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.
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 Poso(@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”.
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…..
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.
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, 1 Paul 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.
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.”
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)
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
DLC’s concluding remark:
“Off to Moderna we go”
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.
