As ICAN Warned, RSV Vaccine for Pregnant Women May Pose Risks

Three years ago, ICAN sent a letter to members of FDA’s vaccine committee warning of the dangers of Pfizer’s RSV pregnancy vaccine, Abrysvo. A recent study supports ICAN’s position that those concerns were warranted.

In May of 2023, ICAN’s legal team sent a letter to the Vaccines and Related Biological Products Advisory Committee (VRBPAC), the FDA committee that makes recommendations on whether or not a new vaccine should be approved. In the letter, ICAN asked the committee to hold off on recommending the approval of Abrysvo until concerning safety signals from the clinical trials had been further investigated. The committee ignored ICAN’s warnings and, shortly after, FDA approved the vaccine.

ICAN’s letter highlighted the following concerns from the Abrysvo clinical trial: “In mothers, serious adverse events included prolonged labor, premature delivery, postpartum hemorrhage, arrested labor, and gestational hypertension, the most frequent of which were preeclampsia and fetal distress.”

A recent study shows safety signals for pregnancy-associated hypertensive disorders (including gestational hypertension), premature rupture of membranes (PROM), and preterm PROM, after receipt of the Abrysvo vaccine. In fact, even though this study was sponsored by Pfizer, the study authors couldn’t avoid stating that “[f]urther epidemiological studies are needed to refine risk estimates….”

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What are these ‘calamari-like’ clots that embalmers keep finding?

Retired Air Force Major Thomas Haviland’s peer-reviewed research exposes a persistent phenomenon that the mainstream medical establishment continues to ignore.

A new peer-reviewed paper published July 1 in the International Journal of Innovative Research and Medical Science breaks down what embalmers across English-speaking countries have discovered in recent years: tough, rubbery, white fibrous clots appearing in a significant percentage of bodies long after the COVID-19 pandemic and vaccine rollout.

Thomas Haviland, a retired U.S. Air Force Major, began investigating this phenomenon after watching the 2022 documentary Died Suddenly. He has since conducted annual surveys of embalmers in the United States, Canada, the UK, Australia, and New Zealand. His latest analysis of 808 responses from 2022 through 2025 found that 75% of embalmers reported seeing the unusual clots.

“The embalmers are seeing these white fibrous clots in an average of 23% of their corpses,” Haviland stated.

A separate, more recent, 2026 survey of Tennessee embalmers showed roughly 70% still observing the clots in 18% of cases, according to Haviland.

Notably, these structures differ sharply from clots seen before 2020. “Many of these embalmers have 20 or 30 years of experience, never saw this phenomenon before,” Haviland explained.

“Prior to COVID, they would see two types of clots. What’s called grape jelly clots… And they also see what’s called chicken fat clots… Much, much different than these large white fibrous clots, which are really tough and rubbery and hard to break.”

Haviland also shared the account of an endovascular specialist and cardiologist in Jacksonville, Florida, who contacted him about removing similar clots from living patients at his lab. “He actually refers to the clots as devious clots,” Haviland said. After sharing images and angiograms, the doctor emailed in March 2024 to tell Tom that he had been instructed to terminate communication immediately.

“Somebody, his hospital administrator probably got to him, right? Told him to shut up, stop talking about this, or else we’ll go after your medical license,” Haviland observed. “So it’s a shame. That’s what’s happening. People are staying silent about this when they should be speaking out.”

Laboratory tests on the clots, including Raman spectroscopy and others, point to the spike protein — whether from the virus, modified RNA injections, or both — sticking to a blood protein called fibrinogen and creating unusual structures. “It makes that fibrinogen all misfolded and twisted… So then it becomes almost impossible to break down the clot. It becomes this rubbery polymer instead,” Haviland said.

Despite repeated submissions of survey results to the FDA, CDC, and NIH, and the publication of supporting papers, major health agencies and institutions including the Mayo Clinic, Cleveland Clinic, Johns Hopkins, and Stanford have shown no interest in obtaining samples for further study.

Although Haviland’s initial preprint was rejected by one platform as “not novel enough,” four years later, embalmers continue to report the never-before-seen clots into 2026.

Haviland and others behind his research are calling for forensic pathologists and independent researchers to examine the structures directly and for congressional hearings to investigate what embalmers have been documenting for years.

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Here’s why Fauci can’t chicken out and plead the ‘Fifth’ during upcoming hearing…

Anthony Fauci thinks Biden’s last-minute “autopen” pardon is his golden parachute.

But he could be very, very wrong.

In reality, that so-called pardon might turn out to be a pair of golden handcuffs instead.

Americans have sat back and watched Fauci play a lot of games. He’s dodged, danced, redefined words, split a lot of hairs, and acted like the rest of the country (and the world) was way too stupid to understand what really went down during the COVID circus. He became the face of the “pandemic” response, and according to the media and liberals, he was the patron saint of “trust the science.”

Who can forget these absurd candles?

As you likely know by now, Senator Rand Paul says Fauci will testify publicly before his committee on July 29th, and this time, the “fifth” escape hatch might not be so easy to open…

That’s because Biden gave Fauci that sweeping preemptive “autopen” pardon before leaving office. The pardon was supposed to protect him. But legally, it screws up Fauci’s ability to sit there, twiddle his thumbs, and plead the Fifth when the questions get uncomfortable.

A lot of Americans believe Fauci should’ve faced real legal consequences a long time ago for what he did to humanity. They look at COVID, the lockdowns, deaths, mandates, ruined businesses, lost years, and all the sketchy questions about Wuhan and the endless array of smug lectures from “experts,” and they don’t see a humble public servant who deserves yet another theatrical political hearing… they see a criminal.

A criminal who got protected.

And let’s be honest here, a blanket pardon doesn’t exactly scream “innocence,” does it? Normal people see something like that and ask the obvious question: if nobody did anything wrong, why did Biden’s autopen feel the need to pardon him before anyone was even charged with anything?

And again, that’s what makes this hearing interesting.

Because if Fauci can’t hide behind the Fifth, then he may be forced into a very ugly corner. He can tell the truth or risk lying to Congress (again). And if Republicans actually have the balls to press hard, follow up, and refuse to let him bluster his way through the hearing, this could become more than another useless Swamp show.

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Correcting the New York Times ACIP Reporting on Vaccine Injury

Seeing Sunday’s New York Times headline titled “Confidential Report Calls for Sweeping Changes to Track Covid Vaccine Harms,” a reflexive question flashed in the minds of even the most staunch defenders of legacy vaccine policy – is the NY Times about to dismiss the Covid vaccine-injured?

For those who don’t care to read the outlet’s reporting, here are what the authors chose to add as closing words:

“The basis of supposed Covid vaccine injury syndrome is even less persuasive and thus even less directly relevant to vaccine policy…”

For experienced readers, seeing who the article’s lead author is should have caused pause immediately. When it comes to journalistic integrity, Apoorva Mandavilli is not who comes to mind.

In an October 6, 2021 NYT article titled ”A New Vaccine Strategy for Children: Just One Dose, for Now,” Mandavilli stated that 900,000 US children have been hospitalized due to Covid. She was forced to correct the glaring error when the real number was found to be slightly more than 63,000.

In 2022 Mandavilli reported on the US Centers for Disease Control and Prevention’s (CDC) recommendation of Pfizer’s Covid shot for kids aged 5-11. The NY Times initially reported, “Nearly 4,000 children aged 5 to 11 have died from a Covid-related condition called multisystem inflammatory syndrome during the pandemic.”

Mandavilli was again forced to add a correction

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If a SIDS-vaccine study offends, remove it

In 2021 Toxicology Reports published Neil Miller’s results of his examination of VAERS reports of 2,605 SIDS deaths between 1990 and 2019:

The peer-reviewed paper found that 75% of SIDS reports occurred within seven days of vaccination, with the highest number on day two. [snip] The journal removed the paper April 9, 2026, citing “serious methodological flaws” and “potential implications for medical practice.” Miller said the journal never specified what those flaws were, despite repeated requests.

Sen. Ron Johnson (R-Wis.) wrote a letter on June 29 demanding that “Toxicology Reports and its parent company Elsevier release all records related to the decision to remove the paper. HHS Secretary Robert F. Kennedy Jr. HHS also wrote to the journal June 11 seeking clarification.”

Neil Miller is careful to say that his paper correlating vaccines with SIDS does not prove causation. But reclassifying ICD codes to remove vaccine-related deaths and purging papers that expose shocking statistics to the contrary smacks of the deliberate suppression of information unfavorable to the vaccine industry.

This is not to damn vaccines: in the first half of the 20th century alone, smallpox is credited with killing 254 million people. Vaccines eliminated that disease. Although tuberculosis can be treated by medicine, the scourge of that devastating disease was largely vanquished by vaccines.

Multi-billion-dollar industries engender powerful — some may say insurmountable — incentives to grow and continue to grow, continuously. The vaccine industry is no exception.

The CDC maintains that children need vaccines starting within 24 hours of birth through age 18, comprising approximately 15-17 vaccines across 26-30 doses. The CDC fails the public when they create the impression of stacking the deck in favor of the industry by “reclassifying” or withholding contradictory information. Absence of absolute proof of harm is no excuse when the degree of safety remains unproven. Parents are entitled to access to all available information regarding the risks as well as the benefits of vaccines.

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Brian Hooker’s paper showing vaccines increase mortality was REMOVED from preprints.org

They censored this paper as a danger to public safety. This means they know the paper is incorrect and can explain the observed data. But they are keeping their analysis a secret. From everyone, including the authors.

So Karl wrote the entire advisory board. Only ONE member bothered to respond with the reasoning. The rest ghosted him.

But the BIG problem is that the “reasoning” does not EXPLAIN what the study observed. At all. We are left clueless. If the vaccines didn’t increase the mortality, then what did? All we have is COMPLETE SILENCE.

In this article I’ll post what the Advisory Board member wrote and what I wrote back.

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Sen. Ron Johnson Demands Journal Turn Over Records Related to SIDs and Vaccines Study

In a letter made public today, Sen. Ron Johnson called on the editor-in-chief of Toxicology Reports and the CEO of Elsevier, which owns the journal, to release all records related to the decision to remove vaccine researcher Neil Z. Miller’s peer-reviewed analysis of VAERS data showing that many more SIDS reports were filed in VAERS in the first few days after vaccination compared to later on after vaccination.

Sen. Ron Johnson (R-Wis.) is demanding to know why a 2021 peer-reviewed paper that presented data suggesting a possible link between vaccination and sudden infant death syndrome (SIDS) was recently removed from the Toxicology Reports website.

In a letter dated June 29 and made public today, Johnson called on the editor-in-chief of Toxicology Reports and the CEO of Elsevier, which owns the journal, to release all records related to the decision to remove vaccine researcher Neil Z. Miller’s analysis: “Vaccines and sudden infant death: An analysis of the VAERS database 1990-2019 and review of the medical literature.”

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DARPA Project ‘PROPHECY’ Reengineered Vaccine Development by Building Future Pathogen Blueprints First and Systems to ‘Validate’ Them Later

The Defense Advanced Research Projects Agency (DARPA) spent the early 2010s constructing what may have been the most ambitious predictive vaccine-development infrastructure ever attempted: a sprawling, multi-institution effort designed to determine the future characteristics of purported pathogens before they emerged and ultimately use those predictions to develop drugs and vaccines before they were needed.

The program, known as PROPHECY—short for Pathogen Defeat—was announced in 2010 under Broad Agency Announcement DARPA-BAA-10-93 and was managed by DARPA’s Defense Sciences Office.

DARPA itself described the vaccine-centric purpose of the program unambiguously.

According to the agency:

“The Prophecy (Pathogen Defeat) program will explore the evolution of viruses in the hopes of predicting viral mutations and ultimately developing drugs and vaccines in advance of need.”

The effort was not limited to coronaviruses, influenza, or any other single disease category.

DARPA repeatedly stated that the goal was understanding:

“the natural evolution of any virus.”

The result was a massive architecture that brought together machine learning researchers, statisticians, bioinformaticians, computational biologists, laboratory scientists, surveillance specialists, universities, contractors, and national laboratories into a single “predictive” framework.

Yesterday, this website reported that DARPA’s PROPHECY program expanded into the laboratory of coronavirus researcher Ralph Baric years before the COVID-19 pandemic and nearly a decade before the DARPA/DEFUSE proposal documented all three defining structural features of the SARS-CoV-2 spike protein prior to the outbreak.

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DARPA’s Chilling Pre-COVID Blueprint: Predict, Manufacture, & Deploy Pandemics On Demand

A sprawling, multi-institution effort for “predicting” future pathogen characteristics, developing vaccines “in advance of need,” and building the very systems intended to validate those predictions.

The Defense Advanced Research Projects Agency (DARPA) spent the early 2010s constructing what may have been the most ambitious predictive vaccine-development infrastructure ever attempted: a sprawling, multi-institution effort designed to determine the future characteristics of purported pathogens before they emerged and ultimately use those predictions to develop drugs and vaccines before they were needed.

The program, known as PROPHECY—short for Pathogen Defeat—was announced in 2010 under Broad Agency Announcement DARPA-BAA-10-93 and was managed by DARPA’s Defense Sciences Office.

DARPA itself described the vaccine-centric purpose of the program unambiguously.

According to the agency: “The Prophecy (Pathogen Defeat) program will explore the evolution of viruses in the hopes of predicting viral mutations and ultimately developing drugs and vaccines in advance of need.”

The effort was not limited to coronaviruses, influenza, or any other single disease category.

DARPA repeatedly stated that the goal was understanding: “the natural evolution of any virus.”

The result was a massive architecture that brought together machine learning researchers, statisticians, bioinformaticians, computational biologists, laboratory scientists, surveillance specialists, universities, contractors, and national laboratories into a single “predictive” framework.

Yesterday, this website reported that DARPA’s PROPHECY program expanded into the laboratory of coronavirus researcher Ralph Baric years before the COVID-19 pandemic and nearly a decade before the DARPA/DEFUSE proposal documented all three defining structural features of the SARS-CoV-2 spike protein prior to the outbreak.

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RFK Jr. Plans To Create A List Of Injuries Caused By COVID-19 Vaccines

Health officials are proposing a plan to clarify which COVID-19 vaccine side effects would be eligible for government financial compensation, according to a new notice.

The Department of Health and Human Services (HHS) and one of its divisions said in a description of a proposed rule released on July 1 that they plan to establish an injury table for COVID-19 vaccines through the Countermeasures Injury Compensation Program (CICP).

“The Table will list and explain injuries that, based on compelling, reliable, valid, medical, and scientific evidence, are presumed to be caused by covered COVID-19 countermeasures, and set forth the time periods in which the onset of these injuries must occur after the administration or use of these covered COVID-19 countermeasures,” a summary of the rule, which has not been made public, stated.

COVID-19 vaccines fall under the CICP because previous health secretaries declared and extended emergency declarations for COVID-19, which opened up the option of emergency clearance of vaccines and other countermeasures under the Public Readiness and Emergency Preparedness Act.

Health Secretary Robert F. Kennedy Jr., who just announced that he was ending the emergency declaration, is authorized under the declarations to provide benefits to people injured by the vaccines under the act, HHS officials noted in the proposal summary.

“Under the leadership of Secretary Kennedy, HHS is restoring transparency and accountability because the American people deserve clear, evidence-based information about both the benefits and the known risks associated with medical countermeasures,” an HHS spokesperson told The Epoch Times in an email.

The spokesperson said that more information will be available when the notice is published in the Federal Register.

Aaron Siri, Kennedy’s former lawyer, wrote to Kennedy in 2025, urging him to create a COVID-19 vaccine-injury table. He pointed to the readiness and preparedness law, which states that the health secretary “shall by regulation establish a table identifying covered injuries that shall be presumed to be directly caused by the administration or use of a covered countermeasure.”

An injury table would help people injured by vaccines apply successfully to the congressionally created program, which requires “compelling, reliable, valid, medical, and scientific evidence” that an injury was a direct result of a countermeasure, Siri wrote on behalf of the Informed Consent Action Network, which advocates for government transparency and change.

A well-constructed injury table is needed for the CICP,” Richard Hughes IV, a former Moderna executive who is representing health groups in litigation against the administration that has halted some of its changes to vaccine guidance, told The Epoch Times in an email. “The real question is whether this administration would promulgate such a table or weaponize it to further platform misinformation.

Dr. Joel Wallskog, who suffered the neurological disorder transverse myelitis and other issues from COVID-19 vaccination and has sued the government over the CICP, told The Epoch Times in an email that the HHS proposal “is more appearance than substance.”

It appears to do little more than streamline the process for the relatively small number of individuals whose injuries – primarily anaphylaxis and myocarditis/pericarditis – are already recognized under the current system,” added Wallskog, also the co-chair of the React19 nonprofit, which offers support to people injured by COVID-19 vaccines. “For everyone else who has been denied, nothing changes.”

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