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COVID-19

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

Published

7 months ago

9 minute read

From LifeSiteNews

By Calvin Freiburger

“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.

“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.

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Conservatives demand probe into Liberal vaccine injury program’s $50m mismanagement

Published on July 15, 2025

By

From LifeSiteNews

By Clare Marie Merkowsky

The Liberals’ Vaccine Injury Support Program is accused of mismanaging a $50-million contract with Oxaro Inc. and failing to resolve claims for thousands of vaccine-injured Canadians.

Conservatives are calling for an official investigation into the Liberal-run vaccine injury program, which has cost Canadians millions but has little to show for it.

On July 14th, four Conservative Members of Parliament (MPs) signed a letter demanding answers after an explosive Global News report found the Liberals’ Vaccine Injury Support Program (VISP) misallocated taxpayer funds and disregarded many vaccine-injured Canadians.

“The federal government awarded a $50 million taxpayer-funded contract to Oxaro Inc. (formerly Raymond Chabot Grant Thornton Consulting Inc.). The purpose of this contract was to administer the VISP,” the letter wrote.

“However, there was no clear indication that Oxaro had credible experience in healthcare or in the administration of health-related claims raising valid questions about how and why this firm was selected,” it continued.

Canada’s VISP was launched in December 2020 after the Canadian government gave vaccine makers a shield from liability regarding COVID-19 jab-related injuries.

However, mismanagement within the program has led to many injured Canadians still waiting to receive compensation, while government contractors grow richer.

“Despite the $50 million contract, over 1,700 of the 3,100 claims remain unresolved,” the Conservatives continued. “Families dealing with life-altering injuries have been left waiting years for answers and support they were promised.”

Furthermore, the claims do not represent the total number of Canadians injured by the allegedly “safe and effective” COVID shots, as inside memos have revealed that the Public Health Agency of Canada (PHAC) officials neglected to report all adverse effects from COVID shots and even went as far as telling staff not to report all events.

The PHAC’s downplaying of vaccine injuries is of little surprise to Canadians, as a 2023 secret memo revealed that the federal government purposefully hid adverse effect so as not to alarm Canadians.

The letter further revealed that former VISP employees have revealed that the program lacked professionalism, describing what Conservatives described as “a fraternity house rather than a professional organization responsible for administering health-related claims.”

“Reports of constant workplace drinking, ping pong, and Netflix are a slap in the face to taxpayers and the thousands of Canadians waiting for support for life altering injuries,” the letter continued.

Regardless of this, the Liberal government, under Prime Minister Mark Carney, is considering renewing its contract with Oxaro Inc.

Indeed, this would hardly be the first time that Liberals throw taxpayer dollars at a COVID program that is later exposed as ineffective and mismanaged.

Canada’s infamous ArriveCan app, which was mandated for all travelers in and out of Canada in 2020, has cost Canadians $54 million, despite the Public Health Agency of Canada admitting that they have no evidence that the program saved lives.

Details regarding the app and the government contracts surrounding it have been hidden from Canadians, as Liberals were exposed in 2023 for hiding a RCMP investigation into the app from auditors.

An investigation of the ArriveCan app began in 2022 after the House of Commons voted 173-149 for a full audit of the controversial app.

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COVID-19

Trump DOJ dismisses charges against doctor who issued fake COVID passports

Published on July 14, 2025

By

From LifeSiteNews

By Calvin Freiburger

Attorney General Pam Bondi has ended the federal prosecution of Dr. Michael Kirk Moore for giving ‘patients a choice when the federal government refused to do so.’

The Utah plastic surgeon who issued fake COVID-19 vaccine passports to help patients get around COVID vaccine mandates will no longer be prosecuted, U.S. Attorney General Pam Bondi announced Saturday.

During the COVID pandemic, Dr. Michael Kirk Moore Jr. and employees at his Salt Lake private practice developed a plan to provide patients who objected to being forced to take the vaccine with ineffectual, harmless saline injections instead and give them COVID vaccination cards that would satisfy (since rescinded) mandates to take the shot as a condition of employment, public facilities, mass gatherings, and more.

For his efforts, he was indicted for allegedly “endanger[ing] the health and well-being of a vulnerable population” and “undermin[ing] public trust and the integrity of federal health care programs.” The government also accused him of doing so for profit, but several sources attested off the record that Moore not only issued the cards for free but actually refused offers of compensation.

“They broke no laws and harmed no person,” the defendants’ legal team said in 2023. “Dr. Moore, specifically, abided by his long held Hippocratic oath to First Do No Harm. We believe he and his co-defendants will be found innocent of all charges.”

Last month, LifeSiteNews reported that Moore’s trial was set to begin on July 7, which could have potentially ended with him facing 35 years in jail and a $125,000 penalty. Supporters of the doctor had expressed worry that the change in presidential administration had not yet halted the prosecution.

Over the weekend, however, Bondi announced that at her direction it has now done exactly that.

“Dr. Moore gave his patients a choice when the federal government refused to do so,” she said. “He did not deserve the years in prison he was facing. It ends today.”

 

The federal Vaccine Adverse Event Reporting System (VAERS) reports 38,709 deaths, 221,030 hospitalizations, 22,331 heart attacks, and 28,966 myocarditis and pericarditis cases as of June 27, 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 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 2024, the U.S. Centers for Disease Control & Prevention (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 January, a long-awaited Florida grand jury report on the COVID vaccine manufacturers found that while only a miniscule percentage of the millions of vaccinations resulted in serious harm based on the data it had access to, such events do occur, and there are “profound and serious issues” in pharmaceutical companies’ review process, including reluctance to share what evidence of adverse events they did find.

In May, Trump administration U.S. Food & Drug Administration (FDA) Commissioner Dr. Marty Makary and vaccine chief Dr. Vinay Prasad announced that there would no longer be blanket recommendations for all Americans to receive the shot, but the “risk factors” it would still be recommended for include asthma, cancer, cerebrovascular disease, chronic kidney diseases, a handful of chronic liver and lung diseases, diabetes, disabilities such as Down’s syndrome, heart conditions, HIV, dementia, Parkinson’s, obesity, smoking, tuberculosis, and more. Health & Human Services (HHS) Secretary Robert F. Kennedy Jr. subsequently announced COVID vaccines will not be recommended to healthy children or pregnant women.

The Trump administration has approved a new mRNA-based COVID-19 vaccine from Moderna, suggesting the federal government’s overall view of the shots will remain favorable, albeit without mandates of any kind. At the same time, it does require mRNA COVID shots to carry a new warning about the danger of heart damage in young men.

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