS DEATHS OR ADVERSE REACTIONS! This is the NEXT MEETING:

June 10, 2021

Discussing Pediatric Use of COVID-19 Vaccines

The Committee will meet in open session to discuss, in general, data needed to support authorization and/or licensure of COVID-19 vaccines for use in pediatric populations.
Meeting Materials
FDA intends to make background material available to the public no later than 2 business days before the meeting. If FDA is unable to post the background material on its website prior to the meeting….
FDA

Now we come to the meat, exactly who is at those meetings?

The VRBPAC Advisory Committee

The Committee reviews and evaluates data concerning the safety, effectiveness, and appropriate use of vaccines and related biological products which are intended for use in the prevention, treatment, or diagnosis of human diseases, and, as required, any other products for which the Food and Drug Administration has regulatory responsibility. The Committee also considers the quality and relevance of FDA’s research program which provides scientific support for the regulation of these products and makes appropriate recommendations to the Commissioner of Food and Drugs.
The Committee shall consist of a core of 15 voting members including the Chair. Members and the Chair are selected by the Commissioner or designee from among authorities knowledgeable in the fields of immunology, molecular biology, rDNA, virology; bacteriology, epidemiology or biostatistics, vaccine policy, vaccine safety science, federal immunization activities, vaccine development including translational and clinical evaluation programs, allergy, preventive medicine, infectious diseases, pediatrics, microbiology, and biochemistry.
FDA

Applying for Membership on FDA Advisory Committees

As part of the Food and Drug Administration’s (FDA’s) ongoing efforts to recruit qualified experts with minimal conflicts of interest who are interested in serving on FDA advisory committees, FDA is requesting nominations for members to serve on its advisory committees….
Conflicts of Interest:
Potential candidates are asked to provide detailed information concerning such matters as financial holdings, employment, and research grants and/or contracts in order to permit evaluation of possible sources of conflict of interest.
FDA

Oooh Boy, they do not sound good. I am digging up and placing here a lot of info on each individual. However I have screened out much much more. What struck me, is out of the sixteen only three do not have major expertise in pediatrics. ALL have ties to NIH/Fauxi or the FDA or the CDC. Some have ties to drug companies and more than one has ties to China. Most are women and three are foreign educated and probably not American born. Out of over 300 million people, you would think they could find Americans.

First a cameo of each of the players, and then if you wish you can look at some of the other information I dug out. If you click on the name it takes you to the information they provided to the FDA, often pages and pages citing the papers they wrote and who they worked for. This is the information I used with some added from other sources.

CAMEOS

DIRECTOR
Prabhakara Atreya, Female connected to Fauci She has no FDA bio.

Ph.D. biochemistry Memorial University of Newfoundland, in Canada 1987

Wayne State University, School of Medicine, Detroit, MI 1989 – 1990 (messing with fiber cell membranes of frog, chick, bovine, rabbit and human lenses)

Plant Pathology, University of Kentucky, Lexington KY – Papers 1990 &1995

FDA since 2010 per BIO but actually a paper shows she was working @ FDA in 1999.

NIH paper shows she was at NIH in 1998
Plant Pathology, University of Kentucky, Lexington KY – Papers 1990 &1995 (Only 13 papers found)

…..

Chair
Hana El Sahly, M.D.
Baylor College of Medicine (Woman)

Wrote paper on Remdesivir used by Fauci to trick President Trump. The one referred to by DR. McCullough

…..

Paula Annunziato, M.D. ***
Vice President and Therapeutic Area HeadVaccines Clinical ResearchMerck

Seems to specialize in Pediatric Vaccines.

Archana Chatterjee, M.D., Ph.D.
Dean Chicago Medical School (Woman)

specialises Pediatrics Vaccines

Pune University, Maharashtra, India 1979-1983

Army Medical Corps, Military Hospital, Gaya, India, 1985 -1988

She is nationally recognized for her work in vaccine development for human papilloma viruses – think Gardasil. I wonder how well acquainted she is with Gregg Sylvester, below & Bill Gates? – Controversial vaccine studies: Gates and Infertility

…….

CAPT Amanda Cohn, M.D.
Expertise: Pediatrics, Vaccines

Chief Medical Officer – National Center for Immunizations and Respiratory Diseases – CDC
The mission of the National Center for Immunization and Respiratory Diseases (NCIRD) is the prevention of disease, disability, and death through immunization

59 Scientific papers: many authored with Nancy E Messonnier

Time to check the Atlantia graveyards… And I am NOT kidding.

…..

Hayley Gans, M.D. (woman)
Expertise: Pediatrics, Infectious Diseases
Department of Pediatrics
Stanford University Medical Center

Author with a bunch of Chinese with FUNDING from China, using the bogus PCR test to say people who have recovered can catch Covid again and re-infect others. This is WHY natural immunity was never on the table and vaccines were.

….

Holly Janes, Ph.D.
Expertise: Biostatistics
Professor – Fred Hutchinson Cancer Research Center
Vaccine and Infectious Disease Division
Division of Public Health Sciences – Seattle, WA

Holly is a biostatistician working on the design and analysis of vaccine studies, with a particular expertise in HIV prevention and vaccine science. Worked for NIH and Bill & Melinda Gates Foundation.

…..

Michael Kurilla, M.D., Ph.D.
Expertise: Infectious Diseases, Pathology
Director, Division of Clinical Innovation National Center for Advancing Translation Sciences
National Institutes of Health (NIH <– He works for Fauci)
Bethesda, MD 20852

….

Myron Levine, M.D., D.T.P.H., F.A.A.P

Expertise: Infectious Diseases

Associate Dean for Global Health – Vaccinology and Infectious Diseases

Center for Vaccine Development – University of Maryland School of Medicine Baltimore, MD

Faculty at CVD have served in critical leadership roles in U.S. and international research and policy efforts. For example, Neuzil co-chaired the COVID-19 Prevention Trials Network, a research network established by the National Institute of Allergy and Infectious Diseases [ Dr. Fauci was appointed director of NIAID in 1984.] in response to the pandemic. Vaccine research at CVD continues, with an emphasis on reaching the populations most impacted by COVID-19 and testing pediatric vaccines.
University of Maryland

….

H. Cody Meissner, M.D. (Male)
Expertise: Infectious Diseases

Professor of Pediatrics – Tufts University School of Medicine
Director, Pediatric Infectious Disease

H. Cody Meissner, MD, is a leading national expert on childhood vaccinations who consults with the Centers for Disease Control and Prevention on periodic updates to the recommended immunization schedule for newborns through 18-year-olds. At Tufts Children’s Hospital at Tufts Medical Center he heads the Division of Pediatric Infectious Diseases…
H. Cody Meissner, MD, Vice Chair (’19)
H. Cody Meissner, MD | Tufts Medical Center

…..

Paul Offit, M.D.

Expertise: Infectious Diseases

Professor of Pediatrics, Division of Infectious Diseases, The Children’s Hospital of Philadelphia

Paul A. Offit, MD is the Director of the Vaccine Education Center at the Children’s Hospital of Philadelphia as well as the Maurice R. Hilleman Professor of Vaccinology and a Professor of Pediatrics at the Perelman School of Medicine at the University of Pennsylvania. He is a recipient of many awards including the J. Edmund Bradley Prize for Excellence in Pediatrics from the University of Maryland Medical School, the Young Investigator Award in Vaccine Development from the Infectious Disease Society of America, and a Research Career Development Award from the National Institutes of Health. Dr. Offit has published more than 160 papers in medical and scientific journals in the areas of rotavirus-specific immune responses and vaccine safety….
FDA

In 2017, Dr. Offit was a weekly columnist for The Daily Beast.

A look at his recent peer-reviewed papers shows he is targeting vaccine hesitant parents.

https://pubmed.ncbi.nlm.nih.gov/?term=Offit+PA&cauthor_id=24011750&size=20

This says it all:

Plotkin SA, Offit PA, Reiss D.: Important New Resource for Clinicians Giving Expert Witness Testimony on Vaccines. Pediatr Infect Dis J. 37(12), Dec. 2018.

To the Editors:

Vaccination is under attack by individuals who occasionally use the legal system to oppose mandatory vaccination laws and in some cases to obtain exemptions for particular children whose parents are opposed to vaccination. During the legal proceedings, as we have witnessed, experts testifying in favor of vaccination may be challenged with references from journals of doubtful quality that oppose vaccination.
To provide important references that discuss and disprove claims made against vaccines, the Vaccine Education Center at the Children’s Hospital of Philadelphia has created a library of references addressing certain safety issues that may be useful as an aid and refresher to clinicians giving expert testimony on the safety of vaccines and to lawyers defending vaccination of children.
The Children’s Hospital of Philadelphia legal library may be entered through the web address vaccine.chop.edu/safety-references.
We would be grateful if you could inform your colleagues about the availability of this resource, which should be of great value for experts testifying for vaccination and for clinicians who need to convince parents about vaccine safety. https://journals.lww.com/pidj/Fulltext/2018/12000/Important_New_Resource_for_Clinicians_Giving.42.aspx
The Pediatric Infectious Disease Journal

………..

Steven Pergam, M.D.
Expertise: Infectious Diseases
Medical Director
Infection Prevention
Seattle Cancer Care Alliance — Seattle, WA

He seems to specialize in cancer and immuno-compromised and seems to be the best of a bad bunch, until you see he is tied at the hip to NIH & CDC from 2009 to present as well as to various drug companies.

….

Jay Portnoy, M.D.

Expertise: Consumer Representative (This is the guy representing the public)

Professor of Pediatrics

Medical Director of Telemedicine Section of Allergy, Asthma and Immunology

Children’s Mercy Hospital Kansas City, MO

150 papers mainly on allergies. American College of Allergy, Asthma & Immunology – “…a professional medical association of more than 6,000 allergist-immunologists and allied health professionals…” AND if you search long enough…. You find the American College of Allergy, Asthma & Immunology wrote an Article urging allergists to support more funding for NIH (Fauci)

He is also on a Task Force Paper recommending those with severe egg allergies to go ahead and get the Flu vaccine, just do it at the allergist because “… personnel to recognize and equipment to treat anaphylaxis need to be immediately available…”

….

Andrea Shane, M.D., M.P.H., M.Sc.

Expertise: Pediatric & Infectious Diseases

Professor of Pediatrics, Director Division of Pediatric Infectious Diseases – Emory University School of Medicine – Atlanta, GA

International exchange fellowship, Children’s Hospital at Montefiore and Beijing Children’s Hospital, Beijing, China October-November, 1999

Lieutenant Commander, United States Public Health Service, 2001-2003;

Inactive Reserve Corps (IRC) 2003-until IRC dissolved in 2010.

Centers for Disease Control and Prevention, Advisory Committee on Immunization Practices (ACIP) respiratory syncytial virus (RSV) immunoprophylaxis working group, appointed member, 2009-until committee dissolved by CDC in 2011.

01 August 2007- 01 August 2016 Co- investigator, NIH/NIAID/DMID Vaccine and Treatment Evaluation Unit (VTEU)

influenza vaccine to breastfeeding women trial, DMID#09-007;

…..

Paul Spearman, M.D.
Expertise: Pediatric & Infectious Diseases

Director, Division of Infectious Diseases
Albert B. Sabin Chair in Pediatric Infectious Diseases
Cincinnati Children’s Hospital Medical Center
Professor, Department of Pediatrics
University of Cincinnati School of Medicine Cincinnati, OH

This guy is a really big heavy weight.

There is cross-over with the lady above, Andrea Shane. Any bets he pulled her in to be his ‘female puppet’ – a good little government soldier?

03/2009-09/2016: Vice Chair for Research Department of Pediatrics Emory University School of Medicine

03/2009-09/2016: Chief Research Officer Children’s Healthcare of Atlanta Atlanta, GA

[Andrea Shane is Attending Pediatrician Children’s Healthcare of Atlanta Emory Healthcare Grady Health 2006 – present ]

This guy has a full page of COMMITTEE MEMBERSHIPS, National and International, and a whole section for NIH Councils and Study Sections AND… NIH/NIAID HIV Vaccine Trials Network – Protocol Chair, HVTN 088 Protocol 2010-present

Not to mention his connections to the drug companies and China.

………

Geeta K. Swamy, M.D.
Expertise: Infectious Diseases
Senior Associate Dean Vice Chair for Research & Faculty Development
Associate Professor, ObGyn, Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine
Duke University, Durham, NC

2004 – 2006 Duke University Associate Faculty Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine & Division of Clinical & Epidemiological Research

2009 – present Duke University Vaccine Trials Unit Investigator Duke Translational Research Institute Durham, NC

Grants from, NIH-NIAID, GlaxoSmithKline, CDC-NCIRD, ACOG/Merck & Company,

2015

Consultative Workshop: Immunology Research Gaps Related to Maternal Immunization – Bill & Melinda Gates Foundation

WHO Brighton Collaboration Global Alignment of Immunization Safety Assessment in Pregnancy – Chair, Fetal Distress Working Group

…

Gregg Sylvester, M.D., M.P.H. +
Expertise: Alternate Industry Representative
Vice President – Medical Affairs, Seqirus Inc., Summit, NJ

• Launched Pfizer’s Pediatric and Adult Pneumococcal conjugate vaccine,

Spearheaded science-based rationale to preserve Pfizer’s Prevnar 13 infant schedule in US recommendations

• Launched Merck’s HPV4 vaccine in over 100 countries

• Partnered with community organizations in Delaware to reduce infant mortality, teen pregnancy rates and HIV rates

Created the medical affairs strategy for Merck’s HPV4 vaccine, Gardasil

….

Vaccine Approval For Children

Now, if you have time & stomach, a deeper dive into the people who unleashed the Clot Shot on babies.

DIRECTOR
Prabhakara Atreya, Ph.D.
Division of Scientific Advisors & Consultants
Center for Biologics Evaluation & Research
Food and Drug Administration – Silver Spring, MD

Dr. Prabhakara Atreya, an Indian American scientist is a 10 year veteran at the US Food and Drug Administration which she joined in 2010. Prior to this appointment, Atreya worked at the National Institutes of Health, leading the Office of Scientific Review. She has a PhD in biochemistry, biophysics and molecular biology from the Memorial University of Newfoundland, in Canada. She was one of the team of US regulators and independent experts of Vaccines and Related Biological Products Advisory Committee (VRBPAC). At the time of emergency use authorization for Pfizer’s Covid-19 vaccine, she was the Acting Designated Federal Officer of VRBPAC.
LINKED-IN

Thesis:
Atreya, Prabhakara Lakshmi (1987) Conformational aspects of proline hydroxylation in collagen biosynthesis : studies with synthetic peptides. Doctoral (PhD) thesis, Memorial University of Newfoundland.

Probable Papers (13):
Affiliation: Department of Plant Pathology, University of Kentucky, Lexington
I think this paper is what Fauci Spotted:
Construction of in-frame chimeric plant viral genes by simplified PCR strategies.
Atreya CD, Atreya PL, Pirone TP. Plant Mol Biol. 1992 Jun;19

Site-directed mutations in the potyvirus HC-Pro gene affect helper component activity, virus accumulation, and symptom expression in infected tobacco plants.
Atreya CD, Atreya PL, Thornbury DW, Pirone TP.Virology. 1992 Nov

Mutational analysis of the coat protein N-terminal amino acids involved in potyvirus transmission by aphids.
Atreya PL, Lopez-Moya JJ, Chu M, Atreya CD, Pirone TP.J Gen Virol. 1995 Feb;76
…
Her papers then show a move to NIH
Affiliation: Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892-0720, USA.
The NS1 protein of human respiratory syncytial virus is a potent inhibitor of minigenome transcription and RNA replication.
Atreya PL, Peeples ME, Collins PL.J Virol. 1998 Feb;

And then the move to FDA.
Affiliation: Laboratory of Pediatric and Respiratory Viral Diseases, DVP/CBER, Food and Drug Administration, Bethesda, MD 20892, USA.
Respiratory syncytial virus strain A2 is resistant to the antiviral effects of type I interferons and human MxA.
Atreya PL, Kulkarni S.Virology. 1999 Sep 1; (@ FDA)

Role of type I IFNs in the in vitro attenuation of live, temperature-sensitive vaccine strains of human respiratory syncytial virus.
Loveys DA, Kulkarni S, Atreya PL.Virology. 2000 Jun

……..
Her resume STINKS! She has three papers on human respiratory syncytial virus, and a bunch of early papers on cloning and tinkering with plants @ Univ Kentucky and earlier papers messing with fiber cell membranes of frog, chick, bovine, rabbit and human eye lenses @ Wayne State Univ, MI NOTHING ELSE except the Sex Card, Race Card and probably not American born.
……..

These are her picks:

CHAIR:
Hana El Sahly, M.D.
Baylor College of Medicine
May 18, 2020
Hana El Sahly on Remdesivir and the NIH’s Adaptive COVID-19 Treatment Trial (Well that answers WHO set up elders for DEATH!)

On May 15, Texas Monthly reported on their conversation with Dr. Hana El Sahly of Houston’s Baylor College of Medicine. In the coming days, she will begin registering hospitalized participants at Baylor St. Luke’s Medical Center and Ben Taub Hospital for the second phase of the National Institutes of Health’s Adaptive COVID-19 Treatment Trial, or ACTT. She’s Baylor’s lead investigator for participation in the program, which in its first phase analyzed a randomized, controlled trial designed to evaluate the safety and efficacy of the investigational antiviral remdesivir. Preliminary findings suggested that patients treated with remdesivir recovered faster than patients who received a placebo, which led to the May 1 announcement that remdesivir would be the first medication to receive FDA authorization for emergency use for COVID-19.
“We found that for patients who have COVID-19 pneumonia bad enough to get them to the hospital, treatment with remdesivir expedites the time to recovery by an average of four days per patient,” says El Sahly…
Hana El Sahly, M.D.

Education

Undergraduate education American University of Beirut, Lebannon Bachelor of Science, 1987-1990Medical education American University of Beirut, Lebannon School of Medicine, Doctor of Medicine, 1990-1994

Scientific Papers (46)

Several presentations on “HIV vaccines”
Fauci must love her:

Review Panels, Committees
Member, Safety Monitoring Committee, National Institutes of Health-sponsored vaccine clinical trial 05-0011; 2006
Reviewer, Loan Repayment Program, National Institute of Allergy and Infectious Diseases, National Institutes of Health; 2008
Member, Safety Monitoring Committee, National Institutes of Health-sponsored vaccine clinical trial 08-0009; 2009
Reviewer, Scientific Review Program, National Institute of Allergy and Infectious Diseases; 2010
Member, Data Safety Monitoring Board, Protein Sciences Corporation vaccine clinical trial PSC-22; 2010
Member, Safety Monitoring Committee, National Institutes of Health–sponsored study DMID 10-0043; 2011
Member, Safety Monitoring Committee, National Institutes of Health-sponsored study DMID 11-0007; 2011
Reviewer, Scientific Review Program, National Institutes of Health, P01 application “Towards A Universal Influenza Vaccine”; 2012
Member, Safety Monitoring Committee, National Institutes of Health sponsored study DMID 13-0087; 2014
Member, Publications Committee, Infectious Diseases Society of America; 2014-2017
Member, Safety Monitoring Committee, Mercia Pharma Inc-sponsored study NOVA MAS-1; 2015
Member of the Food and Drug Administration Vaccine and Related Biological Advisory Committee; 2016–
Reviewer, Influenza pre-applications, US Army Medical Research and Materiel Command-Congressionally Directed Medical Research Programs, 2016
WHAT THE HECK IS THIS!! => Member, ID week program planning committee, 2017-2019

Is this her daughter: Dr. Hana Mohammed Elsahly, MD 28, practicing in Houston, TX?
……

Paula Annunziato, M.D. ***
Vice President and Therapeutic Area Head
Vaccines Clinical Research
Merck
Seems to specialize in Pediatric Vaccines.
Nuv said…

…..

Archana Chatterjee, M.D., Ph.D.
Dean Chicago Medical School
Vice President for Medical Affairs
Rosalind Franklin University of Medicine and Science
M.B.B.S. (Equivalent to M.D.): Pune University, Maharashtra, India 1979-1983
Army Medical Corps, Military Hospital, Gaya, India, 1985 -1988
Major Scientific Interest: Vaccine development. She forgets to mention her main trial target is infants.

Principal Investigator: Recent Research Projects/Grants
GSK = GlaxoSmithKlinePled Guilty and Pay $3 Billion to Resolve Fraud Allegations & Failure to Report Safety Data – July 2012
(Nice people she worked for.)

Date: 2018-2019 Sponsor: Department of Health and Human Services, Administration For Community Living

Date: 2018-2020 Sponsor: Pfizer A Phase 2, Randomized,Trial ….Pneumococcal Conjugate Vaccine in Healthy Infants.

Date: 2018-2020 Sponsor: GSK …Study to Assess the Safety & Immunogenicity of Meningococcal Vaccine & 1 Pneumococcal Vaccine when Administered Concomitantly with Routine Vaccines to Healthy Infants.

Date: 2018-2020 Sponsor: GSK … dose-escalation study to evaluate safety, reactogenicity and immunogenicity of GSK Biologicals’ respiratory syncytial virus (RSV) investigational vaccine based on the RSV viral proteins F, N and M2-1 encoded by chimpanzee-derived adenovector.. when administered… to RSVseropositive infants aged 12 to 23 months.

Date: 2017-2019 Sponsor: MedImmune ….Study to Evaluate the Safety and Efficacy of MED18897, a Monoclonal Antibody With an Extended Half-life Against Respiratory Syncytial Virus, in Healthy Preterm Infants. [Are they going to give the infants the RSV?]

Date: 10/2015-10/2017 Sponsor: Merck…, Study to Evaluate the Safety, Tolerability, and Immunogenicity of Different Formulations of V114 [15-valent pneumococcal conjugate vaccine ] in Healthy Adults and Infants.

Date: 10/2015-10/2016 Sponsor: Astra Zeneca An observational study of RSV hospitalization in preterm infants.

Date: 9/2014-2017 Sponsor: GSK … multinational study … of GSK Biologicals’ MMR vaccine (209762)… compared to Merck (M-M-R®II or VaxPro), as a first dose, both co-administered with Varivax, Havrix (all subjects) and Prevnar 13 (US subset) in healthy children 12 to 15 months of age.

Peer-Reviewed Articles (120)

Appointments:
2020 – Invited to serve on NIH (NCI) Special Emphasis Panel to evaluate grant applications received in response to the RFA(s) with primary focus on HIV-Associated Malignancy Research

2019 to present – Invited to serve as and appointed a member on the Vaccines and Related Biological Products Advisory Committee (VRBPAC) of the United States Food and Drug Administration (US FDA)

2012 -2019 – Consultant to the US FDA

2014 – Merck Vision 2027 Expert Input Forum on Vaccine Policy

2008 – 2012 – Member, Anti Infective Drug Advisory Committee (AIDAC), Center for Drug Evaluation and Research, US FDA

2008 -2012 – Invited to serve on the National Vaccine Advisory Boards for Merck, GlaxoSmithKline and Novartis Pharmaceutical Companies

2008– Merck Vaccination Service Award, recognition of commitment to improving public health through vaccination.

2006 – Invited member, Sanofi-Pasteur, MedImmune, Abbott Pharmaceutical Companies’ National Advisory Boards

2003 – Invited Session Chair at an International Symposium organized by the Merieux Foundation entitled, “Vaccination in Tomorrow’s Society – New Information Pathways”. Annecy, France

Merieux Foundation …. AND THAT GETS INTERESTING…. WIKI

In October 2004, the FM was the beneficiary of a Franco-Chinese agreement that led to the creation of the Institut Pasteur de Shanghai.…
In 2012, the FM continued its partnership with the Chinese Academy of Medical Sciences.
In 2015, the CAMS-FM partnership founded the Christophe Mérieux Laboratory (CML) at the Institute of Pathogen Biology in Beijing to focus on the study pneumonia and tuberculosis. Researchers at the CML “benefit from and training modules developed by the Emerging Pathogens Laboratory in Lyon”,[5][6] a BSL-4 lab which was also built by the FM in 1999 and since 2005 is now operated by INSERM.[7]
In 2015, the FM participated in the donation by the French government of CIRI’s Biosafety Level 4 expertise to the Wuhan Institute of Virology.
In January 2017, a researcher who was financed by the CAMS-FM partnership participated in a study of human rhinovirus and genotype A21…..
https://en.wikipedia.org/wiki/Fondation_M%C3%A9rieux
WIKI

“Mentorship and sponsorship of faculty and learners has been a hallmark of Dr. Chatterjee’s entire thirty- year career in academic medicine…” LINK [I am sure she has been kissing FauXi’s ass for years to get funding.]
MORE:

….Board certified in general pediatrics and pediatric infectious diseases, she is nationally recognized for her work in vaccine development for human papilloma viruses and in antibiotic resistance. She has completed more than 100 clinical trials and published more than 50 peer-reviewed articles, 23 invited review articles, 17 book chapters and one book.
The first woman and person of color to serve as dean of CMS, Dr. Chatterjee, a native of India, earned her medical degree from the Armed Forces Medical College at Pune University in India and her PhD from the University of Nebraska Medical Center (UNMC) in Omaha….
https://www.rosalindfranklin.edu/news/rfu-announces-selection-of-new-dean-for-chicago-medical-school/

…..

CAPT Amanda Cohn, M.D.
Expertise: Pediatrics, Vaccines
Chief Medical Officer
National Center for Immunizations and Respiratory Diseases
Centers for Disease Control and Prevention

Immunization and Respiratory Diseases (NCIRD) MISSION | CDC
The mission of the National Center for Immunization and Respiratory Diseases (NCIRD) is the prevention of disease, disability, and death through immunization and by control of respiratory and related diseases.
CDC

POSTGRADUATE TRAINING 2004 – 2006 Epidemic Intelligence Service, CDC, Atlanta, GA
WORK EXPERIENCE :
3/2019-present Chief Medical Officer (Acting), Vaccine Policy, Preparedness, and Global Health, Office of the Director, NCIRD, CDC
11/2015-present Executive Secretary, ACIP and Senior Advisor, Vaccines Office of the Director, NCIRD, CDC
5/2014-11/2015 Deputy Division Director, Immunization Services Division, NCIRD, CDC
01/2013-05/2014 Acting Epidemiology Team Lead Meningitis and Vaccine Preventable Diseases, DBD, NCIRD, OD
06/2006-12/2012 Medical Officer, Epidemiology Team Meningitis and Vaccine Preventable Diseases, Division of Bacterial Disease, NCIRD, CDC
07/2004-06/2006 Epidemic Intelligence Service (EIS) Officer, Epidemiology Program Office Centers for Disease Control and Prevention, Atlanta, GA Assigned to: Bacterial Vaccine Preventable Diseases Branch, National Immunization Program

Scientific papers: 59 many authored with Nancy E Messonnier
Great titles like:

Multistate Outbreak of Respiratory Infections Among Unaccompanied Children, June 2014-July 2014.
Conclusions: This respiratory disease outbreak was due to multiple pathogens, including Streptococcus pneumoniae serotype 5 and influenza viruses. Pneumococcal and influenza vaccinations prevented further transmission. Future efforts to prevent similar outbreaks will benefit from use of both vaccines. https://pubmed.ncbi.nlm.nih.gov/27001799/
[How about CLOSING THE DARN BORDERS!]
Understanding Factors Affecting University A Students’ Decision to Receive an Unlicensed Serogroup B Meningococcal Vaccine.
Compliance with recommendations and opportunities for vaccination at ages 11 to 12 years: evaluation of the 2009 national immunization survey-teen.
Adolescent immunizations and other clinical preventive services: a needle and a hook?
Immunizations in the United States: a rite of passage.
Attitudes, practices, and preferences of pediatricians regarding initiation of hepatitis B immunization at birth.
……

Hayley Gans, M.D.
Expertise: Pediatrics, Infectious Diseases
Professor of Pediatrics
Department of Pediatrics
Stanford University Medical Center

Fellowship: Stanford University School of Medicine (1998) CA

Medical Education: State University of New York Syracuse Medical School Registrar (1991) NY
Board Certification: American Board of Pediatrics, Pediatric Infectious Diseases (1999)
Residency: Stanford University Medical Center (1994) CA
Internship: Stanford University Medical Center (1992) CA
M.D., SUNY at Syracuse, Medicine (1991)

Fellowship Program Director, Pediatric Infectious Diseases (2006 – 2017)

Co-director, Pediatric Infectious Diseases Program for Immunocompromised Hosts, Children’s Hospital at Stanford (2013 – Present)
Associate Fellowship Director, Pediatric Infectious Diseases, Stanford University Medical Center (2017 – Present)
Director, Fellowship Education, Department of Pediatrics, Stanford University Medical Center (2017 – Present)

Sort of BLAAaaaah until you look at this paper:

Remember her focus is kids.

July 2020 Lancet preprint.
Kinetics of SARS-CoV-2 Positivity of Infected and Recovered Patients: A Single Center COVID-19 Experience and Potential Implications https://autopapers.ssrn.com/sol3/papers.cfm?abstract_id=3605268

Jia Huang – Southern University of Science and Technology CHINA and 42 other authors with only 7 others not Chinese. The other universities were Sichuan University, China and Sanford.

https://autopapers.ssrn.com/sol3/cf_dev/AbsByAuth.cfm?per_id=4257785

And then it REALLY GETS GOOD:

FUNDING STATEMENT: This work was supported by grants from Sanming Project of Medicine in Shenzhen (Jia Huang, No. SZSM201812065); Bill & Melinda Gates Foundations (Lei Liu); and from National Natural Science Foundation of China (Jia Huang, No. 81501651)

DECLARATION OF INTERESTS: The authors declare no competing interests.

ETHICS APPROVAL STATEMENT: This study was approved by the Ethics Committee of the Second Affiliated Hospital of Southern University of Science and Technology.[CHINA]

Abstract

BACKGROUND: Recurrence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) positive detection in infected but recovered individuals has been reported. Patients who have recovered from coronavirus disease 2019 (COVID-19) could profoundly impact the health care system if a subset were to be polymerase chain reaction (PCR)-positive again with reactivated SARS-CoV-2. We sought to define the kinetics and relevance of PCR-positive recurrence during recovery from acute COVID-19 to better understand risks for prolonged infectivity and reinfection.

METHODS: A series of COVID-19 414 patients, at The Second Affiliated Hospital of Southern University of Science and Technology in Shenzhen, China from January 11 to April 23, 2020. Univariable and multivariable statistical analysis of inpatient data were performed to develop an algorithm to predict patients at risk of recurrence of PCR positivity.
[REMEMBER PCR TESTS RETURN MAJOR FALSE POSITIVES – Reiner Fuellmich say this guy Droston isn’t a Doctor at all, but a bull**** artist. Christian Drosten & the Fraud Behind COVID 19 PCR Testing ]
FINDINGS: 16·7% recovered patients with PCR positive recurring one to three times, despite being in strict quarantine. Younger patients with mild pulmonary respiratory syndrome had higher risk of PCR positivity recurrence. The recurrence prediction model had an area under the ROC curve of 0·786.

INTERPRETATION: This case series provides clinical characteristics of recovered COVID-19 patients with recurrent SARS-CoV-2 positivity, despite strict quarantine, at a 16·7% rate. Use of a recurrence prediction algorithm may identify patients at high risk of recurrent SARS-CoV-2 positivity and help understand reactivation and reinfection possibilities to establish protocols for health policy.
LANCET

This is a very important paper because it REFUTES NATURAL IMMUNITY and green lights MORE DRACONIAN ECONOMY KILLING ‘Health Measures’

……

Holly Janes, Ph.D.
Expertise: Biostatistics
Professor — Fred Hutchinson Cancer Research Center
Vaccine and Infectious Disease Division
Division of Public Health Sciences – Seattle, WA

Dr. Holly Janes is a biostatistician working on the design and analysis of vaccine studies, with a particular expertise in HIV prevention and vaccine science. She also develops and applies statistical methodology for evaluating biomarkers for risk prediction and optimizing treatment decisions

Current Projects

Leadership for the Statistical Data Management Center of the HIV Vaccine Trials Network

Statistical methods for HIV prevention efficacy trials

Statistical methods for human challenge studies

Statistical evaluation of biomarkers for making treatment decisions https://www.fredhutch.org/en/faculty-lab-directory/janes-holly.html

HONORS, AWARDS, SCHOLARSHIPS:

2008 Travel Award, AIDS Vaccine Conference, Global HIV Vaccine Enterprise

2000 Cardiovascular Biostatistics Training Grant, National Institutes of Health

EDITORIAL RESPONSIBILITIES:

Associate Editor Journal of the National Cancer Institute (2015-2018)

Diagnostic and Prognostic Research (2016-present)

Statistical Communications in Infectious Diseases (2019-present)

RESEARCH FUNDING:

Active Funding:

2 UM1 AI068635 (PI: Gilbert P) 01/01/2014 – 11/30/2020 5.4 Calendar NIH/NIAID SDMC HIV Vaccine Trials Network

2 R01 CA152089 (PI: Janes H) 07/01/2010 – 11/30/2021 4.8 Calendar

NIH/NCI

Statistical Methods for Evaluating Markers for Treatment Selection

Interventions for disease treatment and prevention can potentially be made more cost-effective by using markers to identify in advance the individuals most likely to benefit from the treatment, and thus avoid treating those unlikely to benefit. [Rationed Health Care anyone?]

Lots more Mostly NIH and then this goodie:

38744 7/1/2006-4/30/2012

Bill & Melinda Gates Foundation

Vaccine Immunology Statistical Center (VISC) The VISC will provide 1) statistical and study design support for pre-clinical vaccine performance trials, 2) centralized data management services for the standardized evaluation of vaccine candidates, 3) development of new statistical methods for cross-species correlates-of-protection analysis.

Role: Faculty Statistician

BIBLIOGRAPHY Publications in Refereed Journals

1. Pepe MS, Janes H, Longton G, Leisenring W, Newcomb P. Limitations of the odds ratio in gauging the performance of a diagnostic, prognostic, or screening marker. Am J Epidemiol. 2004;159(9):882-90.

2. Janes H, Pepe M, Kooperberg C, Newcomb P. Identifying target populations for screening or not screening using logic regression. Stat Med. 2005;24(9):1321-38.

12. McElrath MJ, De Rosa SC, Moodie Z, Dubey S, Kierstead L, Janes H, Defawe OD, Carter DK, Hural J, Akondy R, Buchbinder SP, Robertson MN, Mehrotra DV, Self SG, Corey L, Shiver JW, Casimiro DR. HIV-1 vaccine-induced immunity in the test-of-concept Step study: A casecohort analysis. Lancet. 2008;372(9653):1894-905. PMCID: 2774110.

13. Pepe MS, Feng Z, Janes H, Bossuyt PM, Potter JD. Pivotal evaluation of the accuracy of a biomarker used for classification or prediction: Standards for study design. J Natl Cancer Inst. 2008;100(20):1432-8. PMCID: 2567415.

21. Barnabas RV, Wasserheit JN, Huang Y, Janes H, Morrow R, Fuchs J, Mark KE, Casapia M, Mehrotra DV, Buchbinder SP, Corey L. Impact of herpes simplex virus type 2 on HIV-1 acquisition and progression in an HIV vaccine trial (the Step study). J Acquir Immune Defic Syndr. 2011;57(3):238-44. PMCID: 3446850.

22. Fitzgerald DW, Janes H, Robertson M, Coombs R, Frank I, Gilbert P, Loufty M, Mehrotra D, Duerr A. An Ad5-vectored HIV-1 vaccine elicits cell-mediated immunity but does not affect disease progression in HIV-1-infected male subjects: Results from a randomized placebo-controlled trial (the Step study). J Infect Dis. 2011;203(6):765-72. PMCID: 3119328.

And many more. I am sure Fauci loves her.

……

Michael Kurilla, M.D., Ph.D.
Expertise: Infectious Diseases, Pathology
Director, Division of Clinical Innovation
National Center for Advancing Translation Sciences
National Institutes of Health

National Center for Advancing Translational Sciences

The National Center for Advancing Translational Sciences (NCATS) is one of 27 Institutes and Centers at the National Institutes of Health (NIH). The focus of NCATS is to advance the science of translation, which is the process of turning observations into interventions to improve health.
National Center for Advancing Translation Sciences

……

Myron Levine, M.D., D.T.P.H., F.A.A.P
Expertise: Infectious Diseases

Simon & Bessie Grollman Distinguished Professor
Associate Dean for Global Health
Vaccinology and Infectious Diseases Center for Vaccine Development
University of Maryland School of Medicine

Center for Vaccine Development and Global Health – UMB …

University of Maryland School of Medicine

For more than a year, researchers at the Center for Vaccine Development and Global Health (CVD) at the University of Maryland School of Medicine (UMSOM) have been working tirelessly on COVID-19 research, helping to pave the way for the use of vaccines and therapies that are being administered across the country.
Under the leadership of CVD director Kathleen Neuzil, MD, MPH, FIDSA, the Myron M. Levine, MD, DTPH, Professor in Vaccinology at UMSOM, researchers quickly pivoted decades of vaccine and infectious disease research experience toward combating this deadly virus, which continues to impact millions of people around the world.
Faculty at CVD have served in critical leadership roles in U.S. and international research and policy efforts. For example, Neuzil co-chaired the COVID-19 Prevention Trials Network, a research network established by the National Institute of Allergy and Infectious Diseases [NIAID Dr. Fauciwas appointed director of NIAID in 1984.] in response to the pandemic. Vaccine research at CVD continues, with an emphasis on reaching the populations most impacted by COVID-19 and testing pediatric vaccines.
CVD experts have launched an expansive grassroots campaign to educate the community and reach those who have been hit the hardest by this terrible virus, including members of the Black and Brown communities, the elderly, and those with underlying health risks.
“Our CVD team has worked tirelessly and meticulously to advance COVID-19 vaccines and to ensure they are reaching the most affected populations,” Neuzil said. “Our work continues as we begin testing vaccines in children and investigate booster vaccines to address the risk of COVID-19 variants.” [Like this Dude is neutral?]

Center for Vaccine Development and Global Health (CVD …

Our research, surveillance and vaccine development focuses on four key areas: Enteric Diseases, Malaria, Influenza and Respiratory Diseases, and Emerging Pathogens.
Overview
Our faculty and staff are experts in the field of global health and vaccinology, and they are dedicated to improving global health by conducting innovative, world-leading research in Baltimore and around the world. Our key mission is to harness the power of vaccines to prevent disease and save lives in the most vulnerable populations.

…….

H. Cody Meissner, M.D.
Expertise: Infectious Diseases
Professor of Pediatrics
Tufts University School of Medicine
Director, Pediatric Infectious Disease
Tufts Medical Center
POST GRADUATE TRAINING

1973 – 1975 Internship and Residency Boston Floating Hospital New England Medical Center Boston, MA

1975 – 1977 Research Associate Public Health Service National Institute of Child Health and Human Development National Institute (NICHD) Bethesda, MD Parent Agency is National Institutes of Health (Fauci)

2008 – Present Advisory Committee on Immunization Practices (ACIP) Centers for Disease Control and Prevention (CDC)

2010 – Present Massachusetts Vaccine Purchasing Advisory Council

2017 – Present National Vaccine Advisory Committee, United States Department of Health and Human Services

2017 – Present Vaccine Injury Compensation Program, United States Department of Health and Human Services

AWARDS

Massachusetts 2017 Recipient of the CDC Childhood Immunization Award

The National Vaccine Injury Compensation Program: Striking a Balance Between Individual Rights and Community Benefit.

Meissner HC, Nair N, Plotkin SA. JAMA. 2019 Jan 29

The Importance of MMR Immunization in the United States.

Perrone O, Meissner HC. Pediatrics. 2020 Aug

Principles of Vaccine Licensure, Approval, and Recommendations for Use.

Pickering LK, Meissner HC, Orenstein WA, Cohn AC. Mayo Clin Proc. Epub 2020 Feb 13.

H. Cody Meissner, MD | Tufts Medical Center

H. Cody Meissner, MD, is a leading national expert on childhood vaccinations who consults with the Centers for Disease Control and Prevention on periodic updates to the recommended immunization schedule for newborns through 18-year-olds. At Tufts Children’s Hospital at Tufts Medical Center he heads the Division of Pediatric Infectious Diseases

….

Paul Offit, M.D.
Expertise: Infectious Diseases
Professor of Pediatrics
Division of Infectious Diseases
The Children’s Hospital of Philadelphia

Paul A. Offit, MD is the Director of the Vaccine Education Center at the Children’s Hospital of Philadelphia as well as the Maurice R. Hilleman Professor of Vaccinology and a Professor of Pediatrics at the Perelman School of Medicine at the University of Pennsylvania. He is a recipient of many awards including the J. Edmund Bradley Prize for Excellence in Pediatrics from the University of Maryland Medical School, the Young Investigator Award in Vaccine Development from the Infectious Disease Society of America, and a Research Career Development Award from the National Institutes of Health. Dr. Offit has published more than 160 papers in medical and scientific journals in the areas of rotavirus-specific immune responses and vaccine safety. He is also the coinventor of the rotavirus vaccine, RotaTeq, recommended for universal use in infants by the CDC….
FDA

In 2017, Dr. Offit was a weekly columnist for The Daily Beast.

Papers:

2018

Plotkin, S.A., P.A. Offit, and P. Bégué, : “Vaccine mandates in France will save lives,” Science 359: 283-284, 2018.

Plotkin SA, Offit PA, Reiss D.: Important New Resource for Clinicians Giving Expert Witness Testimony on Vaccines. Pediatr Infect Dis J. 37(12), Dec. 2018.

To the Editors:

Vaccination is under attack by individuals who occasionally use the legal system to oppose mandatory vaccination laws and in some cases to obtain exemptions for particular children whose parents are opposed to vaccination. During the legal proceedings, as we have witnessed, experts testifying in favor of vaccination may be challenged with references from journals of doubtful quality that oppose vaccination.
To provide important references that discuss and disprove claims made against vaccines, the Vaccine Education Center at the Children’s Hospital of Philadelphia has created a library of references addressing certain safety issues that may be useful as an aid and refresher to clinicians giving expert testimony on the safety of vaccines and to lawyers defending vaccination of children.
The Children’s Hospital of Philadelphia legal library may be entered through the web address vaccine.chop.edu/safety-references.
We would be grateful if you could inform your colleagues about the availability of this resource, which should be of great value for experts testifying for vaccination and for clinicians who need to convince parents about vaccine safety. https://journals.lww.com/pidj/Fulltext/2018/12000/Important_New_Resource_for_Clinicians_Giving.42.aspx

2017

Offit, P.A.: “Commentary: Science Denialism Isn’t New to the Trump Administration,” Philadelphia Inquirer December 22 2017.

Offit, P.A.: “By Regulating Homeopathic Remedies, FDA Holds ‘Modern-Day Snake-Oil Salesmen’ Accountable,“ Philadelphia Inquirer December 28 2017.

2013

Williams SE, Rothman RL, Offit PA. Schaffner W, Sullivan M, Edwards KM. A randomized trial to increase acceptance of childhood vaccines by vaccine-hesitant parents: a pilot study. Academic Pediatrics (2013) 13: 475-480.

A look at his recent papers shows he is targeting vaccine hesitant parents.

https://pubmed.ncbi.nlm.nih.gov/?term=Offit+PA&cauthor_id=24011750&size=20

…..

Steven Pergam, M.D.
Expertise: Infectious Diseases
Medical Director
Infection Prevention
Seattle Cancer Care Alliance — Seattle, WA

He seems to specialize in cancer and immuno-compromised and seems to be the best of a bad bunch. But then we look at this:

SPECIAL NATIONAL RESPONSIBILITIES:

2009–2010 Independent Safety Monitor, NIH/NIAD, DMID Influenza Protocols: 09-0039, 09-0043, 09-0047, 09-0053, and 09-0054: H1N1

2010–2011 Independent Safety Monitor, NIH/NIAID, DMID Protocol 09-0002: Comparison of the Safety and Immunogenicity of Lyophilized IMVAMUNE® (1×108 TCID50) versus Liquid Formulation IMVAMUNE® (1×108 TCID50) Administered by the Subcutaneous Route and a Lower Dose Liquid Formulation IMVAMUNE® (2×107 TCID50) Administered by the Intradermal Route in Healthy Vaccinia-Naïve Individuals (Bavarian Nordic)

2011–2013 Member, Data and Safety Monitoring Board: Effect of tenofovir on genital HSV shedding: a randomized, double-blind, placebo-controlled, clinical trial

2015-present Member, Zoster Working Group, Advisory Committee on Immunization Practices (ACIP), Centers for Disease Control and Prevention, Department of Health and Human Services

2016-present Member, Abstract Selection Committee, Association for Professionals in Infection Control and Epidemiology (APIC)

2016-2017 Independent Safety Monitor, NIH/NAID, DMID Protocol 16-0117: Comparison .of High vs. Standard Dose Flu Vaccine in Pediatric Stem Cell Transplant Recipients

15. RESEARCH FUNDING

Current: Washington Vaccine Alliance (WAVA) Pilot Award (PI: S. Pergam) 10/1/13-6/30/20 Interactions between gastrointestinal microbiota, Influenza vaccine responses and respiratory viral infections in a large cohort of clinic employees

BAA-NIAID [Fauxi Director]-DMID-NIH-AI (PI: M. Ison; Subcontract PI: Pergam) 5/1/16-4/30/20 Phase II Multi-Center, Prospective, Randomized, Double-Blind Study of Nitazoxanide in Acute and Chronic Norovirus in Hematopoietic Stem Cell and Solid Organ Transplant Recipients 1U01AI132004-NIAID (PI: N.Halasa; Subcontract PI: Pergam)

7/5/2017-6/30/20 High vs. Standard Dose Flu Vaccine in Adult Stem Cell Transplant Recipients 1R01AI134808-NIAID (PI: D. Fredricks)

Completed:

NIH/NIAID T32 AI007-044 (PI: W. Stamm) 9/1/05-2/1/07 Host Defense Training in Allergy and Infectious Diseases

Industry Sponsored Clinical Trials:

Chimerix, Inc. (PI: Pergam) 2016-current An Intermediate-size, Expanded Access Protocol to Provide Bincidofovir for the Treatment of Serious Adenovirus Infection or Disease, Protocol CMX001-35”

6/17/2017-present Prior Industry Trials Merck, Sharp & Dohme Co., Inc (PI: Pergam)

2012-2015 Pergam, SA – CV Page 15 A Phase III, Double-Blind, Randomized, Placebo-Controlled, Multicenter Clinical Trial to Study the Safety, Tolerability, Efficacy, and Immunogenicity of V212 in Recipients of Autologous Hematopoietic Cell Transplants (HCT)

Cubist Pharmaceuticals, Inc.* (PI: Pergam) 2013-2015 A Phase IIIb, Multi-Center, Double-Blind, Randomized, Placebo-Controlled Study to Demonstrate the Safety & Efficacy of Fidaxomicin for Prophylaxis against C difficile-Associated Diarrhea in Individuals Undergoing Hematopoietic Cell Transplants (HCT) *formerly Optimer pharmaceuticals

KRT16/26/21, 01:40 PM

$ACXP In December 2014, Merck ($MRK) paid US$9.5 billion for Cubist ($CBST) largely to obtain marketing access to agents daptomycin and fidaxomicin. https://stocktwits.com/symbol/CBST

Chimerix, Inc. (PI: Pergam) 2016 A Multicenter Non-Interventional Study to Obtain Retrospective Data for Subjects Previously Diagnosed with Adenovirus Infection to serve as Matched Historical Controls for Study CMX001-304; Protocol No. CMX001-305

Chimerix, Inc. (PI: Pergam) 2015 – 2017 A Phase 3, Open-label, Multicenter Study of the Safety/Tolerability and Efficacy of Brincidofovir (CMX001) for the Prevention of Adenovirus (AdV) Disease in Subjects with Asymptomatic AdV Infection at Risk of Progression and for the Treatment of Subjects with Localized or Disseminated AdV Disease

Chimerix, Inc.

All that shimmers isn’t … enhanced by lipid conjugate technology. Chimerix is a development-stage biopharmaceutical company, dedicated to accelerating the advancement of innovative for patients living with cancer and other serious diseases. Its two clinical-stage development programs include dociparstat sodium (DSTAT) and brincidofovir (BCV). DSTAT, is a glycosaminoglycan derivative of heparin with known anti-inflammatory properties and BCV is an oral antiviral in development for the treatment of smallpox.

2505 Meridian Pkwy Ste 100 Durham, NC,

https://www.dnb.com/business-directory/company-profiles.chimerix_inc.a1878daaef1b59d25a1d2e8876c4b4bf.html

Chimerix, Inc.’s key principal is Michael A Sherman. Chimerix, Inc. has 54 employees

https://wallmine.com/people/8557/michael-a-sherman

…..

Jay Portnoy, M.D.
Expertise: Consumer Representative (This the guy who is supposed to represent the interests of the Public.)
Professor of Pediatrics
Medical Director of Telemedicine Section of Allergy, Asthma and Immunology
Children’s Mercy Hospital Kansas City, MO

Offices and Board of Directors:

American Board of Allergy & Immunology (ABAI). 2014-present.

Vice President, American College of Allergy, Asthma & Immunology 2005-6.

Board of Directors, Black Healthcare Coalition. 2006-2009. [He is WHITE]

Editorships and Editorial Boards

Regional Editor, World Allergy Organization Journal. 2008 to 2012.

Section Editor, Annals of Allergy and Asthma. Appointed 2002 to 2005

Editor, Current Opinion on Allergy & Asthma. Issue on Pediatric Allergy. 2004 and 2005

Editor, Current Allergy and Asthma Reports. Issue on Pediatric Allergy. 2001-2013

Editorial Board, Allergy Watch. 1998-2001.

Editorial Board, Annals of Allergy and Asthma. 1994 to 2006

Editorial Board, Current Allergy Practice. 1993 to present

Other Appointments

FDA advisory panel (CBER), Allergenic Extracts.

2017-present FDA advisory panel (CDER). Respiratory and allergy drugs.

2010-present FDA advisory panel (CBER), Allergenic Extracts.

2005-2010 Special Emphasis Panel. T-cell Epitopes. NIAID. 2011.

https://www.fda.gov/media/105541/download

The guy has 151 papers mainly dealing with allergy so I am not going to look at all of them.

He seems to work with Environmental Allergens Workgroup. Also with American College of Allergy, Asthma & Immunology – “…a professional medical association of more than 6,000 allergist-immunologists and allied health professionals…” He is a Fellow, American Academy of Allergy, Asthma, and Immunology (AAAAI) …. if you search long enough…. You find an AAAAI Legislative Action article urging Allergists to support Fauci’s funding.

NIAID, NIEHS, NHLBI, MCAN Workshop Report: The Indoor Environment and Childhood Asthma: Implications for Home Environmental Intervention in Asthma Prevention and Management

The National Institute of Allergy and Infectious Diseases (NIAID), National Institute of Environmental Health Sciences (NIEHS), National Heart, Lung, and Blood Institute (NHLBI), and Merck Childhood Asthma Network (MCAN) sponsored a joint workshop to discuss the current state of the science with respect to the indoor environment and its effects…

Adverse reactions to vaccines practice parameter 2012 update

…..Thus although patients with a history of mild reactions to egg ingestion (hives only) can receive their vaccine in a primary care provider’s office, those with a history of more severe reactions (cardiovascular, respiratory, or gastrointestinal symptoms) should receive the influenza vaccine in an allergist’s office. In both cases, personnel to recognize and equipment to treat anaphylaxis need to be immediately available, but the allergist’s office affords additional expertise in this area should it be required…..
…..There has been a great deal of additional information published over the past year demonstrating the safety of influenza vaccination in patients with egg allergy. Health care providers should no longer withhold the vaccine from any patient with egg allergy. In an update to recommendations made in the last year, it is now considered safe for patients even with a history of a severe egg allergy to receive influenza vaccination…..

No worries, we will revive you when you almost die of anaphylaxtic shock, it is utmost importance for us to jab you with a shot that is probably useless so we can get paid our bonus.
…..

Andrea Shane, M.D., M.P.H., M.Sc.
Expertise: Pediatric & Infectious Diseases

Professor of Pediatrics
Director Division of Pediatric Infectious Diseases
Emory University School of Medicine – Atlanta, GA

Joint appointment:
Assistant Professor of Global Health Hubert Department of Global Health, Rollins School of Public Health, Emory University 01 September 2013-present

Military or Government Service: Lieutenant Commander, United States Public Health Service, 2001-2003; Inactive Reserve Corps (IRC) 2003-until IRC dissolved in 2010.
……
The United States Public Health Service is a collection of agencies of the Department of Health and Human Services concerned with public health, containing eight out of the department’s eleven operating divisions. The Assistant Secretary for Health oversees the PHS.
WIKI

ALSO:

OASH oversees the Department’s key public health offices and programs, a number of Presidential and Secretarial advisory committees, 10 regional health offices across the nation, and the Office of the Surgeon General and the U.S. Public Health Service Commissioned Corps. https://www.hhs.gov/ash/index.html
……

Centers for Disease Control and Prevention, Advisory Committee on Immunization Practices (ACIP) respiratory syncytial virus (RSV) immunoprophylaxis working group, appointed member, 2009-until committee dissolved by CDC in 2011.

Infectious Diseases Society of America (IDSA) National Global Public Health Committee (NGPHC), appointed member 2010-2013.

World Society of Pediatric Infectious Diseases (WSPID), Board Member and member of the Education Committee representing the Pediatric Infectious Disease Society (PIDS), appointed 2017; term through 2019.

[THIS IS WHERE SHE HAS A LOT OF POWER]
Manuscript reviewer:
American Journal of Infection Control, 2001-2003
Clinical Infectious Disease Journal, 2003-present
Journal of Infectious Diseases, 2003 – present
Pediatrics, 2006 – present
Journal of Pediatrics, 2006-present
The Pediatric Infectious Disease Journal, 2003-present
Infection Control and Hospital Epidemiology, 2003 – present
Archives of Pediatrics and Adolescent Medicine, 2006 – present
Emerging Infectious Diseases Journal, 2006 – present
Neonatology, 2008 – 2010
Journal of American Medical Association, 2009 – present
JAMA Pediatrics, 2013 – present
Journal of Pediatric Infectious Diseases, 2013-present
Pediatric Research 2017-present
Clinical Therapeutics, 2017-present
Faculty of 1000 (f1000), Public Health and Epidemiology section, post publication peer review of publications, 2009 -2011. [WTF???]
Pediatric Infectious Disease section with creation of the section, 2011-2014.

Honors and Awards:
International exchange fellowship, Children’s Hospital at Montefiore and Beijing Children’s Hospital, Beijing, China October-November, 1999

Department of Health and Human Services, Public Health Service Crisis Response Service Award, 2002

Department of Health and Human Services, Public Health Service Outstanding Unit Citation, 2002

National Foundation for Infectious Diseases (NFID) Advanced Vaccinology Course Travel Grant to attend ADVAC 9, Annecy, France, 2008

National Institute of Allergy and Infectious Diseases, Division of Microbiology and Infectious Diseases, Special Recognition, H1N1 influenza research, 2010

Center for Disease Control and Prevention, National Center for Emerging and Zoonotic Infectious Diseases Award for Excellence in Partnering-Domestic to NETEC (the National Ebola Training and Education Center)…. This award recognizes programs’ initiative and effectiveness through establishing and sustaining a strategic partnership with government, private sector, volunteer, or nonprofit organizations, 24 March 2016.

Contracts:

Co- investigator, NIH/NIAID/DMID Vaccine and Treatment Evaluation Unit (VTEU) – Emory University School of Medicine. Role: Site PI on rotavirus vaccine cross-over trial, DMID #08- 0017 and influenza vaccine to breastfeeding women trial, DMID#09-007; site co- investigator on other trials. Salary support, 01 August 2007- 01 August 2016….

………….

Paul Spearman, M.D.
Expertise: Pediatric & Infectious Diseases

Director, Division of Infectious Diseases
Albert B. Sabin Chair in Pediatric Infectious Diseases
Cincinnati Children’s Hospital Medical Center
Professor, Department of Pediatrics
University of Cincinnati School of Medicine Cincinnati, OH

This guy is a really big heavy weight. There is cross-over with the lady, Andrea Shane above. Any bets he pulled her in to be his ‘female puppet’ – a good little government soldier?

11/2005-09/2016: Professor and Division Director Nahmias-Schinazi Research Chair Pediatric Infectious Diseases Department of Pediatrics Emory University School of Medicine
11/2005-09/2016: Associate Director for Pediatric Studies Emory Vaccine Center Atlanta, GA
03/2009-09/2016: Vice Chair for Research Department of Pediatrics Emory University School of Medicine
03/2009-09/2016: Chief Research Officer Children’s Healthcare of Atlanta Atlanta, GA

[Andrea L. Shane is Attending Pediatrician Children’s Healthcare of Atlanta Emory Healthcare Grady Health 01 August 2006 – present ]

This guy has a full page of
COMMITTEE MEMBERSHIPS:
a. National and International:

NIH Councils and Study Sections Chair, NIH ZRG1 AARR-E (41)
December 2016 Member, NIH ZRG1 AARR-P (02)
December 2016 Chair, NIH SEP: ZRG1 AARR-K (02)M; AIDS and related research SEP
August 2016 Chair, NCI Board of Scientific Counselors, Site Visit Team, Review of HIV DRP, Frederick, MD
July 2016 Chair, NIH SEP: ZDE1; Approaches to Eliminate HIV and Opportunistic Pathogens from Oral Reservoirs
November 2015 Chair, NIH SEP: ZRG1 AARR-E; AIDS and AIDS-related
July 2015 Chair, NIH SEP: Basic Research on HIV Persistence
March 2015 Chair, NIH/NIDCR Review Panel on HIV and Oral
March 2015 Opportunistic Pathogens
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.
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NIH/NIAID HIV Vaccine Trials Network
Protocol Chair, HVTN 088 Protocol 2010-present
Chair, Chiron/Novartis Products Development Team 2000-2007
Chair, Wyeth Products Development Team 2001-2007 Protocol
Chair, HVTN 049 Protocol 2002-2007 Protocol
Chair, HVTN 056 Protocol 2002-2006 Protocol
Chair, HVTN 061 Protocol 2003-2005 Member, HVTN Phase I-II Committee 2002-2005 Protocol
Chair, HVTN 088 Protocol 2010-present
NIH/NIAID/DMID Vaccine and Treatment Evaluation Unit Co-Principal Investigator, Emory VTEU site 2007-present
Protocol Chair, VTEU 0008 Protocol 2009-2014
NIH/NICHD-Westat/NIAID IMPAACT Network Principal Investigator, Emory IMPAACT site 2014-present
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.
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CONSULTANTSHIPS:
Chiron, HIV Vaccines Development Team, Emeryville, CA 2003, 2004
Wyeth, HIV Vaccine Programs, Pearl River, NY 2003, 2004

EDITORSHIPS AND EDITORIAL BOARDS: [Again this is where a lot of power lies.]
Member of Editorial Board, Journal of Virology
Member of Editorial Board, Virology
Member of Editorial Board, Current HIV Research
Academic Editor, PLoS One

MANUSCRIPT REVIEWER: [There is that POWER again]
Journal of Virology (numerous, 1995-present)
Virology (numerous, 1998-present)
Current HIV Research (2001-present)
Ad Hoc reviewer, Biochemistry (2005, 2006)
Ad Hoc reviewer, Traffic (2005, 2006, 2007, 2013)
Ad Hoc reviewer, JAIDS (2004, 2011, 2012, 2013, 2014, 2015)
Ad Hoc reviewer, JBC (1997-present)
Ad Hoc reviewer, Leukocyte Biol (2000)
Ad Hoc reviewer, Vaccine (2000-2016)
Ad Hoc reviewer, Virus Research (2005, 2012, 2012, 2013)
Ad Hoc reviewer, Nature Structural Biology (2005)
Ad Hoc reviewer, PLOs Medicine (2006, 2007, 2008)
Ad Hoc reviewer, J Mol Biol (2007,2012, 2015, 2016)
Ad Hoc reviewer, PNAS (2007, 2008, 2009,2012, 2013, 2014)
Ad Hoc reviewer, JCB (2007, 2008, 2010, 2011,2012, 2013)
Ad Hoc reviewer, PLOs One (2008, 2009, 2010,2011,2012, 2013, 2014) 6
Ad Hoc reviewer, Cell Host and Microbe (2008-present)
Ad Hoc reviewer, Nature Medicine (2009, 2011,2012, 2016)
Ad Hoc reviewer, PLOs Pathogens (2009-present) Ad Hoc reviewer, J Immunology (2010, 2011, 2013) Ad Hoc reviewer, Retrovirology (2011-present)
.
.
GRANT SUPPORT:
a. Active Support

Federally funded:
NIH R01 AI058828: Role of Vpu in HIV Particle Assembly. Funded since 2004, currently in no-cost extension with competing renewal under review.
NIH R01 GM111027-17A1: Viral and Cellular Determinants of HIV-1 Assembly. Funded 9/16/2013-8/31/2017 (Principal Investigator). $200,000 initial period; $800,000 direct costs.
NIH R01AI11863: Mucosal Protection against HIV Generated by PIV5 Priming and VLP Boosting. Funded 4/01/2014-8/31/2018 (Principal Investigator, Multiple PI grant). $351,366/yr.
Private foundation funded:
None presently.
Industry Contracts:
None presently

b. Previous Support:
NIH R01HL125042: HIV-induced Redox Stress and the Alveolar Macrophage as a Resistant Reservoir. Funded 7/01/2014-6/30/2018 (Principal Investigator, Multiple PI grant). $686,584/yr; relinquished upon relocation to Cincinnati.
NIH K12 HD072245: Atlanta Pediatric Scholars Program. Funded 04/01/2011-11/30/2016 (Program Director). $324,000/yr.
HHSN275201300003C: Westat/NICHD Contract- IMPAACT Network; Pediatric and Adolescent HIV/AIDS Research Program at Emory University. Funded 9/01/2014-8/31/2019 (Site Principal Investigator). $450,000/yr estimated.
NIAID-DMID-NIH AI2012144: Vaccine and Treatment Evaluation Units (VTEU). Funded 9/13/2013-9/12/2020. (Co-Principal Investigator). $4-5M/yr estimated. 8
NIH R21 AI098592: HIV-specific B cell repertoire in humans following cross-clade immunization. Funded 7/01/2012-6/30/2014 (Principal Investigator). $150,000 initial period; $275,000 direct costs.

NIH R01 AI090656: Broadly-reactive antibodies against chimeric virus-host antigens. Funded 06/14/2010-05/31/2014 (Co-investigator).

I wonder if he knows Ralph Baric??

NIH U01 AI069418: HIV/AIDS Clinical Trials Unit. Funded 2/01/2007-11/30/2013 (Coinvestigator). HHS N272200800005C: Vaccine and Treatment Evaluation Units. Funded 11/01/07- 10/31/14 (Co-Director), $2,494,361/yr.
NIH U01AI78407 : Clonal Analysis of the Human B Cell Response to HIV. Funded 2/01/08-01/31/13 (Co-Investigator), $150,000/yr (Emory component); $750,000 total.
NIH RO1 AI40338: Viral and Cellular Determinants of HIV-1 Assembly. Funded since 1994; (Principal Investigator). $250,000 initial period; $1,150,000 total- now transitioned to GM111027 (active, above).
NIH R01 CA27834: Genetics of Primate “D” Type Retroviruses. Funded 09/24/07- 11/30/12 (Co-investigator), $250,000/yr, $1,250,000 total.
NIH R01 AI084834: Defining Neutralization Breadth in HIV-positive serum. Funded 9/01/2009-8/31/2011 (Principal Investigator), $250,000 initial period, $500,000 total.

NIH R21 AI65312: Pseudovirion Formation by Live Vector HIV Vaccines. Funded 06/01/2006-05/31/2008 (Principal Investigator), $150,000 initial period; $300,000 total.

NIH R01 AI067101: Novel Assays for Inhibitors of HIV Assembly. Funded 6/15/2005- 5/31/2008 (Principal Investigator), $200,000 initial period; $550,000 total.
NIH U01 AI47985: HIV Vaccine Trials Units. Funded 06/00-05/05. $1,438,628 initial period; $7,637,877 total.
NIH P30 AI054999: Vanderbilt-Meharry Developmental CFAR. Funded 05/01/03-04/30- 06 (Co-investigator), $528,468 initial period; $1,633,442 total.
NIH R29 AI40338-01A1: Membrane Binding and Transport of HIV-1 Pr55Gag. Funded 03/97-03/2002 (Principal Investigator). $ 70,000/ year; $350,000 total.
NIH R21 AI44369 (Innovation Grant): Development of Enhanced HIV-1 Pseudovirion Vaccines. Funded 07/99-06/01(Principal Investigator). $140,000/ year; $260,000 total.
NIH R55 CA83527-01A1: Induction of KSHV replication by HIV-1. Funded 03/00-02/02 (Principal Investigator). $80,000 total.
.
.
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NIH R01 AI52007: Development of Enhanced HIV-1 Pseudovirion Vaccines. Funded 06/2002-05/2007 (Principal Investigator), $225,000 initial period, $1,125,000 total.

NAI113678, GlaxoSmithKline: An open-label, multicenter, single arm study to evaluate the safety and tolerability of intravenous zanamavir in the treatment of hospitalized adult, adolescent, and pediatric subjects with confirmed influenza infection. Funded 10/02/12- 05/01/15. Principal Investigator.
P903-23, Cerexa: A multicenter, randomized, observer blinded, activ-controlled study to evaluate the safety, tolerability, efficacy, and pharmacokinetics of ceftaroline vs. comparator in pediatric subjects with acute bacterial skin and skin structure infections. Funded 01/01/2013-12/31/2014. Principal Investigator.
Merck Contract: Protocol 007: A Probe Study of the Safety, Tolerability, and Immunogenicity of a Three-dose Regimen of the Ad5 Gag Vaccine in Healthy Adults. Funded 04/01-12/02, $113,000 total (Principal Investigator).
Merck Contract: Protocol 012: A Probe Study of the Safety, tolerability, and Immunogenicity of the Ad5 HIV-1 Gag Vaccine. Funded 07/01/01-06/30/2003, $114,000 total (Principal Investigator).
Merck Contract: Protocol 016: A phase I dose-ranging study of the safety, tolerability, and immunogenicity of the Merck trivalent adenovirus serotype 5 HIV-1 gag/pol/nef vaccine in a prime-boost regimen in healthy adults. Funded 05/01/03-04/30/05, $117,000 total.
Basic Research Grant, Elizabeth Glaser Pediatric AIDS Foundation: Pseudovirion formation by live vector HIV vaccines. Funded 03/01/02-02/28/2004, $180,000 total.
.
.

LECTURESHIPS, SEMINAR INVITATIONS, AND VISITING PROFESSORSHIPS:
.
.

Invited speaker, Peking University Department of Biomedical Engineering, Beijing, May 2015: “HIV-1 replication in macrophages”
Invited speaker, Chinese Academy of Sciences, Institute of Biophysics, Beijing, May 2015: “Intracellular trafficking of the HIV envelope glycoprotein”

…………

Geeta K. Swamy, M.D.
Expertise: Infectious Diseases

Senior Associate Dean Vice Chair for Research & Faculty Development
Associate Professor, ObGyn
Department of Obstetrics & Gynecology, Division of Maternal-Fetal Medicine
Duke University, Durham, NC

2004 – 2006 Duke University Associate Faculty Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine & Division of Clinical & Epidemiological Research

2009 – present Duke University Vaccine Trials Unit Investigator Duke Translational Research Institute Durham, NC

2010 – 2018 Duke University Director Duke Perinatal Research Center Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine Durham, NC

2012 – present Duke University Associate Professor Department of Obstetrics & Gynecology Division of Maternal-Fetal Medicine & Durham, NC

2013 – present Duke University Human Vaccine Institute Investigator Durham, NC

2016 – 2017 Duke University Associate Dean for Regulatory Oversight & Research Initiatives in Clinical Research Durham, NC

Professional Awards and Special Recognition

2008 NIH Young Investigator Award Perinatal Research Society Meeting, Santa Fe, New Mexico
2010 NIH – NIAID Special Recognition for H1N1 pandemic
2013 and 2014 “Outstanding Reviewer” (Top 10%), Obstetrics and Gynecology
2014 “Outstanding Reviewer” for Vaccine

RESEARCH

Active Grants:
NICHD Maternal-Fetal Medicine Research Units (MFMU) 4/7/11 – 3/31/21

NIH-NICHD (Swamy) Principal Investigator Participation as a clinical site in the NICHD sponsored MFMU Research Network to investigate treatment strategies for common yet unresolved obstetric conditions through large multicenter collaborative trials

Past Grants:
Health Works for Women, NIH Summer Research Fellowship, University of North Carolina at Chapel Hill, Center for Health Promotion & Disease Prevention, 1994

PiiiTCH Study-Prevention of Influenza in Infants by Immunization of Their Household Contacts (CDC, Walter) Co-Investigator

NIH-NIAID (HHSN272200800057C, Swamy) Duke Site Principal Investigator
Randomized, Double-Blind Trial on Safety & Immunogenicity of Inactivated Trivalent Influenza Vaccine in Pregnant Women

NIH-NIAID (HHSN272200800057C, Swamy) Duke Site Principal Investigator A Phase II Study in Pregnant Women to Assess the Safety and Immunogenicity of an Unadjuvanted Sanofi Pasteur H1N1 Inactivated Influenza Vaccine Administered at Two Dose Levels

GlaxoSmithKline (Swamy) Cost-effectiveness of seasonal influenza vaccination during pregnancy An epidemiological study to develop and validate a model for estimating the costs and outcomes related to seasonal influenza vaccination during pregnancy for both mothers and infants through age 6 months.

Charles Hammond Research Fund (Gray) Mentor Assessing Decision Making & Acceptance of H1N1 Influenza Vaccine Administered in a Research Setting In Pregnancy

CDC-NCIRD – 1U01IP000190-01 (Swamy) Principal Investigator Effectiveness of a Vaccination Program in the Community ObGyn Setting The main objective of this 2-year project is to conduct a clinic-based study to develop and assess the effectiveness of a vaccination program for adolescent and adult women in the community Ob/Gyn setting.

ACOG/Merck & Company Research Award on Immunization (Fortner/Swamy) Mentor/Principal Investigator Compliance with Vaccination in the Obstetrical Setting with Novel H1N1 and Seasonal Influenza Retrospective review of births occurring in Durham, North Carolina during the 2009-2010 influenza season to evaluate influenza vaccination practices during the novel H1N1 pandemic.

Charles Hammond Research Fund (Swamy) Principal Investigator Association of Circulating Mitochondrial DNA Content and Preterm Birth Among Black Mothers

NIH-NIAID (HHSN272200800057C, Swamy) Duke Site Principal Investigator A Randomized, Double-Blind Trial on the Safety and Immunogenicity of Seasonal 2010-2011 Inactivated Trivalent Influenza Vaccine in Pregnant Women
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Vaccine & Treatment Evaluation Units 9/16/13 – 9/15/23
NIAID (HHSN272201300017I, Walter and Swamy)
Co- Principal Investigator Participation as a clinical site in the NIAID sponsored VTEU Network to conduct clinical trials of vaccine and treatments for infectious diseases

Contract PI for the following active trials
 A Phase I, Double-Blind, Dose Escalation Study to Evaluate the Safety and Pharmacokinetics of NTM-1632 vs Placebo Administered Intravenously in Healthy Adults

 Group B Streptococcus (GBS) Colonization and Disease Among Pregnant Women: A Historical Cohort Study

 A Phase I Cohort-Randomized, Double-Blind, Controlled Trial in Healthy Adults to Assess the Safety, Reactogenicity, and Immunogenicity of a Monovalent Inactivated Influenza A/H5N8 Virus Vaccine Administered Intramuscularly at Different Dosages Given With or Without AS03 or MF59 Adjuvants: Assessment of Immunological Responses and Lymphocyte Interplay

 A Phase II, Double-Blind, Randomized, Placebo-Controlled, Multicenter Trial to Assess the Safety and Efficacy of 5% Monolaurin Vaginal Gel Administered Intravaginally for the Treatment of Bacterial Vaginosis

 A Double Blind, Randomized, Placebo-Controlled, Phase I Dose Escalation Trial to Evaluate the Safety and Immunogenicity of an Inactivated West Nile Virus Vaccine, Hydro Vax-001, in Healthy Adults

 An Opportunistic Study to Evaluate the Population Pharmacokinetics of Beta-lactam Antibacterials in Adults Including Elderly Subjects (POPS_SILVER)

 A Population Pharmacokinetic Study to Evaluate Disposition of Azithromycin and Ertapenem in Pregnant Women Undergoing Cesarean Delivery After Failed Labor (POPS_CAN_DO)

 Targeted Reduction of Antibiotics Using Procalcitonin in a Multi-center, Randomized, DoubleBlinded, Placebo-Controlled Non-Inferiority Study of Azithromycin Treatment in Outpatient Adults with Suspect Lower Respiratory Tract Infection (LRTI) and a Procalcitonin (PCT) Level of ≤0.25 ng/mL (TRAP-LRTI)

Phase 3, Randomized, Observer-Blind, Placebo-Controlled, Group-Sequential Study to Determine the Immunogenicity and Safety of a RSV F Nanoparticle Vaccine with Aluminum in Healthy 3rd Trimester Pregnant Women; and Safety and Efficacy of Maternally Transferred Antibodies in Preventing RSV Disease in their Infants Novavax, Inc. (Swamy) 12/1/15 – 7/31/19

Principal Investigator Clinical Immunization Safety Assessment (CISA) 9/29/15 – 9/28/18 Clinical Study of the Safety of Simultaneous Administration of Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine (Tdap) and Inactivated Influenza Vaccine (IIV) in Pregnant Women CDC (HHS200-2012-53663, Swamy) Principal Investigator
.
.
.
GlaxoSmithKline Speaker Services, 2009 – 2012

NIH-NIAID Division of Microbiology & Infectious Diseases Working Group on the Enrollment and Safety Assessments of Pregnant Women in Clinical Trials of Drugs and Vaccines, 2010 to 2015

National Vaccine Advisory Committee – Maternal Immunization Working Group – 2014 to 2016

Appointed Member, February 2017 to present
HPV Working Group, February – June 2018

Consultative Workshop on Immunology Research Gaps Related to Maternal Immunization – Bill & Melinda Gates Foundation, May 25-26, 2015

WHO Brighton Collaboration Global Alignment of Immunization Safety Assessment in Pregnancy (GAIA) – Chair, Fetal Distress Working Group – 2015

Independent Data Monitoring Committee, GlaxoSmithKline, Inc. – RSV vaccines for the protection of children, 2015 to 2017

Data Safety Monitoring Board, Randomized Controlled Trial of Influenza Vaccine and Meningococcal Vaccine in Pregnant Malian Women and Their Infants Up To 6 Months of Age, Sponsor: Bill & Melinda Gates Foundation, 2011-2016

………….

Gregg Sylvester, M.D., M.P.H. +
Expertise: Alternate Industry Representative

Vice President – Medical Affairs
Seqirus Inc., Summit, NJ

Physician | Public Health Expert
Pharmaceutical Executive Expert in vaccine preventable diseases, pediatrics and population health.

Career Highlights
• Head of Medical Affairs for Seqirus, a CSL company
• Launched Pfizer’s Pediatric and Adult Pneumococcal conjugate vaccine, as well as Meningococcal B vaccine in the USA
• Launched Merck’s HPV4 vaccine in over 100 countries, presented to numerous National Immunization Technical Advisory Groups (NITAGs), public health and medical societies
• Partnered with community organizations in Delaware to reduce infant mortality, teen pregnancy rates and HIV rates

Professional Experience
SEQIRUS, a CSL company Summit, N.J Vice President, Medical Affairs 2016 – present
• Responsible for the strategy and implementation of Medical Affairs plan
• Ensures appropriate use of Seqirus’ influenza vaccines
• Overseas Phase IV research and presents data to NITAGs and other key stakeholders.

PFIZER VACCINES Collegeville, Pa
Vice President, Medical and Scientific Affairs: Americas 2013 – 2016
• Spearheaded science-based rationale to preserve Prevnar 13 infant schedule in US recommendations
• Successfully achieved an adult Prevnar 13 recommendation from US Advisory Committee on Immunization Practice
• Accelerated launch of groundbreaking Meningococcal B vaccine to accommodate urgent public health need

Global Head of Medical Affairs for Pediatric Vaccines 2010 – 2013
• Global Medical Lead for Pfizer’s Pediatric vaccine, Prevnar 13
• Created medical strategy for Prevnar 13, an asset exceeding over $5 billion in revenue
• Created innovate systems to improved scientific exchanges in a complex, global environment

MERCK VACCINES West Point, PA
Global Head of Medical Affairs for Adolescent Vaccines 2005 – 2010
• Created the medical affairs strategy for Merck’s HPV4 vaccine, Gardasil
• Spokesperson for all Merck vaccines
• Traveled extensively throughout the world presenting to governmental officials, regulatory agencies and public health/medical congresses

CHRISTIANA CARE HEALTH SYSTEM Greenville, DE
Medical Director, Eugene DuPont Preventive Medicine & Rehabilitation Institute 2001 – 2005
• Led Preventive Medicine for Delaware’s largest health care organization
• Expanded the community-based health programs, serving more than 50,000 people/year

DELAWARE HEALTH & SOCIAL SERVICES New Castle, DE
Cabinet Secretary 1997 – 2001
• Reported directly to Governor of the State of Delaware
• Managed the largest state agency, with more than 5,000 employees and an operating budget of ~$1 billion
• Implemented Medicaid Managed Care and Children Health Insurance Program (sCHIP) in Delaware State

Health Officer 1995 – 1997
• Led Delaware’s Public Health Division
• Formulated Public Health policies and supervised programs addressing high infant mortality rates, teen pregnancy rates, and low childhood immunization rates
• Promoted to Cabinet Secretary within one year

Chief of Community Health & Director of Maternal & Child Health 1993 – 1995
• Directed the development and implementation of community-based public health programs for the state of Delaware
• Managed an annual budget of $30,000,000 and 330 public health professionals

Selected Board Positions
IMA World Health: Chairman of the Board: 2017-2018;
Board Member: 2013 – present

DONORS: The majority of IMA World Health’s projects are funded through grants from generous public funding agencies and foundations.
CORUS INTERNATIONAL
◦ IMA World Health | Corus World Health
◦ Lutheran World Relief
◦ CGA Technologies ==> https://www.cgatechnology.com/
◦ Ground Up Investing
◦ LWR Farmers Market Coffee

Selected Honors and Awards
Merck Global Human Health Awards – 2007 & 2006 Winner: Franchise of the Year; 2006 Winner: Best Support of International Markets and 2008, 2007 & 2006

Education & Training Fellowships:

Public Policy – Joseph P. Kennedy, Jr. Foundation, assigned U.S. Senate, Washington, DC
Epidemic Intelligence Service – Centers for Disease Control & Prevention, Atlanta, GA
General Preventive Medicine Resident – Johns Hopkins School of Hygiene and Public Health, Baltimore, MD
Pediatric Intern, Resident and Chief Resident – Children’s Hospital of Buffalo – State University of New York at Buffalo School of Medicine, Buffalo, NY
Master of Public Health – Johns Hopkins School of Hygiene and Public Health, Baltimore,
MD Doctor of Medicine – Albany Medical College, Albany, NY
Bachelor of Arts – (History) – Ithaca College, Ithaca, NY
Veteran Status Commissioned Officer, United States Public Health Service: Rank – Commander – 1990 -1993

Summary

These are the people who have no problem giving an unvetted vaccine to children and pregnant women before the safety data is available. After all, they have been doing it on a smaller scale most of their careers.

-Gail Combs

GC/wm (written/edited)

DEAR KAG: 20220128 – The Pub is OPEN / Wolf’s Big Howl on January Sixth / Defeat The Mandates Picture Gallery / Why Isn’t Vaccine Localization a Thing?

The Pub is OPEN!

It’s GALLERY NIGHT, wherein our intrepid “print screen photographer” and “substitute bartender” presents his “artistic screen shots” of the Defeat The Mandates rally in Washington, DC.

While our beloved REAL bartender takes a needed break of unknown duration, we will continue to ENDEAVOR TO PERSEVERE.

Tonight’s drink special is not ethanol, but rather a different alcohol – epinephrine – a.k.a. – ADRENALINE.

Stay tuned! We’ll explain later!

Christmas Spirit

It looks like SANTA is still somewhere NORTH of the border, but he’s bringing FREEDOM!

Playing on the Jukebox

Well, we were looking for some stuff that was COMPLETELY DIFFERENT on the persnickety jukebox, and look what we found near the end of the last slider…..

EPIC COWBOY/WESTERN ROCK.

What the FREAKIN’ ‘ELL.

https://youtu.be/I8gr2hmIbew

Not sure what’s wrong enough with me to like this, but if you don’t enjoy this crazed version of cowboy, try an even crazier version of “Indian”.

And I mean that BOTH WAYS.

This stuff looks straight out of Burning Man.

And while that’s kind of interesting, it’s not about the kind of FREEDOM that goes with the ART on the wall tonight.

SO – we add some EPIC FREEDOM MOOD MUSIC for your GALLERY TOUR tonight.

That’s more like it.

And now, the rules of the pub.

HOUSE RULES

Now, back to business.

AMEN!

FREE the JANUARY BROTHERS

Article: Another Witness Tells Mafia Nan To GO TO HELL

And in the following video, you can actually hear the HOWL of WOLF MOON, telling MAFIA NAN exactly how he felt, when her Praetorian guard fired GRENADES upon a crowd filled with GRANDPARENTS, WOMEN and CHILDREN on January 6.

https://youtu.be/27Fci99hGww

Source: Capitol Offense: The Ugly Truth Behind The Five Deaths From January 6th and 7th – https://taylerhansen.substack.com/p/capitol-offense-the-ugly-truth-behind

Hat Tip GA/FL who made me aware of this excellent research.

My experience (including my WOLF HOWL) was documented in Section 4 of the following post, entitled

We Are Mighty To Save This Republic

The Truth About Our January Sixth Protest I was there, and I am PROUD of it. I am proud of the thousands and thousands of patriots who showed up to make an historic statement that the other side could only TRY to stop, by besmirching its beauty with their LIES and TRICKERY. Yes, their LIES …

Current Art On The Wall

We have a really interesting PHOTOGRAPHY exhibit in the bar this week. Consider this to be “gallery night”.

Prints are available FREE by right-clicking – or whatever you need to do on your device.

We have more pictures than just this collection, but these are some of the best. Enjoy a selection of magical moments from the DEFEAT THE MANDATES rally in Washington, DC last Sunday.

Dr. Heather Gessling

Dr. Lynn Flynn

Looking for this lady’s name!

Looking for this gal’s name, too!

Ernest Ramirez (vaccine injured and lost son)

And over in the corner, THIS RIGHTEOUS RANT is playing on a loop on our FREEDOM TV.

If you haven’t seen it, watch it. If you have seen it, watch it AGAIN!

Finally, you can watch the entire video HERE:

From: https://thehighwire.com/watch/

And now for our feature presentation…..

Why Isn’t Vaccine Localization a Thing?

One of the thing that tells me science is really out of whack right now, is the fact that scientists are discouraged from doing simple, plain-Jane things that would actually make vaccines safer for the general public, but are instead encouraged to go off in other, riskier, sexier, more profitable directions, while protected by a kind of “media umbrella of propaganda” which justifies, and rationalizes, but does not convince the HONEST skeptic and investigator.

In a sense, we still have the same sort of “patent medicine killers” of the late 19th century, with their poisonous potions – we’ve just changed WHO it is who is allowed to kill people and make money with bad medicines.

The fact that the very first COVID vaccines were of a risky, barely understood, and rather experimental type (mRNA or viral vector, i.e. genetic, full spike, in humans), while EASIER, FASTER, CHEAPER, SAFER, and much more familiar and better-understood vaccine types (protein or glycoprotein antigen, subunit) were IGNORED and SLOW-WALKED until later – well, it would have boggled my mind a long time ago, but no longer.

In my opinion, the “science”, if you can call it that, was guided by FAUCI PATENTS, rather than by what would have been best for patients AND for vaccine science.

The point about damage to vaccine science ITSELF is a point that Robert Malone often makes, which is critical. The people behind the bad, biased, self-interested, money-making vaccine choices, didn’t just screw THE PEOPLE – they screwed up the SCIENCE.

Let me be blunt. When people LIKE ME attack Tony Fauci, we’re not attacking science.

We’re attacking ABUSE OF SCIENCE by an OUT-OF-CONTROL BUREAUCRAT, aided by MERCENARY GLOBAL CORPORATIONS.

Tony Fauci is biased and corrupted by many sick and damaging compromises and ties to the industry he is SUPPOSED to be countering when necessary on America’s behalf – NOT coddling at every personally beneficial turn.

And all of this WRONGNESS was created under the cover of Francis Collins, who was used as a very phony TOTEM of “ethics” and “morality”. The man was pimped to the masses as a great Christian, as if that meant he WOULD and COULD do something about bureaucratic ethics and morality, while those very virtues he was meant to represent but not interfere with, were UNDONE by a series of corrupt administrations.

There is a LOT that is wrong with government regulation of science and medicine right now, and we need to talk about it.

Tonight, I’d like to talk about just ONE point of vaccine science which is weirdly out of whack, and protected ONLY by propaganda – and that is vaccine localization.

That means MAKING THE VACCINE STAY PUT WHERE YOU INJECT IT.

Obviously this is not working. OK? I’ll just be blunt.

One of the points frequently made against actual science on social media, mostly by CCP propagandists, IMO, is that vaccines simply do not leave the injection site, and thus all these systemic and distant effects which people allege to have been caused by vaccines, could not possibly have been caused by the vaccines. I saw this canard far more often than I should have, because people, generally, are not prepared to debate it.

Even when people just argue the evidence back and forth, because the reality is fuzzy and moves around between “localizes” and “migrates”, the argument itself is a fantastic deflection by the “protectors of vaccines”. Instead of talking about the very real problems caused by even LIMITED MIGRATION of vaccines, we’re one step removed from the problems.

These sorts of arguments – that the spike protein vaccines could NOT be migrating from the injection site – were completely undone by the Pfizer data obtained from Japan.

Yes, it was animals, and yes, it was perhaps at an over-sized dose, but the numbers themselves were SO substantial that these kinds of factors basically “factor out”. There is NO DOUBT from this data that there is a RISK of migration of “vaccine which infects cells and cranks out [highly pathogenic] spike protein which is HOPEFULLY dealt with cleanly by the immune system”.

The propaganda that vaccines don’t migrate was CLEARLY violated by the case at hand. That propaganda disappeared rather quickly, although I still hear it from nurses, and just bite my tongue.

Further – shockingly – the idea that the lipid nanoparticles containing the vaccine mRNA (basically what are called “virus-like particles” when injected as part of wasp venom) could actually have time to persist as part of skin lipids and BE SHED – well, it’s rather obvious from the data that this is a very real possibility.

The SKIN is an organ just like everything else. Everything else meaning all the OTHER organs that were getting the vaccine mixed into THEIR lipids in shocking amounts for a very long period of time.

Suddenly the CRAZIEST of the conspiracy theories about the mRNA vaccines was LITERALLY – and I mean LITERALLY – biophysically possible.

I had previously come up with a marginally feasible idea that maybe the spike protein itself was not just toxic, but HORMONE-LEVEL ACTIVE, to explain what people were reporting. But with the Pfizer data, I didn’t need any of that. The VACCINE ITSELF was ready to be shed.

And Pfizer hid this. Yeah. I can kinda see why.

So – if I may – let’s just set aside this foolishness that vaccines don’t migrate, and never have systemic or distant effects, because they do. It’s VARIABLE, but it’s REAL.

So why don’t people DO anything about this?

Why not do things that would absolutely ensure that vaccines CANNOT leave the injection site?

I can imagine a lot of things that MIGHT do this, but had never heard about any adjuvants or additives or vaccine designs that could effectively localize vaccines to arm or shoulder muscle, and simply make sure they didn’t migrate to even the slightest degree.

Solve THAT problem and pericarditis is GONE – RIGHT?

So why not do it? And why not BRAG about it if you CAN do it? Why not say how it’s done?

CRICKETS.

FAST FORWARD to a recent bit of knowledge that I happened upon IN REAL LIFE.

I noticed that I was somewhat jittery after having some minor dental work done. I was quite numb for the work, but later, after leaving the dentist’s office, with the numbness now faded, I noticed that I was shaky, edgy, and “wired”. That went away over the rest of the day. I just assumed that it was a side effect of the anesthetic.

I mentioned this to an anesthesiologist and a nurse, who both explained to me that it was NOT due to the anesthetic, but rather to epinephrine, which is sometimes ADDED to an injectable anesthetic in order to LOCALIZE it.

They explained to me that by epinephrine constricting the blood vessels in the region where the anesthetic is injected, the body removes less of the anesthetic by drawing it away in the blood stream – so the anesthetic STAYS at the site of the injection, giving a longer duration of anesthesia.

Sure enough, when I looked this up online, I found out it is quite real.

**https://journals.lww.com/anesthesia-analgesia/Fulltext/1998/05000/The_Effect_of_Varied_Doses_of_Epinephrine_on.21.aspx**

So I immediately thought to myself – why not do the same thing with vaccines?

Why not try to localize them with something like epinephrine?

But when I looked THAT up, the only results that I got, were for use of epinephrine (you know, as in the EPI PEN) in treating anaphylactic reactions TO vaccines. I probably didn’t look hard enough, but I’m not trying to get a patent or anything like that.

So who knows? It may be that adding epinephrine to vaccines could actually be GOOD in terms of reducing the severity of anaphylactic reactions – in addition to localizing the vaccine.

However, the possible technical feasibility of doing something isn’t my point.

My main point is simply ADMITTING THERE IS A PROBLEM.

If you could simply make these DAMN mRNA vaccines STAY where you put them, and if they didn’t crank out a bunch of bad stuff into the blood stream, then perhaps the only long-term risk would be something like cancer AT THE SITE OF INJECTION.

However, let’s be real. Nobody even TALKS about the problem. The media just DENIES IT.

In my opinion, “they” aren’t addressing this problem, because it gets on the way of “their” real purpose or purposes.

Vaccine localization is the last thing that these people wanted to “solve” here.

The people who CONTROL science and medicine don’t have to tell us about their entire agenda. They only have to tell us things that are somewhat plausible and rational.

In my opinion, mandatory vaccination is a PLATFORM for SOCIALISTS to do whatever they want to whomever they want. It gives them cart blanche to change society without accountability. That is the big picture, and has been their objective for well over 100 years.

Look at what communists are doing to Uighurs in Communist China RIGHT NOW.

Former #Uyghur camp detainees said they were given injections that stopped their periods or caused unusual bleeding consistent with the effects of birth-control drugs. #China_kills_muslims #EVilCCP https://t.co/xSDOvxS6xL
— Jeshurum david (@DavidJeshurum) July 17, 2020

Of Course: Bill Gates Praises China’s Response to COVID https://t.co/meIzorcKSM
— Sharon (@SweetFreedom29) January 24, 2022

Changing PEOPLE directly changes society FASTER.

They want to keep you alive, they keep you alive.
They want to sterilize you, they sterilize you.
They want to experiment on you, they experiment on you.
They want to kill you, they kill you.

Doing things which do not contribute to, or which would actually IMPEDE their “unholy grail” goal of direct control over humans, is simply NOT going to happen, if THEY can help it.

But that doesn’t mean that WE can’t give them a BAD HAIR DAY, EVERY SINGLE DAY, and fight for WHAT IS RIGHT in science and medicine.

defederalization of science
destalinization of medicine (de-obamatization in practice)
force ethics and transparency where socialists don’t want them
bring anti-deception tools and language INTO science itself
chase politics out of science, acting in both of them
increase citizen science literacy outside compromised institutions
work toward a BOR-compatible medical freedom amendment
many more

SO – just remember this.

Science and medicine won’t change when THEY do something about it.

Science and medicine will change when WE do something about it.

ENJOY THE SHOW.

W

WE HAVE THE COOKIES!

7136ad67c6068a95c5577c9397afad2b

DEAR KAG: 20220121 – The Pub is OPEN / The Anti-Saline Theory and The Toxic Batch Problem

The Pub is OPEN!

Tonight is a special night. We invite ALL SCIENTISTS to come down to the bar for TWO HOURS, and listen to one scientist appeal to our LOGIC and our COMMON SENSE on the TOXIC BATCH PROBLEM.

ALL WHO WISH are invited to sit down, drink in hand, and watch – but it is especially important that ALL SCIENTISTS see this.

It is my contention that if ALL scientists in the world – on this planet – watch this video that I will show you, then the entire WORLD will be QUICKLY AWAKENED to the reality of some kind of systematic problem with the current COVID vaccines – some kind of problem which is evidenced by toxicity showing up with certain batches.

But more about that later.

Right now, come into the bar and find a comfy spot.

While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.

Though we are not especially good at mixing tasty drinks, we can stir some occasional thoughts into a compelling report, argument, recollection, or proposition.

And with that barest promise, we begin.

On the Jukebox

The rare live version of a song rarely found on any bar jukebox – enjoy!

https://vimeo.com/20255791

Psalm 118:19-24

¹⁹Open to me the gates of righteousness, that I may enter and give thanks to the LORD.

²⁰This is the gate of the LORD; the righteous shall enter through it.

²¹I will give You thanks, for You have answered me, and You have become my salvation.

²²The stone the builders rejected has become the cornerstone.

²³This is from the LORD, and it is marvelous in our eyes.

²⁴This is the day that the LORD has made; we will rejoice and be glad in it.

Christmas Spirit

We are going to stretch out Christmas longer than your neighbor who never takes down their Christmas lights.

Enjoy this reminder of how special it was to have the Trumps in the White House.

Will they be back?

STAY TUNED!!!

And now, the rules of the pub.

HOUSE RULES

Now, back to business.

AMEN!

(#FJB = Free the January Brothers)

Current Art On The Wall

We opened this week’s shipment, and there was a note on top of the contents that said:

“DANGER: STEAMPUNK”

Looks like a real Pandora’s box to me!

Sure enough, the very next thing we found was MONDAY’S LEFTOVERS.

Mmmmmmmmm. Remember – if the can isn’t actually bulging, you can ignore the date!

Click it! The music seems useful for viewing the remainder of the art!

MOAR ~~COWBELL~~ GEARS!!!

Yeah, I’m enjoying this timeframe-loosening absinthe of sorts.

Indeed, absinthe per se seems to be a meme in steampunk.

Look for GREENPUNK as a subgenre of STEAMPUNK.

OK – one more image and then back to reality.

LOL. Nope. That’s not it.

Let’s try another.

AYE-YI-YI. That’s not it, either. I get the sentiment, but I tend to think the devil’s in certain details of the genre, and – as always in the art world – one must proceed with caution.

Although I do have a story about a fantastic dream you may have heard. In some ways, it was the opposite of steampunk, but it had a certain similar quality of alternate reality about it.

Let’s try one more.

Hey – that’s not steampunk! That’s REALPUNK.

I’ll let Steve tell us all about it.

In the meanwhile, we take leave of the infinitude of artistic imagination, and find ourselves back at the concrete.

Or so one might think!

And now our feature presentation

The Anti-Saline Theory and The Toxic Batch Problem – Did Somebody Actually Contaminate Lots of the Vaccines?

I never really thought that I might be defending Big Pharma – in whole or in part – at this point in the multiple scandals of the COVID-19 Plannedemic.

Maybe “defending” isn’t the right word. Maybe “presenting a potentially somewhat exonerating theory” IS the right phrase.

In fact, I don’t even know WHO I’m exonerating, or or that matter, WHO I’m accusing. Likewise, I’m not even sure who the TARGETS of the perpetrators in this “theory” actually are.

However, this is not a “conspiracy theory” – something which is generally certain of perpetrators, victims, and motives.

This is a CRIMINAL THEORY. This is a theory which allows us to begin to examine an apparent crime, in order to determine perpetrators, victims, and motives. It’s a theory which may even be wrong.

I ask all of you to briefly set aside prejudices, which is often necessary to do when evidence needs to be viewed as potential exoneration. Feel free to bring your prejudices and prior theories back AFTER you have looked at these possibilities, because you will need to compare theories, and your current favorites need to CONTEND with what I’m proposing here.

Thus, we begin.

The Saline Theory

The SALINE THEORY – which many regard as a criminal theory, and which others regard as a “conspiracy theory”, contends that the reason some people have either NO REACTION or ALMOST NO REACTION to the “clot shot” – meaning all the standard Western COVID-19 vaccines – is that those people are being given medical saline solution instead of actual coronavirus vaccines.

The proposed motives for this, generally speaking, are either to spare particular individuals from the problems of the vaccines, OR to statistically reduce the numbers of people being KILLED or INJURED by the vaccines to acceptable levels.

Now, in full disclosure, I have been generally, if quietly, rather critical of the saline theory, despite the fact that I am very skeptical of Big Pharma in general, and even more skeptical of Pfizer and Moderna.

Why am I skeptical of the theory? Basically, because it doesn’t really change most vaccines. In a sentence, vaccines are DESIGNED to approximate saline.

In the history of vaccines, the GOAL has always been to literally approach the state of “injecting people with saline” – meaning not much of anything is given, and nothing bad happens.

Thus, an ideal vaccine – and in practice most good vaccines – basically do nothing except grant immunity, which until recently was always expected to be inferior to “natural” disease-conferred immunity.

Let me point out AS AN ASIDE right here that the industry lost megatons of credibility by letting the media trot out nonsense about vaccine immunity being better than disease-conferred immunity, allegedly negating centuries of medical knowledge. Foolish to abandon the truth on that one. Clearly the result of Big Pharma now having the upper hand against Big Med, thanks to Big Finance, and the willingness of Big Media to tell any lie. But I digress.

The point is simple. We EXPECT normal, good vaccines to have very few adverse events – so rare that we rarely hear about them – and that people basically ARE getting saline.

In other words, people generally can’t tell the difference between a good vaccine, a “bad because too weak” vaccine, and saline.

THAT’S THE POINT – that the REALITY of rare adverse events is expected to MATCH our experience of almost never hearing about or experiencing first, second, or third-hand, that somebody had a problem with a vaccine.

I myself went through life NEVER connecting a vaccine to any personal injury – that is, until I got over 30 years of flu shots, religiously, but then switched to my dominant shoulder for no particular reason, and experienced subsequent NOTICEABLE inflammatory issues which were very likely connected to the vaccine. All that being said, I was much older at that point, and older people ARE more likely to experience inflammation of joints as part of getting old. Indeed, this didn’t stop me from getting the flu shot for a number of more years – KNOWING that the vaccine might be responsible.

SO – bottom line – I’m not at all skeptical of vaccine injury, from sore arms up to death.

But I remain skeptical of the saline theory – for the stated reasons.

I never throw anything OUT completely – but I have been quite skeptical that there might be ANY kind of conspiracy – even a very realistic one – to replace weak “do-nothing” vaccines that the industry has spent DECADES making, and is quite good at making, with saline that does almost the same thing.

And INDEED – bear the opposite in mind. Bad things happen to people who get placebos, “because math”. And more than that, bad things happen to people who get saline, “because injection”. It’s extremely rare, but it DOES happen. This is an acknowledged truth of Anthony Fauci’s Holy of Holies, the placebo-controlled double-blind study. That’s why researchers factor out the difference which comes simply from “doing the test”.

But the fact is simple. Saline is generally pretty damn safe to inject, because it does nothing. A good vaccine, likewise, does nothing but provide some degree of immunity – hopefully lifelong, but with a number of years generally being acceptable, depending on the vaccine.

SO – if you tell me somebody got saline – I will tell you that they got a “good vaccine”, and we’re left with only some very difficult science to tell which of us is right.

However, all of that has a problem.

A HUGE problem.

The problem is summed up by the fact that almost everybody in the English-speaking world recognizes the term “clot shot” as a grim, joking nickname for the COVID-19 vaccines.

That didn’t happen by accident. Admittedly, it’s an injection for preventing or pre-treating a clotting disease by generating immunity TO a clotting protein WITH that same clotting protein, or something very similar to it. BUT STILL…..

In practice, this is NOT a harmless vaccine. No amount of propaganda changes that.

The Anti-Saline Theory

So what is the ANTI-SALINE THEORY?

The anti-saline theory, based on something called the toxic batch problem, is roughly a mirror image of the saline theory. It thus contends that some of the coronavirus vaccines were the opposite of non-toxic saline which could NOT harm people, and were, in fact, loaded with something nasty which caused illness and death.

Possible motives are likewise mirror images of the saline theory – to either harm certain people, or to INCREASE the number of injuries and deaths from the vaccines.

NOW – let me be clear. In the absence of the “potential evidence” of the toxic batch problem, I would be every bit as skeptical of the anti-saline theory as I am of the saline theory.

Even for a bad, risky, side-effect-prone vaccine, blaming the still-generally-infrequent side-effects on anything BUT the vaccine itself would seem foolhardy. We have MANY “more risky” vaccines for nasty tropical diseases, from yellow fever up to Ebola, which we generally ONLY give to people at high risk of actually getting the disease, because the vaccines may be a LESSER RISK than the disease, but they are an INCREASED RISK over most vaccines.

We normally don’t need to postulate that the cause of that higher risk is adulteration due to a new cause or perpetrator, when we have the vaccine itself and the vaccine makers, presumably fighting the risk but possibly not succeeding as well as we would like, as our primary suspects.

So how does the toxic batch problem change all that?

The Toxic Batch Problem

First, a reflection. A bit of a warning. Something to prepare you.

At the various stages where one understands pieces of this problem, the revelations really cannot be “unseen”. And yet, the fact that this problem WAS unseen by SO many for SO long, raises questions about whether or not we are just now seeing the edges of something which has been with us for far longer than we realized.

I know that sounds a bit fantastic, as well as euphemistic and even a bit “code”, but now you understand why so many people who have gained deep knowledge of problems with the COVID vaccines, have gone through various emotionally jarring moments of realization.

Something is NOT RIGHT, and yet there seems to be INTENTION behind the condition.

SO – if you get HIT by this sort of realization as we are going along, just know that you are not alone.

OK, back to work. Ah, yes. The toxic batch problem.

I can sum it up as this.

Normally, one expects that a consistently produced pharmaceutical has a VERY wide range of reactions in those to whom it is given, BUT that this statistical range of responses (you can imagine a bar graph, a pie chart, a curve, or a whole bunch of all of them) will stay roughly the same from BATCH TO BATCH.

Stated simply, we expect the variation BETWEEN sets of variations to be SMALL, CLOSE, PREDICTABLE, and REPRODUCIBLE.

This is simply the “law of large numbers”. You flip a thousand pennies. I flip a thousand pennies. It’s very unlikely that we’ll get exactly the same numbers, but BOTH OF US will be close to 500 heads and 500 tails. Any deviation from this will be a nice bell curve, perfectly explainable by statistics.

Try any “batch” of pennies – it will be close to 50:50 heads-to-tails because of the consistency of pennies.

The toxic batch problem is that adverse events for the COVID-19 vaccine batches violate this – and in a HUGE WAY.

A small fraction of the batches (about 5%) are STRIKINGLY TOXIC relative to all the other batches.

The differences are too big, the harmless group is too large, the nasty group is too small, and there are additional patterns that are not random and should not be there.

Yes, there will be variation in the exact numbers of deaths and injuries from batch to batch, “because statistics“, but that variation should be small, natural, centered, and understandable mostly in terms of mathematics. If there IS a big difference in the numbers between the batches, then there has to be some kind of systematic difference – most likely either in the contents of the batches, or in the administration of the batches.

Let’s look at the latter first.

As an example of an administration difference, if you give one batch to kids, and another to seniors, you expect differences. However, if the batches are BIG, and they’re used in a lot of different places, and the groups of people those places serve are large and diverse, then the differences from administration will vanish.

And even if those differences DON’T vanish – in FACT, even if you INTENTIONALLY give one batch to kids and another to seniors, those differences cannot be as big as what was observed.

Another administration difference would be to use some batches ONLY for first injections, and others ONLY for second injections.

Again, we do expect differences there, but not nearly as big as what is observed.

IN FACT, the difference between the “good, nearly harmless batches” (doesn’t that sound like saline?) and the BAD batches is SO big, that it is NOT EXPLAINED by ANYTHING seen in the Moderna and Pfizer trials.

THIS is one of our first clues that something is actually wrong with the contents of those toxic batches.

Now – let’s look at the possibility of a difference in contents.

Could it be that the vaccines are “going bad” and turning into something more poisonous?

Yes, this is possible – BUT the fact of the matter is that when drugs degrade, they almost invariably become “less active”, not MORE active – and certainly never MORE active by orders of magnitude.

Rocks just don’t “roll uphill” by themselves.

In fact, there is a great argument you will see later, made about the COVID-19 vaccine data, as compared to the flu vaccine data, which points out that if you remove all the “bad batches” from the COVID-19 vaccine data, it looks almost exactly like the flu shot.

BASICALLY, SALINE.

Like a normal vaccine is supposed to look.

Now, hopefully, you not only understand why I called this the “anti-saline theory”, but you are also “seeing certain things that you cannot unsee”.

Because YES – something is definitely wrong with those batches.

Even if you don’t accept that the majority of batches are “harmless”, something is terribly wrong with the rest.

But before I get into talking about possible reasons as to WHY these “bad batches” are different, I want to thoroughly convince you that they ARE different and that it’s NOT NORMAL.

I want to give you a brief introduction to the toxic batch problem as seen by the people who found it, examined it, and first told the world.

A Pharma Exec & Researcher Examines the Data

We begin with a video of a man who appears to me to be very typical of the scientists that I knew during my career. He does not appear crazy, loony, mentally ill, psychopathic, or even irrational.

He seems, if anything, like somebody who has witnessed institutional madness descending upon their professional world. You know – like what happened to scientists in Russia in the early 1900s, and in Germany and Italy in the 1930s.

As I listened to this guy, he made scientific sense, just like any seminar speaker, invited lecturer, or even an interviewer for student job prospects from a drug company.

In fact, I believe that if most scientists listened to him, they would BELIEVE HIM.

There is something *apparently* wrong with certain specific batches of the COVID vaccines from three companies that were used globally AND specifically in America. And according to the speaker, a retired drug industry executive and research scientist, this difference cannot be random – it must be adulteration of some kind.

Just watch and see what you think.

LINK: https://odysee.com/@Corona-Investigative-Committee:5/Mike-Session-86-en:0

Now – let me summarize.

The most key and salient point is that vaccine side effects vary strongly by batch number – and in a way that the drug companies MUST understand to be REAL and PROBLEMATIC. The variation is NOT merely statistical from a quality-controlled product. It is systematic – meaning it has a CAUSE other than randomness. It is not necessarily intentional (IMO), but it is an OBVIOUS problem.

There is also some argument over how batch toxicity varies across time and batch number – I will leave THAT for the next videos.

The point which the speaker, Dr. Yeadon, made which struck me hardest, was the simple but powerful idea that the individual responses of recipients to a vaccine batch can vary wildly, BUT that the statistical array of responses will NOT vary significantly between batches – that it CANNOT vary – UNLESS there is some REAL, SIGNIFICANT, CONTENT DIFFERENCE between the batches.

The alternative, in my opinion, would be that the batch differences are administration-based – e.g., that batches primarily used for SECOND administrations would have much higher adverse events.

I’m not wed to that thought – but it is an alternative that is every bit as troubling as content differences, and negates the entire strategy of “boosterism”. I also tend to doubt it, both because it does not explain the magnitude of the difference, and is also statistically very unlikely. Content differences just seem more likely to me.

The People Who Found The Toxic Batch Problem

NEXT, I want to deepen the explanation of what Dr. Yeadon was describing. Yeadon provides drug industry credibility to the idea that batch differences are real and almost certainly content-based. They don’t look right to somebody with industry experience.

But NOW we need to explore possible explanations for those differences, based on a closer look at the differences themselves.

SO – next, I want to show you some additional videos and web pages that drill down into the “toxic batch problem”.

We’ll start with the “secondary reporting” and then get to the data itself.

In this video, Stu Peters and Dr. Jane Ruby, who I criticize routinely when they edge toward clickbait, are doing an AMAZING job of reporting on a group of investigators who studied the batch differences. This is excellent journalism. These two can only be as good as their material, but WOW – they have quality material here.

LINK: https://www.brighteon.com/9a45a7a0-e260-4a6c-a251-2b4c139dd211

Now, follow that up with an even deeper examination of the toxic batches.

Jump to 12:50 to continue the discussion. Jane Ruby ends at about 19:00. At 20:00 (to 32:12) it picks back up again with a member of the investigatory group, Team Enigma, who is a pharmaceutical industry bio-statistician. She adds a different perspective on how SMALL any group poisoning the vaccines might be.

This doesn’t require a grand conspiracy of many people. It might involve only a few dedicated and highly skilled saboteurs.

LINK: https://rumble.com/vs59wj-live-hackers-reveal-deadly-jab-lot-numbers-horrific-pfizer-teen-trial-data-.html

Now, let’s look at one of the original presentations of data by Team Enigma.

LINK: https://www.bitchute.com/video/4HlIyBmOEJeY/

Points made in this video:

dosages of pharmaceuticals are normally highly controlled
consistency and purity are also normally highly controlled
COVID vaccines can be readily and correctly compared to flu vaccines
flu vaccines are consistent and low in adverse events
COVID vaccines are NOT consistent, and vary widely between harmless and highly toxic
toxic batches are too wide-spread – problems like refrigeration loss cannot be responsible

Now – here is an EXTREMELY compelling video, which shows in great detail the DIFFERENCE between the “harmless batches” and the “toxic batches”.

LINK: https://www.bitchute.com/video/6xIYPZBkydsu/

Pay special attention to the following ideas:

most batches (roughly 80%) are almost completely harmless
the bad batches produce up to (and in MANY cases) a thousand times more adverse reactions
when viewed geographically in the United States, the bad batches affect every state in America

The latter point proves the generality of the effect – that local differences can’t account for the toxicity of the particular lots. If anything, the high distribution of the batches seems to be used to hide the toxicity.

Next, I want to return you to the PERSONAL REALITY of the toxic batch problem.

A Personal Case of a Bad Batch

It turns out that Dr. Robert Malone got one of the “bad batches” for his second vaccine, and almost died.

Just read here.

LINK: https://rwmalonemd.substack.com/p/how-bad-is-my-batch

ARCHIVE: https://archive.fo/5Q9dx

A Good Review of the Toxic Batch Problem

Lastly, here is a very nice review of work on the toxic batch problem. Very nicely put together, with lots of graphs and key points as quotes. This is a real CONVINCER.

LINK: https://hillmd.substack.com/p/vaccine-batches-vary-in-toxicity

ARCHIVE: https://archive.fo/h0R8Y

Some of the videos in the review have been removed for some reason, but not this one.

This video is truly stunning. This video shows apparent patterns in the deployment of batches. While I am not fully in agreement that this is proven to be the work of the companies themselves, I think that there is overwhelming evidence of “bad batches” and some kind of pattern which looks like the results are being studied.

By the time you’ve gotten here, you very likely think that something is definitely wrong with certain batches.

Next, I want to begin thinking about HOW and WHY somebody might want to do such a thing. In the process, I’m going to “lean into” some current events and statements made by varous people.

This is where things get political, geopolitical, military, and more.

How and Why Would Anybody Poison the West’s Major COVID Vaccines?

This is where we begin to say to ourselves:

Did somebody actually poison various lots of these vaccines? WHO would do it? Who COULD do it? WHY? Why would ANYBODY do this? HOW did they pull it off? WHAT possible benefit could they get from it? WHERE did they do it?

I’m going to leave most of these questions TO YOU ALL.

I want YOU to tell ME.

Now, we have a list of “usual suspects”, but things get interesting when you consider additional motives, additional suspects, and additional opportunities.

MEANS, MOTIVE, and OPPORTUNITY are what turn “conspiracy theories” into CRIMINAL THEORIES.

So I’m going to give you some “kick-starters” to get you seeing some possibilities.

The first thing that got me thinking “HMMMMM……” about things, was when Team Enigma began seeing evidence of coordination between the drug companies, in the chronology of the toxic batches.

As somebody who has been involved with real conspiracies, the idea that drug companies coordinated their plotting to poison the vaccines does NOT sound realistic.

Real conspiracies need compartmentalization. They need as few as possible seeing the big picture.

Thus, it is MUCH more likely, IMO, that there is a SINGLE player who is involved with ALL of the vaccines – a SINGLE player – who would be able to pull off a systematic study of poisoning them.

One such player is the CCP.

BOTH the Pfizer vaccine AND the Moderna vaccine are utterly dependent upon components manufactured in CHINA. Indeed, the “lipid nanoparticle technology” of the mRNA vaccines is pretty much delivered by Chinese companies.

That is how Karen Kingston discovered that components of the “clot shot” vaccines were manufactured by a Chinese company called SINOPEG, which ALSO specializes in something called “PEGylated graphene oxide”, which is further known to temperature-stabilize mRNA vaccines.

I’m not necessarily saying that graphene oxide was used here, although it’s worth considering.

SIDEBAR: For background on graphene oxide (sometimes called graphene hydroxide – it’s the same thing, really), go HERE.

SIDEBAR: For background on the work by Karen Kingston, former Pfizer employee, who figured out the Chinese connection on the lipid nanoparticle components, go HERE.

Moderna executives are also deeply associated with these Chinese companies and their controlling organizations – see photo below. Note what this page (discovered by Karen Kingston) means – you have COVID-19 vaccines, graphene lipid nanotech IN those same vaccines, and pictures of Moderna executives mentioned on the same page.

If this is not a smoking gun, it’s a pretty damn good imitation, suitable for blackmail.

Thus, it sure seemed possible to ME, that if the CCP or PLA wanted to “intervene” in the vaccines, they have MEANS and OPPORTUNITY.

What about MOTIVE?

Well, Deplorable Patriot found something that got me thinking.

So – according to this theory, the US is being blackmailed by the Chinese government.

As soon as I saw this, I realized exactly HOW the ChiComs could have war-gamed this whole thing for some grand-master play.

CCP/PLA + Cabal makes Western pharma weak and dependent upon ChiCom manufacturing
CCP/PLA has total control of Chinese companies and products they ship
CCP/PLA has total control of information within Chinese borders (remember their “rules” which made many SMART companies LEAVE CHINA)
CCP/PLA begins manipulating people to make them RUN FROM TRUTH and into CHINESE CONTROL

To me, this makes CHINA a no-brainer suspect. It doesn’t matter WHO is POTUS – Biden or Trump – if the vaccines have problems in the West, CHINA wins.

China gets power over the American POTUS
China gets power over the American Deep State
China gets power over the global pharmaceutical industry

Basically, it’s a form of entrapment.

And remember – if China gets caught and wants to blamecast, they can say “it wasn’t us – it was this rogue company cheating” – and nobody can prove otherwise on anything within Chinese borders.

NOW – there could be other players. China is not the only player who would benefit by making the West stumble here.

WEF, for instance, strikes me as “guilty as sin”. If the vaccines were really safe, they could not stir up as much division as we’re seeing. To me, KlauSS SSchwab and the WEFFEN SS have to be a suspect.

Depopulationists are also an easy target.

Satanists as well. This is their thing.

“FOREIGN” could also be doing things independently of their pet globalists and depopulationists.

Russia, unfortunately, is also an easy suspect, thanks to their stupid antics with Skripal and other spies. If the Russians wanted to keep America WEAK, causing a mess with the vaccines to keep Americans divided would be one way to do it. However, I tend to think that they don’t have as much MEANS and OPPORTUNITY as China. But to be fair, we have to keep Russia on the list.

Similarly Ukraine – to which Democrat operative Alexandra Chalupa seems to have some kind of weird supreme loyalty – because it doesn’t have a perfectly clean history on poisonings, either.

Ukrainian opposition presidential candidate Viktor Yushchenko, with his face disfigured by illness, during an interview with the Associated Press in Kiev, Ukraine, Thursday, Dec. 16, 2004. Yushchenko said Thursday that he is sure he was poisoned by the Ukrainian government, and for the first time pinpointed the time and place of his dioxin poisoning: a Sept. 5 lunch with the head of the Ukrainian security service and his deputy. (AP Photo/Efrem Lukatsky)

And, of course, there is our own DEEP STATE, still led in truth by Barack Obama.

Obama seems really committed to a kind of Stalinist, utilitarian, “death panel” health agenda, where health-care shuffles off people to their graves to save money.

Obama’s famous academic and New York Times-featured “moral advisors” on healthcare have always been, and remain in my opinion, a litany of granny-snuffers. SO – if Obama’s “worst of the worst of the KGB faction in CIA” wanted to begin testing depopper stuff on us – well – they could be up to tricks.

But none of them has as much MMO as China.

All in all, CHINA looks like my main suspect.

They poisoned our dog treats forever, making it look like greedy little companies was the extent of the problem.

We just put up with it.

Maybe they got ideas from that.

WHAT DO YOU THINK, SUSPICIOUS CAT?

So who is your main suspect?

Or do you have a different explanation of the toxicity of the shots – and especially something that explains the weirdly binary toxicity / non-toxicity of the batches?

I’m interested in your thoughts!

Have a Great Weekend

And don’t forget to…..

ENJOY THE SHOW.

W

Dear KMAG: 20220117 Joe Biden Didn’t Win ❀ Open Topic / 1Q22 / MLKJ Day / Malone & Navarro: Declaration of Vaccine Independence / Fauci Hid Early Knowledge of SARS-CoV-2

Joe Biden didn’t win. This is our Real President:

AND our beautiful REALFLOTUS:

Get your rest NOW, Trumpy Bear! You’re going back to the White House!!!

The Business At Hand

And indeed, it’s Monday…again.

But we WILL get through it!!!

Repeatedly!

And we’ll have a good time doing it!

About Today

Equal rights. Yes. It’s STILL a noble struggle.

Only the STRUGGLE is NOW with those who make sure things remain unequal between “Let’s You All And Them All Fight” groups.

Just sayin’.

It’s also the Qth of January.

Speaking of people who are actually fighting for equal rights.

ThanQ, wherever you are!

The Rules

Boilerplate, more or less, but worth reading again and again, if only for the minor changes, and to stay out of moderation.

The bottom line is Free Speech. Theories and ideas you don’t agree with must be WELCOME here, and you must be part of that welcoming. But you do NOT need to be part of any agreement.

If we err, we’re going to err in the direction of FREE SPEECH and PAINFUL TRUTH.

This is a feisty show, a lot like GAB. You can say what you want, but others can and will correct you, disagree with you, or oppose you – as long as they do so in a civil manner.

And you get to DISAGREE BACK.

You may be FRIENDLY, but you don’t have to be SILENT.

So DO try to be civil, but DON’T stay silent when something needs to be said, and YOU are the person who needs to say it.

FREE SPEECH – USE IT OR LOSE IT.

Civility makes us FIT to inherit the MORAL SYSTEM passed down to us by the Founders.

We must endeavor to persevere to love our frenemies – even here.

So OPPOSE EACH OTHER RESOLUTELY BUT WITH KINDNESS, in the manner of a guy named Paul.

In Wheatie’s words, “We’re on the same side here so let’s not engage in friendly fire.”

That includes the life skill of just ignoring certain other posters.

If the Second Tree goes down, please go to The U Tree, or to our Gab Group, which is located at https://gab.com/groups/4178.

In the words of Wheatie, “Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”

A Moment of Prayer

Our policy on extreme religious freedom on this site is discussed HERE. Please feel free to pray and praise God anytime and anywhere.

Thus, please pray for our real President, the one who actually won the election.

You may also pray for our enemies, whose numbers diminish daily, as they flee to our camp in alliance, from the jabby and murderous designs of ROBBER JOE, WINNIE THE POOH, and the KISSINGER KABAL.

MUSICAL INTERLUDE

For your listening enjoyment, and general encouragement, we continue Wheatie’s tradition of fine music videos, shipped fresh from the seas of information by our intrepid authors.

Let’s finish near where we left off last time…..

So where does that lead?

To a fascinating node in the web of all things Q Tree…..

AUUURRRGGGHHH!!!! I need something with a little more PEP – and maybe a bit less CSNY CHOOMER SOY and BEELZEBUBBA STDs.

But still some estrogen, it would appear.

OK – that does it. Whether plant estrogens or the regular ones, it always leads to the dreaded condition of WAXY SOY FACE, and that is best exemplified by…..

REGRETCHEN WITCHMORE

a.k.a.

WITCHY WOMAN!!!

https://youtu.be/FZFQJg1WV-8

So as an antidote, I think I need THE OTHER GRETCHEN.

And now that we’re cured of all this stuff, let’s see if we can find…..

Some actual WHEATIE MUSIC. You know – epic soundtrack stuff!

How about this?

OK – not quite. Sorry – it’s everything wrong with Hollywood. Epic but not inspiring.

Let’s try THIS.

“Epic Victorian Steampunk” or something like that!

Ah – that’s more like it! THAT is what we need……

Call To Battle

Our beloved country is under Occupation by hostile forces.

Daily outrage and epic phuckery abound.

We can give in to despair…or we can be defiant and fight back in any way that we can.

Joe Biden didn’t win.

And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.

A Declaration of Independence from Immoral and Unconstitutional Vaccine Mandates

by Dr. Robert Malone & Peter Navarro

in Washington, DC – January 12, 2022

from https://www.washingtontimes.com/news/2022/jan/12/just-say-no-to-biden-and-faucis-universal-vaccinat/

In this declaration of independence from a “Forced Universal Vaccination Policy,” we hold these truths to be evident:

SARS-CoV-2 appears to be a bioweapon genetically engineered at the Wuhan Institute of Virology using gain-of-function technologies transferred to China by Dr. Anthony Fauci’s National Institutes of Health bureaucracy and funded in part by both NIH and the threat mitigation branch of the Department of Defense’s Defense Threat Reduction Agency.

China’s virus has killed millions, undermined the economies of China’s rivals and destabilized Western-style democracies through panicky authoritarian measures such as vaccine passports, economic lockdowns and mask/vaccination mandates.

No vaccine exists capable of eradicating the virus comparable to vaccines for diseases like polio and smallpox, and COVID-19 has entered a variety of animal reservoirs. At this point, it cannot be eradicated by any human vaccine.

Furthermore, the public health threat of the omicron variant is minuscule while our national medicine cabinet contains only a very mixed bag of highly leaky and nondurable quasi-vaccines. For example, the Pfizer and Moderna jabs are based on an experimental mRNA technology originally developed by one of this piece’s authors (Malone), are of primitive construction and are associated with the development of vaccine and monoclonal antibody-resistant viral mutations.

With leakiness, vaccinated individuals are becoming infected at increasing rates. With nondurability, the Pied Pipers of forced vaccinations are demanding ever more “booster” jabs.

America’s quasi-vaccines are significantly riskier than public health officials have disclosed. They can trigger serious cardiac and thrombotic conditions, menstrual cycle disruptions, Bell’s palsy, Guillain-Barre syndrome and anaphylaxis. Male children appear particularly prone to myocarditis, while, post-vaccination, individuals may have suppressed immunities that make them vulnerable to other diseases.

Government officials like Dr. Fauci and Big Pharma executives like Pfizer’s CEO Albert Bourla and Scott Gottlieb have fed us a steady diet of “noble lie” assurances to encourage universal vaccination. This propaganda has been disseminated by outlets such as CNN and MSNBC and reinforced by systematic Big Tech censors like Facebook and Google determined to hide reality from the public — even as drug company lawyers work to avoid data disclosure that would inform us otherwise.

The virus is now so thoroughly embedded in global populations that, like the common cold and flu, it will be with us for the foreseeable future. It is long past time to substitute Dr. Fauci’s increasingly frantic “vaccine” as a silver bullet fantasy for this reality: The genetic vaccines and overall Fauci/Biden policies have utterly failed to meet their public health objectives — even as life insurance executives such as OneAmerica CEO J. Scott Davison are on fire concerning the overall high mortality rates they are observing in their data.

Alternatively, we must pragmatically build “herd immunity” against the virus, and the quickest and safest way to do this is to reserve vaccination for the most vulnerable (who are already highly vaccinated) while flooding our communities with cheap, safe and efficacious therapeutics freely prescribed in early treatment by personal physicians.

In this fundamentally conservative strategy, no healthy person below the age of 60 should be enticed — or coerced! — to get vaccinated. This is especially true for healthy children, who are at little risk from the prior higher-risk virus strains and develop more robust, diverse and durable immunity than the quasi-vaccinated.

It should go without saying that healthy normal children should not be treated with experimental medical products. This is particularly true given that over half the nation’s children have already developed the enhanced natural immunity engendered by infection, and the risk of side effects of the Pfizer/BioNTech product is higher in those that have developed natural immunity.

Regarding therapeutics, abundant research now shows hydroxychloroquine and ivermectin, in particular, can significantly moderate symptoms, reduce hospital stays, eliminate the need for a ventilator, and take death off the table when administered in “early treatment” after symptoms begin. Both are not just far cheaper than the new antiviral pills approved by the FDA and pimped by Merck and Pfizer. They are safer and likely more effective.

The biggest health risk from the Biden/Fauci universal vaccination strategy is this doomsday scenario: The more you vaccinate, the more likely you will spawn vaccine-resistant mutations; and the more likely those vaccinated will fall prey to the mutations. A particularly lethal vaccine-resistant mutation in a universally vaccinated world may well wipe out the human race.

This is not science fiction. It is Virology 101 — Black Swan event though it may be. Furthermore, troubling data is emerging from Denmark and the UK that vaccination may increase the risk of omicron infection.

The biggest political risk as America’s mass formation hypnotized bureaucrats ratchet up the universal vaccination pressure are the threats to our jobs and access to schools, shopping, restaurants and sports arenas. Mr. Fauci is now even discussing banning airline travel for the unvaccinated. He seeks to herd us like sheep (or lemmings) towards a vaccine nation ruled by the same kind of overbearing authoritarian apparatchiks epitomized by the very country from which the virus originated.

That Australia, Canada and Europe have already reached a disturbing state of forced vaccination disgrace should be a warning sign to every American still concerned about freedom and the future of American democracy.

If the Biden/Fauci doctrine were based on sound science and a workable strategy, and if omicron were causing severe disease and death, trading freedom for reduced risk might be barely tolerable. But this current frantic madness cuts against the grain of both current data and every scientific principle we know.

The Biden/Fauci administration has become consumed by a mass formation fantasy of safe and effective gene vaccines that can save us from a nonexistent omicron danger.

Accordingly, today we declare our independence from these fools and urge all of our fellow citizens — vaccinated or not — to do the same. This is based on current scientific data, not on a hypnotized fantasy.

• Dr. Robert Malone is the discoverer of in-vitro and in-vivo RNA transfection and the original inventor of the core mRNA vaccine technology. Peter Navarro served in the Trump White House, assisted in rapid development of the gene vaccines and is the author of “In Trump Time: A Journal of America’s Plague Year” (All Seasons Press).

Peter Navarro SCORCHES Anthony Fauci

In this video, J.D. Rucker interviews Peter Navarro on Anthony Fauci.

Just listen to the FIRST TWO MINUTES of this shocking video, which shows that Fauci KNEW from the beginning that this was his virus, and he withheld that information.

Take note – a picture of the WUHAN INSTITUTE OF VIROLOGY is behind Navarro as he speaks.

LINK: https://rumble.com/voeoqq-peter-navarro-drops-bombshell-about-first-time-he-met-anthony-fauci.html

Wolfie’s Wheatie’s Word of the Day:

outré

adjective

violating convention or propriety; bizarre

synonyms: bizarre, cranky, crazy, curious, eccentric, erratic, far-out, funky, funny, kinky, kooky, odd, off-kilter, off-the-wall, offbeat, out-of-the-way, outlandish, peculiar, quaint, queer, quirky, remarkable, screwy, spaced-out, strange, wacky, way-out, weird, wild

Used in a sentence:

**Democrat-favored fashion choices, like their lifestyle preferences, tend toward the outré.**

Used in a picture:

Used in a video:

Wishing you all a great week.

And don’t forget to…..

ENJOY THE SHOW

W

DEAR KAG: 20220107 – The Pub is OPEN / TES Special Edition / Pimp Your Coof Kit / Dealing With Uncertainty / ThEthSkep’s Big Fix of All Things Coof: CCP Hiding Chinese 2018 Release of SARS-CoV-2 Virus

The Pub is OPEN!

Yeah, we still have staffing problems, but who doesn’t under China Joe?

While off to a rocky start, we are staying open as many days of the week as possible, just like some of the small businesses that I patronize.

Keep up that LOCAL PRESSURE on the Biden cabal by going to school board meetings and supporting TRUE non-monopoly capitalism – it SKEERS Kapo and Little Red Jen somethin’ FIERCE.

Merry Christmas and Happy Holidays! To the White House press– thank you for challenging us, for questioning and for holding us accountable as we all work to keep the American people informed. And to the press team–you are simply the best. Grateful every day to work with you. pic.twitter.com/xxBwLMzh2L
— Karine Jean-Pierre Archived (@PressSec46) December 23, 2021

Likewise, patronize those SMALL BLOGS that provide new viewpoints and ideas!

We Serve Whiskey And Guns To Indians Here!

Yup! FREEDOM is GOOD TROUBLE, and we’re in favor of it, for everybody, much to the consternation of our local maskies and vaxxies.

I had the special pleasure of being “refused service” by a maskie recently – he simply walked away from the cash register and went into the back. Some of it was due to race. Having been “not served” because of race before, I can spot that fairly easily, and this person was not exactly “hard to read”.

Three other staffers (all forced to wear masks, sadly) came to my assistance and took my order.

I maintained a pleasant demeanor, as part of one of several psychological warfare tactics that I have adopted recently, in fighting against the VAXZIS and MASKZIS.

While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.

So what’s on the ODD BAR’S CRAZY MENU this week?

We’ve served alcohols our first week, including menthol, ivermectin, and hydroxychloroquine.

Next, we served amines , including second generation antihistamines.

Today, we’ll toast each other with an element that we’ll borrow from Steve…..

…..and some very special natural alcohols and derivatives, including among the 4 of them, 3 terpenoids, 2 phenols, 1 ester, and 1 ether.

More on these wonderful “liqueurs” later!

Christmas Spirit

There’s still time to spread omicron! GET BUSY!!!

While we do have some members out with Omicron now, including Brave and Free, the real question is whether we’re going to see a big peak in March and April, like we did in 2020.

And if you’re gonna get sick, you might at least consider having some willing cohort, looking for that natural immunity, to get sick with you!

thank you pictures

Ah, thanks to SMILEY for reminding me of the goofy fun of these wonderful but stupid GIFs called “Blingees”!

And now, the rules of the pub.

HOUSE RULES

Now, back to business.

AMEN!

Current Art On The Wall

Now for something a bit different…..

Vector background. Molecules and chemical formulas

…..and something a bit more familiar.

David Teniers the Younger (1610–1690), *The Alchemist*, ca. 1643–45. Oil on panel, 20 1/8 x 28 in (51 x 71 cm). Herzog Anton Ulrich Museum, Braunschweig (139)

LINK: https://www.metmuseum.org/blogs/now-at-the-met/2020/alchemy-science-making-marvels

TES Special Edition

As one of the early “discoverers” of The Ethical Skeptic on Twitter, I was happy that I was able to get a few people interested in his precise and well-considered thoughts on things – especially regarding the phony scamdemic. TES was always utterly perturbed by the bad science of the “pandemic”, and worked on a daily basis to “correct the fact checkers” – which was all of hilarious, sad, and joyful.

After I was kicked off Twitter, I rarely saw him, due to my own laziness, really, but in 2021, some GREAT links to The Ethical Skeptic’s work popped up here. THANK YOU, to all who follow him and keep us informed.

THIS was a classic.

LINK: https://theethicalskeptic.com/2019/03/07/nelsonian-inference-and-cultivated-ignorance/

ARCHIVE: https://archive.fo/wZKYb

This work really helped me to GRASP and understand the leftist tactic of “pretending not to know”, and – more importantly – how to spot it.

So let’s look at some of his even more recent stuff.

Pimp Your Coof Kit

LINK: https://theethicalskeptic.com/2021/12/29/our-household-covid-kit-item-listing/

This one got us all thinking about “coof kits”, and GA/FL suggested some of us putting up our own versions. I initially thought that this might not be a good idea, because people’s needs and medical situations really VARY – one of the main reasons that “practicing medicine without a license” is actually a bad idea in normal times. I thought it better to have a broader discussion.

However, I just realized that I did put up a kind of “minimal” kit last week, and it’s worth looking at it.

This kit was designed for people who DON’T have a smart plan already figured out, and don’t want to investigate “hard to find” things like ivermectin and hydroxychloroquine.

Here is what I had, followed by my earlier reasoning. The main change is adding Vitamin C, as discussed below.

Wolf’s COVID Care Package

Thermometer (thermal digital is easiest)
Antigen test kit(s) (yeah, good luck finding one, although they are coming back after New Years)
Antihistamine of your choice (Claritin, Zyrtec, and Allegra are the easiest – 1-2 a day)
Aspirin (regular, or low-dose if your stomach doesn’t like it – 1 a day)
Listerine or Betadine mouthwash/gargle for mouth and throat
Vitamins C and D, Zinc, Calcium, Magnesium, Multivitamin including Selenium.
Quercetin (including natural sources) or Green Tea
Saline or other nasal spray, rinse, or wash of your choice

The thermometer tells you when to use your precious test kit – when you suddenly have a fever and a sore or tingly throat.

The test kit gets you a positive diagnosis that opens doors for things like antibodies, or an official test.

A positive test means you can BEGIN TREATMENT at THERAPEUTIC DOSES.

The antihistamine insures that YOU WILL ALMOST CERTAINLY NOT DIE, because it stops the second, allergic, inflammatory stage of COVID in its tracks.

The aspirin makes doubly sure you won’t get clots, but be careful – don’t take it if you’ve had trouble with aspirin. Talk to your doctor if unsure.

The gargles (Listerine or Betadine) massively reduce viral load and speed time to recovery.

The saline and nasal washes lower viral load, and maintain nasal breathing.

The quercetin and green tea help zinc’s antiviral action by increasing cellular zinc levels.

The vitamins and mineral supplements keep you at antiviral levels of these things. In particular, zinc and vitamin D3 need to be at non-deficient levels.

Please consult authoritative sources from TRUE medical doctors like the ones at https://flccc.net.

Cthulhu noted that I hadn’t mentioned Vitamin C – I have now added that, because it’s likely to help and can’t hurt (“First, do no harm”) and also follows the McCullough Principle (“Signals of Benefit, Acceptable Safety”). I don’t think it’s nearly as important as the antihistamine and “clot-blocker”, but I do have to admit that Vitamin C was certainly far better than nothing when I survived Wuhan with only mild lung damage.

What I’m going to do now is to encourage all of YOU to talk about your “war chests” and “coof kits”, and explain your reasonings about things.

This will help people who are deciding what THEY might want to add to their kits – OR REMOVE, if there is something better for their particular situation.

Remember – everybody has their own unique medical needs.

I will put my thoughts in the comments, just like everybody else.

NOW – about those natural “essential oils” in Listerine.

Let’s look at them.

Menthol

Thymol

Eucalyptol (2 views)

Methyl salicylate

These are all natural substances of roughly the same molecular size and composition (mostly carbon and hydrogen with 1-3 oxygen atoms), all of them being either pungent oily liquids or smelly, vaporous crystalline solids.

There are some relations between these things.

Thymol is basically menthol where the 6-membered ring has been made benzenoid – meaning like benzene – with 3 double bonds.

Notice that methyl salicylate is also benzenoid. Methyl salicylate is related to aspirin, and has similar activities. Don’t drink Listerine, even though the amounts are (believe it or not) rather small.

Eucalyptol is also structurally related to menthol, although it’s harder to see. Try to see it.

All of these natural substances, when isolated from their sources, were very early pharmaceuticals. They ALL have pharmacological activities, which many would regard as “primitive” by today’s standards, and yet, gargling Listerine is PROVEN to be extremely effective in reducing viral load of COVID-19 variants – about 80% as effective as iodine solutions.

Why might this be? Here is just ONE small line of immunological evidence.

LINK: https://pubmed.ncbi.nlm.nih.gov/9810029/

To be honest, we’re a bit late to the game here. Native Australians from the first wave of immigration, roughly 65,000 years ago, discovered the utility of eucalyptol by their own investigations.

LINK: https://successfulaffiliateru.com/medicinal-use-of-eucalyptus-the-australian-aboriginal-way/

Here is some additional information about early Australian medicine using natural products.

LINK: https://theconversation.com/the-art-of-healing-five-medicinal-plants-used-by-aboriginal-australians-97249

There is a great picture of what is essentially a native doctor’s medical bag in the second link. When it freaks you out a bit, let it. This is a way of getting you to appreciate human intelligence outside your modern experience.

Lastly – IODINE.

I have not tried this, and I am not sure I would like it, but it’s a viable option, IMO. I actually like Listerine, and it worked for me on delta, so I’m happy with that. I did NOT try Listerine in the nasal cavity. Not sure that I’d like that. I stuck to saline.

I did find a paper that showed Listerine to be roughly 80% as effective as povidone-iodine.

Here is link to a review which states something similar, and a summary of the review.

LINK: https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7842245/

Executive summary

Methods

A review of literature was conducted regarding the use of commercially available antiseptics and SARS-CoV-2.

Results

Povidone-iodine (betadine), ethanol and essential oils (Listerine) and a combination of xylitol and iota-carrageenan (purified from red marine algae) were shown to reduce viral load of SARS-CoV-2 in vitro by 3–4 log₁₀ in 30 s.
Chlorhexidine, a widely used oral rinse, does not act as quickly in reducing viral load in 30 s as povidone-iodineI, but binds to cell proteins, extending protection.
Hydrogen peroxide is not as effective as other oral rinses in vitro and cell toxicity is a concern.
Hypertonic saline is not directly virucidal, but halts replication by increasing hypochlorous acid inside the cell.

Conclusion

Several commonly used nasal antiseptics and gargles have shown efficacy against SARS-CoV-2 in vitro and clinical trials are currently underway to study their impact on disease course and transmission.

Future perspective

These commercially available products should be further evaluated due to their potential ability to reduce the transmission of SARS-CoV-2 and other viruses that are yet to emerge.

You can also make your own povidone-iodine gargles and nasal rinses – Dr. McCullough has retweeted a nice recipe for this. Click through to Twitter for more information.

pic.twitter.com/JfPLaJgHAd
— Joel "Heart Prevention" Kahn MD, FACC (@drjkahn) December 31, 2021

Here is a great long post on all of these methods, including hydrogen peroxide – an alternative to iodine.

LINK: https://jeffreydachmd.com/2021/09/povidone-iodine-mouth-wash-rinse-gargle-for-c0-ld-prevention/

Do beware that some people need to be careful with iodine, including people with hypothyroid.

LINK: https://www.webmd.com/diet/foods-high-in-iodine#1

LINK: https://www.webmd.com/vitamins/ai/ingredientmono-35/iodine

Dealing With Uncertainty

LINK: https://theethicalskeptic.com/2021/12/24/the-riddle-of-certainty/

ARCHIVE: https://archive.ph/wpfWu

This is another GREAT article, talking about one of my FAVORITE complaints about modern science, which has resulted from a really SICK and UNHEALTHY compartmentalization, as well as insulation of scientists from internal criticism (lack of “herd review”). This condition has allowed all sorts of pathological science to gain ascendancy without check, balance, or proper community criticism.

For example, CLIMATE CHANGE gets more input from FINANCIERS than it does from the many scientists like me who think we are acting irrationally and presumptuously on ERRORS. These errors have been induced by the WRONG forces – beneficiaries not committed to truth – within a small pathologically influenced community – much like what’s going on with improperly influenced government science and the “clot shot”.

This piece by The Ethical Skeptic contains a graphic using a BULLSEYE which you really need to see. It makes a very important point about science – which I can apply DIRECTLY to Anthony Fauci.

Fauci’s extreme focus on antibodies to the spike protein as a nearly sole measure of “success” of the “clot shot”, is a perfect example of what TES is talking about.

I have referred to Fauci’s over-focus as “antibody hypnosis”. In fact, I see this kind of obsession and compulsion repeatedly throughout his career, and would wager that:

it’s why he always “wins” against the Judy Mikovitses and the Kary Mullises
it’s why he’s so highly paid
it’s why he’s tied to so many “grim reaper” experiments
it’s why corrupt industry loves him, and is in bed with him

TES makes a general point about the kinds of information which actually provide STRONGER PROOF – and this set includes something I love – INDEPENDENT CONFIRMATION BY ALTERNATE LINES OF REASONING – not just “duplication of results” and “confirmation of results” – which are both sadly lacking as well, but not nearly as important.

I have powerful, direct experiences in science with the need for RESOLVED DIVERSE INPUTS and AVOIDANCE OF HYPNOTIC REASONING as safeguards against pathological science.

However, THEY (and I mean “they”) are using various forms of hypnosis, including MASS, COMMUNITY, PEER, and INDIVIDUAL to advance science in ways that THEY want.

Human science is far more controlled than we either admit or understand.

Anyway, back to the article.

There is a quote from Elon Musk therein which is really worth your while, and which TES puts in the context of what he is talking about.

Bluntly, it feels wonderful to know that SOMEBODY GETS IT.

What Musk is talking about here is basically the “bullseye” metaphor that TES uses. And THAT is related to the following item.

While Fauci is very committed to the LEVELS of his antibodies, he has not properly processed feedback that would indicate he’s OPTIMIZING THE WRONG THING.

Here is a link to Steve Kirsch’s interpretation of Sucharit Bhakdi’s and Arne Burkhardt’s analysis of people who died after vaccination, showing that these deaths were ALMOST ALL related to the “clot shot”.

LINK: https://stevekirsch.substack.com/p/bhakdiburkhardt-pathology-results

Kirsch REALLY explains this well. Malone takes note of this, too.

IMO, it would appear that Fauci is optimizing the WRONG ANTIBODIES in the WRONG WAY, because the vaccines are CREATING the WRONG ANTIBODIES in the WRONG PLACES.

Please read Kirsch’s article and then the Bhakdi-Burkhardt paper to understand this.

PAPER: https://doctors4covidethics.org/wp-content/uploads/2021/12/end-covax.pdf

Now, Fauci may be optimizing the wrong antibodies in the wrong places for a variety of reasons. Those exact reasons are not nearly as important as the fact that they are simply WRONG.

I believe Bhakdi, Burkhardt, and Kirsch – this is a risky vaccine, and now we begin to understand WHY.

Based on this knowledge, I personally will not be taking these vaccines.

In my opinion, these results CLEARLY show that vaccination against SARS-CoV-2 should not be effected by IM injections of a full SARS-CoV-2 spike protein, and even more emphatically so, NOT by genetic vaccines delivered by IM injections. In my very early opinion, this is going to be a CLASSIC case for using RBD antigen (protein) and/or nasal delivery as a concession to the virus – with nasal delivery being used as a SAFETY feature and NOT merely a convenience.

To have SAFER vaccines for DISCRIMINATING SHOPPERS like me, we’re going to have to compromise with the virus. That’s just the way it is.

There may be SOME who thought that we could arrive at a compromise that would reduce human populations, but frankly I don’t like that deal.

In my opinion, ANYBODY with vascular, cardiac, clotting, or other issues like WANTING TO HAVE KIDS SOMEDAY, or NOT RISKING CANCER, should absolutely avoid the current clot shots.

In my opinion, the clot shot is stupidity advanced by greedy people who are controlled and manipulated by really evil people. In other words, it’s not stupid, greedy, or evil – it’s ALL OF THE ABOVE.

The DISEASE is no picnic, and I can see some people making the risk-benefit calculation in favor of the vaccine – particularly newer RBD antigen vaccines like Corbevax (Hotez/Baylor/India/open-source). But if people are dying in 5 years from experimental mRNA vaccines with the full spike protein – well, that is exactly like the RISK that one takes with SMOKING SOMETHING YOU DON’T UNDERSTAND.

Seriously, most Americans would refuse to take a novel “legal” or illegal designer drug, given stories like the “bath salts” and “Parkinson’s heroin” experiences which shocked the public in horror headlines.

Parkinson’s from Designer Heroin (Ironically related to Paraquat)

LINK: https://www.latimes.com/archives/la-xpm-1985-07-29-me-5136-story.html

LINK: https://pubmed.ncbi.nlm.nih.gov/28282815/

VIDEOS: https://duckduckgo.com/?q=mptp&iax=videos&ia=videos (warning – they’re really sad)

Effects of “Bath Salts” (Euphemism for CCP Designer Drugs)

LINK: https://www.npr.org/sections/parallels/2014/06/16/321779232/how-bath-salts-a-drug-made-in-china-wreaked-havoc-in-the-u-s

LINK: https://www.justice.gov/usao-wdny/pr/akron-man-arrested-importing-bath-salts-china

The CLOT SHOT is a RISK, and not all of us will want to take that risk.

Mandating that risk is EVIL, IMO, and Democrats deserve to DIE AT THE POLLS in November for it.

Period.

They have BLOOD on their hands.

ThEthSkep’s Big Fix of All Things Coof

LINK: https://theethicalskeptic.com/2021/11/15/chinas-ccp-concealed-sars-cov-2-presence-in-china-as-far-back-as-march-2018/

ARCHIVE: https://archive.fo/zww1q

This is what I really wanted to show you, right here.

The Ethical Skeptic, or TES, or “ThEthSkep“, as I sometimes call him, has proven to my satisfaction that CCP lied even MORE than we previously thought possible.

Is this hard to believe? That we got CHUMPED by CHINA yet again?

Yeah. Getting chumped by China YET AGAIN is a thing.

I am tempted to try to construct an “elevator pitch” of ThEthSkep’s argument, and have even asked him (in a moderated comment) if he could provide such a short explanation that I could pitch to others.

If he DOES provide one, I will do an entire post on it.

For the moment, I will just give you my “two paragraph description” of his very long and elegant post, which post I can guarantee most here will have trouble following.

TES argues that setting an earlier date for the actual initial Chinese release of an ancestral pathogen to current SARS-CoV-2, provides a far better explanation of the facts at hand, as well as some facts which he generated through analysis of the genetics of SARS-CoV-2 variants, than does the “standard model” of a late 2019 release, whether that late release is taken from the early Chinese LIES about a zoonotic outbreak in December 2019, or from the October 2019 Wuhan lab activities which have always struck me as potential disinformation.

In particular, an early 2018 release of a less pathogenic ancestor explains the omicron variant’s surprisingly early 2020 appearance and low pathogenicity so well, and China’s population resistance to the more pathogenic Wuhan variant, whether that was a descendant or (my thinking) a new release, that IMO it is the duty of the “standard model” to explain all of the facts better than the TES theory.

Now, like I said, this post by TES is not an easy read, even for those with some knowledge of the field, and even for those experienced in reading the scientific literature. He moves at “review speed” through a lot of reasoning and even his own work, which is not all shown, but which is all fully described and referenced.

I am actually WAITING for my first reading to fully sink in, but I can tell you this. As soon as I “freed myself” from the necessity of a late 2019 release, everything “coof” just started falling into place.

This is one of those things that starts generating RESETS in my mind, on everything I had thought before. Once you see what TES is getting at, it’s almost impossible to unsee it.

AND I CAN GO FURTHER.

I talk to a LOT of people, and listen carefully to their thinking about COVID. One of my sources is somebody who has a lot of contacts in Europe and Asia, especially India, due to working for an international firm.

That person strongly believes, based on illnesses within the corporation as well as associated entities, that something like COVID-19 was already circulating worldwide during ALL of 2019.

I had set this aside, unable to fit it into everything else I knew. NOW, however, it makes easy sense. In fact, the details which I don’t want to give, fit his model of spread EXACTLY.

If TES is correct, and I believe he is, then WE WERE DEALING WITH VARIANTS EVEN BEFORE THE CDC BEGAN TALKING ABOUT VARIANTS. In fact, they never told us that THE ORIGINAL WAS LIKELY JUST A VARIANT OF SOME PRIOR VARIANT.

And THIS explains much better why Fauci, Baric, Dazsak, and all the others were ready to cover up – because a virus related to their research had already gotten out in 2018. Going along with the Chinese story was a RELIEF to them – and they grabbed on tightly.

In other words, a conspiracy of aligning interests, not something discussed on paper or by phone. It’s a brilliant Chinese move, actually. Proffer a lie and see if our own scientists will join them in it.

The USEFUL IDIOT American media? NO PROBLEM.

And not just THAT stuff, but now we have much more evidence that these bugs could have been “in the wild” EVERYWHERE – including possibly just outside the Baric lab, near where Gail Combs picked up a “coofy” bug much earlier than would have been possible with a late 2019 release. (I will let her address the time-frames.)

Consider that China could even have been trying to FRAME or intimidate Baric with a stateside release in the vicinity of his lab. Why? Because NOW we have MOTIVE.

Does it make sense NOW that these highly contagious bugs could have been getting out willy-nilly from these laboratories? Or that China has been playing fast and loose with biological releases?

What does this mean?

It means that the whole NIH-Fauci-Wuhan complex has been in cover-up mode, trying to SAVE THEIR DANGEROUS RESEARCH which they know is VERY likely to be SHUT DOWN BY A CONGRESS RUN BY THE PEOPLE – no matter WHAT THE CAUSE OF THIS RELEASE.

Remember how I said the President Wolf Moon would send a cruise missile into every BSL level 4 that didn’t shut down immediately upon his inauguration? Those missiles armed with whatever insured that all viruses were FRIED?

See the motive to get rid of Trump now? WE THE PEOPLE cannot be allowed to interfere with their “holy” research.

And wait – there’s MOAR.

Somewhere in the years between 2005 and 2010, around the time I got an extremely SARS-CoV-2-like infection, complete with anosmia, exhaustion, and “sore lung”, I took note of the fact that all of my Asian colleagues in the “anti-CCP” camp became very religious about taking COVID-like precautions in our CCP-Chinese-infested workplace. These precautions included isolation, surface and aerosol measures, like wipes, air filters, and even clothing choices.

Most of us dismissed it as an “Asian thing” like masks, even though it was a sudden and new social phenomenon, but because I had contacts in that community who were sometimes sources of insight on CCP skulduggery, I noticed that ONLY the “antis” were engaging in the protective behaviors – the mainlanders and pro-CCP Hong Kongers/Taiwanese were not.

Interestingly, I was not getting any good information on the trend – unlike other scuttlebutt at the time.

Was it real or disinformation? Was it an op to flush out the antis? Was it “anti” paranoia?

I have no idea. But I personally think that China has been up to “bio-tricks” for a LONG time – as in back BEFORE SARS (2003).

If 2018 is the first time China released any biologicals, I would be VERY surprised.

SO – see what you think. Read this sucker, and then think about it.

I think TES is onto something.

A Note About January 6 – and More

I have been avoiding all things January 6, largely because I don’t want to give Nancy Gambino any “lift” as far as her phony “investigation” into HER OWN CRIME.

I understand her game plan, and I’m not going to play along.

I would have loved to have recounted that amazing day in another long, glowing, “all about me and my experiences” post, but no.

THIS IS WAR.

In my opinion, we can bring down these horrible communists faster by focusing on whatever WE want to focus on.

Nancy says “the fight is over here”.

NOPE. Go to hell, Mafia Bitch. We know what you did. With Kapo’s dirty FBI. And the backing of Mitch McConnell and SCOFFLAW SCOTUS.

Some may want to join the fight against Pelosi right now, and please feel free to “follow Darren Beattie into Pelosi’s breach”, but I think that MANDATES are going to kill these bastards at the polls, if we just help them commit electoral suicide.

Expose the “clot shot” risks more fully, and show that the mandates are MORE EVIL.

We need to make Democrats – destroying America for GREED under the cover of virtue signals – absolutely unelectable, and I think we can.

ENJOY THE SHOW.

Thank you all for being here. Have a great weekend.

How a Psycho Vaccine Marrying the Infamous COVID Spike Protein to HIV’s Neurotoxic gp41 Was [Allegedly] Canned by a Mere Testing SNAFU

How Australia Dodged The First Mad Vax Bullet of the WEF Scamdemic / Plannedemic

Darwin Award Vaccine Featured Insane Merger of HIV and COVID But Failed Due to Buggering of AIDS Tests, NOT Because of the Obvious Risks

Was It Ever Really For COVID? The gp41 HIV Protein is a TOP Target For AIDS Vaccines

How Science Monetization and Corruption Has Broken All Vaccine Safety Mechanisms and Made Sneaky Liars Out of Scientists

Mood Music

Intro – Prepare To Be Shocked

BUT NO. NOT NOW.

State of Corruption of Vaccine Science

One of the biggest BOOMS dropped in the video, IMO, is the fact that Robert Malone WARNED the FDA about the toxicity of the spike protein, and they SHRUGGED IT OFF.

The Frankenvax That Almost Was

VolksWackcine 451

So What’s With HIV and the COVID Vaccines?

Rapid Response Subunit Vaccine Design in the Absence of Structural Information

An AIDS Vaccine in Disguise?

“REVERSO”.

Doorless Carp’s Suspicious Cat In A Box

Update on The University of Queensland COVID-19 vaccine. “..trial did not give trial participants HIV”, just a neurotoxic glycoprotein

11 Dec 2020

So What The Heck Is Going On Here?

W

The Pub is *STILL* OPEN!

We are doing our best under the circumstances!

Christmas Spirit

HOUSE RULES

AMEN!

Free the January Brothers

(no matter what the SHANGHAI SLIDER says)

Current Art On The Wall

G-Bay (Gab Marketplace) Is Here

Fake Science Normalized by Fake News and Fake Entertainment

IT IS YOUR DUTY TO PERCEIVE AND REJECT FAKE SCIENCE.

Malone and Bhakdi Validated by “Pro-Vax” Paper

A Health Public Policy Nightmare

WHUUUUUUUUT?????!!!!!

We’re not only the news now.

We’re the science now.

ENJOY THE SHOW.

W

Joe Biden didn’t win. This is our Real President:

AND our beautiful REALFLOTUS.

The Business At Hand

And indeed, it’s Monday…again.

But it doesn’t matter, because with God, every day is glorious!

The Rules

Thus we are assembled here to peacefully address our grievances to whom they may concern, even each other, using both our freedom of speech and of press, as well as our freedom of religion.

A Moment of Prayer

MUSICAL INTERLUDE

Call To Battle

Our beloved country is under Occupation by hostile forces.

Daily outrage and epic phuckery abound.

We can give in to despair…or we can be defiant and fight back in any way that we can.

Joe Biden didn’t win.

Pandemic of the Vaccine

Are mRNA Vaccines Fundamentally Flawed?

Well, is there such a compelling theory?

In my opinion, we’re there.

Innate Immune Suppression by SARS-CoV-2 mRNA Vaccinations: The role of G-quadruplexes, exosomes and microRNAs

The Abstract

Analyzing the Abstract

Analyzing the Paper

Wolfie’s Wheatie’s Word of the Day:

wolven

noun

Of or pertaining to wolves; wolflike; wolfish.

Used in a sentence:

ENJOY THE SHOW

W

The Pub is OPEN!

We may serve “off-label” drinks here, including hydroxychloroquine, ivermectin, and truck diesel, but we don’t serve spike protein, remdesivir, or anything made in Wuhan, Chinazia.

Christmas Spirit

And now, the rules of the pub.

HOUSE RULES

AMEN!

#FJB – Free the January Brothers

Current Art On The Wall

On The Jukebox

And now for our feature presentation…..

The End of the mRNA Vaccines

The TRUTH is a SOLID FORTRESS.

The Pub is STILL OPEN!