Biden’s COVID censorship machine takes a hit: Missouri wins landmark ban on federal threats to Big Tech



A landmark settlement delivered a blow to the censorship industrial complex that silenced Americans during the COVID era.

Sen. Eric Schmitt (R-Mo.) announced Tuesday that Missouri had reached a settlement agreement with the U.S. government in its Missouri v. Biden lawsuit, which accused the Biden administration of violating Americans' First Amendment rights by directing social media companies to censor speech challenging the government's COVID messaging.

'For every working Missouri family tired of being silenced by their own government: this victory is yours.'

Schmitt filed the lawsuit against the Biden administration while serving as Missouri attorney general, before securing his Senate seat.

The agreement included a 10-year Consent Decree that enforces a narrow permanent injunction on the surgeon general, the Centers for Disease Control and Prevention, and the Cybersecurity and Infrastructure Security Agency. The injunction prevents them from threatening social media companies with any form of punishment if those companies fail to remove or suppress content that contains protected speech.

However, this ban applies only to posts made on Facebook, Instagram, X, LinkedIn, and YouTube by the specific plaintiffs in the case, including Missouri and Louisiana government officials and agencies acting in their official capacity. It does not extend to other social media networks or content posted by the general public.

"The Parties also agree that government, politicians, media, academics, or anyone else applying labels such as 'misinformation,' 'disinformation,' or 'malinformation' to speech does not render it constitutionally unprotected," the agreement reads.

The court must first approve this settlement agreement.

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Eric Schmitt. Photo by Anna Moneymaker/Getty Images

"We just won Missouri v. Biden," Schmitt wrote in a post on X. "As Missouri's Attorney General, I sued the Biden regime for brazenly colluding with Big Tech to silence Missouri families — censoring the truth about COVID, the Hunter Biden laptop, the open border, and the 2020 election. They tried to turn Facebook, X, YouTube, and the rest into their private speech police, labeling dissent 'misinformation' while they pushed their narrative on the American people."

Schmitt called the Consent Decree the "first real, operational restraint on the federal censorship machine."

He explained that it "directly binds the Surgeon General, the CDC, and CISA: no more threats of legal, regulatory, or economic punishment. No more coercion. No more unilateral direction or veto of platform decisions to remove, suppress, deplatform, or algorithmically bury protected speech."

"For every working Missouri family tired of being silenced by their own government: this victory is yours. The heartland fought back, and the heartland delivered," Schmitt concluded.

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Photo by Matt Cardy/Getty Images

Benjamin Weingarten, a senior contributor at the Federalist, addressed the victory's narrow application.

"This decree is limited to the plaintiffs, but as precedent, and practically, its impact may prove orders of magnitude more powerful in protecting disfavored speech," Weingarten wrote, calling it "a momentous blow for the First Amendment."

National Institutes of Health Director Jay Bhattacharya, who had to withdraw as a plaintiff in the case after being appointed by the Trump administration, called the settlement "a huge win for all Americans."

"Huzzah! The consent decree in Missouri v. Biden is a historic victory for free speech in the US. Though I had to switch to the government side in the case after I became NIH director, I've never been more pleased by 'losing' in my life," he wrote.

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How ‘structural racism’ came to dominate medical research



President Trump's recent push to send federal health care dollars directly to individuals, rather than insurers, reflects a broader demand for transparency and effectiveness in how public funds are used. Government-funded medical research, which forms the foundation of much clinical care, also requires such scrutiny.

In recent years, academic medicine has advanced a nebulous theory of “structural racism” that echoes the 19th century “miasma” theory, which blamed disease on “bad air.” Despite scant evidence, studies attempting to validate this vague framework have multiplied, often funded by largely unaware taxpayers. Refocusing federal research dollars on rigorous science and evidence-based care is essential to correcting this trajectory.

The incentives were clear: Few researchers — early-career or established — would decline funding in an area where the NIH was investing heavily.

How did this happen? The construct of “structural racism” was virtually absent from medical literature until a decade ago. Since then, it has become the default explanation in academic medicine for differences in health outcomes across racial and ethnic groups. Its rise accelerated during the 2020 anti-racism craze, which swept through corporate boardrooms and university administrations while also becoming a core ideological pillar of Black Lives Matter and other political movements.

Academic medicine was no exception. This philosophy quickly gained favor in medical education, academic health centers, elite journals, and professional associations, eventually influencing federal agencies that distribute research funding.

The result: a surge of grant-funded studies built on the premise that racism causes health disparities. Of the nearly 2,300 articles indexed under the term “structural racism” in PubMed, the U.S. National Library of Medicine’s database of leading biomedical and health journals, 95% were published after Jan. 1, 2020. In 2025 alone, PubMed lists 400 such papers — nearly four times the total published before 2020.

This proliferation has been supported by a tsunami of federal taxpayer dollars coming from the National Institutes of Health. From 2020 to 2025, an NIH database search found nearly 750 projects mentioning “structural racism” in their abstracts, totaling almost $533 million in funding. More than 70 of those projects were funded in 2025 at just under $40 million — significantly down from more than 220 projects in 2024 totaling $150 million, but still far above 2020, when only 12 projects received a little over $12 million in the aggregate. Before 2020, the NIH had funded just 10 such projects at a combined cost of $4 million.

Funding patterns across NIH’s 27 Institutes and Centers from 2020 to 2025 make clear that ideology, not medical science, drove much of this growth. The largest investments came from the National Institute on Drug Abuse ($147 million in total funding), National Institute on Minority Health and Health Disparities ($70 million), and National Institute on Aging ($57 million), each pouring substantial resources into “structural racism” research.

In 2025, for example, NIDA supported a project under the Healthy Brain and Child Development National Consortium that identified “structural racism” as a risk to babies before and after birth, alongside more recognizable factors like maternal health, toxic exposures, and child abuse — thereby conflating an abstract, ill-defined, and ideological social theory with measurable, scientific variables as a threat to child development.

Also in 2025, NIMHD funded the Clinical Research Scholars Training program, a “health-equity focused” initiative created in part due to NIH calls for research on “the impact of structural racism and discrimination on health disparities.” Eligibility for this program was limited to those deemed “underrepresented in biomedical research.” All others need not apply.

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Douglas Rissing / Getty Images

And just last year, a NIA-funded project invoked “interrelated systems of structural racism” and “race-specific stress” as risk factors for Alzheimer’s disease and cognitive decline, diverting attention and resources away from well-established contributors such as genetics, medical conditions, lifestyle and environmental factors, and core biological mechanisms like amyloid plaques and tau tangles.

Unfortunately, a commitment to science gave way to ideology years ago. Under Francis Collins, the NIH “acknowledged and committed to ending structural racism,” without even defining the concept itself. “Structural racism” was accepted despite its questionable validity and lack of explanatory power.

With vague boundaries and mechanisms difficult to measure, claims of “structural racism” far exceeded the empirical evidence. Nevertheless, the idea was accepted wholesale and used to justify a wave of DEI initiatives, effectively recasting the NIH as an “anti-racist” institution in the Ibram X. Kendi mold. Objective science was no longer sufficient; the agency was expected to take an activist stance.

Proponents embraced this shift, seeing an opportunity to move health research from “individual-level risk, health behavior, and functioning” to “structural level concepts” with “structural racism” named specifically. Research dollars supported tools like the Structural Racism Effect Index to “guide policies and investments to advance health equity.”

The incentives were clear: Few researchers — early-career or established — would decline funding in an area where the NIH was investing heavily, especially when that support could provide a path to publication in top journals.

Yet the instruments used to quantify “structural racism” expose a basic flaw: They don’t measure racism.

The SREI’s nine dimensions, for example, largely track socioeconomic conditions — wealth, income, housing, employment. In practice, a high score identifies communities facing poverty. Even researchers linking SREI scores to hypertension, obesity, smoking, and low physical activity concede they “cannot make causal inferences.”

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Deagreez via iStock/Getty Images

These health risks may result from poverty, contribute to it, or arise from entirely different causes. Labeling them as products of “structural racism” adds no explanatory value, miscasts economic hardship as race-based, and downplays individual responsibility. It overshadows far more consequential drivers of outcome disparities, including access to care, personal choice, medical comorbidities, and genetics.

Nonetheless, no alternative explanation for health disparities has received anywhere near the same attention in leading medical journals — such as the New England Journal of Medicine, Lancet, and JAMA — as “structural racism.” This concept has been treated as settled fact, with disparities alone offered as proof: If disparities exist, racism must be the cause. Likewise, many medical organizations have reinforced this view through policies and position papers that embed an anti-racism framework into scientific inquiry.

But change is in the air. The NIH’s recent miasma-like fixation on “structural racism” is finally clearing. Under Director Jay Bhattacharya, the agency is refocusing on its core mission of funding rigorous, evidence-based science rather than ideology-driven research. This shift will direct scarce taxpayer dollars toward work grounded in medical science and its practical application — research that can genuinely improve health rather than feed political currents.

This course correction is timely, and while sustained effort in 2026 will be needed to fully restore the NIH to its rightful mission, taxpayers can take comfort: America’s leading biomedical and medical science research institute will once again prioritize their dollars and their health.

Editor's note: This article was originally published by RealClearPolitics and made available via RealClearWire.

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NIH Director Dr. Jay Bhattacharya addresses Tylenol scandal in Glenn Beck interview



Trump derangement syndrome has reached a fever pitch. Pregnant women taking Tylenol, even intentionally overdosing on the drug, has become a viral trend on social media in the wake of President Trump and Health and Human Services Secretary Robert F. Kennedy Jr.’s announcement cautioning women against using the drug during pregnancy, as it’s been linked to an increased risk of autism in children.

According to recent reports, one woman who partook in this trend is currently on a ventilator. Both she and her baby face critically low survival chances.

On the other side of the spectrum, MAHA devotees view the announcement as a long-overdue breakthrough. They’re celebrating the fact that the government is finally validating long-held suspicions about acetaminophen contributing to autism’s rise, after years of silence and suppression by Big Pharma and health agencies.

To get clarity on what has become yet another divisive issue facing our society, Glenn Beck spoke with NIH Director Dr. Jay Bhattacharya.

Pregnant or not, Tylenol is “well-known to cause liver toxicities if you overdose,” Dr. Bhattacharya says.

“If you’re not pregnant and you have a headache or you have a fever, it’s fine; just take it at the right dose,” he advises.

However, the reason the U.S. Department of Health and Human Services issued a warning about taking Tylenol while pregnant, he says, is simply because recent research has found a correlation.

“There’s been a whole sort of range of research in recent years that establishes that there’s this association between taking Tylenol late in pregnancy and subsequent neurodevelopmental conditions like autism, like ADHD,” Dr. Bhattacharya says.

The reason the medical community is so divided on this issue is because “there’s a big fight in the literature over how strong that association is.” But Dr. Bhattacharya’s personal opinion after looking at the available evidence is that “there’s enough there to tell people, especially pregnant women, to be careful with it.”

And that is precisely what President Trump’s announcement was: a warning for pregnant women to be cautious about taking Tylenol.

But lefties, in their commitment to demonize everything associated with President Trump, have predictably raged over what is nothing more than a cautionary warning meant to prevent potential harm.

When Glenn first heard the Tylenol announcement, he thought it would be nothing more than “a blip,” but now that it’s turned into a “nightmare,” he fears what other crazy stunts the left will pull as HHS continues to uncover what’s fueling the autism epidemic.

The announcement “was the least autocratic thing I’ve seen in probably 20 years, and it was like Hitler himself made this declaration,” he says.

And yet the people — regular citizens and medical professionals alike — who are up in arms over Trump’s Tylenol warning are the same people who happily kowtowed to and endorsed mask, lockdown, and vaccine mandates during the COVID-19 pandemic.

Will blind opposition to Trump cost more lives in the quest for truth?

To hear more of Glenn and Dr. Bhattacharya’s conversation, watch the full interview above.

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COVID wasn’t the only virus. Arrogance infected public health.



America doesn’t have a science problem. It has a trust problem.

The collapse of trust didn’t happen in a vacuum. It happened because the people running our institutions — government agencies, public health bureaucracies, and elite media — chose fear over facts, power over principle, and silence over accountability.

Truth alone won’t restore trust. We need courage. We need accountability. And above all, we need to stop pretending that silence keeps the peace.

I’ve spent more than three decades in life sciences, investing in innovation and funding companies that bring real cures to market. Bureaucracy can slow progress. But during COVID-19, the damage went farther. It wasn’t just red tape. It was arrogance, censorship, and the collapse of debate inside institutions once devoted to transparency and truth.

We told Americans to “trust the experts,” then changed the story every few weeks. We locked down playgrounds while allowing political protests. We shut down small businesses while rewarding massive platforms. We punished skepticism, not misinformation. We arrested surfers, fired nurses, and drove policemen and military personnel out of their jobs for refusing a vaccine. Where were the “my body, my choice” voices then?

Now Americans don’t just question mandates — they question everything: the data, the motives, the science itself.

Who can blame them? Childhood vaccination rates are falling because public health failed. An entire generation lost precious developmental time in isolation. Families grieved alone. And the same bureaucrats behind those mandates persuaded us to blame COVID, when in fact it was their decisions that did much of the damage. No one has been questioned. No one has been punished. Not one county health official has been held accountable.

A recent Gallup poll showed trust in institutions like the CDC and FDA has collapsed by more than 30 points in just a few years. That trust won’t be restored by press conferences or new slogans. It will only be restored when real leaders tell the truth about what went wrong and take responsibility to make sure it doesn’t happen again.

Dr. Scott Atlas put it plainly: The lockdowns weren’t the result of the virus. They were the result of decisions — decisions made by people who ignored known data, silenced dissent, and wielded authority like a weapon. And they got it wrong. Pretending otherwise only guarantees the disaster repeats.

So where do we start if we want to rebuild trust?

End the illusion of absolute authority. The CDC, NIH, and FDA must return to their proper role: advisory. They don’t make laws. They don’t issue mandates. They provide information — period.

Impose term limits on public health leadership. No more 30-year bureaucratic dynasties. Power without turnover hardens into ideology.

Ban conflicts of interest. No royalty payments to government scientists from the very companies they regulate. No revolving door between regulators and pharma.

Demand transparency. Every agency meeting, vote, and decision should be public and immediate. If they work for us, we should know what they’re saying.

These aren’t partisan talking points. They’re common-sense reforms. The stakes are too high to shrug and “move on.” Parents who lost a year of their children’s development, the elderly who died alone, the small business owners who lost everything — they deserve accountability. This isn’t about public policy. It’s about principle.

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Eric Lee/Bloomberg via Getty Images

And here’s the deeper truth: Fixing this mess isn’t just government’s job. It’s up to us — the entrepreneurs, innovators, parents, doctors, investors, and voters — to become stewards of truth. Not because we crave power, but because we believe in clarity. Because we still believe in the ideals America was built on.

I came to the United States at 15 after fleeing war in Beirut. I’ve seen what happens when fear and control override freedom and reason. I’ve spent my life betting on better — on ideas, on people, and on this country.

Truth alone won’t restore trust. We need courage. We need accountability. And above all, we need to stop pretending that silence keeps the peace.

It doesn’t. It only postpones the next disaster.

Researchers tied to Fauci’s COVID cover-up still scoring big NIH grants



The Trump administration's National Institutes of Health is still funding some medical researchers who suppressed debate about the possibility of a lab leak as the origin of COVID-19.

Following the outbreak, then-National Institute of Allergy and Infectious Diseases Director Anthony Fauci and then-NIH Director Francis Collins strongly condemned allegations that the virus was the result of a lab leak, primarily citing a March 2020 peer-reviewed article from National Medicine titled "The proximal origin of SARS-CoV-2."

'How do you put all this together, whether you believe in this series of coincidences, what you know of the lab in Wuhan, how much could be in nature — accidental release or natural event?'

However, released emails revealed that the scientists involved in drafting the Proximal Origin initially had concerns that the virus had leaked from a lab.

Kristian G. Andersen, who would go on to be listed as the primary author of the article, wrote in an email to Fauci on January 31, "The unusual features of the virus make up a really small part of the genome (<0.1%) so one has to look really closely at all the sequences to see that some of the features (potentially) look engineered."

Andersen further noted that he, Edward Holmes, Robert Garry, and Michael Farzan "all find the genome inconsistent with expectations from evolutionary theory."

"But we have to look at this much more closely and there are still further analyses to be done, so those opinions could still change," he added.

Holmes and Garry also helped draft the Proximal Origin.

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Photo by Jane Barlow - WPA Pool/Getty Images

In an email to Fauci and Collins on February 2, 2020, Farzan was quoted as saying, "Nothing seems to specifically suggest whether this virus was most likely to be 'adapted,' 'evolved,' or maybe even 'engineered.' So I think it becomes a question of how do you put all this together, whether you believe in this series of coincidences, what you know of the lab in Wuhan, how much could be in nature — accidental release or natural event?"

"I am 70:30 or 60:40," he concluded. Farzan later backtracked, claiming those numbers were "inverted."

A House subcommittee found that the report was created after Fauci and Collins held a conference call in February with roughly a dozen scientists, four of whom drafted the paper days later. That draft was reportedly sent to Fauci and Collins "for editing and approval" before it was published.

During a 2023 congressional hearing, Andersen denied allegations that Fauci prompted researchers to write the Proximal Origin report and rejected claims that grants were used to persuade scientists to dismiss the lab-leak theory.

Despite early suspicions about the virus' origins, the final published version of the paper stated that the scientists' "analyses clearly show that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus."

The report sparked allegations that the once-skeptical authors were now complicit in the cover-up of the virus' origins.

Yet grant records show that Andersen, Garry, and Ian Lipkin are still receiving taxpayer-funded grants, several of which are being used to conduct COVID-related research.

Andersen is receiving a few grants from the NIAID: one worth over $2.5 million, another for $319,000, and a third for $602,000.

The first grant provides funding to the Center for Viral Systems Biology. Andersen is the director and principal investigator of CViSB, while Garry is the co-director.

The project's summary states, "The COVID-19 pandemic is a stark reminder of the threat posed by infectious diseases, but other priority pathogens, such as Lassa and Ebola viruses, continue to pose significant challenges in endemic areas."

"Our central hypothesis remains that complex networks of viral and human factors, including distinct clinical, immunological, genetic, virological, and physiological attributes play key roles in determining the outcome and spread of Lassa, Ebola, and COVID-19," it continues. "Our overall goal is to identify these molecular networks and provide a deep system-level understanding of the virus, host, and environmental drivers of disease severity and spread to discover predictive markers of human disease."

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Anthony Fauci. Photo by J. Scott Applewhite-Pool/Getty Images

The second grant provides funding for the CViSB's Administrative Core, led by Andersen, which includes support for all of the center's research projects to ensure its goals are successfully met.

The third grant funds "Project 2," which aims to "investigate the complex interplay of virus genetics and host immunity in determining epidemiology and outcome of infection with Lassa virus, Ebola virus, and SARS-CoV-2."

Garry was listed as the project leader on a separate grant for "Project 1," totaling nearly $515,000. The project's goal is "to generate an integrated, systems-level dataset that will enable development of models that predict disease severity or long-term sequelae in individuals infected with Lassa virus, Ebola virus or SARS-CoV-2, and protective responses to vaccines."

Another separate grant, totaling over $1.9 million, went to Columbia University's Center for Infection and Immunity for a project to study "gene-environment interactions between the immune system and infectious agents." The project lead and investigator was listed as Ian W. Lipkin, another co-author of the Proximal Origin.

Lipkin informed Blaze News that he is not pursuing SARS-CoV-2 research.

"Unless new data are uncovered that unequivocally demonstrate a point source, I don’t see how there will be resolution of this contentious and destructive debate," Lipkin said. "What is unequivocal is that wild animal markets and unregulated research with known or potential pandemic pathogens pose unacceptable risks to public health."

According to the NIH RePORTER, Holmes and Andrew Rambaut, also a Proximal Origin co-author, do not appear to have any active projects that are receiving grants at this time.

Dr. Richard H. Ebright of Rutgers University told Blaze News that there is "compelling evidence" that the authors of the Proximal Origin knew the paper's conclusions were "invalid at the time it was submitted for publication, at the time it was accepted for publication, and at the time it was published."

He accused the authors of committing "science fraud by publishing conclusions they knew to be invalid" and then "compound[ing] that science fraud by publishing patently unsound follow-up papers purporting to support the invalid conclusions."

Ebright called for the NIH Office of Research Integrity and the Department of Health and Human Services to investigate and "pursue retraction of their fraudulent paper and unsound follow-up papers, termination and clawback of their federal funding, and debarment from eligibility for future federal funding."

An NIH spokesperson told Blaze News, "NIH does not discuss grants compliance reviews on specific funded awards, recipient institutions, or supported investigators, whether or not such reviews occurred or are under way."

Andersen and Garry did not immediately respond to a request for comment.

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