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COVID-19

Consent of the Governed, Where Art Thou?

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22 minute read

From the Brownstone Institute

BY Robert MaloneROBERT MALONE  

The essay was prompted by a midnight Saturday evening Zoom call with a Canadian physician who was pleading for me to help intervene with the Canadian authorities overseeing the “vaccine” campaign.

I am often asked some form of the question “What caused you to come out of the closet and start criticizing the vaccines?” On a related note, when interviewed by a reporter from the infamous Atlantic August 2021 hit piece, Stan Gromkowski (a former Vical colleague of mine) prophetically opined, “He’s fucking up his chances for a Nobel Prize.”

The answer to this persistent question is nicely summarized in the first essay which I wrote in objection to what was being done, titled “COVID Vaccine Deployment under EUA: It’s time we stop and look at what’s going down.” published in Trial Site News on May 30, 2021 (three months before the defamatory Atlantic attack). I guess that article struck a nerve, because it currently has over 19,000 likes; pretty good for an article on a specialty paid site targeting the clinical research industry.

The essay was prompted by a midnight Saturday evening Zoom call with a Canadian physician who was pleading for me to help intervene with the Canadian authorities overseeing the “vaccine” campaign. This specific physician later had his office raided and office computers damaged by the Canadian government for prescribing early treatment and writing vaccine exemptions, and has now being required to submit to the Canadian government re-education and contrition program for his sins if he wishes to retain the ability to practice medicine, just as has been required of Jordan Peterson. But that was all in the future.

Talking until midnight Saturday, he had described what was being done in Canada to force toxic COVID “vaccines” on an unwitting population including children, imploring me to somehow intervene with Health Canada to stop the madness. I told him I did not have the necessary connections, and there was nothing much I could do to help.

Waking early the following Sunday, I realized there was something I actually could do to advance his cause. I could dip into my extensive training in bioethics and write about the fundamental breaches of established biomedical ethics that were going on in Canada, and would soon migrate to USA, Australia, New Zealand, the United Kingdom, and across the western “democracies.”

The following is the core of my argument back then (May 2021), which I assert has withstood the test of time much better than the notorious Atlantic hit piece published three months later.

I believe that adult citizens must be allowed free will, the freedom to choose. This is particularly true in the case of clinical research. These mRNA and recombinant adenovirus vaccine products remain experimental at this time. Furthermore, we are supposed to be doing rigorous, fact-based science and medicine. If rigorous and transparent evaluation of vaccine reactogenicity and treatment-emergent post-vaccination adverse events is not done, we (the public health, clinical research and vaccine developer communities) play right into the hands of anti-vaxxer memes and validate many of their arguments.

The suppression of information, discussion, and outright censorship concerning these current COVID vaccines which are based on gene therapy technologies cast a bad light on the entire vaccine enterprise. It is my opinion that the adult public can handle information and open discussion. Furthermore, we must fully disclose any and all risks associated with these experimental research products.

In this context, the adult public are basically research subjects that are not being required to sign informed consent due to EUA waiver. But that does not mean that they do not deserve the full disclosure of risks that one would normally require in an informed consent document for a clinical trial. And now some national authorities are calling on the deployment of EUA vaccines to adolescents and the young, which by definition are not able to directly provide informed consent to participate in clinical research – written or otherwise.

The key point here is that what is being done by suppressing open disclosure and debate concerning the profile of adverse events associated with these vaccines violates fundamental bioethical principles for clinical research. This goes back to the Geneva convention and the Helsinki declaration.

There must be informed consent for experimentation on human subjects. The human subjects – you, me, and the citizens of these countries – must be informed of risks. As a community, we have already had a discussion and made our decision – we cannot compel prisoners, military recruits, or any other population of humans to participate in a clinical research study. For example, see the Belmont report, which provided the rationale for US federal law Code of Federal Regulations 45 CFR 46 (subpart A), referred to as “The Federal Policy for the Protection of Human Subjects” (also known as the “Common Rule”).

Quoting from the Belmont Report:

“Informed Consent. — Respect for persons requires that subjects, to the degree that they are capable, be given the opportunity to choose what shall or shall not happen to them. This opportunity is provided when adequate standards for informed consent are satisfied.

While the importance of informed consent is unquestioned, controversy prevails over the nature and possibility of an informed consent. Nonetheless, there is widespread agreement that the consent process can be analyzed as containing three elements: information, comprehension and voluntariness.”

Information, comprehension, and voluntariness. To my eyes, it appears that in many regions public health leadership has stepped over the line and is now violating the bedrock principles which form the foundation upon which the ethics of clinical research are built. I believe that this must stop. We must have transparent public disclosure of risks – in a broad sense – associated with these experimental vaccines. It is either that, or the entire modern bioethical structure which supports human subjects research will have to be re-thought.

This was not a major intellectual leap. It was a simple restatement of the training in clinical research bioethics which I had received and which had been repeatedly reinforced over the prior decade. No big deal, except that few if any were willing to make such a statement at that time. Long before the infamous Dark Horse or Rogan podcasts.

The failure to disclose the risks of the gene therapy-based COVID vaccines by the US and other “Western” governments became widespread, chronic, and well-documented. Fast forwarding to the present, on December 22, 2023 investigative journalist Greg Piper of the alternative “Just The News” published yet another chapter in the abundant library of documented government withholding of key information concerning COVID genetic “vaccine” harms.

Misinformation for thee, not me? FDA had similar concerns as COVID vaccine skeptics, docs suggest

FOIA production shows the agency wasn’t impressed by Pfizer’s plan to mitigate “endotoxins,” complained about insufficient cleaning in manufacturing, and had no basis to claim post-vax heart inflammation was rare.

If an outsider raises questions about contamination of COVID-19 vaccines or how closely the Food and Drug Administration monitors for severe adverse events, the agency considers it a boon to misinformation that lowers vaccine uptake and hence kills people.

If the FDA itself raises these issues, that’s a different story…

The FDA documents, some heavily redacted under the FOIA exemption for trade secrets, show less daylight than may be thought between the agency and critics of federal COVID policy such as Florida Surgeon General Joseph Ladapo.

Mr. Piper went on to summarize a range of recent freedom of information act and court-ordered document disclosures which clearly demonstrate a systematic and intentional failure by the US Government to properly inform the public of the risks associated with accepting gene therapy-based COVID “vaccine” products.

  • The CDC had no scientific research to back its public claim in January that people can safely get their COVID, flu, and monkeypox vaccines “at the same time.”
  • “Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, didn’t just tell Florida Surgeon General Joe Ladapo last week his concerns about DNA contamination were “quite implausible” but also shamed him for feeding what he considered misinformation that will cause preventable deaths. Yet an Aug. 6, 2021 email to Pfizer from CBER Senior Regulatory Review Officer Mike Smith about “endotoxins” – potential contaminants introduced in pharmaceutical manufacturing – shows the feds had similar concerns as they considered full approval for Pfizer’s Comirnaty.”
  • “A month before then-acting FDA Commissioner Janet Woodcock told the media that post-vaccination heart inflammation “appears to be very low,” a CBER “surveillance” scientist made clear that the leader was not relying on the agency’s own data. Joyce Obidi reviewed how well CBER’s Sentinel Program, created under a 2007 law to monitor drug safety through electronic healthcare data, could “evaluate the serious risk for myocarditis and pericarditis” following Pfizer COVID vaccination in recipients 16 and older, the first population authorized for emergency use. “Post-authorization safety data identified serious risks for myocarditis and pericarditis after COMIRNATY, with increased risk in males under 30 years of age,” Obidi wrote in the May 18, 2021, memo, which is also buried in the agency’s 246-document public folder on materials related to Comirnaty’s approval.”
  • Obidi also stated that “Available data sources in the CBER Sentinel Program are NOT sufficient to identify the outcomes of myocarditis and pericarditis” and not “sufficiently powered to assess the magnitude of risk” for ages 12-30. She wrote. The program would need a minimum of 3-6 months follow up data to check for “long-term sequelae,” and it cannot study subclinical myocarditis “because of the absence of a definition of subclinical myocarditis and unknown background incidence of troponin abnormalities,” according to Obidi. Sentinel’s data sources at full approval of Comirnaty did not have “sufficient power to assess the magnitude of risk in patients 12-30 years of age” and hence cannot assess the “serious risks of myocarditis and pericarditis, and subclinical myocarditis” associated with the vaccine.”
  • “In another May 18, 2021, memo reviewing Pfizer’s proposed pharmacovigilance plan for its vaccine, Analytic Epidemiology Branch Medical Officer Deborah Thompson evaluated the company’s claim that “vaccine-associated enhanced disease” is just a “theoretical risk.” She cited Vaccine Adverse Events Reporting System reports of deaths in “fully vaccinated” patients at that early stage of vaccination. “Severe manifestations and death from COVID-19 raise the possibility” of VAED because it has “overlapping clinical manifestations with natural SARS-CoV-2 infection, making it difficult to differentiate VAED from severe” infection in VAERS reports.”
  • Despite assurances otherwise from Peter Marks in his letter to the Florida Surgeon General, major manufacturing process good practices were breached. “In a Form 483 to Pfizer following inspections that uncovered possible or actual product adulteration, FDA investigators made 13 observations about procedures at Pfizer’s Andover, Massachusetts, manufacturing facility. They include “insufficient data to support product quality prior to the release” of vaccine batch FA8057. The observation says “a deviation [redacted] was initiated due to the multiple control limit excursions during [redacted]” and the “affected batch was manufactured with a process that deviated from the validated process parameters” and was “not put on stability until July 22, 2021.” It was released on a redacted date. An observation on “inadequate quality oversight” implies that Pfizer was late in adding a notation to a batch record that        “[redacted] exceeded the allowable [redacted].” The company’s quality assurance does not review “electronic data/reports” from a redacted manufacturing process “during batch record review or prior to batch release.” <Note: No clinical trial I have ever been involved in has been associated with an FDA 483 warning letter. This is no small matter.>
  • Just the News asked the FDA prior to publication of this report on 22 December for its characterization of the FOIA-disclosed and related documents in light of Marks’ comments to Ladapo about feeding misinformation. A spokesperson responded two days later, saying the agency was working to provide an answer. As of 27 December, the FDA still has not provided a response.

At this point, the burden of publicly available documentation clearly demonstrates multiple examples of intentional breaches of informed consent by both the US government and the pharmaceutical industry manufacturers of these products. It is difficult to dispute that the US government and the pharmaceutical industry sponsors are colluding in a public-private partnership to suppress information concerning risks of these products. Likewise, there has been an agreement between the UK and US governments to suppress disclosure of information concerning risks and adverse events associated with these products.

In a normal, historic regulatory and bioethical environment, this breach of international bioethical norms concerning informed consent would rise to the level of a clear-cut crime against humanity. But in the “through the looking glass” world of COVID post-late 2019, established legal, moral, and ethical norms concerning patient and citizen rights to proper informed consent have all been turned upside down. All of these clear-cut breaches ostensibly being actively “justified” by mockingbird media, the massive censorship-industrial complex, and government officials as being in service of the public interest and the greater good.

The western Five Eyes alliance participants, deferring to the leadership of the US government, are all acting in coordination and cooperation to disregard and hide the implications and consequences of their illegal and unethical actions. This is being justified based on the following oft-repeated catechism, each element of which is demonstrably false or opposed to established Western bioethical consensus:

  1. COVID-19, the disease caused by infection with SARS-CoV-2, is highly pathogenic with a case fatality rate of 3.4 %. <The actual case fatality rate was approximately 0.02% when this disease was first “modeled” in 2020 and is much lower now>
  2. The gene therapy-based COVID-19 “vaccines” are safe and effective, are effective as prophylactics, are effective in preventing infection and spread of COVID-19 disease, and if taken by a sufficient fraction of the population <a moving goalpost> can be used to achieve herd immunity. <all of these previous claims are now clearly demonstrated unsupported falsehoods>
  3. The gene therapy-based COVID-19 “vaccines” are effective at preventing severe disease and death from SARS-CoV-2, and have saved 14 million lives. <this 14 million lives saved claim turns out to be based on flawed mathematics, and all cause mortality data analysis indicates something more like 17 million lives lost globally due to the products>
  4. Fully disclosing actual risks, morbidity and mortality data concerning the COVID-19 genetic vaccines will result in “increased vaccine hesitancy” and avoidable harm due to reduced “vaccine” (booster) uptake. <at this point in the outbreak, multiple data sources indicate that acceptance of boosters is associated with “negative effectiveness,” meaning that after a 2-3 month lag period (shorter in some studies) you are more likely to suffer death or severe COVID-19 disease – and other diseases- if you accept injection with these products than if you do not.>

This fourth point is a clear-cut example of flawed logic. Flawed both in terms of the data on morbidity, mortality, and immune imprinting, as well as flawed bioethical reasoning.

Think this through with me. The essence of the statement is essentially the governments’ assertions that “if the public knew about the risks that we know about, then they would choose not to accept those risks based on their assessment of the effectiveness of the product and the clinical risks of infection with the virus. Therefore there would be much more avoidable disease, disability, and death from COVID-19 than would be saved from vaccine products not administered.”

And on the basis of this ill-logic, governments and Pharma are withholding adverse event data, and thereby are unilaterally making medical decisions for sovereign individuals and their children. This is what we have come to. The ultimate embodiment of the nanny state, with corporatist allies. The State knows best, and will withhold medical information from the public which would cause members of that public to question its wisdom and decision-making.

Basically, the State is asserting that it has the right to sentence you to increased risk of death and disease by purchasing (using tax dollars), mandating (vaccines for children program), distributing, enticing, and marketing an injectable product while censoring or defaming (using modern psychological warfare technologies) any and all who disagree or even have the temerity to question the decisions and rights of the State to do so.

Republished from the author’s Substack

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  • Robert Malone

    Robert W. Malone is a physician and biochemist. His work focuses on mRNA technology, pharmaceuticals, and drug repurposing research. You can find him at Substack and Gettr

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Censorship Industrial Complex

Scott Atlas: COVID lockdowns, censorship have left a ‘permanent black mark on America’

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From LifeSiteNews

Editor’s note: The following text is taken from a speech delivered by radiologist and political commentator Scott Atlas to the Independent Medical Alliance conference in Atlanta, Georgia, on April 5, 2025. Transcription provided by Dr. Robert Malone.

ATLANTA (Robert Malone) — First, thank you to the organizers, and to my many friends and supporters here. It’s great to be here – surrounded by people who believe in personal freedom!

At the recent international Alliance for Responsible Citizenship (ARC) forum in London, I was invited to address the question, “Can Institutions be Reformed?” Begun with Jordan Peterson, ARC joins voices from all over the world to discuss how to refresh the institutions and best values of Western heritage, values that provided the world with history’s most successful societies, particularly the commitment to freedom.

I asked that audience to first consider:

Why, at this moment in history, are we finally focusing on how institutions should be reformed, or if institutions can even be reformed?

After all, for decades we have been aware that our institutions were failing – editorialized, dishonest journalism; wasteful, corrupt government; and agenda-driven schools and universities increasingly unbalanced toward the left, with many conservative faculty and students often self-censoring, afraid to offer unpopular views.

The answer? It is COVID, the pandemic mismanagement specifically – the most tragic breakdown of leadership and ethics that free societies have seen in our lifetimes.

COVID fully exposed the massive, across-the-board, institutional failure – including the shocking reality of overt censorship in our country, the loss of freedoms and the frank violation of human rights – in this country, one explicitly founded on a commitment to freedom.

Yet, oddly, the pandemic remained invisible at the ARC conference, unmentioned by dozens of speakers addressing freedom. It was the elephant in the room – just as explaining the truth about lockdowns, the pseudoscience mandates on masks and social distancing, closing churches and businesses, prohibiting visits to elderly parents in nursing homes while they die – all are missing from post-election discussions today in the United States, including, notably, any of the very public statements and proclamations from the new administration about health care today.

Today, in the wake of COVID, we are left with an undeniable crisis in health. Trust in health guidance has plummeted more rapidly since 2019 than any other government institution, with almost two-thirds now rating the FDA and the CDC as “only fair or poor.”

Half of America no longer has much confidence in science itself. Trust in our doctors and hospitals dropped from 71 percent in 2019 to 40 percent in 2024. The loss of trust is part of the disgraceful legacy of those who held power, who were relied upon to use critical thinking and an ethical compass on behalf of the public, who were handed the precious gift of automatic credibility and almost blind trust.

To understand how to move forward to restore trust, it’s important to first acknowledge basic facts about the pandemic, and keep repeating them, because truth serves as the starting point of all rational discussion. And we must live in a society where facts are acknowledged.

Remember – lockdowns were not caused by the virus. Human beings decided to impose lockdowns.

Indeed, lockdowns were widely instituted, they failed to stop the dying, and they failed to stop the spread – that’s the data: Bjornskov, 2021; Bendavid, 2021; Agarwal, 2021; Herby, 2022; Kerpen, 2023; Ioannidis, 2024; Atlas, 2024.

Lockdowners ignored Henderson’s classic review 15 years earlier showing lockdowns were both ineffective and extremely harmful. They rejected the alternative, targeted protection, first recommended on national media in March 2020 independently by Ioannidis, by Katz, and by me (Atlas) – and then repeatedly for months – based on data already known back then, in spring of 2020. It was not learned 7 months later in 2020, when the Great Barrington Declaration reiterated it, or in 2021, or 2022, or more recently.

And the Birx-Fauci lockdowns directly inflicted massive damage on children and literally killed millions, especially, sinfully, the poor. “The U.S. alone would have had 1.6 million fewer deaths (through July 2023) if it had the performance of Sweden,” according to a review of 34 countries.  Bianchi calculates that over the next 15-20 years, the unemployment alone will cause another million additional American deaths – from the economic shutdown, not the virus.

Beyond a reckless disregard for foreseeable death from their policies, America’s leaders imposed sinful harms and long-lasting damage on our children, the totality of which may not be realized for decades. Mandatory school closings, forced isolation of teens and college students, and required injections of healthy children with experimental drugs attempting to shield adults will be a permanent black mark on America.

It is also worth remembering that this was a health policy problem.

While credentials are not the sole determinant of expertise, I was the only health policy scholar on the White House Task Force and advising the president. Virology is not health policy; epidemiology is not health policy. And while physicians are important in contributing, they are not inherently expert in health policy. Those are only pieces of a larger, more complex puzzle. The stunning fact is – I was the only medical expert there focused on stopping both the death and destruction from the virus and the death and destruction from the policy itself.

As Hannah Arendt observed in “Eichmann in Jerusalem”:

What has come to light is neither nihilism nor cynicism, as one might have expected, but a quite extraordinary confusion over elementary questions of morality.

More than massive incompetence, more than a fundamental lack of critical thinking, we saw the disappearance of society’s moral compass, so pervasive that we have rightfully lost trust in our institutions, leaders, and fellow citizens, trust that is essential to the function of any free and diverse society.

Why did free people accept these draconian, unprecedented, and illogical lockdowns?

This is the question. And the answer reveals the reason for today’s silence on the pandemic.

Clearly, censorship and propaganda are key parts of the explanation, tools of control that convinced the public of two fallacies – that a consensus of experts on lockdowns existed, and dissenters to that false consensus were highly dangerous.

Censorship first was done by the media companies themselves – when it counted most:

  • In 2020, before the Biden administration, when school closures and lockdowns were being implemented;
  • May 2020, YouTube bragged about its “aggressive policies against misinformation”;
  • August 2020, Facebook shamelessly admitted to the Washington Post it had already taken down 7 million posts on the pandemic;
  • My interviews as advisor to the president were pulled down by YouTube on September 11, 2020, by Twitter blocking me on October 18, 2020.

You might think the public – in a free society – should know what the advisor to the president was saying?

And what was the response to truth at America’s universities, our centers for the free exchange of ideas, including Stanford, my employer?

Censorship: character assassination, intimidation, and to me, formal censure.

Why is censorship used? To shut someone up, yes; but more importantly, to deceive the public – to stop others from hearing, to convince a naïve public there is a “consensus on truth.”

Truth is not a team sport.

Truth is not determined by consensus, or by numbers of people who agree, or by titles. It is discovered by debate, proven by critical analysis of evidence. Arguments are won by data and logic, not by personal attack or censoring others.

I am proud to be an outlier – happily proven right when the inliers are so wrong – but Cancel Culture is effective because it stops others from speaking. I received hundreds of emails from doctors and scientists all over the country, including from Stanford, from other professors, and from inside the NIH, saying, “Keep talking, Scott, you’re 100 percent right, but we’re afraid for our families and our jobs.”

And indeed, no one at Stanford Medical School – not a single faculty member there – spoke publicly against their attack on me. Only Martin Kulldorff, then a Harvard epidemiologist, wrote in and publicly challenged the 98 signatories at Stanford to debate on whether I was correct or not (none accepted that challenge!).

But that alone doesn’t explain today’s silence about that extraordinary collapse. It is not simply “issue fatigue.”

It is also that so many smart people, including many claiming to support the new “disruptors,” bought into the irrational measures when it counted most, when our kids and particularly the poor were being destroyed in 2020, uncomfortable to discuss and admit, but far more fundamental than the Sars2 origin, or Fauci, or the vaccine. That acquiescence, that silence, that cowardice, and that failure to grasp reality are inconvenient truths that no one wants to admit.

Today, disruption is sorely needed, and many are basking in the resounding victory of history’s most disruptive politician, President Donald J. Trump.

As promised, his new administration is moving quickly, disrupting on several fronts: national security, energy, trade, justice, immigration, and perhaps most importantly with Elon Musk’s effort to eliminate government waste and fraud, and protect our money. After all, the government has no money – it’s all our money, taxpayers’ money!

In health care, important changes in the status quo have also begun, first with Elon Musk’s much needed DOGE, streamlining tens of thousands of Department of Health and Human Services (HHS) bureaucrats while exposing massive fraud and waste in programs like Medicaid.

And Secretary of HHS Bobby Kennedy has also provoked an important, new national dialogue with his “Make America Healthy Again” mantra focused on wholesome foods to achieve the goal everyone readily supports – good health for themselves and their children. And no doubt, ensuring safety of all drugs and eliminating corruption in pharma and the food industry are also crucial to health. I am a strong supporter of those ideas.

We also have two excellent appointments in health – my friends and colleagues, Marty Makary to FDA and Jay Bhattacharya to NIH. Both Marty and Jay are highly knowledgeable, have top training and expertise, and are committed to critical thinking, to legitimate science, and most importantly to free scientific debate.

But I am concerned that most are simultaneously eager to “turn the page” on the human rights violations, the censorship, the true “constitutional crisis” – no setting the record straight, no official recognition of facts, no accountability? The ultimate disruptor won, and his disruptor appointees will now be in charge – so all is well?

Silently turning the page on modern history’s most egregious societal failure would be extraordinarily harmful. Failure to issue official statements of truth by the new government health agency leaders about the pandemic management would prevent closure for the millions who lost loved ones and whose children suffered such harms. And it would completely eliminate all accountability. Remember, only public accountability will prevent recurrence, and accountability is necessary to restore trust in institutions, leadership, and among fellow citizens.

My second concern: the era of trusting experts based solely on credentials must be over. But will that backlash against the failed “expert class” usher in a different wave of false belief? We cannot forget that legitimate expertise is still legitimate; that known, solid medical science is still valid; that unfounded theories based on simple correlations are not scientifically sound.

And we do not want to inadvertently replicate the cancel culture that harmed so many, with another wave of demonizing anyone who doesn’t 100 percent support the new narratives. It’s already begun – that if you disagree with any of the incoming opinions, then you must be “bought by pharma!” Blind support is just as bad as blind opposition; critical thinking must prevail.

What reforms are needed now?

  • The first step to restore trust is formal, official statements of truth on the COVID lockdowns, masks, and other pseudoscience mandates from new HHS, NIH, FDA, CDC, CMS leaders.
  • We need to forbid – by law – all shutdowns and reset that the CDC and other health agencies are (only) advisory. They recommend; they give information – they don’t set laws. They don’t have the power to set mandates. And if our guaranteed freedoms are not always valid, especially during crises, then they are not guaranteed at all.
  • We need to add term limits (5 years?) to all mid- and top-level health agency positions. We cannot continue the perverse incentives of career bureaucrats accruing personal power, like Anthony Fauci and Deborah Birx with their 30-plus years in government.
  • All new heads of HHS, FDA, NIH, CDC, and CMS should be prohibited from post-government company board positions in health sectors they regulate for ~5 years. It’s unethical, an overt conflict-of-interest. Why hasn’t that been announced?
  • We need to forbid drug royalty sharing by employees of the NIH, the FDA, and the CDC. $325 million of royalties were shared with pharma by those people over the 10 years prior to the pandemic. That’s a shocking conflict of interest.
  • We should forbid all mandates forcing people to take drugs. First, the essence of all ethical medical practice is informed consent. And what kind of a “free country” requires you to inject a drug into your child or yourself? No – that’s antithetical to freedom. In public health, you give the information… you shouldn’t need to force anything legitimate, but you do need to prove the case.
  • We need to require the immediate posting of discussions in all FDA, CDC, and NIH meetings. They work for us. What are they saying? We should know in real-time.
  • We need accountability for all government funding. We have 15+ universities getting >$500M/year from NIH alone. The essence of research is free debate. If they’re thwarting that with intimidation, like faculty censures, why would they be entitled to U.S. taxpayers’ money?

More broadly, I and others are working on policies to ensure the free exchange of ideas – the essence of all legitimate science, the basis for the mission of education.

Ideological gatekeeping in public discourse has no place in free societies, especially in science and health.

Here’s the point – the solution to misinformation is more information. No one should be trusted to be the arbiter of truth.

Ultimately, most solutions come from individuals, and ultimately, it is individuals, not institutions, who will save freedom.

I fear we still have a disastrous void in courage in our society today.

To quote CS Lewis, “Courage is not simply one of the virtues, but the form of every virtue at the testing point.”

We cannot have a peaceful, free society if it’s filled with people who lack the courage to speak and act with certainty on Hannah Arendt’s “elementary questions of morality.”

Finally, to the young people here, never forget what GK Chesterton said:

Right is right, even if nobody does it. Wrong is wrong, even if everybody is wrong about it.

Reprinted with permission from Robert Malone.

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Alberta

Medical regulator stops short of revoking license of Alberta doctor skeptic of COVID vaccine

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From LifeSiteNews

By Anthony Murdoch

The Democracy Fund has announced that COVID-skeptic Dr. Roger Hodkinson will retain his medical license after a successful appeal against allegations of ‘unprofessional conduct’ by the College of Physicians and Surgeons of Alberta.

A doctor who called for officials to be jailed for being complicit in the “big kill” caused by COVID measures will get to keep his medical license thanks to a ruling by a Canadian medical regulator.

The Democracy Fund (TDF) announced in an April 4 press release that one of its clients, Dr. Roger Hodkinson, will retain his medical license after filing an appeal with the College of Physicians and Surgeons of Alberta (CPSA) over allegations of “unprofessional conduct regarding 17 public statements made in November 2020 and April 2021.”

Hodkinson had routinely argued against the dictates of public health and elected officials and “presented an alternative perspective on COVID-19, including the efficacy of masking and vaccines,” TDF noted.

In 2021, Hodkinson and Dr. Dennis Modry publicly blasted the then-provincial government of Alberta under Premier Jason Kenney for “intimidating” people “into compliance” with COVID-19 lockdowns.

In 2022, Hodkinson said that leaders in Canada and throughout the world have perpetrated the “biggest kill ever in medicine’s history” by coercing people into taking the experimental COVID injections and subjecting them to lengthy lockdowns.

These statements, among others, led the CPSA to claim that Hodkinson had promoted inaccurate or misleading information. “However, following negotiations with lawyers for The Democracy Fund, the CPSA limited its claims to arguing that Dr. Hodkinson’s comments violated the ethical code and extended beyond the scope of a general pathologist.”

Thus, Hodkinson did not “concede that any of his statements were false,” but “acknowledged that his criticisms of other physicians technically breached the Code of Ethics and Professionalism,” the group explained. “He also admitted that he should have clarified that his views were outside the scope of a general pathologist.”

Instead of having his license revoked, TDF stated that Dr. Hodkinson received a “caution” and will have to “complete an online course on influence and advocacy.”

“However, he did not concede that any of his statements were misinformation, nor did the tribunal make such a determination,” noted lawyer Alan Honner.

Some of Hodkinson’s warnings seem to have been vindicated by the current Alberta government under Premier Danielle Smith, who commissioned Dr. Gary Davidson to investigate the previous administration’s handling of COVID-19.

Davidson’s report, which was made public earlier this year, recommended the immediately halt of the experimental jabs for healthy children and teenagers, citing the risks the shots pose.

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