Tag: pandemic

Pfizer COVID-19 “Vaccine” Plasmid DNA Found Inside Lethal Turbo Cancer of the Heart

We have just completed a new case report that presents one of the most striking findings yet in the debate over COVID-19 “vaccine” turbo cancers: vaccine spike-encoding plasmid DNA was recovered directly from an extremely rare, hyper-aggressive heart tumor.

The McCullough Foundation paper is titled, “Fatal Cardiac Intimal Sarcoma in a 35-Year-Old Male Following COVID-19 mRNA Vaccination: Plasmid DNA Fragments Encoding the S-Protein Detected in Tumor Tissue.”

The patient was a 35-year-old man with no personal or family history of cancer and no identified hereditary cancer predisposition. He received Pfizer-BioNTech BNT162b2 on April 10 and May 4, 2021. Just 170 days after the first dose, doctors discovered a large tumor filling the left atrium of his heart along with multiple brain metastases.

Three days later, surgeons removed a 9.0 × 7.0 × 5.3 cm mass from his heart. Pathology confirmed a high-grade cardiac intimal sarcoma, an exceptionally rare and aggressive cancer. Molecular testing found the characteristic abnormalities MDM2 and KDR amplification, while whole-body PET/CT found no other primary tumor elsewhere in the body.

The cancer progressed at an extraordinary pace. Despite open-heart surgery, chemotherapy, radiation, gamma knife treatment, and four brain surgeries, new metastases continued to appear. He ultimately suffered bleeding into a brainstem tumor and died 675 days after diagnosis.

What makes this case especially important is that the growth rate could actually be measured. One brain metastasis grew from about 4 millimeters to 35 millimeters in only 94 days. That works out to a tumor volume doubling time of roughly 10 days.

Then came the most remarkable finding. Archived tissue from the original heart tumor was tested for vaccine components.

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Mortality Data Reveal ‘Screaming Safety Signals’ Following COVID Vaccine Rollout

Excess mortality researcher Denis Rancourt, Ph.D., on Tuesday told Canadian lawmakers that national mortality statistics show “screaming safety signals” following the rollout of COVID-19 vaccines — including increases in deaths among infants and children and increases in turbo cancers.

Testifying at Canada’s Allison Inquiry, Rancourt also argued that COVID-19-era government interventions — including lockdowns, isolating the elderly, closing businesses and withdrawing government support programs — also drove excess mortality during the pandemic.

Rancourt based his arguments on his analysis of official mortality data from Statistics Canada and in the U.S., the Centers for Disease Control and Prevention (CDC). He described how COVID-19 vaccines directly harmed individuals, and how specific pandemic policies caused broader societal harm.

His presentation came on the opening day of the Allison Inquiry, a four-day hearing chaired by Canadian Member of Parliament Dean Allison. The inquiry collected testimony from 50 Canadians injured by COVID-19 vaccines, along with testimony from physicians, scientists and other witnesses.

4,000 excess infant deaths in the U.S. alone

Infant mortality had been declining in the U.S. before the pandemic. That trend reversed during the pandemic, according to Rancourt’s data — but not until 2022, nine months after COVID-19 vaccination was recommended for pregnant women.

Rancourt estimated the change represented approximately 4,000 excess infant deaths in the U.S. from 2022 to 2024.

He presented a similar case for Canada, although the raw numbers were much lower due to the smaller population. After Canada issued its vaccine guidance for pregnant women on May 28, 2021, he said mortality rose among infants, with a marked increase nine months after the recommendations.

He estimated there were 200 excess infant deaths in Canada during that time, with 10 excess pregnancy-related deaths.

Data show 2,000+ excess deaths among 1- to 4-year-olds in U.S.

Rancourt identified more than 2,000 excess deaths among children ages 1-4 in the U.S. between 2021 and 2024.

He attributed an initial increase in 2021 partly to the abrupt withdrawal of federal financial assistance in some states.

But Rancourt said the largest increase coincided with the June 17, 2022, authorization of COVID-19 vaccines for young children. Excess deaths peaked precisely with the vaccine rollout.

Canadian mortality data showed a similar age-specific pattern. Rancourt shared mortality trends for Canadian children ages 1-4, 5-9 and 10-14, showing each group experienced a pronounced increase during the year COVID-19 vaccines became available for that particular age group.

The spikes in excess mortality were “very sudden,” he said. The increases did not occur during the first two years of the pandemic, he emphasized.

“As soon as you vaccinated these age groups and not before, not when there was COVID, not in the first two years of the pandemic. But when you started vaccinating them, that is the signature that you see in the mortality [data],” Rancourt said. “It’s absolutely stunning.”

He estimated 410 excess deaths among Canadian children ages 1-14.

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Inside the Safety Record Behind Israel’s Early Myocarditis Warning to Global Health Authorities

On February 28, 2021, Israel’s Ministry of Health alerted health authorities on both sides of the Atlantic to an emerging cardiac safety signal following the Pfizer Covid-19 vaccine.

The warning came just over two months after Israel had launched one of the fastest vaccination campaigns in the world, placing the country at the forefront of the global rollout.

That day, the Ministry informed the European Medicines Agency that it was investigating a “safety signal of myocarditis/peri-myocarditis in the younger population (16–30 years old)” and had already received reports of around 40 cases. A CDC internal tasking memo from the same day recorded that Israel was seeing “a large number of reports of myocarditis, particularly in young people,” and was seeking contacts at the CDC and FDA to discuss the issue. The message was marked “Importance: High.” 

Three days later, Dr. Roee Singer, Deputy Director of Epidemiology at Israel’s Ministry of Health, wrote directly to the CDC: “We are seeing a large number of myocarditis and pericarditis cases in young individuals soon after Pfizer COVID-19 vaccine. We would like to discuss the issue with a relevant expert at CDC.”

It was, in every sense, a “Houston, we have a problem” moment.

The alarm had been sounded. But what, exactly, had Israeli health officials seen that prompted it? And when, and how, was that warning communicated to physicians and the public?

Our newly published study in EXCLI Journal discloses and analyzes an internal Israeli Ministry of Health pharmacovigilance dataset that had never been made public. The dataset was provided to us by a whistleblower whose identity we are protecting. The file itself was titled, in Hebrew, “Reports of Hospitalizations and Deaths to Pfizer,” and contains detailed case-level reports documented by the Ministry of Health during the vaccination campaign.

The record was not reconstructed years later, after vaccine-associated myocarditis had become an established safety concern. It was being built in real time as the signal emerged. 

The dataset provided to us comprised eight cumulative versions, all sharing an original creation date of March 25, 2021. The record was updated repeatedly for more than a year as new cases were added and existing reports were revised with additional clinical information. The final version extends through May 9, 2022.

Already on March 25, just over three weeks after Israel first sounded the international alarm, the record contained 157 hospitalization reports and 46 death reports. Sixty-five of the hospitalization reports involved myocarditis or pericarditis.

By the final version of the dataset, myocarditis or pericarditis appeared in 250 of 531 hospitalization reports, nearly half. Among patients under 30, it appeared in 151 of 211 reports, more than 70%.

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Evidence Continues to Emerge Linking COVID-19 Shots to Rising Cancer Risks

For the last five years, the War Department has largely overlooked whistleblower warnings about the adverse effects of the COVID-19 shot on military personnel, which include rising cancer rates and even death. This total disregard by the Biden administration has long raised concerns regarding the health and safety of those who serve.

In light of this, Dr. Theresa Long, an Army doctor board-certified in aerospace medicine, has recently been appointed as the senior medical military adviser to Health and Human Services Secretary Robert F. Kennedy Jr. Her role includes examining whether COVID-19 shots contributed to the deaths of more than 2,500 military personnel.

The previous administration may have attempted to conceal the health conditions initially identified in the Defense Medical Epidemiology Database (DMED), even in the face of a “notable rise in several serious medical diagnoses,” including cancer.

Given that the military is a subset of the broader U.S. population, it is likely that Dr. Long will discover that cancer has contributed to some of these fatalities.

Cancer among service members has made the headlines on more than one occasion, as evidenced by the subsequent health struggles of key military officials in recent years. Former Secretary of Defense Lloyd Austin was diagnosed with prostate cancer in December 2023 but kept it hidden for months.

Shortly after Austin revealed his condition, Col. Tara Lunardi, Deputy Commander of the Air Force Office of Special Investigations, passed away from cancer.

In October 2023, retired Navy Medical Service Corps officer Lt. Ted Macie warned Chief of Naval Operations Adm. Lisa Franchetti about potential cancer risks potentially linked to the shot. Ironically, in June 2024, she found a lump in her breast during a routine screening.

Research published in peer-reviewed journals, which consists of scholarly and scientific articles assessed and approved by experts in the relevant field before publication, indicates an increase in cancer cases following the distribution of the COVID-19 shots.

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Ignored for years, Canada’s vaccine-injured finally get their day in Parliament

The idea of two solitudes in Canada is typically understood as the great divide between Anglophones and Francophones who cannot see eye-to-eye due to cultural and linguistic differences, the latter preventing any meaningful communication to bridge the gap.

But in the post-COVID era, “two solitudes” could just as easily describe the chasm between lawmakers, legacy media and its subscribers who remain uninterested in the suffering that COVID vaccines caused, and the camp of vaccine-injured, their advocates and members of the public who saw through the “safe and effective” lies, understand the damage caused and now want accountability.

While any accountability for the human toll that experimental COVID vaccines wrought has been non-existent in Canada, on Tuesday, Conservative MP Dean Allison’s COVID vaccine injury hearings – dubbed The Allison Inquiry – began on Parliament Hill in Ottawa. Whether it will bring Canada’s two COVID solitudes any closer together remains to be seen.

Legacy media journalists were absent, as were any MPs from the governing Liberal Party, which bears ultimate responsibility for these injuries. Of the four Conservative MPs who attended, Mike Dawson (Miramichi–Grand Lake, NB) told the Inquiry he believed his daughter-in-law’s baby died in the womb following a COVID vaccination in the second trimester, and Essex MP Chris Lewis (Ontario) said he believed his mother suffered from turbo esophageal cancer after taking the COVID shot.

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U.S. Supreme Court Rejects New York Healthcare Workers’ Bid to Revive COVID Vaccine Mandate Lawsuit

The U.S. Supreme Court today declined for a second time to take up a case brought by New York healthcare workers who lost their jobs after the state denied their requests for religious accommodations from its COVID-19 vaccine mandate, SCOTUSblog reported.

The justices rejected a petition asking them to reconsider their June decision not to hear Does 1-2 v. Hochul, the lawsuit healthcare workers brought against the state. The court denied the request without asking New York Gov. Kathy Hochul to respond.

“This ruling is definitely a sad day for the workers who stood up and said no,” said Michael Kane, Children’s Health Defense (CHD) director of advocacy and member of New York’s Teachers for Choice, which also challenged New York’s vaccine mandate in the courts.

Kane said he was “not surprised” by the decision.

The plaintiffs represented a handful of healthcare workers, he said. “But over 30,000 were fired in New York state because of this horrendous policy from Gov. Hochul. The policy didn’t allow for any religious exemption from vaccination. On its face, it is illegal. It is unconstitutional, but the politics of the thing seems to be playing out instead.”

The workers filed their lawsuit in 2021, challenging a now-repealed New York state law mandating that workers in some healthcare-related positions get the COVID-19 vaccine.

In 2022, a federal court dismissed the lawsuit, and in 2024, the 2nd U.S. Circuit Court of Appeals upheld the dismissal. In 2025, the workers appealed to the U.S. Supreme Court.

In an unusual move, the Supreme Court asked the U.S. Department of Justice solicitor general to weigh in. In May 2026, Solicitor General D. John Sauer wrote an amicus brief recommending the court deny the appeal.

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US Army doctor claims 28 troops died from Covid vaccines – Politico

A US Army doctor has testified that she knows of 28 US military deaths caused by Covid-19 vaccines, Politico has reported citing a court deposition. The US government is investigating 2,544 deaths reported following the jabs, the official has said.

Theresa Long, who also serves as an adviser to US Health Secretary Robert F. Kennedy Jr., reportedly gave the testimony during an August 14 deposition in a federal court case in Virginia. Neither her testimony nor her role at the Department of Health and Human Services (HHS) had previously been reported.

Long allegedly said that the 2,544 unverified deaths were reported to the department’s Vaccine Adverse Event Reporting System (VAERS).

Former US President Joe Biden ordered all US military staff to be vaccinated or be discharged from service, resulting in over 9,000 dismissals. After returning to office, President Donald Trump ordered the Pentagon to offer reinstatement to those who had been discharged for refusing a vaccine.

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2026 Chicago Socialism Conference Features Covid Masking Requirements

The 2026 Chicago Socialism Conference is requiring all attendees to wear N-95 or K-95 masks – and organizers will provide them for those without.

A description on the conference website adds:

“Please note: this requirement applies only to formal conference spaces and sessions—attendees should be aware of the possibility that attendees will be unmasked elsewhere in the conference hotel (or beyond) where they may informally congregate.”

Attendees are encouraged to test themselves for Covid ahead of time, and free tests will also be available on site.

The conference, which begins on Friday, will host a number of socialist speakers including Hasan Piker and DSA president Megan Romer.

In an about section, the conferences states “Socialism 2026 is a four-day conference bringing together thousands of socialists and radical activists from around the country to take part in discussions about social movements, abolition, Marxism, decolonization, working-class history, and the debates and strategies for organizing today.”

Continuing, it states, “Every year, the Socialism conference is a place where activists share lessons from their struggles—from anti-ICE organizing to the fight for gender liberation, from striking workers to Palestine solidarity campaigns, the struggle to stop the destruction of the planet, the fight against racism, and more.”

A conference agenda lists a number of programs including a “Marxism Education Series,” “Reproductive Justice Strategy Session,” “Sing, Struggle, Organize: Movement Songs, Political Education, and Collective Power,” and “Abolition Judaism: The Revolutionary Possibilities of Diaspora.”

Sponsors of the conference includes the DSA and the Palestinian Youth Movement among many other radical left organizations.

A code of conduct for the conference says they are committed to “uplifting and centering the voices and organizations of oppressed people and we know that interpersonal harm and harassment are pervasive in our society, and the left is not immune to these behaviors.”

Continuing, they state, “Our goal is to have a conflict- and crisis-free conference, and we are committed to working to de-escalate and resolve any problems that may arise.”

What is not clear from the code of conduct is whether the calls of political violence from Piker or other featured speakers violates the code of conduct or if threats towards conservatives and Republicans are allowed.

Tickets for the full conference range from $250 to $500 but if you identify as a student or low income, a subsidized option at $65 is also available.

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Ex-FDA Commissioner Privately Told CIA That Up to 25% of Americans Had Already Achieved Natural Immunity Through Exposure to COVID by May 2020, Unclassified Document Reveals

Newly released documents are raising explosive questions about what pharmaceutical insiders and America’s intelligence community knew about COVID-19 immunity during the earliest months of the pandemic and why Americans were hearing a dramatically different story in public.

Senator Rand Paul (R-KY) released records detailing a May 7, 2020, CIA briefing involving Dr. Scott Gottlieb, the former FDA commissioner who had joined Pfizer’s board of directors the previous year.

Paul announced on X:

“I released documents showing Pfizer and the CIA privately acknowledged high population immunity as early as May 2020, while the public heard a different story. Americans deserve the truth.”

He pointed to reporting at Brownstone Institute on a newly unclassified CIA meeting summary buried in the latest tranche of records Paul entered into the congressional record.

The date on the briefing is May 7, 2020.

That is two months after the country was shut down. Churches closed. Small businesses crushed. Kids locked out of school. Fauci and Deborah Birx still talking as if this was a rare, novel threat that required indefinite emergency rule until a pharmaceutical product arrived.

Inside the CIA, they were already talking seroprevalence. Seroprevalence is the percentage or proportion of people in a specific population who have antibodies against a specific disease or infectious agent in their blood serum.

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FDA Approves Moderna XFG COVID Vaccines 81 Days Before Teen/Adult Safety Study, 126 Days Before Children’s Study

The U.S. Food and Drug Administration approved Moderna’s new XFG-formulated COVID-19 vaccines on August 27, 81 days before a human study specifically designed to evaluate the safety and immune response of the new formulations was scheduled to begin.

Pfizer’s XFG COVID vaccine formulation was approved on the same day, equally without safety data for its new formulation.

FDA approved the 2026–2027 formulas for Moderna’s SPIKEVAX and mNEXSPIKE vaccines, which are claimed to contain genetic instructions corresponding to the alleged JN.1-lineage XFG subvariant.

But FDA’s own Aug 27 approval letters show that a Phase 3b/4 human study specifically evaluating the “Immunogenicity and Safety of MNEXSPIKE and SPIKEVAX 2026-2027 Formula” is not scheduled to begin until November 16.

The first interim results are not due until March 26, 2027.

For younger children eligible to receive the new SPIKEVAX formulation, a separate human safety and immunogenicity study is scheduled to begin even later.

In other words, FDA approved Moderna’s new XFG vaccines first.

The human studies specifically evaluating the new formulations come afterward.

The regulatory pathway allows FDA to rely on claimed evidence from previously licensed formulations rather than require a new human safety trial of every updated formulation before approval.

But that raises consequential health, informed-consent, regulatory, and accountability questions:

  • How can FDA determine that a newly reformulated vaccine is safe before formulation-specific human safety data exist?
  • What evidence justifies carrying earlier safety findings forward to a changed product?
  • And why is FDA requiring a Phase 3b/4 study specifically to evaluate the new formulas’ “Safety” only after Americans are permitted to receive them?
  • And most fundamentally, if FDA is approving a newly reformulated vaccine before human safety data specific to that formulation exist, is the agency fulfilling its responsibility to independently establish that products are safe before Americans receive them, or shifting that uncertainty onto the public and collecting the answers afterward?

Congressional committees have confirmed that the FDA “is not meeting important federal safety requirements to protect its employees and the public while also failing to prioritize scientific data quality delivered from FDA laboratories.”

You can contact the FDA here.

And Moderna here.

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