COVID-19
Undue Censorship Still Skews COVID Treatments
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.
COVID-19
Trump DOJ seeks to quash Pfizer whistleblower’s lawsuit over COVID shots
From LifeSiteNews
The Justice Department attorney did not mention the Trump FDA’s recent admission linking the COVID shots to at least 10 child deaths so far.
The Trump Department of Justice (DOJ) is attempting to dismiss a whistleblower case against Pfizer over its COVID-19 shots, even as the Trump Food & Drug Administration (FDA) is beginning to admit their culpability in children’ s deaths.
As previously covered by LifeSiteNews, in 2021 the BMJ published a report on insider information from a former regional director of the medical research company Ventavia, which Pfizer hired in 2020 to conduct research for the company’s mRNA-based COVID-19 shot.
The regional director, Brook Jackson, sent BMJ “dozens of internal company documents, photos, audio recordings, and emails,” which “revealed a host of poor clinical trial research practices occurring at Ventavia that could impact data integrity and patient safety […] We also discovered that, despite receiving a direct complaint about these problems over a year ago, the FDA did not inspect Ventavia’s trial sites.”
According to the report, Ventavia “falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial.” Overwhelmed by numerous problems with the trial data, Jackson filed an official complaint with the FDA.
Jackson was fired the same day, and Ventavia later claimed that Jackson did not work on the Pfizer COVID-19 shot trial; but Jackson produced documents proving she had been invited to the Pfizer trial team and given access codes to software relating to the trial. Jackson filed a lawsuit against Pfizer for violating the federal False Claims Act and other regulations in January 2021, which was sealed until February 2022. That case has been ongoing ever since.
Last August, U.S. District Judge Michael Truncale dismissed most of Jackson’s claims with prejudice, meaning they could not be refiled. Jackson challenged the decision, but the Trump DOJ has argued in court to uphold it, Just the News reports, with DOJ attorney Nicole Smith arguing that the case concerns preserving the government’s unfettered power to dismiss whistleblower cases.
The rationale echoes a recurring trend in DOJ strategy that Politico described in May as “preserving executive power and preventing courts from second-guessing agency decisions,” even in cases that involve “backing policies favored by Democrats.”
Jackson’s attorney Warner Mendenhall responded that the administration “really sort of made our case for us” in effectively admitting that DOJ is taking the Fair Claims Act’s “good cause” standard for state intervention to mean “mere desire to dismiss,” which infringes on his client’s “First Amendment right to access the courts, to vindicate what she learned.”
Mendenhall added that in a refiled case, Jackson “may be able to bring a very different case along the same lines, but with the additional information” to prove fraud, whereas rejection would send the message that “if fraud involves government complicity, don’t bother reporting it.”
That additional information would presumably include the FDA’s recent admission that at least 10 children the agency has reviewed so far “died after and because of receiving COVID-19 vaccination.”
“The truth is we do not know if we saved lives on balance,” admitted FDA Chief Medical Officer Vinay Prasad in a recent leaked email. “It is horrifying to consider that the U.S. vaccine regulation, including our actions, may have harmed more children than we saved. This requires humility and introspection.”
The COVID shots have been highly controversial ever since the first Trump administration’s Operation Warp Speed initiative prepared and released them in a fraction of the time any previous vaccine had ever been developed and tested. As LifeSiteNews has extensively covered, a large body of evidence has steadily accumulated over the past five years indicating that the COVID jabs failed to prevent transmission and, more importantly, carried severe risks of their own.
Ever since, many have intently watched and hotly debated what President Donald Trump would do about the situation upon his return to office. Though he never backed mandates like former President Joe Biden did, for years Trump refused to disavow the shots to the chagrin of his base, seeing Operation Warp Speed as one of his crowning achievements. At the same time, during his latest run he embraced the “Make America Healthy Again” movement and its suspicion of the medical establishment more broadly.
So far, Trump’s second administration has rolled back several recommendations for the shots but not yet pulled them from the market, despite hiring several vocal critics of the COVID establishment and putting the Department of Health & Human Services under the leadership of America’s most prominent anti-vaccine advocate, Robert F. Kennedy Jr. Most recently, the administration has settled on leaving the current jabs optional but not supporting work to develop successors.
In a July interview, FDA Commissioner Marty Makary asked for patience from those unsatisfied by the administration’s handling of the shots, insisting more time was needed for comprehensive trials to get more definitive data.
COVID-19
Canadian Health Department funds study to determine effects of COVID lockdowns on children
From LifeSiteNews
The commissioned study will assess the impact on kids’ mental well-being of COVID lockdowns and ‘remote’ school classes that banned outdoor play and in-person learning.
Canada’s Department of Health has commissioned research to study the impact of outdoor play on kids’ mental well-being in light of COVID lockdowns and “remote” school classes that, for a time, banned outdoor play and in-person learning throughout most of the nation.
In a notice to consultants titled “Systematic Literature Reviews And Meta Analyses Supporting Two Projects On Children’s Health And Covid-19,” the Department of Health admitted that “Exposure to green space has been consistently associated with protective effects on children’s physical and mental health.”
A final report, which is due in 2026, will provide “Health Canada with a comprehensive assessment of current evidence, identify key knowledge gaps and inform surveillance and policy planning for future pandemics and other public health emergencies.”
Bruce Squires, president of McMaster Children’s Hospital of Hamilton, Ontario, noted in 2022 that “Canada’s children and youth have borne the brunt” of COVID lockdowns.
From about March 2020 to mid-2022, most of Canada was under various COVID-19 mandates and lockdowns, including mask mandates, at the local, provincial, and federal levels. Schools were shut down, parks were closed, and most kids’ sports were cancelled.
Mandatory facemask polices were common in Canada and all over the world for years during the COVID crisis despite over 170 studies showing they were not effective in stopping the spread of COVID and were, in fact, harmful, especially to children.
In October 2021, then-Prime Minister Justin Trudeau announced unprecedented COVID-19 jab mandates for all federal workers and those in the transportation sector, saying the un-jabbed would no longer be able to travel by air, boat, or train, both domestically and internationally.
As reported by LifeSiteNews, a new report released by the Justice Centre for Constitutional Freedoms (JCCF) raised alarm bells over the “harms caused” by COVID-19 lockdowns and injections imposed by various levels of government as well as a rise in unexplained deaths and bloated COVID-19 death statistics.
Indeed, a recent study showed that COVID masking policies left children less able to differentiate people’s emotions behind facial expressions.
COVID vaccine mandates and lockdowns, which came from provincial governments with the support of the federal government, split Canadian society.
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