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COVID-19

Large new study finds COVID jabs carry increased risks of heart, brain, blood diseases

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From LifeSiteNews

By Calvin Freiburger

The study of 99 million jabbed people found ‘significantly higher risks of myocarditis’ after mRNA COVID shots, as well as increased risks of pericarditis, Guillain-Barré syndrome, and other diseases.

A new COVID-19 jab study being billed as the largest to date has found increased risks of rare heart, brain, and blood disorders, yet the organization behind the controversial shots continues to defend them.

The study, published this month in the journal Vaccine, looked for 13 neurological, blood, and heart related medical conditions in 99 million jabbed people across eight countries, according to a press release from the Global Vaccine Data Network (GVDN). It “confirmed pre-established safety signals for myocarditis, pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis,” as well as identifying “[o]ther potential safety signals that require further investigation.”

“[W]e observed significantly higher risks of myocarditis following the first, second and third doses of BNT162b2 and mRNA-1273” (both mRNA shots), the study says, “as well as pericarditis after the first and fourth dose of mRNA-1273, and third dose of ChAdOx1 [adenovirus-vector vaccines], in the 0–42 days risk period.”

“Another potential safety signal was identified for ADEM after the first dose of mRNA-1273 vaccine, with five more observed than expected events based on 1,035,871 person-years and 10.5 million doses administered,” it continued. ADEM stands for acute disseminated encephalomyelitis, an autoimmune disease that involves serious brain and spinal cord inflammation. “[H]owever, the number of cases of this rare event were small and the confidence interval wide, so results should be interpreted with caution and confirmed in future studies.”

The study also found a 2.5 times higher risk of the immune disorder Guillain-Barré syndrome associated with the AstraZeneca shot, as well as potential signs of increased risk of ​transverse myelitis, another type of spinal cord inflammation, associated with the viral-vector jabs.

It further noted that “[p]otential underreporting across countries may have led to an underestimation of the significance of potential safety signals. It is important to recognize the potential for false negatives, especially when detecting associations with lower confidence intervals below 1.5 that maintain statistical significance.”

Yet on February 12, GVDN also published a blog post doubling down on the dominant medical establishment positions that the COVID shots “reduce the incidence of infection,” despite the jabs’ failure to stop transmission, and that fears about dangers “are often based on misinterpretation of data, anecdotal evidence, or preliminary research that does not stand up to rigorous scientific scrutiny.” The author of the post, Helen Petousis-Harris, was one of 35 authors to whom the new study is credited.

The first in a series of reports by a Florida grand jury impaneled to investigate the COVID jabs recently concluded that COVID was “statistically almost harmless” to children and most adults and that it is “highly likely” that COVID hospitalization numbers were inflated, seriously undermining the presumed need for vaccines.

The federal Vaccine Adverse Event Reporting System (VAERS) reports 37,100 deaths, 214,248 hospitalizations, 21,431 heart attacks, and 28,121 myocarditis and pericarditis cases as of January 26, among other ailments. An April 2022 study out of Israel indicates that COVID infection itself cannot fully account for the myocarditis numbers, despite common insistence to the contrary.

Jab defenders are quick to stress that reports submitted to VAERS are unconfirmed, as anyone can submit one, but 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 overreporting.

2010 report submitted to the U.S. Department of Health & Human Services’ (HHS’s) Agency for Healthcare Research and Quality (AHRQ) warned that VAERS caught “fewer than 1% of vaccine adverse events.” On the problem of underreporting, the VAERS website offers only that “more serious and unexpected medical events are probably more likely to be reported than minor ones” (emphasis added).

In 2021, Project Veritas shed light on some of the reasons for such underreporting with undercover video from inside Phoenix Indian Medical Center, a facility run under HHS’s Indian Health Service program, in which emergency room physician Dr. Maria Gonzales laments that myocarditis cases go unreported “because they want to shove it under the mat” and nurse Deanna Paris attests to seeing “a lot” of people who “got sick from the side effects” of the COVID shots but adds that “nobody” is reporting them to VAERS “because it takes over a half hour to write the d–mn thing.”

Further, VAERS is not the only data source containing red flags. Data from the Pentagon’s Defense Medical Epidemiology Database (DMED) shows that 2021 saw drastic spikes in a variety of diagnoses for serious medical issues over the previous five-year average, including hypertension (2,181%), neurological disorders (1,048%), multiple sclerosis (680%), Guillain-Barre syndrome (551%), breast cancer, (487%), female infertility (472%), pulmonary embolism (468%), migraines (452%), ovarian dysfunction (437%), testicular cancer (369%), and tachycardia (302%).

Leading COVID shot manufacturer Pfizer donated more than $8.5 million to political candidates, leadership PACs, trade associations, and party committees representing both parties last year, fueling suspicion as to why only a handful of nationally prominent GOP officeholders, such as Florida Gov. Ron DeSantis and Wisconsin’s Sen. Ron Johnson, are opposed to the company’s shot.

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COVID-19

FDA requires new warning on mRNA COVID shots due to heart damage in young men

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From LifeSiteNews

By Doug Mainwaring

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:

  1. the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
  2. 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.

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COVID-19

Court compels RCMP and TD Bank to hand over records related to freezing of peaceful protestor’s bank accounts

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Justice Centre for Constitutional Freedoms

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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