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COVID shots have 200-times higher risk of brain clots than other jabs: new report

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Dr. Peter McCullough

From LifeSiteNews

By Calvin Freiburger

A new review by Dr. Peter McCullough and other medical experts found 5,137 cases of cerebral thromboembolism since the COVID-19 shots have been available, compared to less than 400 for the previous three decades.

The COVID-19 shots carry increased risks of creating blood clots to the brain, according to a newly-published study by a team of experts that includes prominent critics of the COVID establishment such as Dr. Peter McCullough.

The study by Drs. McCullough, Kirstin Cosgrove, James Thorp, and Claire Rogers examined data on reports of cerebral thromboembolism, blood clots that block cerebral veins or brain arteries (interfering with blood and oxygen flow to the brain), following COVID shots submitted to the U.S. Centers for Disease Control & Prevention (CDC) and federal Vaccine Adverse Event Reporting System (VAERS) from January 1990 all the way through December 2023.

It found 5,137 cases reported in the three years the COVID injections have been available, compared to just 52 associated with influenza vaccines and 282 for all other vaccines over the past three decades, for a risk more than 200 times greater from the new shots.

“An immediate global moratorium on the use of COVID-19 vaccines is necessary with an absolute contraindication in women of reproductive age.”

“There is an alarming breach in the safety signal threshold concerning cerebral thrombosis AEs [adverse events] after COVID-19 vaccines compared to that of the influenza vaccines and even when compared to that of all other vaccines,” the authors conclude. “An immediate global moratorium on the use of COVID-19 vaccines is necessary with an absolute contraindication in women of reproductive age.”

McCullough, a widely-published cardiologist, added on his personal Substack that the report “did not capture the level of permanent neurologic devastation and disability suffered by these patients. I can tell you that the rates must be very high given the extensive nature of the blood clots reported. These data among others strongly support removing all COVID-19 vaccines and boosters from the market. No one should be put at risk for a serious stroke with any vaccine.”

large body of evidence identifies significant risks to the COVID shots, which were developed and reviewed in a fraction of the time vaccines usually take. Among it, VAERS reports 37,647 deaths, 216,757 hospitalizations, 21,741 heart attacks, and 28,445 myocarditis and pericarditis cases as of May 31, among other ailments. 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.

READ: Kansas AG sues Pfizer for misrepresenting COVID shot as ‘safe and effective’

In Florida, a grand jury impaneled by Republican Gov. Ron DeSantis is currently investigating the manufacture and rollout of the COVID jabs. In February, it released its first interim report on the underlying justification for Operation Warp Speed, which determined that lockdowns did more harm than good, that masks were ineffective at stopping COVID transmission, that COVID was “statistically almost harmless” to children and most adults, and that it is “highly likely” that COVID hospitalization numbers were inflated. The grand jury’s report on the shots themselves is highly anticipated.

On Monday, Kansas Attorney General Kris Kobach announced a lawsuit against pharmaceutical giant Pfizer over “multiple misleading statements” about the health risks and ineffectiveness of its mRNA-based COVID-19 shot as violations of the Kansas Consumer Protection Act.

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COVID-19

Employee wins lawsuit filed by gov’t agency after losing job for refusing COVID shot

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From LifeSiteNews

By Emily Mangiaracina

The federal government successfully sued on her behalf, citing a Title VII violation.

A former assistant manager who was fired after applying for a religious accommodation to refuse the COVID shot has been awarded a six-figure payout after a federal government agency filed a lawsuit on the employee’s behalf.

Federal Judge M. Casey Rodgers on Thursday ordered the Pensacola, Florida store Hank’s Fine Furniture (HFI) to pay a former manager, identified in the lawsuit as “K.M.O.,” $110,000 for refusing to accommodate her request for exemption from the COVID shot due to her “sincerely held Christian beliefs.”

“HFI is permanently enjoined from discriminating against any employee on the basis of religion in violation of Title VII,” Rodgers wrote, the Pensacola News Journal reported Monday. He further declared that HFI “will reasonably accommodate employee and prospective employee religious beliefs during all hiring, discipline and promotion activities,” and “any activity affecting any other terms and conditions of employment.”

Significantly, the store also “cannot require proof that an employee’s or applicant’s religious objection to an employer requirement be an official tenet or endorsed teaching of said religious belief,” according to Pensacola News Journal.

Hank’s Furniture must also adopt a written policy, disseminated to all employees, declaring that HFI “will not require any employee to violate sincerely held religious beliefs, including those pertaining to vaccinations, as a condition of his/her employment.”

The U.S. Equal Employment Opportunity Commission (EEOC) sued on behalf of K.M.O. (EEOC v. Hank’s Furniture, Inc., Case No. 3:23-cv-24533-MCR-HTC) in the U.S. District Court for the Northern District of Florida after it was unable to reach a pre-litigation settlement “through its administrative conciliation process.”

According to Pensacola News Journal, about two weeks after HFI implemented a policy mandating that its employees receive a COVID shot, K.M.O. told the company she would not get the shot due to her “sincerely held religious beliefs,” and then requested a religious exemption.

According to the lawsuit, HFI ignored her request and asked if she would comply with their COVID shot policy, and K.M.O. then told HFI she planned to submit a written religious accommodation request, asking “whether HFI had a particular form she should use.”

HFI reportedly did not respond to her request. When K.M.O. complained that HFI’s unwillingness to grant her a religious exemption was “unjust,” her new supervisor reportedly told her that “HFI did not care why she would not take” the COVID shot and that HFI “would never grant an accommodation.”

When K.M.O. emailed HMI on September 6, 2021, asking for the status of her religious exemption request, HFI informed her that her religious exemption request was “severely lacking,” and then denied it.

K.M.O. then “asked for help to submit an acceptable religious exemption request,” but HFI refused to discuss any accommodation, according to the lawsuit. Then on October 31, she was fired by HFI because she did not comply with their COVID “vaccination” policy.

Birmingham District Director Bradley Anderson remarked regarding the case for an EEOC press release, “Employees should not have to renounce their religious beliefs in order to remain employed. Let this case serve as a reminder that employers should afford accommodation for religious beliefs unless doing so would cause an undue hardship.”

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Undue Censorship Still Skews COVID Treatments

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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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