Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

The Pub is OPEN!

And we’re finally serving a NORMAL DRINK tonight. Even though it’s a SECOND ROUND.

STAY TUNED…..

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

and what time of year is it now???

Christmas Spirit

We continue our WAAAAAY too-long celebration of Christmas by noting that some of our neighbors STILL have their lights and decorations up.

We saw a nice red Christmas bow laying in somebody’s yard by their driveway.

We ourselves just got rid of our tree.

And TODAY is the 25th of the month. That’s VERY “Christmassy”.

So yeah. Given that there are a few ~~days~~ ~~weeks~~ months AFTER Christmas where it’s STILL Christmas, that means we have a few more weeks left. Riiiiiiight?

Sure! So have some hot CHRISTMAS chocolate!

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!

Current Art On The Wall

We’re just gonna segue into the next item with our selection, if that’s OK.

This gets a bit “planetary”…..

**Christiaan Huygens, Saturn, and Something**

https://owlcation.com/stem/Huygens-Mission-on-Titan

**LINK: https://www.instagram.com/p/BAOVsasAXhl/**

**Mercury**, the old cure for ***grandgore***.

COVID-19 Vaccine Interference With AIDS and Syphilis Tests

Earlier this week, RAC brought a news item from CTH, which really got me thinking:

FDA Warns of Vaccine Induced Positive Syphilis Test

This had to do with a CDC alert…..

LINK: https://www.cdc.gov/std/FDA-alert-12-20-2021.pdf

…..which was based off of an FDA alert (sketchy link)…..

…..which actually links back to a different CDC alert (even sketchier link)…..

WHATEVER.

Here is that final CDC alert. Only the top 3 paragraphs are important here.

Let me quote the text of those first 3 paragraphs for Zoe. I will make BOLD what is important.

Dear Partners in Prevention,

December 20, 2021

I’m writing to share the U.S. Food and Drug Administration (FDA) alert sent to clinical laboratory staff and health care providers about a syphilis test. The alert reports that false reactivity, or “false-positive,” Rapid Plasma Reagin (RPR; non-treponemal) test results, when using the Bio-Rad Laboratories BioPlex 2200 Syphilis Total & RPR kit, can occur in some people who received a COVID-19 vaccine and includes recommendations for addressing these potential false positives.

Historically, false-reactive RPR test results have been observed in people with systemic infections unrelated to syphilis, such as tuberculosis, rickettsial diseases, and endocarditis. False-reactive RPR testing also has been previously observed following immunization (specifically following smallpox vaccine). False reactivity with RPR can also occur during pregnancy.

Per CDC’s 2021 STI Treatment Guidelines, reactive RPR results should always be confirmed with treponemal testing (e.g., Treponema pallidum particle agglutination, TP-PA). This is, in part, because of the above-mentioned issue: false-positive nontreponemal test results can be associated with multiple medical conditions and factors unrelated to syphilis. According to FDA’s alert, treponemal testing for syphilis does not appear to be impacted by this issue.

Allow me to translate.

It turns out that “being vaccinated for COVID-19” throws off an ANTIBODY-BASED SYPHILIS TEST, and can give false positives.

The reason is that these are a sort of antibodies against substances released from cells attacked by certain diseases and conditions. Thus, they’re not exclusively the downstream product of syphilis.

Normally, certain diseases, certain vaccines, and pregnancy can all throw off this more rapid but less conclusive syphilis test, and that is part of the reason why people are supposed to follow up this easier test, with a test that looks for the actual organism which causes syphilis.

Thus, we have added one more cause for the test to be thrown off.

This is not the same as the HIV test that was thrown off by a particular Australian vaccine, because the antigen in the vaccine actually contained an HIV protein (gp41) as part of the vaccine, and created antibodies against HIV. I talked about that last week. That was a much more direct test interference, easily expected.

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 …

What I find interesting is that one of the things that normally sets off the syphilis test is endocarditis.

Endocarditis, which is inflammation of the inner surfaces of the heart, is one of the three main heart inflammations, thus being pretty damned close to myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the outer sac), both of which have very prominent correlations to the jabs.

So while this means that – NO – the shots are not giving people syphilis – the shots ARE basically acting like an illness, and very much like a known cardiac illness.

You were warned.

Now – while I was researching syphilis, I became interested in the treatment with compounds of mercury.

Traditional mercury-based pastes were used in cures. Whilst this was partially effective, the toxic side effects of the mercury probably outweighed any advantages.

This is actually a HUGE understatement.

It turned out that arsenic was considerably better.

The first effective treatment for syphilis was arsphenamine, discovered by Sahachiro Hata in 1909, during a survey of hundreds of newly synthesized organic arsenical compounds led by Paul Ehrlich. It was manufactured and marketed from 1910 under the trade name Salvarsan by Hoechst AG.^[88] This organoarsenic compound was the first modern chemotherapeutic agent.

It wasn’t too long after that success, that penicillin took over as the real cure for syphilis.

I will come back to MERCURY in a future post, because I found something quite amazing in its history.

But if you look ONE COLUMN TO THE LEFT and TWO ROWS UP…..

COPPER is also bacteriostatic and algicidal – and at concentrations below where it is a health risk. And THAT leads back to a DRINK that Grandmaintexas introduced us to……

Moscow Mule Revisited

Based upon my reading of Grandma’s post on the subject, the Moscow Mule simply is not a proper Moscow Mule unless it is served in copper vessels.

The health effects of COPPER are about as debatable as the effects of mercury – although, in general, copper is much less toxic, so when it’s being “not good for you”, it’s a lot less “not good for you” than lead. At the same time, copper is much MORE toxic to things like algae, fungi, plant roots, and other “pests”, than it is to us, and that is why it is found among the gardening pesticides in hardware stores. The antimicrobial activity of copper is extremely well-documented, but appears to be complex. Simply having copper in the household or workplace environment seems to have health benefits – and this was particularly noted back in the days of less sanitary environments. Water passing through copper fixtures tended not to spread disease.

We tend to forget about OLD SCIENCE, so we can’t put new things into good perspective.

LEAD and other CHEMICAL ADVANCES saved us from the horrible BIOLOGICAL diseases and maladies of the uncivilized life.

Did they have chemical consequences? Yes. The TRICK is REMEMBERING AND ADMITTING OLD RISKS AND BENEFITS while also DISCOVERING AND ADMITTING NEW RISKS AND BENEFITS, then BALANCING HONESTLY with the PROPER PRIORITIES which put PEOPLE FIRST.

It is VERY easy to see where CDC went off the rails with the COVID-19 vaccines, being unable to admit old benefits (of lasting immunity to caught and treated diseases), while also being unable to admit new risks (of vaccines using untested and immature technologies).

Likewise, looking back, it is easy to see that basic sanitation – not vaccination – REALLY conquered diseases. Vaccines came in, mopped up, and took all the credit, by design, because bad people realized that vaccines in the hands of a technological elite, combined with an ignorant populace they can essentially murder and experiment on at will, allow them to basically FARM HUMANITY.

Sorry, Bill Gates. We understand your social engineering of us. We know your M.O. We know your real intentions. Including for the “people of color” you pretend to care about.

You will note that, in general, the further down the periodic table one goes, the more toxic the metals. Surprisingly, the second-lightest one – beryllium – is quite toxic, but even lightweight aluminum simply isn’t all that bad, in the big picture (but you’ve got to keep it on the OUTSIDE). In contrast, if you get down and heavy there with mercury, thallium and lead, or even as far down the table as cadmium and indium, the metals can be quite toxic.

Lead used to be used for plumbing – enough to lend its name to the profession. Copper then took over – before plastic began to displace copper. Nevertheless, copper is still highly valued for plumbing, as well as for electrical wiring.

As noted above, copper in drinking water is an interesting beast. Lead and copper in drinking water are controlled by the EPA under something called the Lead and Copper Rule, or LCR. Note that the linked document, which talks about the most recent “upgrade” to the rule, is over 400 pages. Yeah – there is a MESS of goofiness outside the actual rule there. Most of the concern is about lead, which is now highly restricted. Here is all that is said about copper’s toxicity in the linked explainer:

Acute copper exposure causes gastrointestinal distress. Chronic exposure to copper is particularly a concern for people with Wilson’s disease because they are prone to copper accumulation in body tissue, which can lead to liver damage, neurological, and/or psychiatric symptoms. For a more detailed explanation of the health effects associated with copper see Appendix E of the final rule Economic Analysis (USEPA, 2020). EPA did not propose revisions to the copper requirements; thus, the final rule does not revise the copper requirements.

Copper is basically off the hook at 1.3 ppm or below. That number has not been upgraded. Why is that level important? In my opinion, it’s because copper is bacteriostatic and algicidal in practice at between 0.1 and 1.0 ppm. Thus, one can SAFELY DRINK water which is being purified against microorganisms with copper.

And THAT would include the Moscow Mule, depending upon how long it sits.

I refer you now to an excellent article, which relies on a breathless scaremongering headline, but actually DOES provide a balanced set of viewpoints on both the DANGERS and BENEFITS of dietary copper.

Sipping This Popular Cocktail Is a “Health Hazard,” Experts Say

AFTER 27 MINUTES, YOU MAY BE AT RISK OF HEAVY METAL POISONING.

LINK: https://bestlifeonline.com/moscow-mule-copper-news/

ARCHIVE: https://archive.fo/6YT3X

First of all, copper isn’t really a “heavy metal” IMO, but whatever. It’s heavier than some.

You will note, after reading at the link, that you have to drink a ton of Moscow Mules, or a few that have sat around for a very long time, to MAYBE get sickened by them.

In general, avoid drinking acidic things that have been in contact with copper for a long time, and you will be OK.

Remember – most household water has sat around in copper pipes for quite a while at neutral pH, and it’s simply not toxic (due to copper). You DO get less lead if you flush your water 30 seconds before getting drinking water, but again – we’re talking about levels that would make Romans, Victorians, and even people from 70 years ago howl with laughter at our prissy over-concern – even knowing the science.

Perspective is very important – as you are about to see in a beautiful example of the failure of modern science, thanks to CCP socialism infecting both global science and science publishing.

Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

The fact that Pierre Kory now calls JAMA “PHAMA” is a nice short way of saying that medicine has been utterly taken over by the pharmaceutical industry, and IMO set back several thousand years. Hippocrates would be HORRIFIED by what has happened to medicine – and I say that as somebody OUTSIDE medicine, and a lot closer to the pharmaceutical industry.

IMO it’s too late to save the pharmaceutical industry from scandalous criminal survival – but it’s not too late to save the profession of medicine from utter moral death. And thus, you will be treated to my following scientific opinion.

Steve Kirsch doesn’t play defense. He saw how JAMA (the Journal of the American Medical Association) completely FUMBLED an ivermectin paper, and how Pierre Kory picked it up off the ground, taking complete control, but more or less just standing there, lamenting the bad refs and horrible cheating. So Kirsch did the only thing he does. He grabbed the ball from Kory and ran it back for a touchdown.

“New JAMA paper show Ivermectin blows the COVID vaccines out of the water”

This is an utter reversal of the conclusion of the paper.

All because some guy in the stands named “Massimaux” spotted the free ball and yelled “FUMBLE!!!”

If you understand science, and science publishing, then you will see that what Kirsch did here was BRUTAL. And I’m gonna show you where all the bruises and black eyes are.

I almost feel sorry for JAMA, but not enough to miss this opportunity to LEAP ONTO THE DOGPILE and give AMA’s hare-brained PC leadership a good WEDGIE.

Don’t worry about the AMA. They’re protected by Pfizer, Biden, and the media. And just like any good mafia arrangement, as long as AMA keeps saying the right things, and not saying the wrong things, everything is gonna be OK.

Everything but science. But that’s OK, too.

We’ll take care of things. Just like we did here.

Here is the Kirsch gab that grabbed my attention.

Repeating for Zoe, as well as our silicon friends…..

Steve Kirsch
@stkirsch
22h·

New JAMA paper show Ivermectin blows the COVID vaccines out of the water

https://stevekirsch.substack.com/p/new-jama-paper-show-ivermectin-blows?r=o7iqo&utm_campaign=post&utm_medium=web

New JAMA paper show Ivermectin blows the COVID vaccines out of the water

Whoops! How embarrassing! The CDC gave you bad advice. If you want to survive COVID, you should use the drug they said to avoid, and avoid the drug they said to…

stevekirsch.substack.com

View Link Feed

2,589 likes
208 comments
1,670 reposts
42 quotes

Now, as soon as I saw this, I was going….

“Wait a second. I thought there was some paper just out that Alex Berenson said was basically the end of ivermectin, although scientifically, I know that’s pretty much impossible. I know there is SOME explanation for why this paper (which I have not read yet) has to be deviating in some way from the MANY papers that show limited but solid efficacy – and especially against DEATH – just like HCQ. But this CANNOT be the same paper. No way! Kirsch would not be saying this unless the results were stunningly IN FAVOR of ivermectin, and there is no WAY that some authors with a NEGATIVE-LEANING study would be……. I mean….. WHAT THE HELL????”

SO – I just stopped to see what in the hell paper Kirsch was talking about.

YUP.

This is the SAME PAPER.

ARTICLE: https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/2789362

SUPPLEMENTARY: https://cdn.jamanetwork.com/ama/content_public/journal/intemed/0/ioi220006supp2_prod_1644957301.65433.pdf

This is the SAME PAPER that caused Alex Berenson to issue TWO articles:

Ivermectin fails

To the ivermectin fanatics

Now we’ve discussed (in the comments on this site) Berenson’s very weird attack on Robert Malone when they appeared together on Fox News, which didn’t make sense THEN, but which does NOW – and I will explain that momentarily. But first, back to Kirsch.

Kirsch explains that – YES – this paper states in BOTH its abstract and its conclusion the following:

“The study findings do not support the use of ivermectin for patients with COVID-19.”

However, that is NOT what the data says.

Certainly not to everybody.

Certainly not to me.

In other words, DIFFERENT scientists (like Kirsch, Kory, me, and an anonymous Twitter poster names Massimaux, who found the key issue) have looked at the data, and see something quite different.

Kory goes into a rather long analysis of the whole war against ivermectin, but Kirsch digs into Kory’s article and then finds and elucidates the key nugget – discovered by Massimaux – that just ends the arguments.

It helps to read this in Kirsch’s article, but if you’re going to be lazy, I’ll explain here.

Here is Massimaux’s tweet:

In the I-TECH study, of 490 patients, 241 got Ivermectin and 331 were vaccinated.

Can we compute the vaccine effectiveness AGAINST DEATH and Ivermectin effectiveness AGAINST DEATH? Yes, we can! See the figure.

Which prevented more deaths, The Vaccine or Ivermectin? pic.twitter.com/WszQMQkAYX
— Massimaux (@masimaux) February 20, 2022

Look at the bottom line in the two tables and compare. Not only is ivermectin CLEARLY better than the vaccine at preventing death – the significance of the result is significantly greater.

If the efficacy of ivermectin against death is not true, then very little else in the study is true.

This data says that ivermectin is exactly what we’ve been saying it is. It’s not a miracle cure, but it WORKS – particularly in preventing DEATH – its only real purpose. That result is IN THE PAPER. It is IN THE DATA. And if the authors want to argue that it’s not in the data, because it’s not significant enough, then nothing ELSE is in the data, because most everything else is even LESS significant.

Now it’s very important to realize that this nice little pair of tables FROM THE DATA is not due to the original authors – it’s due to a POST-PUBLICATION “peer review” by somebody who looked at the very same data, and PROVED using the authors’ own data that they were WRONG to say that the data didn’t support use of ivermectin.

So why did the authors tack on that wrong statement?

Did the EDITORS make them tack on that statement?
Did the AUTHORS tack it on to get the paper to publish?
Or is the “peer bias” against ivermectin, mostly due to the media, SO STRONG that scientists didn’t even look through their own data to see a conclusion they didn’t want to see?

Or is it a combination of ALL of these?

It is clearly in the data that ivermectin is three times as effective as the vaccines in preventing death. Even more importantly, if you add in what is known OUTSIDE the paper in question – namely the adverse effects of the vaccine and the safety of ivermectin, then it’s a no-brainer to NOT take the vaccine and to just use ivermectin. And Kirsch explains THAT rather nicely.

The data LITERALLY justify our position.

This was my hunch all along, and as vaccine side effects loomed larger and larger, and ivermectin proved to be rather shockingly harmless, even at antiviral doses comparable to large-animal systemic antiparasitic doses. All ivermectin had to do was prevent death to some moderate extent, and it was a no-brainer that people should take it.

To conclude anything else, based on the data, is murderous folly, in my opinion.

When I was a young lad – a mere student – but also one who WROTE PAPERS (because I had a great professor who TRAINED US to be full-blooded scientists), we EXPECTED to be CRITICIZED in peer review by people exactly like Steve Kirsch, Pierre Kory, and myself. We expected that others would look at data and see it completely differently.

And we would then have to ACKNOWLEDGE the alternative interpretations, or convince the editors that the criticism was not even worth acknowledging (a VERY rare occurrence in any legitimately contested field).

My lab had PRACTICE criticizing other people’s work – and we expected it in return. I personally found quite a few errors in the literature. Most were small – mostly problems of the writing – but some were huge and affected the science. Sometimes the big errors would only partially alter the author’s conclusions, but other times they had a significant impact.

However, I have to admit that I never ran into data which PROVED THE OPPOSITE of the authors’ main conclusion – even if only to the critic – and THAT is what we have here.

PEER REVIEW is designed to subject a paper to (hopefully at least TWO) critical readers who will very likely DEMAND improvements. Those improvements often mean acknowledging DIFFERENT views of the data as being possible and maybe even reasonable.

That kind of QUALITY peer review was VERY OBVIOUSLY not done here.

What we have RIGHT HERE is a demonstration that HERD REVIEW is much more important than PEER REVIEW.

PEER REVIEW is subject to BIAS. It is subject to SUBVERSION and GAMING.

I go back to the Zhang mask paper, for crying out loud.

To me, this will always remain a horrifying example of “fitting the data to the theory”, rather than looking to see what the data says. You can just look at this graph and see the crime.

I lay this stuff SQUARELY at the feet of SOCIALISM, which has politicized science and removed control of science from the people of science themselves, investing much of it in a media which WILL NOT question government narratives. People raised under socialism who become “go-alongers” – and so SOME degree that is everybody – stop questioning things that need to be questioned.

I have WATCHED and I have SEEN how WEF and CCP corruption have degraded science everywhere.

They’re not going to fix this stuff – at least not yet.

But until then, know this:

Ivermectin WORKS, and it was just proven by people who said it doesn’t work.

Thanks to HERD REVIEW.

One last point.

Why did Alex Berenson not see this?

IMO, it’s because Berenson is simply not a scientist – he’s an investigative journalist. Thus, his virtue-signaling attack on Malone was meant to show “journalistic balance”, NOT that he himself had deeply researched the history of the topic, in which case he (Berenson) would have likely said “Yes, Malone really is the most foundational of the founding fathers of the tech.”

But let’s not blame Alex too hard. THE AUTHORS OF THIS STUDY – that’s right – the authors themselves – didn’t see it, either.

See what I’ve always said? Real science is contentious.

But it has a good heart.

It wants the TRUTH.

ENJOY THE SHOW.

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

W

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

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

NATTOKINASE for COVID and CLOT-SHOT HIGH BLOOD PRESSURE! JUST DO IT!

A couple of days ago there was some more discussion of nattokinase for helping lower the blood pressure spike many people are seeing after Covid or unfortunately having taken the vaxx. Some here, including RAC and TradeBait2 have had success with it, and I take it daily for general cardiovascular health.

Today, I talked to another man I know who had the shots (sick wife, long story) and had a high blood pressure episode two weeks ago that put him in the emergency room. He was already on Losartan, but it failed to keep his pressure down. He was in the 200/170 range, stroke territory.

I recommended that he try nattokinase, as I mentioned here in comments a few days ago. His pressure dropped 20 points within a few days. It’s now been a week on the natto. His pressure this morning was down 60 points, and in the normal range!

Gail Combs posted this information about nattokinase a few days ago:

Nattokinase | Memorial Sloan Kettering Cancer Center

Nattokinase is an extracelluar enzyme secreted by the bacterium Bacillus subtilis, used to ferment boiled or steamed soybeans resulting in a preparation called nattō. Nattō has been consumed as food in Japan for several centuries. Nattokinase is also available as a supplement and is most known for its effects on prevention and treatment of clots and to improve blood circulation.
Nattokinase may help prevent clot formation and reduce blood pressure. It has not been tested as a cancer treatment in humans.
Nattokinase is an enzyme produced from nattō, a traditional Japanese food made from soybeans fermented with the bacterium, Bacillus subtilis. Lab studies suggest it can break down fibrin in the blood that forms clots or affect some factors that characterize Alzheimer’s disease. Human studies are limited, and suggest nattokinase may reduce high blood pressure. Although nattokinase has been promoted as an alternative anticancer treatment, clinical studies have not been conducted.
Nattokinase may increase the risk of bleeding in patients when used with blood-thinning drugs….

I know this is anecdotal information, but I think it is fantastic! Nattokinase is natural and much less likely to have side effects than a pharmaceutical, so if you have high blood pressure issues, from Covid, clot-shot, or otherwise, you might want to take a good look at the research and try it!

The Nuremberg Code vs US Law and The Push For World Government

TradeBait2 Made the comment:

I have been reminding folks on here – the Fed has to be bankrupted at some point. It will either be by the white hats or the black hats. The Gab post you show is correct for the most part IMO. The Fed has fueled the Great Reset, which is why they could care less about how much debt we have in America because we will not exist as an independent nation in their black hat world.
Digital one world currency is the plan. Why do you think there were coin shortages recently? Why do you think they hate crypto and parallel economies so much? Why do they want America at odds with Russia, but falling right in line with China? Where Xi falls in this I am not certain. But I do know China and the Chi-coms are a CB [central bank] creation.
The linchpin is digital currency.
Follow the money….

That is the first half of the comment

Actually I can see where he is going since I also have warned of this much earlier.

The Push For World Government

A few years ago Soros directed the USA to overthrow the ELECTED government in both Syria and Ukraine. (Trump side stepped both.)

Why? Because the EU is the model for a global government. Soros wanted the EU to annex the Ukraine. The elected president said HE!! NO! so he was ousted and a pro-EU puppet was put in his place who has since been voted out while Trump was in the White House.

Russia tossed Soros out and put out a warrant for him. Russia makes much of their money selling gas to Europe. It also gives them leverage to keep the EU from expanding into their sphere of influence. Soros wants to remove Russia’s leverage by putting in a pipeline from the middle east to Europe. ALL the countries that were opposed to that pipeline have been overthrown EXCEPT for Syria.

If you want a World Government similar to the European Union then you are on Soros side. If you want sovereign nations you are on the side of Russia….. AND I am still of that opinion.

BREXIT THE MOVIE will give you the details on how the EU is actually run.

https://www.youtube.com/watch?v=UTMxfAkxfQ0

Former World Trade Organization Director-General Pascal Lamy tells you point blank that the EU is the template for the desired World Government and it has been the plan since the 1930s.

All had lived through the chaos of the 1930s — when turning inwards led to economic depression, nationalism and war. All, including the defeated powers, agreed that the road to peace lay with building a new international order — and an approach to international relations that questioned the Westphalian, sacrosanct principle of sovereignty…
Pascal Lamy, Whither Globalization

Lamy is quite blunt in stating national sovereignty is passé:

…more than half a century ago that the Frenchman Jean Monnet, one of the shapers of post-war Europe, said, “The sovereign nations of the past can no longer provide a framework for the resolution of our present problems. And the European Community itself is no more than a step towards the organizational forms of tomorrow’s world.” His assessment was as valid then as it is now….
Pascal Lamy, Global Governance: Lessons from Europe

Lamy indicates that a super state fashioned after the European Union is the goal and he calls for European-Inspired Global Governance:

This is what Global Warming was really about. We have all seen the political message morph over the decades from Global Warming to Climate Change to Weather Weirding.

As H.L. Mencken said:

“The whole aim of practical politics is to keep the populace alarmed — and hence clamorous to be led to safety — by menacing it with an endless series of hobgoblins, all of them imaginary.”

In other words, create a crisis to order to implement Diocletian’s Problem-Reaction-Solution

Mencken also warns:

“The urge to save humanity is almost always only a false face for the urge to rule it.”

The UN put the concept into practice via the IPCC. The IPCC mandate states:

The Intergovernmental Panel on Climate Change (IPCC) was established by the United Nations Environmental Programme (UNEP) and the World Meteorological Organization (WMO) in 1988 to assess the scientific, technical and socio-economic information relevant for the understanding of human induced climate change, its potential impacts and options for mitigation and adaptation. http//www.ipcc-wg2.gov/ (No longer available)
IPCC

Notice the IPCC ASSUMES the hypothesis of human induced climate change IS TRUE and goes from there.

With Reagan killing off the Cold War, Pascal Lamy takes ‘Practical Politics’ the next step, by telling us about a “new enemy to unite us” (Global Warming) A global enemy needed to create Legitimacy, one of the ‘four legs’ needed to implement a global government…

I see four main challenges for global governance today.
The first one is leadership, i.e. the capacity to embody a vision and inspire action, in order to create momentum. Who is the leader? Should it be a superpower? A group of national leaders? Selected by whom? Or should it be an international organization?
The second one is efficiency, i.e. the capacity to mobilize resources, to solve the problems in the international sphere, to bring about concrete and visible results for the benefit of the people. The main challenge here is that the Westphalian order gives a premium to “naysayers” who can block decisions, thereby impeding results. The ensuing viscosity of international decision-making puts into question the efficiency of the international system.
The third one is coherence, for the international system is based on specialization. Each international organization focuses on a limited number of issues. The World Trade Organisation deals with trade, the International Labour Organisation with labour issues, the World Meteorological Organisation with meteorology and so the list continues. It is a fact: the UN is not really overarching, assuming this was the initial intention.
The last challenge that I see is that of legitimacy— for legitimacy is intrinsically linked to proximity, to a sense of “togetherness”. By togetherness, I mean the shared feeling of belonging to a community. This feeling, which is generally strong at the local level, tends to weaken significantly as distance to power systems grows. It finds its roots in common myths, a common history, and a collective cultural heritage. It is no surprise that taxation and redistribution policies remain mostly local!
There is one place where attempts to deal with these challenges have been made and where new forms of governance have been tested for the last 60 years: in Europe. The European construction is the most ambitious experiment in supranational governance ever attempted up to now. It is the story of a desired, delineated and organized interdependence between its Member States…. http://www.wto.org/english/news_e/sppl_e/sppl220_e.htm
Pascal Lamy

In another presentation Lamy again addresses the problem of legitimacy:

It gives me great pleasure to be here today to participate in this thematic debate on the United Nations in global governance, an issue of the utmost importance given the urgency of the global challenges we are facing… As for legitimacy, I see two avenues to strengthen it. First, domestically, by increasing the visibility of international issues and giving citizens a greater say…. https://archive.globalpolicy.org/social-and-economic-policy/the-three-sisters-and-other-institutions/global-governance-and-the-three-sisters-1-11/50398-lamy-urges-raising-un-ecosoc-profile.html%3Fitemid=id.html
Pascal Lamy

By now, with Al Gore exiting stage left, Trump entering stage right, it is pretty obvious that ‘Global Warming’ has lost its high panic factor and the climb down is in progress. However the need for a ‘Crisis to Unite Us’ and a reason to implement ‘Agenda 21 – Sustainability’ and ‘Global Governance’ still remains. WORSE for the Globalists the fiat currency central banking system is on its last legs and about to IMPLODE, as many people like Dave of the X22 Report and Clif High and others have been warning us. Up to now we have been wondering what the next hobgoblin would be. And now we know it’s COVID -19!!! A Bio-Weapon and a Poison Jab that kills off a lot of the population, crashes the world economy and ushers in a Vaccine Digital Passport soon to be linked to the BRAND NEW DIGITAL WORLD CURRENCY and Social Credit Score.

And that brings us to the second part of TradeBait2’s comment.

…… You do not want to use the Nuremberg Code as your get out jail free card from jabs. You fall into the hands of international law superseding national law. It’s a set up, don’t fall for it.
Cannot tell you the number of times I have prepared a post and deleted it because I doubted folks on here would pay attention or believe it. This is the world I lived in for 35 years and escaped.

As I showed above that “international law superseding national law” is exactly what Pascal Lamy was yammering about a decade ago and what Klaus Schwab is threatening us with now.

So how do we escape this TRAP if it is being set?

Use USA LAW!

I find it interesting that the internet is FULL of the Nuremberg Code…….

……and the GERMAN/CALIFORNIA LAWYER Reiner Füllmich and 50 Lawyers, but I went nutz trying to find the US LAWS. It took me over ½ hour.

And WHY does Reiner Füllmich have no problem with YouTube???? When everyone else gets the boot?

https://duckduckgo.com/?q=Reiner+F%C3%BCllmich+youtube&t=brave&ia=videos&iax=videos

JW in Germany even brought us this comment:

I watched it for about half an hour and thought it was important enough to post here. The dozens of witnesses/experts that will be speaking in the next days are from around the world…many of the names you may already know.
Day 1 Opening Session of the Grand Jury Proceeding
A group of international lawyers and a judge are conducting criminal investigation modeled after Grand Jury proceedings in order to present to the public all available evidence of Covid 19 Crimes Against Humanity to date against “leaders, organizers, instigators, and accomplices” who aided, abetted, or actively participated in the formulation and execution of a common plan for a pandemic
https://gettr.com/post/psoiulc122

Those are things that make you go HMMMmmm…..

I think Reiner Füllmich and his group is sincere but it is very very possible they are being used.

So after a LOT of digging at Cornell Law I found the provision that covers the situation for the military: 10 U.S.C. § 1107. “This provision prohibits the administration of investigational new drugs, or drugs unapproved for their intended use, to service members without their informed consent.”

And finally after a lot more searching I stumbled across the information that civilians are covered under a FDA Regulation and not a law:
CFR – Code of Federal Regulations Title 21 as of January 6, 2022

Subpart B – Informed Consent of Human Subjects
   § 50.20 – General requirements for informed consent.
   § 50.23 – Exception from general requirements.
   § 50.24 – Exception from informed consent requirements for emergency research.
   § 50.25 – Elements of informed consent.
   § 50.27 – Documentation of informed consent.

[Code of Federal Regulations]
[Title 21, Volume 1]
[CITE: 21CFR50.20]

TITLE 21–FOOD AND DRUGS
CHAPTER I–FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES

SUBCHAPTER A – GENERAL
PART 50 — PROTECTION OF HUMAN SUBJECTS
Subpart B – Informed Consent of Human Subjects
Sec. 50.20 General requirements for informed consent.
Except as provided in §§ 50.23 and 50.24, no investigator may involve a human being as a subject in research covered by these regulations unless the investigator has obtained the legally effective informed consent of the subject or the subject’s legally authorized representative. An investigator shall seek such consent only under circumstances that provide the prospective subject or the representative sufficient opportunity to consider whether or not to participate and that minimize the possibility of coercion or undue influence. The information that is given to the subject or the representative shall be in language understandable to the subject or the representative. No informed consent, whether oral or written, may include any exculpatory language through which the subject or the representative is made to waive or appear to waive any of the subject’s legal rights, or releases or appears to release the investigator, the sponsor, the institution, or its agents from liability for negligence.
[46 FR 8951, Jan. 27, 1981, as amended at 64 FR 10942, Mar. 8, 1999]

BUT there is a cockroach in the ointment.

§ 50.24 – Exception from informed consent requirements for emergency research.

[Code of Federal Regulations]
[Title 21, Volume 1]
[CITE: 21CFR50.24]

TITLE 21–FOOD AND DRUGS
CHAPTER I–FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES

SUBCHAPTER A – GENERAL
PART 50 — PROTECTION OF HUMAN SUBJECTS
Subpart B – Informed Consent of Human Subjects
Sec. 50.24 Exception from informed consent requirements for emergency research.
(a) The IRB responsible for the review, approval, and continuing review of the clinical investigation described in this section may approve that investigation without requiring that informed consent of all research subjects be obtained if the IRB (with the concurrence of a licensed physician who is a member of or consultant to the IRB and who is not otherwise participating in the clinical investigation) finds and documents each of the following:
(1) The human subjects are in a life-threatening situation, available treatments are unproven or unsatisfactory, and the collection of valid scientific evidence, which may include evidence obtained through randomized placebo-controlled investigations, is necessary to determine the safety and effectiveness of particular interventions.
(2) Obtaining informed consent is not feasible because:
(i) The subjects will not be able to give their informed consent as a result of their medical condition;
(ii) The intervention under investigation must be administered before consent from the subjects’ legally authorized representatives is feasible; and
(iii) There is no reasonable way to identify prospectively the individuals likely to become eligible for participation in the clinical investigation.
(3) Participation in the research holds out the prospect of direct benefit to the subjects because:
(i) Subjects are facing a life-threatening situation that necessitates intervention;
(ii) Appropriate animal and other preclinical studies have been conducted, and the information derived from those studies and related evidence support the potential for the intervention to provide a direct benefit to the individual subjects; and
(iii) Risks associated with the investigation are reasonable in relation to what is known about the medical condition of the potential class of subjects, the risks and benefits of standard therapy, if any, and what is known about the risks and benefits of the proposed intervention or activity.
(4) The clinical investigation could not practicably be carried out without the waiver.
(5) The proposed investigational plan defines the length of the potential therapeutic window based on scientific evidence, and the investigator has committed to attempting to contact a legally authorized representative for each subject within that window of time and, if feasible, to asking the legally authorized representative contacted for consent within that window rather than proceeding without consent. The investigator will summarize efforts made to contact legally authorized representatives and make this information available to the IRB at the time of continuing review.
(6) The IRB has reviewed and approved informed consent procedures and an informed consent document consistent with § 50.25. These procedures and the informed consent document are to be used with subjects or their legally authorized representatives in situations where use of such procedures and documents is feasible. The IRB has reviewed and approved procedures and information to be used when providing an opportunity for a family member to object to a subject’s participation in the clinical investigation consistent with paragraph (a)(7)(v) of this section.
(7) Additional protections of the rights and welfare of the subjects will be provided, including, at least:
(i) Consultation (including, where appropriate, consultation carried out by the IRB) with representatives of the communities in which the clinical investigation will be conducted and from which the subjects will be drawn;
(ii) Public disclosure to the communities in which the clinical investigation will be conducted and from which the subjects will be drawn, prior to initiation of the clinical investigation, of plans for the investigation and its risks and expected benefits;
(iii) Public disclosure of sufficient information following completion of the clinical investigation to apprise the community and researchers of the study, including the demographic characteristics of the research population, and its results;
(iv) Establishment of an independent data monitoring committee to exercise oversight of the clinical investigation; and
(v) If obtaining informed consent is not feasible and a legally authorized representative is not reasonably available, the investigator has committed, if feasible, to attempting to contact within the therapeutic window the subject’s family member who is not a legally authorized representative, and asking whether he or she objects to the subject’s participation in the clinical investigation. The investigator will summarize efforts made to contact family members and make this information available to the IRB at the time of continuing review.
(b) The IRB is responsible for ensuring that procedures are in place to inform, at the earliest feasible opportunity, each subject, or if the subject remains incapacitated, a legally authorized representative of the subject, or if such a representative is not reasonably available, a family member, of the subject’s inclusion in the clinical investigation, the details of the investigation and other information contained in the informed consent document. The IRB shall also ensure that there is a procedure to inform the subject, or if the subject remains incapacitated, a legally authorized representative of the subject, or if such a representative is not reasonably available, a family member, that he or she may discontinue the subject’s participation at any time without penalty or loss of benefits to which the subject is otherwise entitled. If a legally authorized representative or family member is told about the clinical investigation and the subject’s condition improves, the subject is also to be informed as soon as feasible. If a subject is entered into a clinical investigation with waived consent and the subject dies before a legally authorized representative or family member can be contacted, information about the clinical investigation is to be provided to the subject’s legally authorized representative or family member, if feasible.
(c) The IRB determinations required by paragraph (a) of this section and the documentation required by paragraph (e) of this section are to be retained by the IRB for at least 3 years after completion of the clinical investigation, and the records shall be accessible for inspection and copying by FDA in accordance with § 56.115(b) of this chapter.
(d) Protocols involving an exception to the informed consent requirement under this section must be performed under a separate investigational new drug application (IND) or investigational device exemption (IDE) that clearly identifies such protocols as protocols that may include subjects who are unable to consent. The submission of those protocols in a separate IND/IDE is required even if an IND for the same drug product or an IDE for the same device already exists. Applications for investigations under this section may not be submitted as amendments under §§ 312.30 or 812.35 of this chapter.
(e) If an IRB determines that it cannot approve a clinical investigation because the investigation does not meet the criteria in the exception provided under paragraph (a) of this section or because of other relevant ethical concerns, the IRB must document its findings and provide these findings promptly in writing to the clinical investigator and to the sponsor of the clinical investigation. The sponsor of the clinical investigation must promptly disclose this information to FDA and to the sponsor’s clinical investigators who are participating or are asked to participate in this or a substantially equivalent clinical investigation of the sponsor, and to other IRB’s that have been, or are, asked to review this or a substantially equivalent investigation by that sponsor.
[61 FR 51528, Oct. 2, 1996]

And now we go to USA lawyer, Attorney Thomas Renz and his interview on Bannon’s War Room.

Episode 1,619 – Beijing Olympics Fail; Legal/Financial Investigations Of Big Pharma

https://rumble.com/vu5amo-episode-1619-beijing-olympics-fail-legalfinancial-investigations-of-big-pha.html

ROUGH TRANSCRIPT (start at 18:15)

ATTORNEY THOMAS RENZ: We have to get it to the public and that is where the War room is so important.
Se are going to be submitting this to a case in Alabama. We are going to be submitting ths to a number of different places in the military, ahhh I guess law enforcement world. And we are looking to bring this into the civilian law enforcement as well. There is no question as to what is happening. These are major crimes and you know Steve, I don’t know if you have got this but we just yesterday, dated February 4th, got a document from the CDC that re-affirms everything we said last week when we said they know this. If you are interested that document actually says it is was in the meeting yesterday, it was presented yesterday it says the CDC is working to monitor these things and they are monitoring the DOD data. Which indicates to me, I don’t know if you have heard the DOD s response? DOD to me has committed fraud and conspiracy. They have said there baseline data from 2016 to 2020 was wrong. They didn’t notice it until we pointed it out in the whistle blower testimony. But some how even though they didn’t notice it, it magically got corrected in 2021.

I mean seriously, How stupid do they think the American people are?

STEVE BANNON: What about adjudicating this. What about Alabama? (21:40)

RENZ: We have a case in Alabama where we are challenged the EUA authorization of the vaccine….. Balance of harm tests…. Generally you have to show more benefit than injury… we are also challenging on mis branding, because the CDC changed the definition of vaccines so they could call these gene therapies a vaccine. BTW Pfizer and Moderna have admitted they are gene therapy in their documents. And we have challenged it on several other fronts so that’s in court. This document and all this DOD stuff just came to us. We have declarations under penalty of perjury and those declarations will be submitted to the court. They are getting updated right now because we’ve had this new data come forward related to this…. We have been working with attorneys all over the world and around the country… and we have been getting this data out and we are giving it to anyone who wants to use it anywhere they can. And we believe it will help. We have to find the right court like you said. Until we find a court that is willing to listen and have an evidentiary hearing, it’s tough. We are going to have more info on that coming up…..

STEVE: asks about military JAG system and Senator Johnson. Senator Johnson first.

RENZ: The problem for Senator Johnson is he is not getting enough support from other Senators. He has gotten NO RESPONSE from anyone else [including Rand Paul but he does not say that.]

STEVE: What about JAG? [24:50]

RENZ: Since the data has only been out for a week or two, we are working thru a number of JAG officers….. I got another letter this week…. From all places the Texas National Guard, one of the people there saying they are going to reject all the religious exemptions and we don’t want doctors giving medical exemptions. They actually say they view it as a COMMAND ISSUE and not a medical issue. So if a doctor thinks a soldier should not have this for a medical reason, they are to shut-up and take orders according to this document. We submitted that to Senator Johnson as well as some others.

This is a disaster in the military and they have created a situation where it is very very difficult for our solders to fight this. We do however have quite a number of military personnel stepping forward. And quite a number of JAG officers and others who, because of the publicity we have gotten on this, in the last week or so, are now wiling to step up and do something so we’ll see.

It goes on to Edward Dowd about the insurance industry data about unexpected deaths in working age people from there. Steve Bannon mentions that Zero Hedge covered the information given too. Suicide? How Some Life Insurance Companies Are Dealing With Experimental Vaccines Deaths

A very informative earlier video from the War Room showing the DOD changing the data from Thomas Renz. It also has Ed Dowd, a Financial guru who worked for Blackrock…. Yeah, Blackrock. He is calling out not only the vaccine manufacturers but the FDA for massive FINANCIAL fraud similar to ENRON. The video also has an interview with Dr Malone.

From 27:00 to 35:15 minutes

https://rumble.com/vtkou8-episode-1602-the-big-short-pfizer-and-moderna-the-new-enron-are-criminal-ch.html

-GC

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

Big Pharma – Government – University Collusion on COVID Vaccines

Newly Uncovered COVID Vaccine Contracts Lead Unexpectedly to Academic Corruption and Shill Science Attacks on Honest, Skeptical Scientists

A Gail Combs deep dive into a tangent of Karen Kingston’s latest revelation on Pfizer Comirnaty vaccine deaths and injuries, leads back to the war against truth-telling doctors and scientists – this time by their own CORRUPT university employers.

PREFACE by Wolf Moon

Remember people saying that there was no such thing as the “FDA-approved” Comirnaty version of the Pfizer vaccine in existence?

Well, it turns out that REAL, LIVE COMIRNATY is out there, it has already killed over 50 people [in VAERS – yeah – do the math – x20 (1000), x40 (2000), or x100 (5000)], and – now even more shocking – there was some kind of bureaucratic screw-up in the contract and approval process which makes Pfizer LIABLE for all the deaths and injuries.

Look – I don’t know about the latter part – that’s “the law”, which is basically filled with LIES at this point. Whether any of these people will ever answer for anything is highly debatable, in my opinion.

But that’s not where this goes.

Gail Combs started looking at this video, and discovered ANOTHER scandal – the fact that universities which are silencing and firing honest doctors and scientists are not doing so from some misperception or moral high ground. These universities are turning on honest doctors and scientists because the universities themselves are COMPROMISED – by money, corruption, and the involvement of OTHER scientists at those same universities in the “scamdemic”.

We don’t yet know how deep this goes, but we do know this – the universities are clearly in cover-up mode. It’s not just limited to the vaccines. Fauci’s horrifying executioner remdesivir was forwarded past Trump, thanks to “work” done at one such university.

Follow along with Gail and you’ll see the SHAME of what has happened to many American universities, once bastions of free thinking and HONESTY – now CORRUPT and enemies of TRUTH.

-Wolf

START HERE….

FDA Broke Pfizer’s EUA Shield: Liability Protection Gone, Time To Bring Down The Gavel (10 minutes)

Stew Peters Show, Published January 26, 2022

LINK: https://www.redvoicemedia.com/2022/01/fda-broke-pfizers-eua-shield-liability-protection-gone-time-to-bring-down-the-gavel/

LINK: https://rumble.com/vtcugv-fda-broke-pfizers-eua-shield-liability-protection-gone-time-to-bring-down-t.html

Stew Peters interviews former Pfizer employee and analyst Karen Kingston, who does deep dives into patents and contracts. She found the three major contracts for Moderna, J&J and Pfizer.

Stew: “Karen says she found contracts showing the DOD was in control of what data went to the FDA from vaccine trials. If that is true, then DOD not Big Pharm, was the central figure in any vaccine cover-up…. Military leaders maybe exposed as well…. When the FDA approved the Pfizer vax under the name Cormirnaty, it somehow broke their immunity shield.”

That is not exactly correct. DOD delegated it to Pfizer. With the Pfizer contract with the US Army, it appears that, it was delegated to Pfizer to have the ability to manipulate the data that was submitted to the FDA.

With the Moderna contract for example it shows HHS [US Dept of Health & Human Services] had the authority to manipulate the data that was submitted to the FDA. The contract date is 4/03/2020 for ½ billion $$$ with NIH subsidizing a lot of the contract. It was for producing 100 million mRNA vaccines. The contract (shown) states:

* Contractor shall submit draft FDA submission to BARDA at least 15 days prior to FDA submission
* BARDA will provide feedback to Contractor within 10 days of receipts
* The Contractor MUST address, in writing its consideration of all concerns raised by BARDA prior to FDA Submission.

NOTICE THE DATE 4/03/202. No wonder they wanted to kill HCQ in April!

April 7, 2020 Trump’s Critics Attack His Optimistic Case for Hydroxychloroquine

Karen goes on to say that the contract says that BARDA can provide EDITS to the Data and THAT gets submitted to the FDA. She has never seen anything like this before. This [editing] is why the data was so phenomenally positive. This explains why the Whistle Blowers at Ron Johnson’s Formun found the DOD data had been ‘edited’ to remove the tons of adverse events.

She also said a lot of that contract is redacted including the Key personnel at BARDA .

The J&J contract of an mRNA vaccine was signed 08-Apr-2015 and 60 out of the 90 pages are redacted.

She then goes into the most recent contract. It is a joint mission of Dept of Defense and Dept of Health & Human services who contract with Pfizer/BoiNTech “for the co-development and distribution (excluding China) of a potential mRNA-based Coronavirus vaccine aimed at preventing Covid-19 infection“….. LOTS OF REDACTION….

The Research Collaboration & License Agreement
by and between
PFIZER INC.
and
BIONTECH RNA PHARMACEUTICALS GmbH [Germany]
and
BIOTECH AG
July 20, 2018

Again the DATE July 20 2018 shows mRNA vaccines for the next outbreak of Covid WAS A DONE DEAL!

@5:00 Karen EXPLAINS the OOPS in the Contract. You can not have a contract for commercialization WITHOUT A FDA APPROVAL DATE!!! So how in Hades did they KNOW there would be FDA APPROVAL? This shows it was PRE-PLANNED IN 2018.

@7:00 She also found the Cormirnaty lots used in the USA and the VAERs data

LOT NUMBERS
FD7220
FE3592
FF2587
FF2588
FF2590
FF2593
FF8841
VAERS Dec 2021
Deaths = 51
Disabilities = 94
Hospitalizations 415

So who is BARDA?

Biomedical Advanced Research and Development Authority (BARDA)

WE ARE BARDA
The Biomedical Advanced Research and Development Authority (BARDA), within the Office of the Assistant Secretary for Preparedness and Response in the U.S. Department of Health and Human Services, provides an integrated, systematic approach to the development of the necessary vaccines, drugs, therapies, and diagnostic tools for public health medical emergencies such as chemical, biological, radiological, and nuclear (CBRN) accidents, incidents and attacks, pandemic influenza, and emerging infectious diseases.
Together with our industry partners, BARDA promotes the advanced development of medical countermeasures to protect Americans and respond to 21st century health security threats.

About NIH | National Institutes of Health (NIH)
A part of the U.S. Department of Health and Human Services, NIH is the largest biomedical research agency in the world

So there is your Fauci connection.

And that brings me to the digging I have been doing.

I start with the Chair of the COVID VACCINE ADVISORY BOARD, Hana El Sahly, M.D. of Baylor College of Medicine. She is the one who wrote the Remdesivir paper for Fauci, just in the nick of time so he could get that toxin approved for the use in hospitalized elderly Covid patients.

Baylor College rang a major bell with me. This Yahoo News articles shows why:

August 2, 2021

Dr. Peter McCullough Sued by Baylor After Appearance on Stew Peters Show…

Dr. Peter McCullough is being sued by the healthcare system that just mandated 40,000 employees to get the jab, and they’re doing it out of spite. Here’s the list of emails to those targeting him, if you wish to let them know how you feel….

Sidebar by Wolf – Dr. McCullough on Stew Peters

I dare anybody to watch this and find anything wrong with anything that Peter McCullough is saying. He is basically admitting – at a time when social media was still removing people for saying as much – that the vaccines seemed to no longer be working. And NOW we know why – because of the delta variant.

LINK: https://www.redvoicemedia.com/2021/08/stew-peters-show-dr-peter-mccullough-destroys-vaxx-efficacy-narrative-united-pilots-file-suit-to-stop-mandate/

LINK: https://rumble.com/vlblnr-dr.-peter-mccullough-destroys-vaxx-efficacy-narrative-united-pilots-file-su.html

Dec 20 2021

Doctor fired for spreading COVID misinformation finds supportive Crowd in Bartlesville.

Dr. Peter McCullough, a Dallas cardiologist who is largely discredited by the scientific community [Remember Dr McCullough is the MOST PUBLISHED AUTHOR OF SCIENTIFIC PAPERS IN THE USA.] for his assertions that the COVID-19 vaccines are unsafe and that early treatment options have been suppressed….
While McCullough said that doctors were probably afraid to show up to the event, one of Oklahoma’s top infectious disease physicians, Dr. Anuj Malik, director of infection prevention and control at Ascension St. John, said that the doctors he spoke to were not afraid to attend. They were just not interested in sitting through what would be seen as a “politically-motivated, ideological speech by a modern-day quack.”
Malik said. “With all due respect, none of McCullough’s ideas have been supported by any randomized, double-blind, controlled clinical trials,” [<=== THIS IS ALWAYS THE EXCUSE! NO data is allowed except that PAID FOR BY BIG PHARMA/NIH.]
McCullough shared what he said was a threatening letter from the American Board of Internal Medicine warning that he could lose his certification for spreading misinformation.
There is likely a good reason for his concern about losing certification. A Dallas County court granted a temporary restraining order against him in July on behalf of Baylor Scott & White Health for continuing to claim titles, including vice chief of internal medicine at Baylor University Medical Center, even after he was fired from Baylor in February.
In addition, an article in Medscape, an online global news source for physicians and healthcare professionals, reported that Texas A&M College of Medicine, Texas Christian University and University of North Texas Health Science Center School of Medicine have also cut ties with McCullough for spreading misinformation….

So the Baylor Connection made me curious.

And looky what I found! No wonder Baylor sued Dr McCollough in the hopes of shutting him up as they entice people to be lab rats!

June 8, 2021

Baylor launches clinical trial for COVID-19 vaccine booster

Researchers at the Vaccine and Treatment Evaluation Unit at Baylor College of Medicine have launched a clinical trial to study the safety and efficacy of a booster dose of the Moderna-mRNA-1273 COVID-19 vaccine…. The study is being conducted by the Infectious Disease Clinical Research Consortium in collaboration with the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health…. “It’s important to determine the magnitude of the immune response after a booster dose in persons who received different vaccines in their initial vaccine regimen. We will also be looking at the safety of a booster dose,” said Dr. Robert Atmar, professor of infectious diseases at Baylor and co-principal investigator of the national study.
This activity is supported by the Infectious Diseases Clinical Research Consortium (IDCRC) through the National Institute of Allergy and Infectious Diseases (NIAID) (UM1AI148684). The IDCRC, consisting of the Vaccine Treatment and Evaluation Units (VTEUs) and the IDCRC Leadership Group, was formed in 2019 to support the planning and implementation of infectious diseases clinical research that efficiently addresses the scientific priorities of NIAID. The consortium includes infectious diseases leaders and clinical researchers from Emory University, University of Maryland School of Medicine, Baylor College of Medicine, Cincinnati Children’s Medical Center and University of Cincinnati, FHI360, Fred Hutchinson Cancer Research Center, Johns Hopkins University, Kaiser Permanente Washington Health Research Institute, New York University, Saint Louis University, Vanderbilt University Medical Center, University of Alabama at Birmingham, University of Rochester, University of Washington, and NIAID. For more information about the IDCRC, please visit www.IDCRC.org.

https://idcrc.org/_includes/images/group_fullv2.jpg

January 21, 2020, Rockville, MD [Above photo]

With presentations from members of the NIAID, the Infectious Diseases Clinical Research Consortium (IDCRC) Leadership Group, and VTEU PIs, the inaugural meeting of the IDCRC began with opening remarks from Anthony Fauci, MD, NIAID director. Session topics featured details on working with the NIAID, the Division of Microbiology and Infectious Diseases, and grants management. Breakout sessions facilitated thoughtful discuss on the consortium’s scientific agenda, flu, STIs, malaria, enteric, and emerging diseases, mentoring and career development, special populations, emerging lab sciences, and operations.
https://idcrc.org/about/index.html

Leadership Operations Center

The IDCRC institutions are leaders of influential infectious diseases, immunology and clinical research programs focused on vaccines and STIs at eight top academic institutions and affiliates across the country. The programs, faculty and collaborators at these institutions have exceptional NIH/NIAID network and international connectivity, a history of performing outstanding ID clinical research and the experience and capability of rapidly responding to ID threats.

Bio Robert Atmar

Dr. Atmar is a member of the Baylor Vaccine Research Center and the federally funded Vaccine Treatment and Evaluation Unit (VTEU). This research group performs Phase I to Phase IV studies of experimental and licensed vaccines, and Dr. Atmar serves as Principal Investigator or Co-Investigator for the clinical trials. Dr. Atmar and the research group have been involved in important studies that led to the licensure of live attenuated and high dose inactivated influenza virus vaccines. They also have performed many studies evaluating vaccines targeting pandemic influenza, including H5N1, H9N2 and H7N9 viruses, and they have evaluated methods to improve vaccine immunogenicity, including delivery of vaccine by different routes of administration, different dosages, and with different adjuvant preparations. The group has also evaluated vaccines targeting other pathogens, including those with importance to biodefense.

NIH Clinical Trials Baylor: LINK

484 ACTIVE Studies found for: Baylor College of Medicine | Recruiting, Enrolling by invitation Studies

2,625 studies found in data base [Baylor College] and 4195 for just Baylor.
24,250 studies – Just college

224,279 studies – University

SEE:
https://clinicaltrials.gov/ct2/results/details?cond=&term=university&cntry=&state=&city=&dist=&Search=Search

>

So is there a Robert Atmar – Hana El Sahly connection???

PubMed(dot)Gov lets you search by author name. So I went looking to see if those two authored papers together.

Search for Atmar R
https://pubmed.ncbi.nlm.nih.gov/?term=Atmar+R&sort=date&size=50

AND WELL WELL WELLL the first two out of the BOX!!!

2022 Jan 26.

SARS-CoV-2 Omicron Variant Neutralization after mRNA-1273 Booster Vaccination.

Pajon R, Doria-Rose NA, Shen X, Schmidt SD, O’Dell S, McDanal C, Feng W, Tong J, Eaton A, Maglinao M, Tang H, Manning KE, Edara VV, Lai L, Ellis M, Moore KM, Floyd K, Foster SL, Posavad CM, Atmar RL, Lyke KE, Zhou T, Wang L, Zhang Y, Gaudinski MR, Black WP, Gordon I, Guech M, Ledgerwood JE, Misasi JN, Widge A, Sullivan NJ, Roberts PC, Beigel JH, Korber B, Baden LR, El Sahly H, Chalkias S, Zhou H, Feng J, Girard B, Das R, Aunins A, Edwards DK, Suthar MS, Mascola JR, Montefiori DC.

N Engl J Med.

And the Affiliations:

• Moderna, Cambridge, MA.
• National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, MD.
• Duke University Medical Center, Durham, NC.
• NIAID, Bethesda, MD.
• Emory University School of Medicine, Atlanta, GA.
• Fred Hutchinson Cancer Research Center, Seattle, WA.
• Baylor College of Medicine, Houston, TX.
• University of Maryland School of Medicine, Baltimore, MD.
• National Institutes of Health, Bethesda, MD.
• Los Alamos National Laboratory, Los Alamos, NM.
• Brigham and Women’s Hospital, Boston, MA.
…..

2022 Jan 26.

Homologous and Heterologous Covid-19 Booster Vaccinations.

Atmar RL, Lyke KE, Deming ME, Jackson LA, Branche AR, El Sahly HM, Rostad CA, Martin JM, Johnston C, Rupp RE, Mulligan MJ, Brady RC, Frenck RW Jr, Bäcker M, Kottkamp AC, Babu TM, Rajakumar K, Edupuganti S, Dobrzynski D, Coler RN, Posavad CM, Archer JI, Crandon S, Nayak SU, Szydlo D, Zemanek JA, Dominguez Islas CP, Brown ER, Suthar MS, McElrath MJ, McDermott AB, O’Connell SE, Montefiori DC, Eaton A, Neuzil KM, Stephens DS, Roberts PC, Beigel JH; DMID 21-0012 Study Group.N Engl J Med.

Affiliation
• From the Departments of Medicine and Molecular Virology and Microbiology, Baylor College of Medicine, Houston (R.L.A., H.M.E.S.), and Sealy Institute for Vaccine Sciences, University of Texas Medical Branch, Galveston (R.E.R.); the Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore (K.E.L., M.E.D., K.M.N.), and the Division of Microbiology and Infectious Diseases (S.C., S.U.N., P.C.R., J.H.B.) and the Vaccine Research Center (A.B.M., S.E.O.), National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda; Kaiser Permanente Washington Health Research Institute (L.A.J.), the Departments of Medicine (C.J., T.M.B., M.J. McElrath) and Laboratory Medicine and Pathology (C.J., C.M.P.), University of Washington, the Vaccine and Infectious Disease Division (C.J., C.M.P., C.P.D.I., E.R.B., M.J. McElrath) and the Statistical Center for HIV/AIDS Research and Prevention (D.S., J.A.Z.), Fred Hutchinson Cancer Research Center, and Seattle Children’s Research Institute (R.N.C.) and the Department of Pediatrics (R.N.C.), University of Washington School of Medicine, Seattle; the Department of Medicine, Division of Infectious Diseases, University of Rochester, Rochester (A.R.B., D.D.), NYU Langone Vaccine Center and Division of Infectious Diseases and Immunology, Department of Medicine, NYU Grossman School of Medicine, New York (M.J. Mulligan, A.C.K.), and NYU Langone Hospital-Long Island Vaccine Center Research Clinic and the Division of Infectious Disease, Department of Medicine, NYU Long Island School of Medicine, Mineola (M.B.) – all in New York; the Departments of Pediatrics (C.A.R.), Microbiology and Immunology (M.S.S.), and Medicine (S.E., D.S.S.), the Center for Childhood Infections and Vaccines (C.A.R.), Hope Clinic of Emory Vaccine Center (S.E.), Emory Vaccine Center, and Yerkes National Primate Research Center (M.S.S.), Emory University School of Medicine, Emory University, and Children’s Healthcare of Atlanta (C.A.R.) – all in Atlanta; the Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh (J.M.M., K.R.); Cincinnati Children’s Hospital Medical Center, Division of Infectious Diseases, University of Cincinnati College of Medicine, Cincinnati (R.C.B., R.W.F.); and FHI 360 (formerly Family Health International) (J.I.A.) and Duke Human Vaccine Institute (D.C.M.) and the Department of Surgery (D.C.M., A.E.), Duke University Medical Center, Durham, NC.

2021 Oct 15

Heterologous SARS-CoV-2 Booster Vaccinations – Preliminary Report.

Authors: Atmar RL,….. El Sahly HM…

EPub 2021 Sept 22
Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase.

El Sahly HM, … COVE Study Group. N Engl J Med. 2021 Nov 4….. Epub 2021 Sep 22….

PubMed lists: COVE Study Group [Corporate Author]

COVE STUDY GROUP:

Hana M. El Sahly, MD is principal investigator for Baylor and under her is listed
Jennifer A. Whitaker, C. Mary Healy, Christine Akamine, Wendy A Keitel, Robert L Atmar, Annette Nagel, Sandra Francisco, Thea Marie Cordero, Janet Brown, Jennifer Christensen, Caroline Doughty-Skierski, Connie Rangel, Carrie Kibler, Coni Cheesman, Lisreina Toro, Chanei Henry, Chianti Wade Bowers, Pedro Piedra, Kathy Bosworth, Kayla Burrell, Jesus Banay, Tykel Eddy, Trent Davis, Shetel Anassi, Yvette Rugeley, Olga Rybina-Willis
…..

So what about the OTHER 15 on the ‘Advisory Board’ I checked, none are in the COVE study group.

….

And one last Baylor – Atmar paper:

SARS-CoV-2 Vaccination During Pregnancy: A Complex Decision.

Wang EW, Parchem JG, Atmar RL, Clark EH.Open Forum Infect Dis.

2021 Apr 10

Abstract
As the first severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines passed UK and US regulatory milestones in late 2020 and early 2021, multiple professional societies offered recommendations to assist pregnant and breastfeeding people as they choose whether to undergo vaccination. Despite such guidance, the lack of data describing vaccine safety, immunogenicity, and efficacy in pregnant and breastfeeding people has made this decision challenging for many. However, even considering the paucity of data, the known risks of coronavirus disease 2019 during pregnancy likely outweigh the not yet fully elucidated risks of SARS-CoV-2 vaccines, which have reassuring safety and efficacy profiles among nonpregnant people.

The Chair of the FDA Vaccines and Related Biological Products Advisory Committee is so compromised she should NEVER have been anywhere near the approval process!

-GC

Summary

After viewing the tape of Dr. Peter McCullough on Stew Peters, I’m both shocked and disappointed that Baylor (IMO both the College of Medicine and the allied University) would do anything except DEFEND Dr. McCullough for simply speaking TRUTH when nobody else dared to say it.

At a time when all of social media was defending what now amounts to SCIENTIFIC ERROR, Baylor – a renowned institution – accused a TRUTH-TELLER of “misinformation” for being on the cutting edge.

To borrow from Trump…… “SAD!”

We know now that everything Dr. Peter McCullough said was not only true, but that the science he cited was LEADING EDGE – pointing in the direction of future findings.

It is not “misinformation” to state scientific and medical findings which are both TRUE and in the process of CHANGING narratives. That IS what science is supposed to do.

China won’t have to fire a SHOT to steal academic leadership from the United States, if Baylor – in TEXAS of all places – is going to hand them scientific superiority on a silver platter.

Get the politics and the self-dealing OUT OF YOUR SCIENCE, BAYLOR.

It is a TRAVESTY for you, Baylor, to let your “big money scientists” force out your TRUTH-TELLERS based on POLITICS and motivated by their own SCIENTIFIC MISJUDGMENTS.

W

**A Book of Some Importance to Baptists**

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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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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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)
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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.
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LECTURESHIPS, SEMINAR INVITATIONS, AND VISITING PROFESSORSHIPS:
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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
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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.

The Pub is OPEN!

And we’re finally serving a NORMAL DRINK tonight. Even though it’s a SECOND ROUND.

STAY TUNED…..

and what time of year is it now???

Christmas Spirit

And now, the rules of the pub.

HOUSE RULES

AMEN!

Free the January Brothers!

Current Art On The Wall

COVID-19 Vaccine Interference With AIDS and Syphilis Tests

Moscow Mule Revisited

Sipping This Popular Cocktail Is a “Health Hazard,” Experts Say

Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

“New JAMA paper show Ivermectin blows the COVID vaccines out of the water”

YUP.

The data LITERALLY justify our position.

It wants the TRUTH.

ENJOY THE SHOW.

W

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

The Pub is STILL OPEN!