COVID-19
Mandating COVID shots ‘one of the greatest mistakes,’ former CDC chief says

From LifeSiteNews
By John-Michael Dumais, The Defender
In a Senate hearing July 11, ex-CDC Director Robert Redfield said mRNA COVID-19 vaccines are ‘toxic’ and should not have been mandated. He also called for a pause on gain-of-function research.
Former Centers for Disease Control and Prevention (CDC) Director Robert Redfield confirmed the dangers of mRNA COVID-19 vaccines in a U.S. Senate hearing on July 11, calling them “toxic” and saying they should never have been mandated.
Redfield’s admissions came during a Senate Committee on Homeland Security and Governmental Affairs hearing on government oversight of taxpayer-funded high-risk virus research.
The late admission of vaccine injuries underscores the failure of public health agencies and the medical establishment to provide informed consent to the billions of vaccine recipients worldwide.
“It’s important that he is telling the truth now,” vaccine researcher Jessica Rose, Ph.D., told The Defender. “Adverse events were hidden and still are being hidden to prevent injection hesitancy.”
Redfield, who led the CDC from 2018 to 2021, didn’t stop there. He declared biosecurity “our nation’s greatest national security threat,” calling for a halt to gain-of-function research pending further debate.
The hearing, which featured contentious exchanges between senators and witnesses, also touched on controversial topics such as the COVID-19 origins lab-leak theory and allegations that health agencies suppressed data.
mRNA vax ‘should have been open to personal choice’
During the hearing Redfield, who oversaw the CDC during the crucial early months of the COVID-19 pandemic, elaborated on his recent statements about mRNA vaccine safety.
“I do think one of the greatest mistakes that was made, of course, was mandating these vaccines,” Redfield said. “They should have never been mandated. It should have been open to personal choice.”
Redfield went further, admitting that the spike protein produced by mRNA vaccines is “toxic to the body” and triggers “a very strong pro-inflammatory response.”
He noted that in his own medical practice, he doesn’t administer mRNA vaccines, preferring “killed protein vaccines” instead.
Redfield’s statements stand in stark contrast to the CDC’s official stance during his tenure, which strongly promoted mRNA vaccine uptake as safe and effective.
Sen. Ron Johnson (R-WI) pressed Redfield on the issue, highlighting concerning data from the Vaccine Adverse Event Reporting System (VAERS). Johnson presented figures showing over 37,000 deaths reported following COVID-19 vaccination, with 24 percent occurring within two days of injection.
Redfield acknowledged there was “not appropriate transparency from the beginning about the potential side effects of these vaccines.” He criticized attempts to “underreport any side effects because they argued that would make the public less likely to get vaccinated.”
I truly appreciated Dr. Redfield’s honesty at the hearing today. pic.twitter.com/X06znrxe12
— Senator Ron Johnson (@SenRonJohnson) July 12, 2024
‘FDA should release all of the safety data’
Redfield’s criticism of data withholding extended beyond vaccine side effects. He expressed disappointment in the U.S. Food and Drug Administration‘s (FDA) handling of vaccine safety information.
“The FDA should release all of the safety data they have,” Redfield said. “I was very disappointed to hear that they were planning to hold on to that until 2026. That really creates a sense of total lack of trust in our public health agencies towards vaccination.”
Johnson echoed these concerns, revealing his frustration with the lack of follow-through by health agencies and the committee itself.
“I’m not getting cooperation out of the chairman of the permanent subcommittee investigation to issue subpoenas to get this,” Johnson said, referring to unreleased data and documents.
The senator displayed a chart comparing adverse event reports for various drugs, including ivermectin and hydroxychloroquine, to those for COVID-19 vaccines. The stark contrast in reported deaths from these therapeutics – with COVID-19 vaccines showing significantly higher numbers – fueled Johnson’s demand for more transparency.
“As important as the cover-up of the origin story is, there’s a lot more that’s being covered up,” Johnson asserted. “The public has a right to know. We pay for these agencies. We pay their salaries. We fund these studies.”
Redfield agreed with Johnson’s assessment, stating that withholding the information is “counterproductive.”
Redfield doubtful of ‘any benefit from [gain-of-function] research’
Redfield’s testimony took another controversial turn when he called for a pause on gain-of-function research, experiments that involve making pathogens more infectious or deadly.
“I’m not aware of any advanced therapeutic or vaccine that has come to pass because of gain-of-function research,” Redfield said. “I do think there has to be a very aggressive debate of whether there’s any benefit from that research.”
Sen. Rand Paul (R-KY) seized on this point, introducing his Risky Research Review Act. The bill aims to establish an independent board within the executive branch to oversee federal funding for high-risk life sciences research.
“If the Risky Research Review Act had been in place, it might have prevented the COVID-19 pandemic,” Paul said, citing Redfield’s endorsement.
MIT’s Kevin Esvelt, Ph.D., inventor of a technique for rapidly evolving proteins and other biomolecules who was also instrumental in developing CRISPR gene-editing technology, reinforced these concerns.
Highlighting gaps in current oversight, he described an experiment where his team – with FBI approval – successfully ordered DNA fragments of the 1918 influenza virus from 36 of 38 providers.
“Everything that we did and the companies did was entirely legal,” Esvelt said, underscoring the potential for misuse. “There are no laws regulating DNA synthesis, even though the industry group, the International Gene Synthesis Consortium, has requested congressional regulation.”
The hearing revealed a growing consensus among witnesses for stricter oversight of potentially dangerous research, with Redfield suggesting such studies should be “highly regulated” to protect national security.
Redfield reaffirms COVID lab-leak theory
The hearing reignited debate over the origins of COVID-19, with Redfield reaffirming his belief in the lab-leak theory.
“Based on my initial analysis, I believe then, and I still believe today, that the COVID infections were the direct result of a biomedical research experiment and subsequent lab leak,” Redfield stated.
This assertion led to a heated exchange between Sen. Josh Hawley (R-MO) and Carrie Wolinetz, Ph.D., former chief of staff to then-director of the National Institutes of Health (NIH) Francis Collins. Hawley accused NIH officials of deliberately suppressing the lab-leak theory.
“Your office, Dr. [Anthony] Fauci and others tried to actively censor them,” Hawley said. “There was a propaganda effort that this paper was the center of, and now everybody says, ‘Oh, well, we just weren’t sure at the time.’”
Hawley referred to the 2020 “Proximal Origin” paper that argued against the lab-leak hypothesis.
Wolinetz defended the NIH’s actions. “I do not believe censorship took place, sir.” She maintained that discussions about the virus’s origins were part of normal scientific discourse.
Redfield, however, criticized the lack of thorough investigation into both natural origin and lab-leak hypotheses. “Unfortunately, this didn’t happen,” he said, adding that four years later, he believes there’s no meaningful evidence supporting a natural origin.
The former CDC director also revealed that he did not learn about concerning biodistribution studies of the vaccine’s lipid nanoparticles until as late as the summer of 2021, suggesting a delay in critical information reaching top health officials.
‘Biosecurity is our nation’s greatest national security threat’
Redfield emphasized the critical importance of biosecurity in national defense.
“In 2024, 2025, biosecurity is our nation’s greatest national security threat,” Redfield stated. “You need to think of it the same way we thought about the verge of nuclear atomic [sic] in the late ‘40s, ‘50s, and ‘60s.”
He called for a proportional response to the threat, suggesting the creation of a dedicated agency within the U.S. Department of Energy to address biosecurity concerns.
“We have a $900 billion Defense Department for the threat of China, North Korea, and Russia,” Redfield noted. “We don’t have really any systematic agency or network of private sector contractors to help us with the biosecurity threat.”
Sen. Roger Marshall (R-KS) echoed this sentiment. “In my humble mind, a viral biosecurity issue is a bigger issue than China’s military threat to us.”
Gerald Parker, DVM, Ph.D., associate dean for Global One Health at Texas A&M University, supported the call for enhanced oversight, recommending “an independent authority to consolidate secure functions in a single entity with a dedicated mission.”
The hearing also touched on the potential for future pandemics, with Redfield repeating his warnings about the potential spread of H5N1 bird flu.
As the hearing concluded, senators from both parties expressed concern over the lack of transparency and oversight in high-risk research.
Paul summarized the sentiment: “We cannot stand idly by. We must demand accountability, strive for transparency, and ensure the safety of our citizens is never again compromised by negligence or deceit.”
This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.
COVID-19
US Government ADMITS It Approved Pfizer’s COVID “Vaccine” Despite Knowing About a Long List of Trial Violations

The Vigilant Fox
The US government just admitted something shocking.
They KNEW Pfizer’s COVID “vaccine” trials were a complete sham back in 2020.
But they didn’t pursue fraud because exposing it would blow up the very health policy they’re still clinging to today.
This revelation comes from the whistleblower case of Brook Jackson, a former regional director at Ventavia, the company that ran Pfizer’s clinical trials.
In 2021, Jackson filed a lawsuit under the False Claims Act, alleging that Pfizer, Ventavia, and others committed fraud by falsifying data and violating clinical trial protocols.
And now, the government refuses to investigate further—because doing so would expose that they knowingly pushed a harmful product onto the American people.
We’ll show you the court filings with Brook Jackson in this report.
Here’s what Brook Jackson witnessed firsthand.
As regional director at Ventavia, the company running Pfizer’s vaccine trial sites, Jackson said the entire operation was riddled with serious violations. She saw falsified data, trial participants who were unblinded, staff who were poorly trained, and vaccines that were improperly stored.
Worse, she claimed the company FAILED to follow up on adverse events, including serious, potentially life-threatening ones—which recklessly endangered patients and destroyed the integrity of the entire trial.
“We were so inundated with the number of adverse events that we could not keep up,” she said. Pfizer even called asking what the plan was to handle the flood of safety reports.
She said patients weren’t even given full informed consent—her “number one concern.”
Jackson reported these issues to Ventavia. When nothing changed, she went to the FDA.
Six hours later, she was fired. The reason? “I was not a good fit,” she said. “I was not a good fit for reporting fraudulent conduct in a clinical trial.”
Jackson worked at Ventavia for just 18 days but says that’s all it took to get a grasp of the fraud she witnessed.
The court documents reveal a disturbing admission: the government KNEW about ALL the previously listed issues before granting Emergency Use Authorization for Pfizer’s COVID shot.
“The FDA was aware of the protocol violations allegedly witnessed by relator BEFORE it granted Pfizer emergency use authorization for its vaccine.”
That’s the quote from page 19 of the court documents.
The “Relator” they’re referring to is Brook Jackson.
If Jackson’s allegations were true, it would completely undermine the trial’s integrity.
So what did the FDA do with that knowledge?
According to Jackson, nothing.
“I called them. I filed a report. Did they investigate the allegations I was making? The answer is no,” she said.
In a second slap in the face to the American people, the government claimed they moved forward with the COVID shots because they had “continued access” to Pfizer’s vaccine clinical trial data.
That’s the same data the FDA tried to hide for 75 years.
Now that it’s been forced into the light, we know exactly what they were trying to cover up—data showing:
• Heart damage in young people
• A massive volume of adverse events
• Biodistribution to vital organs and dangerous accumulation
• Reproductive harm affecting fertility and pregnancy outcomes
• Deaths and severe injuries linked directly to the shot
• COVID-19 listed as a side effect
• Complete failure to stop transmission
• And much, much more.
They had access to it all. And they pushed the shots anyway.
The most disturbing admission of all comes in the third point of the case.
The court filing states:
“The government further explained that discovery and litigation obligations associated with the case would place significant burdens on FDA, HHS, and the Department of Justice and that the government should not be required to bear such burdens on a case ‘inconsistent with its health policy.’”
In plain English: the government didn’t want to investigate Pfizer, not because the fraud claims lacked merit, but because digging deeper would conflict with its official narrative that the COVID shots are “effective.”
That’s the health policy they’re clinging to.
And they’d rather bury anything that threatens to expose flaws, fraud, or harm from these shots than face the fallout of their own actions.
Jackson emphasized that her lawsuit is about one thing: fraud.
She questioned how exposing fraud could possibly go against public health policy, especially when that policy has never even been clearly defined.
“These were our taxpayer dollars used to fund their experiments,” Jackson said, adding, “these [COVID shots] are not safe or effective products. They’re contaminated, they’re dangerous, and they need to be stopped immediately.”
She called for a full recall, congressional investigations, and accountability for the dangerous experiment that’s been carried out on the American people.
“Fraud should not be allowed to be a part of a clinical trial. Period.”
Thanks for reading.
Subscribe to this page for more COVID reports and stories that matter.
Watch the full conversation with Brook Jackson and Maria Zeee below.
COVID-19
Former Australian state premier accused of lying about justification for COVID lockdowns

Daniel Andrews, Premier of Victoria
From LifeSiteNews
By David James
Monica Smit said she is launching a private criminal prosecution against Daniel Andrews based on ‘new evidence proving they enforced lockdowns without medical advice or evidence.’
The fiercest opponent of the former Victorian premier Daniel Andrews during the COVID crisis was activist Monica Smit. The government responded to her advocacy by arresting her for participating in anti-lockdown protests. When she refused to sign her bail conditions she was made, in effect, a political prisoner for 22 days.
Smit subsequently won a case against the Victoria Police for illegal imprisonment, setting an important precedent. But in a vicious legal maneuver, the judge ensured that Smit would be punished again. She awarded Smit $4,000 in damages which was less than the amount offered in pre-trial mediation. It meant that, despite her victory, Smit was liable for Victoria Police’s legal costs of $250,000. It was not a good day for Australian justice.
There is a chance that the tables will be reversed. Smit has announced she is launching a private criminal prosecution against Andrews and his cabinet based on “new evidence proving they enforced lockdowns without medical advice or evidence.”
The revelation that the savage lockdown policies made little sense from a health perspective is hardly a surprise. Very little of what happened made medical sense. For one thing, according to the Worldometer, about four-fifths of the people who tested positive for COVID-19 had no symptoms. Yet for the first time in medical history healthy people were treated as sick.
The culpability of the Victorian government is nevertheless progressively becoming clearer. It has emerged that the Andrews government did not seek medical advice for its curfew policies, the longest in the Western world. Andrews repeatedly lied when he said at press conferences that he was following heath advice.
David Davis, leader of the right wing opposition Liberal Party, has made public a document recording an exchange between two senior health officials. It shows that the ban on people leaving their homes after dark was implemented without any formal input from health authorities.
Davis acquired the email exchange, between Victorian chief health officer Brett Sutton and his deputy Finn Romanes, under a Freedom of Information request. It occurred two-and-a-half hours after the curfew was announced.
Romanes explained he had been off work for two days and was not aware of any “key conversations and considerations” about the curfew and had not “seen any specific written assessment of the requirement” for one.
He added: “The idea of a curfew has not arisen from public health advice in the first instance. In this way, the action of issuing a curfew is a mirror to the State of Disaster and is not occurring on public health advice but is a decision taken by Cabinet.” Sutton responded with: “Your assessment is correct as I understand it.”
The scale of the deceptions is becoming harder for most Australians to avoid if they are paying attention. The mainstream media, for example, is now running stories that the virus originated in a laboratory. Those who have memories will recall that in 2020 anyone suggesting that the virus was artificially made were accused of anti-China racism, especially the state broadcasters SBS and the ABC. Likewise, most politicians and academics dismissed the lab leak theory. To say the least, no one is holding up their hand to take responsibility for their errors.
The email exchange, compelling evidence of the malfeasance of the Andrews government, raises further questions. If Smit’s lawyers can get Andrews to respond under oath, one ought to be: “If you were lying about following medical advice, then why were you in such a hurry to impose such severe measures and attack dissenters?”
It remains a puzzle. Why did otherwise inconsequential politicians suddenly turn into dictatorial monsters with no concern for what their constituents thought?
The most likely explanation is that they were told it was a biowarfare attack and were terrified, ditching health advice and applying military protocols. The mechanism for this was documented in a speech by Queensland senator Malcolm Roberts.
If so, was an egregious error of judgement. As the Australian Bureau of Statistics showed, 2020 and 2021 had the lowest level of respiratory diseases since records have been kept. There was never a pandemic.
There needs to be an explanation to the Australian people of why they lost their liberty and basic rights. A private prosecution might achieve this. Smit writes: “Those responsible should face jail time, nothing less. The latest revelation of ‘document 34‘ is just the beginning. A public criminal trial will expose truths beyond our imagination.”
-
Business2 days ago
Welcome to Elon Musk’s New Company Town: ‘Starbase, TX’ Votes To Incorporate
-
COVID-192 days ago
US Government ADMITS It Approved Pfizer’s COVID “Vaccine” Despite Knowing About a Long List of Trial Violations
-
Health2 days ago
Jay Bhattacharya Closes NIH’s Last Beagle Lab
-
Alberta1 day ago
Premier Smith seeks Alberta Accord: Announces new relationship with Ottawa
-
Artificial Intelligence1 day ago
The Responsible Lie: How AI Sells Conviction Without Truth
-
Energy2 days ago
Is the Carney Government Prepared to Negotiate a Fair Deal for the Oil, Gas and Pipeline Sectors
-
Business2 days ago
‘Got To Go’: Department Of Energy To Cut Off Billions Of Dollars’ Worth Of Biden-Era Green Energy Projects
-
Alberta22 hours ago
Saudi oil pivot could shake global markets and hit Alberta hard