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Undue Censorship Still Skews COVID Treatments

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7 minute read

From the Frontier Centre for Public Policy

By Lee Harding

The censorship and institutional capture evident in the pandemic should be an ongoing concern for policy-makers, scientists, and the medical field. Someone who encountered this first-hand was clinical trials researcher Sabine Hazan, who testified to the National Citizens Inquiry on COVID-19.

Hazan, the CEO and principal investigator at Venture Clinical Trials is also the founder and CEO of Progena Biome, a genetic sequencing lab. Starting in 2020, she subjected stool samples of COVID-19 patients’ to next-generation sequencing (NGS) of the entire genome of the virus.

It wasn’t long before the tests, which were $3,000 each, showed the virus mutating into four different spike proteins. Patients had anywhere from one to all of them.

“‘How is the vaccine going to work if the spike protein itself is mutating into multiple combinations?’” she asked herself.

“Vaccinating against viruses is not a really a good idea because unfortunately, viruses mutate more than bacteria.”

Hazan was curious about three cases where the virus had completely disappeared by day five. Two of these patients said they had been taking hydroxychloroquine and azithromycin.

On April 2, 2020, Hazan submitted a protocol to treat COVID-19 consisting of hydroxychloroquine, azithromycin, vitamins C, D, and zinc. The Food and Drug Administration (FDA) approved a request to do clinical trials within 24 hours, yet Facebook, Twitter, and Instagram blocked her advertisements for patients.

The few patients Hazan could recruit faced another hurdle as medical authorities warned pharmacists not to prescribe hydroxychloroquine and azithromycin together because of cardiac problems. Her monitoring of patients never revealed such problems.

“These drugs have been given to millions of people with arthritis, and all of a sudden, they’re bad?” she asked.

In the first 16 of 17 patients, the virus disappeared from stool samples between 5 to 8 days after being on the regimen. Hazan applied for a patent for her protocol in July 2020 and received it in December 2020. An unnamed party or parties offered her $10 million, then $40 million for her patent, but refused the money to continue her research.

Hazan found newborns have a lot of bifidobacteria and the elderly have little to none. Her research suggests that boosting a person’s microbiomes can address c difficile, anxiety, Lyme Disease, Crohn’s, psoriasis, Alzheimer’s, and cancer, while its deficiencies may be related to autism.

She had concerns from the vaccines from the start, but authorities kept doctors in California like her from warning patients about possible side effects.

“What I realized doing clinical trials is I couldn’t always trust pharmaceutical companies,” she said.

“When people are coming at me with a new medication that has been tested on animals for one week, I start freaking out.”

Some of her studies waited 6 to 8 months to get published, while 52 have not yet found a journal willing to print them.

“I’m trying to publish the data on the messenger RNA [of COVID vaccines] affecting the microbiome, which won a Research Award at the American College of Gastro[enterology], and nobody’s interested in publishing that.”

This study of more than 150 vaccine-injured patients found the entire phylum of bifidobacteria had been “wiped” out.

Frontiers in Microbiology published her most popular paper, Microbiome-Based Hypothesis on Ivermectin’s Mechanism in COVID-19: Ivermectin Feeds Bifidobacteria to Boost Immunity in July of 2022. The paper received 47,000 views before a complaint led to its retraction in May of 2023.

Twitter deemed her hypothesis as “misinformation” long before the retraction and blocked her account. Some of Hazan’s own patients who worked for Twitter helped get her account reinstated but could not keep her from a ‘misinformation’ label on her posts.

“I was doing the clinical trials. I was treating the patients, I was analyzing the stools. I was working with the FDA. Who’s giving misinformation? I’m publishing. You’re telling me I’m misinforming people?” she recalled thinking.

Hazan expressed concern that a “movement” to retract papers has yanked more than 14,000 of them and artificial intelligence will ignore them.

“What’s interesting about these papers is they all go against the narrative that is meant to sell you something. So that’s dangerous…if you’re trying to push a drug, or biologic, and now you’re removing everything else,” she said.

Such one-sided medical dogma is wrong, she insisted.

“That’s not science. That’s propaganda. That’s what we saw this pandemic,” said Hazan.

“Now I’m blacklisted from a lot of pharmaceutical companies…It actually killed my business of doing clinical trials.”

The fact that mRNA vaccines are still being pushed concerns the Moroccan-born doctor.

“You talk to scientists who do animal studies on the mRNA, they will tell you that the rats are eating their arms. So that’s all I need to hear,” she said.

“The technology may be promising, maybe, but it’s not there yet. It’s still very much experimental.”

Let’s hope more scientists, doctors, and journal publishers will find the integrity and courage of Hazan. Citizens have reason for concern that regulators have pushed risky mRNA vaccines while undermining the legitimacy of other promising options. When will honest science prevail?

Lee Harding is a Research Fellow at the Frontier Centre for Public Policy.

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

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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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Trump DOJ dismisses charges against doctor who issued fake COVID passports

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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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