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Brownstone Institute

Three Medical Policies that Need Immediate Changing

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From the Brownstone Institute

BY Pierre KoryPIERRE KORY

You can’t make this up: The same cast of characters who erred so badly on COVID-19 want a do-over. A head-turning essay in The Atlanticwent so far as to plead for “pandemic amnesty.” For many in the medical community who have been derided by the likes of Dr. Anthony Fauci and his fanatics, these words ring hollow. Talk, as they say, is cheap, especially with the benefit of hindsight. Before a COVID-19 mulligan can be considered, here are three policies that must change.

First, “vaccine or bust” proponents must admit their approach overpromised and underdelivered. President Biden has repeatedly declared COVID-19 a “pandemic of the unvaccinated,” despite the science indicating otherwise. His claim that the vaccinated “do not spread the disease to anyone else” was rated “mostly false” by PolitiFact. Simply lowering the goalposts about less severe symptoms is insufficient. This is not what we were promised.

Making matters worse was the weaponization of this misinformation to influence public policy. It wasn’t just a smug Rachel Maddow telling her audience in March 2021 that the “virus stops with every vaccinated person.” This so-called science was used to pit Americans against one another, keep children out of school and force personnel out of critically important positions in the military, schools and first responders. Last fall, 5% of unvaccinated adults reported leaving their jobs.

I should know. I’ve been on the receiving end of threats to my livelihood.

This brings us to point two: The new California law empowering the punishment of doctors deemed guilty of spreading “misinformation” must be repealed before it can inflict further damage. Signed by Gov. Gavin Newsom, California Assembly Bill 2098 enables the state to strip the medical licenses of professionals who veer from the preferred political party line.

It’s a disturbing trend taking hold across the country. The American Board of Internal Medicine (ABIM) recently voted to remove Dr. Peter McCullough, one of the nation’s leading cardiologists, from his certifications in cardiovascular disease. Mr. McCullough’s sin had nothing to do with his performance in caring for patients, but rather with questioning the necessity of the COVID-19 vaccine for younger populations. With their far-reaching certification authority, the ABIM has the power to make any doctor’s life a living hell. Mr. McCullough’s fate now hangs in the balance until his Nov. 18 appeal date. This dangerous precedent must be nipped in the bud in the nation’s most populous state (governed by an oft-mentioned future presidential candidate) before it can take hold elsewhere.

Third, the District of Columbia must scrap its vaccine mandate for children in schools once and for all. Last week’s vote to delay compliance until January 3, 2023, is not enough. DC is one of the only school districts in the country with this type of requirement, going further than their counterparts in New York City or Los Angeles.

Last month, nearly half (44.7%) of DC school students fell short of COVID-19 compliance, according to Axios. In a city where 60% of the school-age population is Black, this mandate is not only unnecessary but is perpetuating further inequity. The pandemic has already taken an incredible toll on our children’s education, with math and reading scores falling to astonishing new lows. It is beyond misguided to bar children from attending school unless they receive a vaccine for an illness that poses a far smaller hazard to their health than the soaring crime rates in our cities.

From masks to breakthrough cases to alternative treatments, the so-called experts have amassed a track record of incorrect judgments that make political pollsters look good by comparison. Even in the fog of a once-in-a-century pandemic, these decisions were not just borne of inexpert and incorrect scientific knowledge but rather driven by a rush to push a medical agenda.

Our organization, the Front Line COVID-19 Critical Care Alliance (FLCCC) practices what we preach. As data evolved over time, we updated our recommendations and approaches accordingly. It wasn’t luck. We were following the science. Sadly, government agencies stuck with their unceasing policy recommendations that were increasingly divorced from the science.

One thing most people can agree on: COVID-19 won’t be the last public health emergency. There are already concerning headlines about an early spike of RSV impacting children. The leaders of captured health agencies must learn from their mistake of allowing the pharmaceutical industry unimpeded control of pandemic health policy. Americans are incredibly forgiving people willing to show grace, but step one in that process is a willingness for those in charge to admit their mistakes.

Republished from Washington Times

Author

  • Pierre Kory

    Pierre Kory is a Pulmonary and Critical Care Specialist, Teacher/Researcher. He is also the President and Chief Medical Officer of the non-profit organization Front Line COVID-19 Critical Care Alliance whose mission is to develop the most effective, evidence/expertise-based COVID-19 treatment protocols.

After 15 years as a TV reporter with Global and CBC and as news director of RDTV in Red Deer, Duane set out on his own 2008 as a visual storyteller. During this period, he became fascinated with a burgeoning online world and how it could better serve local communities. This fascination led to Todayville, launched in 2016.

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Brownstone Institute

The WHO: Our New Overlords

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From the Brownstone Institute

BY John Mac GhlionnJOHN MAC GHLIONN

According to its website, the World Health Organization (WHO), a specialized agency of the United Nations, “works worldwide to promote health, keep the world safe, and serve the vulnerable.” In recent times, however, the organization has become a vehicle for corruptiondeceit, and Chinese propaganda.

The WHO is an incredibly powerful organization with 194 member states. When the WHO speaks, the world listens. When the WHO decides on a plan of action, the world changes.

As the piece demonstrates, the WHO has aspirations of becoming even more powerful than it already is. If successful, the consequences could prove to be severe.

Last year, Henry I. Miller, a physician and molecular biologist, wrote a stinging piece that took direct aim at the WHO’s “bungled response to the coronavirus.” Miller, like so many others around the world, was particularly disillusioned about the “misplaced trust” placed in the Chinese Communist Party (CCP). As many readers no doubt recall, the CCP did its very best to conceal the COVID-19 outbreak that originated in Wuhan.

Because of the WHO’s numerous failures, Miller argued persuasively that the United States, whose “funding of UN activities exceeds that of every other country,” should refrain from financing the organization unless an “effective oversight and auditing entity” can be created to oversee operations.

In 2020, shortly after suspending financial support, the Trump administration began initiating a process to withdraw the United States from membership in the WHO. However, upon taking office in January 2021, President Joe Biden quickly reversed that decision and restored funding practices.

A few weeks after Miller’s well-argued piece, Sen. Rick Scott (R-Fla.) introduced a bill designed to prevent the WHO from unilaterally imposing public health restrictions on the United States and violating the country’s national sovereignty. The legislation came after the decision-making body of the WHO, the World Health Assembly, met to discuss a “pandemic treaty.” If introduced, such a treaty would give the WHO far greater control over public health decisions in the United States.

Scott said: “The WHO’s radical ‘pandemic treaty’ is a dangerous globalist overreach. The United States of America must never give more power to the WHO.” He added that the bill would “ensure that public health matters in the country remain in the hands of Americans,” and it needed to be passed immediately. It wasn’t. It should have been.

From Jan. 9–13, clandestine meetings took place in Geneva, Switzerland. Those in attendance discussed the possibility of amending the WHO’s International Health Regulations (IHR). For the uninitiated, the regulations are considered an instrument of international law, a legally binding agreement of basically every country in the world (except Liechtenstein) that calls on members to detect, evaluate, report, and respond to public health emergencies in a coordinated manner.

Michael Nevradakis, a senior reporter for The Defender, warned that if the proposed IHR amendments are made, then WHO members would essentially be stripped of their sovereignty. As Nevradakis previously reported, the IHR framework already allows Dr. Tedros Adhanom Ghebreyesus, the WHO director-general, “to declare a public health emergency in any country, without the consent of that country’s government.” The proposed amendments would give even more power to the director-general.

Francis Boyle, a professor of international law at the University of Illinois, told Nevradakis that the proposed changes could violate international law.

Boyle, a legitimate expert who played a pivotal role in drafting the Biological Weapons Anti-Terrorism Act of 1989, believes we are heading toward “a worldwide totalitarian medical and scientific police state,” which the WHO directly controls. That’s because the IHR regulations “are specifically designed to circumvent national, state and local government authorities when it comes to pandemics, the treatment for pandemics and also including in there, vaccines.”

It’s clear to Boyle that the WHO is preparing to adopt the regulations in May of 2023, just a few months from now.

The brilliant researcher James Roguski also shares Boyle’s concerns. He claims that the WHO is attempting a global power grab by morphing from an advisory organization into what can only be described as a global law-enforcement agency. If introduced, the IHR changes, he suggested, “would institute global digital health certificates, dramatically increase the billions of dollars available to the WHO and enable nations to implement the regulations WITHOUT respect for the dignity, human rights and fundamental freedoms of people.”

Although COVID-19 is now a distant memory for many, another pandemic, we’re told, is just around the corner. When it comes, the WHO may very well be in a position to order you, dear reader, to do exactly what it wants, when it wants. If these amendments are made in May, resistance may prove to be utterly futile.

Reposted from Epoch Times

 

Author

  • John Mac Ghlionn

    With a doctorate in psychosocial studies, John Mac Ghlionn works as both a researcher and essayist. His writing has been published by the likes of Newsweek, NY Post, and The American Conservative. He can be found on Twitter: @ghlionn, and on Gettr: @John_Mac_G

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Brownstone Institute

FOIA Doc Shows BioNTech Founders Postdated Start of C19 Vax Project

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From the Brownstone Institute

BY Robert KogonROBERT KOGON

As noted in my last article on BioNTech’s “brazen” avoidance of safety testing of its Covid-19 vaccine, BioNTech founders Ugur Sahin and Özlem Türeci claim in their book The Vaccine that the company’s Covid-19 vaccine project got underway on January 27, 2020. But documentary evidence released in response to a FOIA request (and included in the so-called “Pfizer documents”) shows that this is not true and that the company had in fact already begun preclinical, i.e. animal, testing nearly two weeks earlier, on January 14.

BioNTech R&D STUDY REPORT No. R-20-0072 is available here. The report is also referenced and discussed in an FDA submission on the preclinical study program that is available here. The below screenshot shows the study dates from p. 8 of the report.

In the book, Sahin claims furthermore that he only even became interested in the outbreak in Wuhan on January 24, after reading an article in the German weekly Der Spiegel (p. 4) and/or a submission to The Lancet (p. 6). But look again at the study dates above. BioNTech had already completed the first preclinical study for its Covid-19 vaccine the day before!

January 24, 2020 was a Friday. On Sahin’s account, he took the decision to launch his Covid-19 vaccine project over the weekend and unveiled his plans to his collaborators at BioNTech’s headquarters in Mainz, Germany on the following Monday: January 27 (ch. 2 passim and p. 42; see screencap below).

Sahin claims (p. 33) that it was at this January 27 meeting that he asked BioNTech’s animal testing team to prepare the preclinical program that was in fact already underway!

It should be noted that January 14, 2020, the start-date of the first preclinical study, was just two weeks after the first report of Covid-19 cases in Wuhan and just a day after the release of the full SARS-CoV-2 genome (drafts had been released previously).

BioNTech’s first preclinical study was evidently prepared before publication of the genome and in anticipation of it. As explained in the summary of the study (p. 6), its purpose was to test BioNTech mRNA formulated in lipid nanoparticles produced by the Canadian firm Acuitas. But the mRNA was here encoding a proxy antigen (luciferase), not the spike protein of SARS-CoV-2 that would later serve as the target antigen.

The study looked at both biodistribution and immune system activation. As the FDA submission on the preclinical program puts it, “Platform properties that support BNT162b2 were initially demonstrated with non-SARS-CoV-2 antigens” (2.4 NONCLINICAL OVERVIEW, p. 7).

In The Vaccine, which was written with the journalist Joe Miller, Sahin and Türeci talk about the need to obtain the Acuitas lipids, which, they say, were more suitable for intramuscular injection than BioNTech’s own in-house lipids. But, again, they postdate the matter. Thus, on p. 52, we read: “The missing piece was still Acuitas, who had not yet consented to the use of their lipids. Then, on the morning of Monday 3 February, [Acuitas CEO] Tom Madden offered his help.” But BioNTech was already running tests using the Acuitas lipids three weeks earlier!

Furthermore, BioNTech was not able to formulate its mRNA into the lipids itself, but depended on the Austrian company Polymun to do this for it. As noted in The Vaccine (p.51), Polymun’s facilities are an 8-hour drive from BioNTech’s headquarters in Mainz. In the book, Sahin and Türeci describe the first batch of mRNA for the vaccine tests proper being packed up and driven by car to Polymun outside Vienna: “A couple of days later, a small Styrofoam box containing frozen vials full of vaccine would be driven back over the border to BioNTech” (pp. 116-117).

But presumably this same back-and-forth had to have occurred with the mRNA encoding the luciferase. This means that as a practical matter “Project Lightspeed” must have gotten underway even earlier: at least several days before the January 14 start date of the study.

Why did Sahin and Türeci postdate the launch of their Covid-19 vaccine project in their book? Well, undoubtedly because the actual start date – and we do not know when exactly the actual start date was – would have seemed far too soon. Based on the above considerations, it must have been at the latest just days after the first December 31, 2019 report of Covid-19 cases in Wuhan.

Author

  • Robert Kogon

    Robert Kogon is a pen name for a widely-published financial journalist, a translator, and researcher working in Europe. Follow him at Twitter here. He writes at edv1694.substack.com.

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