COVID-19
US House COVID report vindicates lab leak theory but tries to defend ‘success’ of the jabs

From LifeSiteNews
“the federal government supported dangerous gain-of-function research in Wuhan, China without adequate transparency or oversight, and that former White House COVID adviser and National Institute of Allergy & Infectious Diseases (NIAID) director Dr. Anthony Fauci “played semantics with the definition of gain-of-function research” to deny it
The U.S. House Oversight & Accountability Committee’s Select Subcommittee on the Coronavirus Pandemic has released its long-awaited After Action Review on COVID-19 and the government response, which affirms the verdict that COVID most likely originated in a lab through gain-of-function research and broadly condemns the lockdowns of personal freedom and economic activity but attempts to walk a far finer and sometimes contradictory line on the COVID vaccines.
Worked on for almost two years, the 520-page report is billed as the “single most thorough review of the pandemic conducted to date,” according to a press release from the committee.
“This work will help the United States, and the world, predict the next pandemic, prepare for the next pandemic, protect ourselves from the next pandemic, and hopefully prevent the next pandemic. Members of the 119th Congress should continue and build off this work, there is more information to find and honest actions to be taken,” said Republican Rep. Brad Wenstrup of Ohio, the chairman of the subcommittee. “The COVID-19 pandemic highlighted a distrust in leadership. Trust is earned. Accountability, transparency, honesty, and integrity will regain this trust. A future pandemic requires a whole of America response managed by those without personal benefit or bias. We can always do better, and for the sake of future generations of Americans, we must. It can be done.”
The report concludes that COVID most likely “emerged as the result of a laboratory or research related accident,” that the federal government supported dangerous gain-of-function research (that entails intentionally strengthening viruses to better study their potential effects) in Wuhan, China without adequate transparency or oversight, and that former White House COVID adviser and National Institute of Allergy & Infectious Diseases (NIAID) director Dr. Anthony Fauci “played semantics with the definition of gain-of-function research” to deny it, as well as prompting creation of the controversial “Proximal Origins” paper to attempt to discredit the lab-leak theory.
It further found that officials within NIAID actively attempted to flout Freedom of Information Act (FOIA) requests for documents on the matter, such as by intentionally misspelling various names and terms so they would be harder to find in word searches.
The report goes on to conclude that the enormous sums of money the government doled out in the name of COVID relief was rife with waste and abuse, including more than $191 billion in unemployment fraud, $64 billion worth of fraud in the Paycheck Protection Program, and the loss of $200 billion due to the Small Business Administration failing to implement proper oversight and controls.
Meanwhile, the infamous “social distancing” guidance for people to stand at least six feet apart was based on “no scientific trials or studies,” but despite admitting as much, Fauci declined to push back because, in his words, it was “not appropriate to be publicly challenging a sister organization.” Face masks were similarly unsupported by the science and ultimately proven to be ineffective at limiting COVID’s spread, and widespread lockdowns of businesses and public gatherings caused significant harm to the economy, to physical and mental health, and to children’s education and social development far outweighing whatever good they may have done.
On the subject of the controversial COVID vaccines, however, the report is far more deferential. It acknowledges that the shots “had adverse events that must be thoroughly investigated,” and discusses various shortcomings in the government’s reporting systems for adverse vaccine events but still concludes that, overall, the vaccines were “largely safe and effective,” and credits them with saving “millions” of lives.
Operation Warp Speed, the Trump administration initiative to develop vaccines for COVID in a fraction of the time vaccines usually take, “was a tremendous success,” the subcommittee says, and the resulting vaccines “undoubtedly saved millions of lives by diminishing likelihood of severe disease and death.” It even faults President Joe Biden and Vice President Kamala Harris, who were running against Donald Trump for the White House at the time, for “question(ing) the safety and efficacy of COVID-19 vaccinations” before they were released.
At the same time, the report faults the following Biden administration for mandating the shots and rushing approval of vaccine booster doses, downplaying natural immunity, failing to properly adjudicate vaccine injuries, and exaggerating the vaccines’ value.
“COVID-19 vaccines were tremendously important in reducing the severity of COVID-19 symptoms and were extremely effective in doing so,” the report claims. “However, the Biden Administration oversold the power of these vaccines. On more than one occasion, President Biden himself overstated the vaccine’s ability to prevent infection and transmission. These false statements likely contributed to Americans’ confusion about COVID-19 vaccines and reduced overall vaccine confidence.”
The subcommittee report largely reiterates and aligns with a wealth of previous findings on the failures of lockdowns and forced masking, as well as the origins of COVID-19. On the subject of the vaccines, however, it neglects a large body of evidence of far more widespread harm.
The federal Vaccine Adverse Event Reporting System (VAERS) reports 38,068 deaths, 218,646 hospitalizations, 22,002 heart attacks, and 28,706 myocarditis and pericarditis cases as of October 25, among other ailments. U.S. Centers for Disease Control & Prevention (CDC) researchers have recognized a “high verification rate of reports of myocarditis to VAERS after mRNA-based COVID-19 vaccination,” leading to the conclusion that “under-reporting is more likely” than over-reporting.
An analysis of 99 million people across eight countries published February in the journal Vaccine “observed significantly higher risks of myocarditis following the first, second and third doses” of mRNA-based COVID vaccines, as well as signs of increased risk of “pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis,” and other “potential safety signals that require further investigation.” In April, the CDC was forced to release by court order 780,000 previously undisclosed reports of serious adverse reactions, and a study out of Japan found “statistically significant increases” in cancer deaths after third doses of mRNA-based COVID-19 vaccines and offered several theories for a causal link.
In Florida, an ongoing grand jury investigation into the vaccines’ manufacturers is slated to release a report on the safety and effectiveness of the COVID vaccines, and a lawsuit by the state of Kansas has been filed accusing Pfizer of misrepresentation for calling the shots “safe and effective.” The findings of both efforts are highly anticipated.
All eyes are currently on returning President Trump, and whose health team, which will be helmed by prominent vaccine critic Robert F. Kennedy, Jr. as his nominee for Secretary of Health & Human Services, has given mixed signals as to the prospects of reconsidering the shots for which he has long taken credit, and has nominated both critics and defenders of establishment COVID measures for a number of administration roles.
COVID-19
FDA requires new warning on mRNA COVID shots due to heart damage in young men

From LifeSiteNews
Pfizer and Moderna’s mRNA COVID shots must now include warnings that they cause ‘extremely high risk’ of heart inflammation and irreversible damage in males up to age 24.
The Trump administration’s Food and Drug Administration (FDA) announced it will now require updated safety warnings on mRNA COVID-19 shots to include the “extremely high risk” of myocarditis/pericarditis and the likelihood of long-term, irreversible heart damage for teen boys and young men up to age 24.
The required safety updates apply to Comirnaty, the mRNA COVID shot manufactured by Pfizer Inc., and Spikevax, the mRNA COVID shot manufactured ModernaTX, Inc.
According to a press release, the FDA now requires each of those manufacturers to update the warning about the risks of myocarditis and pericarditis to include information about:
- the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
- the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 injection.
The FDA has also required the manufacturers to describe the new safety information in the adverse reactions section of the prescribing information and in the information for recipients and caregivers.
Additionally, the fact sheets for healthcare providers and for recipients and caregivers for Moderna COVID-19 shot and Pfizer-BioNTech COVID-19 shot, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax prescribing information and information for recipients and caregivers.
In a video published on social media, Dr. Vinay Prasad, director of the Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, explained the alarming reasons for the warning updates.
While heart problems arose in approximately 8 out of 1 million persons ages 6 months to 64 years following reception of the cited shots, that number more than triples to 27 per million for males ages 12 to 24.
Prasad noted that multiple studies have arrived at similar findings.
COVID-19
Court compels RCMP and TD Bank to hand over records related to freezing of peaceful protestor’s bank accounts

The Justice Centre for Constitutional Freedoms announces that a judge of the Ontario Court of Justice has ordered the RCMP and TD Bank to produce records relating to the freezing of Mr. Evan Blackman’s bank accounts during the 2022 Freedom Convoy protest.
Mr. Blackman was arrested in downtown Ottawa on February 18, 2022, during the federal government’s unprecedented use of the Emergencies Act. He was charged with mischief and obstruction, but he was acquitted of these charges at trial in October 2023.
However, the Crown appealed Mr. Blackman’s acquittal in 2024, and a new trial is scheduled to begin on August 14, 2025.
Mr. Blackman is seeking the records concerning the freezing of his bank accounts to support an application under the Charter at his upcoming retrial.
His lawyers plan to argue that the freezing of his bank accounts was a serious violation of his rights, and are asking the court to stay the case accordingly.
“The freezing of Mr. Blackman’s bank accounts was an extreme overreach on the part of the police and the federal government,” says constitutional lawyer Chris Fleury.
“These records will hopefully reveal exactly how and why Mr. Blackman’s accounts were frozen,” he says.
Mr. Blackman agreed, saying, “I’m delighted that we will finally get records that may reveal why my bank accounts were frozen.”
This ruling marks a significant step in what is believed to be the first criminal case in Canada involving a proposed Charter application based on the freezing of personal bank accounts under the Emergencies Act.
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