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COVID-19

The Biden-Harris Administration Wasted Nearly One Billion on Misinformation

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From the Brownstone Institute

By Ian Miller 

Biden, CDC Partners Literally Wasted a Fortune to Lie to the American People

The party of “Science” apparently misled hundreds of millions of people on the actual science surrounding the Covid-19 pandemic. Stop the presses.

Starting in early 2020, the combined efforts of Dr. Anthony Fauci, the CDC, the Department of Health and Human Services, and their partners in the media caused an untold amount of damage to society and public health and might have even created conditions for increased Covid spread. How? By repeatedly, profoundly, and often purposefully communicating inaccurate information while spending hundreds of millions of dollars to get their preferred messages across.

Now, a new, massive 113-page report from the US House of Representatives Energy & Commerce Committee has detailed the remarkable abuses from the Biden-Harris administration and the manner in which they communicated during Covid. 

Biden, CDC Partners Literally Wasted a Fortune to Lie to the American People

The report details a number of unbelievable inaccuracies in 2021 coming from the Biden administration’s communications team and the CDC’s messaging apparatus. Fauci and Francis Collins’ National Institutes of Health were also responsible, creating guidance using taxpayer money, nearly $1 billion per the report, that misled millions of people and caused unimaginable harm in the process.

While the Biden-Harris administration’s public health guidance led to prolonged closures of schools and businesses, the NIH was spending nearly a billion dollars of taxpayer money trying to manipulate Americans with advertisements—sometimes containing erroneous or unproven information. By overpromising what the Covid-19 vaccines could do—in direct contradiction of the FDA’s authorizations—and over emphasizing the virus’s risk to children and young adults, the Biden-Harris administration caused Americans to lose trust in the public health system,” Committee Chair Cathy McMorris Rodgers (R-WA) said after the report’s release. “Our investigation also uncovered the extent to which public funding went to Big Tech companies to track and monitor Americans, underscoring the need for stronger online data privacy protections.”

One of the most damaging, and woefully incorrect messaging campaigns centered on vaccine efficacy against infection. As the report details, Biden’s “Stop the Spread” campaign was a pervasive marketing effort in conjunction with the CDC that claimed vaccines would end the pandemic by reducing infections. That had enormous knock-on effects, including decreasing trust in all vaccinations and ultimately harming public health.

“The entire premise of the Biden-Harris ‘Stop the Spread’ campaign was that if you got vaccinated for COVID-19, you could resume daily activities because they said vaccinated people would not spread the disease,” said Subcommittee on Oversight and Investigations Chair Morgan Griffith (R-VA). “Despite lacking scientific basis, the administration bought into this CDC claim and misled the American public. As a result, vaccination coverage with other vaccines appears to have declined, I believe because of a growing distrust of information coming from our public health institutions.”

This campaign was even more disingenuous and purposefully misleading than previously realized. The “Stop the Spread” publicity blitz hid in plain sight a message from the CDC that even they didn’t know whether the vaccines actually stopped infection or transmission. The report shared a screenshot of a page from the Biden administration’s marketing that specifically said “science” wasn’t sure how well the vaccines worked against infection.

Yet the Biden administration made life-altering policy decisions such as vaccine mandates, discriminatory entry processes, and military vaccination requirements regardless. And that was in addition to the less quantifiable impacts like nudging millions of people to follow their preferred course of action.

CDC Guidance Exacerbated Existing Problems

The report also explains how the Biden administration relied heavily on guidance from the CDC, an organization that thoroughly disgraced itself during the pandemic. There were several examples highlighted, chief among them that CDC “experts” went far beyond what even the FDA claimed Covid vaccines could do.

Without evidence, the report says Biden’s marketing claimed that “COVID vaccines were highly effective against transmission.” Within just a few months, it was clear that all the available evidence pointed towards the exact opposite direction. Per the report, this had a “negative impact on vaccine confidence and the CDC’s credibility when proven untrue.”

The CDC also had “inconsistent and flawed messaging about the effectiveness of masks,” which created seemingly endless mandates and, again, overconfidence in an ineffective policy. Some of those mandates even continue to this day.

That’s just the tip of their misinformation. A wealth of data and public embarrassments for the CDC confirmed that the organization “consistently overstated the risk of COVID-19 to children,” the report states. That fear-mongering had disastrous consequences, from unnecessarily terrifying parents to prolonged school closures and lack of socialization—setting an entire generation of children back in the process.

Still, after being repeatedly and profoundly proven wrong, the CDC has demonstrated they’ve yet to learn their lesson. In late 2024, the CDC continues to recommend Covid-19 vaccines for babies starting at six months old. That makes the US a global outlier compared to European nations that have maintained at least some level of intellectual honesty.

How Do We Fix CDC Abuses?

The report detailed several recommendations to fix these organizations after their disastrous work during the pandemic. Even implementing just a select few, listed below, would do wonders for fixing the institutional rot that influenced these mistakes.

  • Congress should consider clarifying responsibility for evaluating the safety of vaccines and streamlining existing reporting systems for capturing vaccine injuries and adverse reactions.
  • HHS and its agencies should embrace a culture of transparency and accountability.
  • The CDC and federal public health officials should not attempt to silence dissenting scientific opinions.

Also highlighted in the report is how the CDC and NIH used their weight in their attempts to censor scientists who dissented from their preferred narratives. Beyond their mistakes, profound inaccuracies, and nearly unlimited spending, their censorship efforts are equally concerning.

As we learned during Covid, if there’s one thing “experts” hate, it’s being told that they were proven wrong. Instead of learning, adjusting, and apologizing, they move to censor, criticize and mislead. This new report is the latest confirmation of these unacceptable “mistakes.” And reaffirms the importance of ensuring they never happen again.

Republished from the author’s Substack

Author

Ian Miller is the author of “Unmasked: The Global Failure of COVID Mask Mandates.” His work has been featured on national television broadcasts, national and international news publications and referenced in multiple best selling books covering the pandemic. He writes a Substack newsletter, also titled “Unmasked.”

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COVID-19

Why FDA Was Right To Say No To COVID-19 Vaccines For Healthy Kids

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From the Daily Caller News Foundation

By Monique Yohanan

The FDA’s decision not to authorize COVID-19 vaccines for healthy children has drawn criticism. Some argue: If parents want the shot, why not let them get it for their kids? That argument misunderstands what FDA authorization means — and why it exists.

The FDA often approves drugs that carry risks or have imperfect evidence of effectiveness. This is a tradeoff we sometimes accept for people who are ill: when someone is already sick, the alternative is untreated disease. Vaccines are different. They are given to millions of healthy children. This requires a higher standard, not just evidence for safety and immune response, but clear, durable clinical effectiveness. Approval for optional use isn’t neutral; once the FDA authorizes a vaccine, it carries the full weight of institutional endorsement.

Measles provides an example for how the FDA approaches vaccine approvals. Before the measles vaccine was introduced in 1963, the U.S. saw 3 to 4 million infections, ~48,000 hospitalizations, ~1,000 cases of encephalitis, and 400-500 deaths each year. Infants bore the brunt of the most severe outcomes.

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That created a natural instinct: why not vaccinate the youngest and most vulnerable? The initial measles rollout was to 9-month-olds, but within two years that timing was changed to children who were at least 1 year of age. This was not because younger babies were not at risk or that the vaccine was riskier for them, but because it just didn’t work well enough to justify a universal campaign.

The knowledge of the particular risk younger infants face has led to continued research on the effectiveness of measles vaccination in that group. A 2023 trial of the combined measles/mumps/rubella (MMR) vaccine in infants aged 5-7 months, and subsequent safety and immune studies in 2024 and 2025, produced consistent results—safety and the ability to generate antibodies were demonstrated, but a durable response and protection against hospitalization were not.

That is why the FDA does not approve MMR for routine use in healthy children younger than 12 months of age. It is also precisely why getting back to herd immunity for measles is so essential: the youngest infants can only be protected if the rest of us are immunized.

What’s the evidence for COVID-19 vaccination in infants and children? It generates robust antibodies, often higher than in adults. But clinical benefits are modestshort-lived, and inconsistent. It is nowhere near the level of proof U.S. regulators require before making a vaccine universally available to healthy kids.

Some argue that even if benefits are modest, parents and pediatricians should be free to choose. But FDA authorization is not about personal preference; it is a stamp of approval for more than 70 million healthy children. Statistical safety is not enough. At that scale, even rare risks mean real harm to real children. COVID-19 vaccines were originally authorized in the hope that immune responses would translate into population-level benefits. For healthy children, the initial optimism sparked by early encouraging signals has steadily given way to three years of disappointing clinical results.

The lessons from measles are clear: safe but minimally effective isn’t enough. We don’t authorize MMR for 5-month-olds, even to parents who might want their children to get it. COVID-19 vaccines for healthy children should be judged similarly. This is not because there is a lack of any benefit, but because it doesn’t rise to the level we use for other vaccines. Only if and when proof of clinical effectiveness becomes available should authorization be reconsidered. At this time, the FDA is right to say no.

Monique Yohanan, MD, MPH, is a senior fellow at Independent Women, a physician executive and healthcare innovation leader, and Chief Medical Officer at Adia Health.

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COVID-19

The Persecution of Canada’s “Other” Freedom Convoy Truckers

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While thousands of serious criminal cases across Canada are dropped merely due to delays, many Convoy-related prosecutions on trivial charges continue more than three-and-a-half years later. The cases of Freedom Convoy truckers (left to right) Bern Bueckert, Clayton McAllister and Csaba Vizi (whose Volvo is shown at bottom) are still not fully resolved. (Sources of photos: (top left and right) screenshots from documentary Unacceptable?; (top middle) ThankYouTruckers.Substack; (bottom) Donna Laframboise)

By Donna Laframboise

On September 8, three and a half years after the 2022 Freedom Convoy departed Ottawa, and five long, stressful months after his trial actually ended, Robert Dinel walked out of court a free man.

Dinel, a Quebec heavy equipment operator who’d behaved entirely peacefully during the protest over Covid restrictions, had been charged with mischief and obstruction of police. Court proceedings were repeatedly delayed — four times alone just this year — until judge Matthew Webber of the Ontario Court of Justice finally stayed the charges on the grounds that Dinel’s Charter rights to a timely trial had been violated.

For Dinel, it was a relief. For Canadians concerned about freedom and justice, his legal ordeal was yet another example of a system gone off the rails.

Most Canadians are aware of the trials of convoy leaders Tamara Lich and Chris Barber, which ended in conviction; they are to be sentenced in October. Few may realize that many more protestors were charged, most for the relatively innocuous infraction of mischief, and have had their cases drag on and on through the courts for more than three years.

The record of Canada’s legal system clearly shows that mischief charges are routinely withdrawn before scarce and expensive court time is expended on relative trivialities. But when it comes to the truckers, the Crown attorneys at the Ottawa courthouse – employees of the Government of Ontario, not the federal government – appear to have lost all perspective. They are on a mission. The sheer intensity of the prosecution of Convoy members looks less like the fair administration of justice than revenge upon people who dared protest the arbitrary and oppressive measures of the Covid years.

The initial police crackdown itself was a mess. Those arrested were passed from police officer to police officer. Officials writing up the paperwork had no direct knowledge of what had actually transpired; extra charges appear to have been tacked on willy nilly. In Dinel’s case, the prosecution doesn’t even know the identity of the tactical officer who pointed a gun at his head and hauled him out of his vehicle on February 18, 2022.

In a police processing trailer four hours after his arrest, Dinel received a medical assessment from a paramedic. Seated and hand-cuffed throughout, the five-foot-three Dinel calmly and repeatedly told police he was in no fit state to be making decisions and that he wanted to speak to a lawyer. “I want to know what I’m signing,” he insisted. But the police officers, who outnumbered him ten-to-one, kept pushing him to sign an undertaking that he wouldn’t return to the protest area. The fact he never got his phone call – that he was denied his Charter right “to retain and instruct [legal] counsel without delay” – should have stopped this case in its tracks. The Crown chose to pursue it, anyway.

A week after Dinel’s mother died in July 2023, he suffered the first of four strokes. In December 2023, one occurred in the courtroom. “My whole face just seized up,” he recalls. “I had another stroke. My whole face drooped, then the judge freaked right out.” An ambulance was summoned and his trial was adjourned. “I hate court,” says Dinel. “It’s hard, you know. It’s stressful, it’s exhausting.” Rather than staying the charges on  compassionate grounds, the prosecution continued, with Dinel accompanied by a service dog.

Nova Scotia trucker Guy Meister spent hours in the same paddy wagon as Dinel the day they were arrested. After travelling from his Nova Scotia home to Ottawa for court appearances more than a dozen times – at considerable expense – in May of this year Meister was found guilty of mischief, but not of obstructing police. In late July, he was sentenced to 20 hours of community service, six months’ probation, and ordered to pay a $100 victim surcharge.

The trial for Windsor, Ontario trucker Csaba Vizi began just this month, the same day Robert Dinel’s charges were stayed. Video broadcast around the world in February 2022 shows him being assaulted by multiple police officers after he’d exited his truck and knelt down in the snow with his hands behind his head. None of those officers were themselves charged following this violence. None were forced to raise tens of thousands in lawyers’ fees, as Vizi has. Even protesters who have endured the stress of a trial and been acquitted have still not always walked free and clear, because the Crown has often insisted on filing appeals. As a result, defence lawyers routinely advise Freedom Convoy protesters that their legal nightmare isn’t actually over until an additional 30 days have come and gone. In one instance, the Crown waited until the last afternoon of the last permissible day to file its appeal.

These are just a few examples of what’s been going on in Canada’s justice system, one already beset by long delays for cases involving far more serious crimes. Credible news reports suggest that the majority of criminal cases in Ontario aren’t even making it to trial, with sexual assault
charges dropped because of delays. Yet the Convoy prosecutions continue.

Many people insist Covid is over, that we should all move on. But the legal persecution of the truckers who bravely protested government overreach in the bitter winter of early 2022 is far from over.

Donna Laframboise is an independent journalist and photographer. A former vice-president of the Canadian Civil Liberties Association, she is the author of Thank You, Truckers! Canada’s Heroes & Those Who Helped Them.

The original, full-length version of this article was recently published in C2C Journal.

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