Vaccination Injuries On Record for Covid19

[ExomatrixTV]

• Conservative MP Dean Allison provides update on inquiry into COVID-19 vaccines – August 13, 2026:

Source: https://youtube.com/watch?v=oqxIMYEb7Zk

Conservative MP Dean Allison holds a news conference on Parliament Hill to comment on the inquiry he is spearheading regarding Canadians who report being injured by COVID-19 vaccines.

The most important and eye opening 6 minutes you will listen to today.

• source

Dr. Charles Hoffe who is a family doctor from Southern British Columbia describes how he was told never to speak badly about the vaccine even though his patients were experiencing adverse reactions to them. On top of it, all of is adverse side effects reports he submitted were censored. What went on during this time was criminal.

The side effects of the coronavirus vaccines are finally the subject of an official parliamentary inquiry in Canada — while most politicians in the Netherlands continue to anxiously avoid the issue. More than a thousand Canadian citizens have come forward to testify about serious health damage they sustained after a coronavirus jab. In the Netherlands, you hardly hear a word about this in the House of Representatives.

• Parliamentary inquiry with hundreds of witnesses

The initiative comes from Dean Allison, a Conservative MP for the Niagara West constituency. He is organizing the so-called Allison Inquiry : a preliminary inquiry that gives affected Canadians the chance to tell their story. The hearings are scheduled from September 8 to 11 on Parliament Hill in Ottawa. About fifty people are expected to testify.

During a press conference in Ottawa , Allison indicated she was completely surprised by the enormous response. Over a thousand people signed up — a multiple of what the organizers had expected. Many of them have been struggling with serious health problems for years and say they feel the medical system has let them down.

• Doctor restricted by own professional association

The most shocking moment of the press conference was the speech by GP Charles Hoffe from southern British Columbia. Hoffe has been working in the same practice since 1993 and primarily serves the First Nations community, the indigenous population. His story shows how far censorship has gone at the medical level.

As soon as the vaccination programs began, Hoffe tried to warn his colleagues about what he was seeing in his own practice: a patient who died suddenly shortly after the jab, three people who became permanently disabled, and several others with serious complaints. He sent an open letter to the provincial health authority of British Columbia, Dr. Bonnie Henry. The response? A vaccine expert declared, without any investigation, that it was all a coincidence.

Hoffe subsequently filed fourteen reports of side effects. All fourteen were dismissed without substantive assessment. He then received a warning letter from the College of Physicians and Surgeons — the professional association of doctors in British Columbia. That letter was sent not only to him, but to every registered doctor in the province: anyone who spoke negatively about the vaccines risked disciplinary proceedings. A collective order to remain silent for the entire medical profession.

• Charges withdrawn — but the damage had already been done

Hoffe was eventually formally charged with spreading disinformation. Shortly before the trial, the professional association withdrew the case — thanks in part to a strong lawyer and eight international experts ready to defend him. The official explanation for withdrawing the charges was that the proceedings had already achieved their goal: deterring other doctors from speaking critically.

In other words: it was never about establishing the truth. It was about stifling dissenting voices. By putting pressure on doctors, an artificial consensus was created that gave the impression that the medical field unanimously supported the vaccines.

• Excess mortality only after vaccination program

In his speech, Hoffe also pointed out a telling pattern in the mortality figures. In the first year of the pandemic, there was no measurable increase in the total number of deaths in Canada. The so-called excess mortality — more deaths than statistically expected — only began after the vaccination programs had been launched.

In the United States, the open adverse events reporting system VAERS has now registered nearly 39,000 cases of people who died unexpectedly within 28 days of receiving their coronavirus shot, and more than 72,000 cases of permanent disability. Yet the official message remains unchanged: safe and effective. Hoffe wondered aloud how many more victims must fall before action is taken.

• The Netherlands remains silent, other countries act

What is now recognized in Canada and the United States as a serious societal problem is being politically hushed up in the Netherlands. Neither the House of Representatives, nor the RIVM or the health authorities have ever initiated an independent investigation into side effects on the scale on which they are being reported by affected individuals. Citizens who have suffered harm are often not taken seriously by doctors who themselves—just as in Canada—felt no room to be critical.

The Allison Inquiry shows that things can be done differently: ordinary citizens are given a platform, doctors like Hoffe finally get a microphone, and parliamentarians take their oversight role seriously. Whether the Netherlands will ever reach that point remains the question for now.

• dutch 🇳🇱 (+ Multi-Language Options). 🦜🦋🌳

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[ExomatrixTV]

• The study that was supposed to dispel vaccine doubts is now under fire itself:

This is going to be a scientific story, but it needs to be covered. Because the regulators think they can get away with it, and we cannot just let that happen. First, all sorts of “fact checks” appeared claiming that there was no DNA in the mRNA vaccines. It is now acknowledged that there is indeed DNA in those vaccines, but it is said to remain within limits. DNA contamination in mRNA vaccines is at the center of a scientific battle — and now independent researchers are delivering scathing criticism of a study used by regulators to dismiss concerns. Immunologist Jessica Rose, along with Kevin McKernan and David Speicher, published a critical analysis in the journal Oncotarget showing that the study by Achs et al. (2025) is riddled with methodological errors that systematically lead to an underestimation of DNA contamination.

• What was the claim of Achs et al.?

The study by Achs and colleagues claimed to have demonstrated, using four independent measurement methods, that there are no excessive DNA contaminants in the COVID-19 mRNA vaccines from Moderna and BioNTech/Pfizer. Regulators seized upon this conclusion as evidence that the vaccines fall within the applicable limits. That limit is set at 10 nanograms of DNA per dose — a standard that had already been exceeded by multiple independent laboratories in previous analyses. But according to McKernan, Speicher, and Rose, there is little truth to the measurement methods followed. One of the most glaring errors concerns the calculation of molecular weight when converting measured values ​​to DNA nanograms. Achs et al. used the molecular weight of an intact plasmid, while their own data showed that the DNA fragments were on average only 130 to 200 base pairs long. Without the mandatory correction factor for fragmentation, the underestimation can amount to a factor of 120. With the correct correction, even the smallest measured value would exceed the legal limit of 10 nanograms.

• The most dangerous piece of DNA was measured the worst.

Particularly alarming is that the primer set used to measure the spike-coding DNA was much larger than the typical fragment size in the vaccines. Detecting a fragment of 233 base pairs while most fragments are only 150 base pairs long is like looking for a key that is larger than the keyhole. The consequence: precisely the most biologically relevant and potentially most dangerous DNA sequence was systematically underestimated. Researchers who did work with comparable sizes consistently found 4 to 6 times more spike DNA than background DNA — a finding that Achs et al. completely ignored.

• Heating destroys the evidence

To release DNA from the lipid nanoparticles, Achs et al. heated the samples to 95 degrees Celsius for ten minutes. That sounds practical, but scientifically speaking, it is disastrous: heating in an aqueous environment fragments DNA through chemical degradation of base pairs. The measurement method thereby actively destroys the evidence one is trying to quantify. Researchers such as McKernan and Speicher used a technology that requires no heating and can detect DNA fragments up to 5,300 base pairs long. Achs et al. demonstrably possessed this technology but deliberately chose not to use it.

• Moderna itself already acknowledged the risk in patents.

What makes the case even more explosive is that Moderna states in black and white in its own patents that residual DNA in vaccines can activate the innate immune response and be cancer-promoting. The same company acknowledges that introduced DNA can integrate into the genome of host cells and can even be passed on to daughter cells. The SV40 elements present in the production plasmids carry multiple specific risks: they can inactivate the tumor suppressor p53, initiate mutagenic processes via enzymes, and introduce DNA into the cell nucleus. All of this is completely ignored in the study by Achs et al.

• RNA:DNA hybrids: the forgotten danger

The biggest blind spot in the study by Achs et al. is the complete lack of any measurement of RNA:DNA hybrids. During the production of mRNA vaccines, so-called RNA:DNA hybrids are formed—structures in which the spike-coding DNA attaches to the mRNA. BioNTech itself acknowledged in published research that DNase I, the enzyme typically used to degrade residual DNA templates, is at least a hundred times less effective on these hybrids. McKernan and colleagues demonstrated that spike sequences occur 10 to 100 times more frequently in hybrid form, fully protected from degradation by lipid nanoparticles. Achs et al. did not measure this, did not acknowledge it, and nevertheless drew conclusions regarding safety.

• Regulators must take another look

The joint conclusion of McKernan, Speicher, and Rose is unequivocal: the study by Achs et al. contains not minor technical imperfections, but major design flaws that leave the research question unanswered. All errors systematically point in the same direction—underestimation. This inevitably raises questions about the independence of the methodology employed. As long as there are no robust studies that measure RNA:DNA hybrids, map long DNA fragments, and employ correct computational methods, the issue of DNA contamination in mRNA vaccines will remain unresolved. Regulators who rely on Achs et al. to dismiss concerns are standing on quicksand.

• dutch 🇳🇱 (+ Multi-Language Options). 🦜🦋🌳

[ExomatrixTV]

• Corona-shots. Tissue analysis never performed despite WHO instructions.

29 Juni 2026, by Maurice van Ulden
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In December 2020, the WHO issued a manual aimed at the monitoring of the safety of the Covid-19 shots. The full name of the document is: Covid-19 vaccines safety surveillance manual. The autor of this article only recently discovered the existence of this very important document, after already having been active for years in the field of tissue analysis following the corona shot together with a Dutch foundation for biomedical auditing (BMRK). This was after a targeted search using the search term 'covid-19 vaccines safety manual'. The idea to search in this way stemmed from the knowledge that numerous international safety manuals exist in the aviation industry that prescribe what aviation companies must incorporate into their standard operating procedures. Perhaps the WHO has written such a safety manual regarding the corona shots? And indeed it has!

• Why is that so important?

The manual states that new vaccine technology may be deployed about which we still have little knowledge. Therefore, argued entirely logically, it is extremely important that safety monitoring is properly set up. Paragraph 5 of chapter two, page 50, is titled: 'Deaths after immunisation'. The first sentence states: 'All countries must establish protocols to investigate death after covid-19 vaccination.' :

„All countries must establish protocols to investigate death after covid-19 vaccination.“

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Subsequently, autopsy and targeted tissue examination are mentioned as preferred methods. As a tool to develop such a protocol, reference is made to a protocol that already existed at the time which was used for targeted investigation in cases of death in correlation with a corona infection. This protocol explicitly mentions the use of technology to stain specific proteins. This technique is called immunohistochemistry and has been widely applied since the 1980s.

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Following communication with the Dutch Society of Pathology (NVVP), Agnes Kant of Lareb (Dutch registration of adverse events), and the Dutch Medicines Evaluation Board (CBG), it can be stated with certainty: to date, there is no protocol in the Netherlands for targeted tissue examination following death after the COVID-19 vaccine. Without human tissue examination following the COVID-19 vaccine, it is impossible to properly determine the effects of these injections on people's bodies. The fact that this examination, which is so obvious to experts in the field, has not been carried out demonstrates the failure of the medical academy and the healthcare institutions of the Netherlands. It is a criminal failure of the duty of care. This is not something that was forgotten during the turbulent COVID-19 years, but something that, given the content of the safety manual and common sense, was willfully and knowingly not carried out.
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The limited number of publications on this specific subject suggests that the guidelines in the aforementioned WHO manual have not been followed worldwide. This demonstrates the unnecessary endangerment of billions of lives, something that can only be interpreted as a crime against humanity.
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How it is possible that very important and obvious instructions from a WHO safety manual have not been followed in a modern Western country such as the Netherlands is a matter that must be investigated to the bottom and for which absolute accountability must be given. To bring this to the attention of the Dutch parliamentary inquiry committee, a demonstration was held in front of the door in The Hague on June 5 from 8:00 AM to 10:00 AM. Three arriving members of the committee were briefed for five minutes about the lack of pathological investigations. The action has been recorded and circulated on social media. The BMRK foundation has sent a follow-up letter to the committee. If the committee and responsible authorities do not provide sufficient follow-up to the subject, legal proceedings will be considered.
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In recent years, targeted tissue research following the covid-shots was carried out by a few courageous German researchers. Among them was Professor Pathology Arne Burkhardt (79), who died in 2023 after unexpectedly falling into the water. Burkhardt examined the tissues of approximately one hundred people who died unexpectedly after receiving the covid-shot. Burkhardt observed a pattern of multiple inflammations in their tissues in the presence of spike protein and the absence of another coronavirus-related protein; this is a strong indication that the inflammations are linked to the spike protein produced by body cells based on the injected genetic instruction. Burkhardt considered it likely that the vaccination played a role in the deaths of three-quarters of the deceased examined. An explanation by Professor Burkhardt himself can be seen at histopathology.nl
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When asked what the Dutch Society for Pathology thinks of Burkhardt's results, secretary Vincent Smit replied: “I am not impressed.” To the question of whether the NVVP, as a professional group, has an academic responsibility to perform this specific tissue examination, the answer was: “We are a demand-driven organization.” A significant role can lay by the fact that health insurance ceases upon death. Pathology examinations after death are paid for from the hospital budget, and this is clearly an anti-incentive to conducting research. Agnes Kant (director of the dutch adverse events registration) stated in a personal conversation that autopsy and tissue examination are difficult because families generally do not want them. The experience of the BMRK foundation is different. In collaboration with German scientists, several bereaved relatives have been guided to investigate the death of their loved ones in greater depth. This involves collaboration with the German pathologist Michael Mörz from Dresden and the German research lab Inmodia.de
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[1] COVID-19 vaccines: safety surveillance manual, second edition. Geneva: World Health Organization; 2021. Licence: CC BY-NC-SA 3.0 IGO.

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[ThePythonicCow]

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This is perhaps the finest essay I've read yet, on the complex depth of the "virus, vaccine, and cancer" campaign commenced in 1966 with a Nobel prize to Peyton Rous, against humanity.

(This virus, vaccine, and cancer narrative in turn funds major pharmaceutical and medical profits, which in turn help fund the deep corruption of American news media and politicians world wide, but that's beside the primary point of this essay.)

It's a bit longish, as Unbekoming's essays often are, but quite well written and quite insightful.

What Is SV40? An Essay on Bubbles, Chemicals, and the Manufactured Cancer Industry

His article begins (I added the bold highlighting):

=== ===

Two groups argue online about SV40, and neither has the whole story.

One group says SV40 is imaginary. A monkey virus that was never isolated and never shown to cause disease. The other waves plasmid maps and points to Kevin McKernan’s laboratory findings of “SV40 promoter sequences” inside Pfizer mRNA vials, and calls the first group unhinged.

Sasha Latypova, a former pharmaceutical industry executive who has spent the last four years documenting the manufacturing fraud behind the covid injections, has done something more useful than pick a side. She has explained what both groups are actually looking at.¹

The natural monkey virus called SV40 was never isolated. The bubbles the Merck scientists photographed in 1960 and named “vacuolating virus” were cellular debris in a dying culture of the wrong species of monkey. Nothing was purified from a sick person and shown to cause disease.

The chemical compound sold today under the label “SV40 promoter” is an industrial construct. It has almost nothing in common with the 1960 bubbles except the name. It is a stack of synthetic DNA sequences built on ceramic beads through automated washes of acids, solvents, and corrosive reagents, designed to force a target cell into rapid, chaotic division.

Both truths point in the same direction. The story of SV40 is the story of an industry that learned how to manufacture cancer by injection and built a regulatory framework to protect the practice.

=== ===

Well worth a full read ... and Unbekoming's Substack is well worth signing up for. He's been on a tear, having produced some 1,400+ essays, interviews, book summaries, and original books in recent years, investigating what medicine got wrong.

[ExomatrixTV]

Philippe Carillo is a French award-winning filmmaker and investigative journalist who spent 14 years in Hollywood. He started his career in France as a sound editor for films and documentaries and worked on more than 65 major documentaries for the BBC, 20th Century Fox, and different French productions. He moved to Hollywood in 2003, made his first major investigative documentary in 2014 called "Inside the Garbage of the World," and won three awards. He moved to Vanuatu in 2017 and created a film production company called Fusion Productions Limited. Since then, Philippe has produced and directed more than 160 short and feature films in the country. The last major investigative documentary, "The Fukushima Disaster: The Hidden Side of the Story," has made its way to worldwide distribution and already won palms at different film festivals around the world.

• IMDb

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Source: https://youtube.com/watch?v=Z8A791RZI9s

Source: https://youtube.com/watch?v=y3AmnOFOr_Q

Uncovering the Hidden Story Behind the “Pandemic”. In 2020, as the world grappled with what seemed like an unprecedented health crisis, many of us felt a shift—something bigger than just a virus. But what if the story we were told wasn’t the full truth? What if, beneath the headlines and official reports, there was something far more complex, even darker? This is where Dr. Reiner Fuellmich enters the picture. A respected international lawyer, he refused to accept the narrative at face value. Alongside other experts and legal minds, he launched the Corona Investigative Committee, determined to dig deeper. Their investigations gathered testimonies that challenged the fundamental truths behind the „pandemic“. Fuellmich's conclusion shook many: the COVID crisis, as painted by governments and media, might have been a carefully orchestrated event—designed to coerce people into receiving injections containing undisclosed substances. For countless people around the world, Fuellmich became more than just a lawyer. He became a beacon of hope—a voice standing up against lockdowns, vaccine mandates, and what many saw as violations of personal freedom and human rights. Questions swirled: was this a breach of the Nuremberg Code? Were governments and corporations committing crimes against humanity? But voices of dissent often meet resistance. Behind the scenes, powerful forces allegedly worked to silence Fuellmich and his allies. Then came the shocking news: in October 2023, Dr. Fuellmich was kidnapped in Mexico and illegally imprisoned in Germany. Who had the power to go beyond borders and laws to make this happen? And how many others might have suffered similar fates, swept away for political reasons? The story of Reiner Fuellmich isn’t just about one man—it’s about the fight for transparency, justice, and truth in a world where shadowy interests often dictate what we believe. “Free Reiner” invites you to look beyond the headlines, to question, to understand, and to join a conversation that’s as urgent as it is unsettling. Because at the heart of it all lies a simple but profound question: what happens when those who speak out are silenced? Discover the full story in this hard-hitting documentary, and decide for yourself—what can truth really tell us, and who decides what we get to know?

• youtube.com/@carillofilm/videos

• Help get Dr. Reiner Fuellmich out of Jail fast

[ExomatrixTV]

• The Reckoning Begins: Vaccine-injured Canadians Take Parliament Hill For The Allison Inquiry!!:

Source: https://youtube.com/watch?v=FGYd0PXOO_A

The silence is finally breaking! From September 8 to the 11th 2026 on Parliament Hill: The Allison Inquiry will hear sworn testimony from Canadians injured by the COVID-19 vaccines! The first time lawmakers are forced to listen. I warned about this from day one and for telling the truth, YouTube terminated my entire channel in July 2020. They tried to erase me… but they failed. Now I’m going to Ottawa in person to cover the Allison Inquiry and interview the key people involved. Please watch this video and share it far and wide! And if you value independent journalism that refuses to stay silent, please support this work so I can be there on the ground, links in description, the reckoning starts now!

[ExomatrixTV]

• The Allison Inquiry:

On September 8, 9, 10 and 11, 2026, the Allison Inquiry will be listening to the testimony of Canadians injured by a Covid-19 vaccine. The Inquiry will be broadcast live from Parliament Hill in Ottawa. The Allison Inquiry represents the first time that Canadian lawmakers will be listening to Canadians about their experiences with the Covid-19 vaccines. The Allison Inquiry will be chaired by Member of Parliament Dean Allison and is non-partisan. Members of Parliament and Senators from all parties are eligible to sit as panel members. The Inquiry is being held with the cooperation of the Covid Testimony Association, a not-for-profit set up to assist in running the Inquiry.

• covidtestimony.com/faq

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[ExomatrixTV]

• I Have Never Seen This Before': Gynecologist Reveals Dramatic Rise In Miscarriages:

Miscarriage rates in the practice of an American gynecologist skyrocketed to an unprecedented 30 percent following the rollout of COVID vaccinations — while top officials in Washington admitted among themselves early on that this risk could be real. This is now evident from released reports by former NIAID Director Anthony Fauci, which Senators Ron Johnson and Rand Paul brought to light.

• Private message versus public reassurance

On January 25, 2021, Fauci sent a message in a group chat with then-CDC Director Rochelle Walensky and then-Surgeon General Vivek Murthy. In it, he suggested that the fever many patients experienced after the second shot could theoretically be linked to first-trimester miscarriages. Walensky called it a good point. Murthy indicated hearing similar concerns about mRNA potentially reaching a fetus.





Just a week later, Fauci stood before the cameras to declare that there were “no red flags” for pregnant women. The experts resolved the matter behind closed doors by advising women to take paracetamol after the vaccination. That was the official response to a potential life-ending risk for unborn children.

• What Dr. Biss saw in her own practice

Kimberly Biss, a gynecologist in the Tampa Bay region of Florida, published her own data as early as 2022. Her findings were alarming. During 2020 — the entire coronavirus year without vaccinations — her miscarriage rate remained stable at an average of 4 percent per month. In fact, that year saw a peak in pregnancies and births.
After approximately 65 percent of her pregnant patients had been vaccinated, 80 percent of them with Pfizer, the picture changed drastically:

• 2021: average 8 percent miscarriage per month
• 2022: 15 to 16 percent
• Early 2023: 30 percent

“I have never seen those numbers in all my years as a doctor,” says Biss in a video from the Independent Medical Alliance . She also reports a sharp increase in dangerous pregnancy complications such as pre-eclampsia and severe postpartum bleeding, for which she had to administer blood transfusions significantly more often than before 2021.

• Dr. Kim Biss: The Precautionary Principle Was Abandoned With COVID-19 Shots in Pregnancy:

Source: https://youtube.com/watch?v=LLL_dWUUSoo

Recently revealed text messages between Drs. Anthony Fauci, Rochelle Walensky, and Vivek Murthy show that in early 2021, top American health officials were privately discussing concerns that COVID-19 mRNA shots could pose risks to pregnancy, including possible miscarriage.

But the public message was very different. All three doctors—and the major public health agencies—publicly urged pregnant women to get vaccinated.

Few physicians publicly challenged this guidance. IMA Senior Fellow, Obstetrics and Gynecology Dr. Kimberly Biss was one of the few in her specialty who began speaking up and asking questions after seeing troubling changes among patients in her own practice.

Here, Dr. Biss examines what health officials knew about COVID-19 shots during pregnancy, the warning signals that were overlooked, and why pregnant women deserve rigorous safety data and full transparency before any new medical intervention.

• imahealth.org/fauci-hid-texts-about-miscarriage-risk-our-doctors-were-saying-it-out-loud

Manipulated research data and a paid professional association

The scientific basis for the safety of mRNA vaccines in pregnant women was fragile from the outset. Pfizer did not include pregnant women in its clinical trial, yet 144 participants became pregnant anyway. Of these, 17 lost the child — roughly double the normal rate of 5 to 6 percent in the first trimester. A report by Pfizer followed 32 of 270 reported pregnant patients. Of those 32, 26 lost their babies. The article in The New England Journal of Medicine that served as the central safety argument for years contained a methodological error that distorted the outcome: of the 827 vaccinated women, at least 700 were vaccinated late in pregnancy, meaning that loss during the first trimester simply could not be recorded. Consequently, the cited miscarriage rate of 12.6 percent was statistically meaningless as evidence of safety. Professional association ACOG launched a vaccination campaign targeting pregnant women in April 2021. Through a FOIA request, it was later established that ACOG received $11 million for this, funds that had been channeled from the U.S. Department of Health and Human Services via a scheme. To this day, ACOG still recommends vaccination for all pregnant women.

• What this means for confidence in public health policy

The released reports confirm what critical doctors have been saying for years: the precautionary principles that protected the medical world for decades were thrown overboard regarding coronavirus vaccinations for pregnant women. Normally, a new drug must be extensively tested on pregnant women before administration is recommended — and the mother, child, and future fertility must be taken into account. None of that happened here.

Dr. Biss now gives her patients simple but concrete advice: ensure you get enough vitamin D, exercise, eat real food, and know that early treatment is available if a respiratory infection strikes. No experimental drug, no marketing campaign. Meanwhile, the US government has removed mRNA vaccines from the vaccination schedule for children and pregnant women — but a formal explanation from the officials involved is still awaited.

In the Netherlands, the discussion is still not being held, and a new round of vaccinations has simply started again. This is happening even though we also have “tens of percent more miscarriages than before the corona period,” as confirmed by retired midwife Jan Koning. Salient detail: the Perined system that was supposed to track miscarriages in the Netherlands was broken during the corona years, Koning knows.

• dutch 🇳🇱 (+ Multi-Language Options). 🦜🦋🌳

[ExomatrixTV]

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[ExomatrixTV]

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[Raskolnikov]

Graphene oxide may prove to be a real Trojan Horse with the potential to target people one by one or en masse for the so-called reset.


🚨GRAPHENE IS ALIVE — AND IT’S LISTENING

This isn’t a static particle.

It’s moving. Twisting. Reacting on command to external frequencies — like it’s programmed.

Graphene oxide, found in the shots millions took, behaves like a living antenna inside the body.

One signal and it reorganizes. What happens when they broadcast the right frequency?

Your blood. Your brain. Your future. They didn’t just inject you. They installed hardware.

Short video at link (is there a way to embed substack videos?):
https://substack.com/@stopthoseshots/note/c-329431963

[Raskolnikov]

BREAKING: STUDY FINDS mRNA “VACCINES” COULD INDUCE OR ACCELERATE CANCER VIA 35 DISTINCT MECHANISMS

We conducted the most comprehensive analysis to date examining the link between mRNA “vaccines” and cancer.

The convergent mechanistic, clinical, and population evidence is now clear: TURBO CANCER IS REAL.

We analyzed CDC mortality data and found an estimated 153,000–197,000 EXCESS U.S. CANCER DEATHS since the 2021 mRNA injection rollout.

Here’s a concise breakdown of our findings:

MECHANISTIC EVIDENCE:

35 distinct cancer-promoting mechanisms converge through 4 major routes: (1) protooncogene activation, (2) mutation pressure, (3) protein–protein interaction network interference, and (4) cancer stem-cell clonal acceleration.

Key mechanisms include EGFR/RAS/MAPK and STAT3–MYC activation, p53/BRCA suppression, impaired DNA repair, residual plasmid DNA and SV40 regulatory elements, LINE-1 reverse transcription, m1Ψ-associated frameshifting, chronic LNP inflammation, immune suppression, and cancer stem-cell expansion—pathways capable of promoting genomic instability, uncontrolled growth, immune escape, dormancy reactivation, and metastatic outgrowth.

Our central concurrent-hit model proposes that these processes do not necessarily operate independently or sequentially. Multiple cancer-promoting hits overlap in the same susceptible host, compressing the time required for dormant, indolent, or microscopic disease to become clinically aggressive.

CLINICAL EVIDENCE:

The published clinical literature includes 333 documented turbo cancer cases across 27 countries, involving lymphomas, leukemia, melanoma, breast cancer, lung cancer, glioblastoma and other glial tumors, sarcomas, and pancreatic cancer. The vast majority of these cases occurred following COVID-19 vaccination, with a minority following SARS-CoV-2 infection.

Approximately 86% of the post-vaccination cases occurred after nucleoside-modified mRNA products—about 56% after Pfizer-BioNTech, 25% after Moderna, and another 5% after exposure to both mRNA products across different doses.

Across these cases, recurring patterns include rapid cancer progression, short-latency recurrence, reactivation of previously controlled disease, and tumors involving the injection site or nearby draining lymph nodes.



https://substack.com/@stopthoseshots/note/c-330179413

[Eva2]

Further to Exomatrix post above, this is Day 1 and 2 of Allison Inquiry - its really shocking how denial is still so prevelent:

https://rumble.com/v7f9t34-ottawa-po...als-durin.html

https://rumble.com/v7f8ici-live-alli...ment-hill.html

https://rumble.com/v7fa0am-day-2-the...ment-hill.html

[ExomatrixTV]

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[ExomatrixTV]

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[ExomatrixTV]

• Explosive Dossier Published After Years Of Censorship: What Were Doctors And Citizens Not Allowed To Know About Myocarditis After Vaccination?

Data on myocarditis following coronavirus vaccination — withheld from the general public for years — have finally been published in a scientific journal. An internal file from the Israeli Ministry of Health, provided by a whistleblower, reveals hundreds of hospitalizations and dozens of deaths that were systematically reported to Pfizer, while doctors and citizens were kept silent.

• What the whistleblower revealed

Researchers Yaffa Shir-Raz (University of Haifa) and Yaakov Ophir (Ariel University) published their findings in the scientific journal EXCLI Journal (Experimental and Clinical Sciences Journal). The internal file contains detailed case descriptions maintained by the Israeli Ministry of Health between March 2021 and May 2022. The document was updated in eight successive versions as new cases emerged. The file reveals that as early as March 25, 2021 — barely three weeks after Israel sounded an international alarm — 157 hospital admissions and 46 deaths had been documented. Of those admissions, 65 involved cases of myocarditis or pericarditis. In the final version of the file, with data up to May 9, 2022, this rose to 250 of the 531 admission reports — nearly half.

• Young men hardest hit

The concentration of heart problems among young people is striking. Of all admitted patients under the age of thirty, over 70 percent presented with myocarditis or pericarditis. Among men under twenty, that percentage rose to 85 percent, and among men between twenty and twenty-nine, to 82 percent. Even among girls under twenty, 11 of the 16 admission reports concerned heart inflammation. The youngest documented case was a nine-year-old girl who was admitted after her second dose. Two of the nine deaths among people under fifty were linked to myocarditis. One of them was a 22-year-old woman who developed fulminant myocarditis after her second dose and died of cardiogenic shock.

• Israel warned early — and was ignored

On February 28, 2021, the Israeli Ministry of Health sent an official signal to both the European Medicines Agency (EMA) and the US CDC. Three days later, the Ministry’s Deputy Director of Epidemiology wrote directly to the CDC: large numbers of myocarditis and pericarditis cases were observed among young people shortly after administration of the Pfizer vaccine. The internal CDC note was marked “Importance: High”.



Yet, it was not until May 28, 2021 — three months later — that American doctors received formal guidelines from the CDC on recognizing and reporting vaccine-related myocarditis. The FDA did not add official warnings to the package inserts until late June. In the meantime, vaccination was extended to children aged twelve to fifteen, a group with a particularly low risk of a severe course of COVID-19, but precisely the group in which the heart signal was most pronounced.

• The official reassurance that was incorrect

When the authorities finally informed the public, the message was unambiguous: myocarditis after vaccination was rare, mild, and transient, and did not outweigh the risks of COVID-19 itself. But that picture does not align with the available science, the researchers state. A Hong Kong study found myocarditis after the second dose in approximately 1 in 2,700 male adolescents — serious enough that Hong Kong decided in September 2021 to give young people only one dose. Examination of MRI images of sixteen young people showed that abnormalities were still visible in eleven of them three to eight months later.

• Pfizer knew — and now what?

The detailed files were reported to Pfizer one by one. What the company did with that information remains unclear to this day. Senator Ron Johnson lashed out: “This confirms once again that they knew the injections could kill and injure, but kept it hidden. And they are still doing so.” Robert F. Kennedy Jr., currently US Secretary of Health and Human Services, called the withholding of this data “downright criminal.”

Retsef Levi, a member of the CDC advisory committee on vaccine programs, emphasizes that the FDA and CDC are still withholding data on deaths from myocarditis following COVID vaccination even today. Shir-Raz is clear about what needs to happen now: the public has never been given access to these files, and that is precisely why publication in the scientific literature is so important. The central question now is: what has Pfizer done with the information? As Wierd Duk would say : sometimes you have to cover up the truth a little.

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Allison Inquiry Final Report: 4 Days Of Testimony The Media Ignored!! Share This Video Far And Wide!:

Source: https://youtube.com/watch?v=EVuPzAujVf0

The Allison Inquiry has concluded. Four days of sworn testimony in Ottawa. 50 Canadians out of 1,400 who came forward finally had their stories heard. This final report features firsthand accounts of life-altering injuries and deaths following COVID-19 vaccination, paralysis, neurological damage, cardiac events, and families left without answers. In this video Dan Dicks of Press For Truth covered the hearings after mainstream outlets stayed away. MP Dean Allison explains why he launched the inquiry: too many people were suffering in silence. The injured describe being dismissed by the medical system, denied support through Canada’s vaccine injury program, and treated as if their experiences didn’t count. Watch the testimonies and share them!

[onawah]

The Silent Aftershock of Vaccination
September 22, 2026
Dr. Mark Sircus
https://drsircus.com/vaccines/the-si...f-vaccination/

"A vaccine can prevent disease and still initiate a medical cascade: inflammation becomes “cellulitis,” an urgent visit becomes an antibiotic prescription, and altered microbial ecology produces changes that ordinary adverse-event tables rarely describe. These effects do not prove that vaccines broadly increase infection. They show that surveillance should measure healthcare visits, antibiotic prescribing, colonization, transmission, and strain replacement—not merely immediate symptoms or sudden death.

39.4 fever after the shot, not counted as an adverse event,
gets labeled as an “ear infection,” gets antibiotics, which then
disrupt the gut and lower the response to the next vaccine.

Fever is among the most common systemic reactions to vaccination. Depending on the product and how fever is defined, it occurs in approximately as many as 20% of recipients. Because it is considered expected “reactogenicity,” it is rarely treated as a significant safety outcome—even though it may provoke medical visits, diagnostic testing, or inappropriate antibiotic treatment.

An under-reported middle ground exists between “perfectly safe” and “serious injury.” Mild vaccine reactions aren’t in VAERS because they aren’t counted as adverse events, but pediatricians see them every day. This describes something the surveillance systems are structurally blind to, not something they are hiding.

The problem with the middle ground: it’s the easiest thing in the world to dismiss, because the symptoms overlap with other things. Fever, irritability, sleep disruption, feeding changes, transient regression — these happen constantly in infants for many reasons but become suspicious when they happen soon after vaccination.

A medically meaningful cascade can therefore run through a child’s first two years without generating a single entry in any safety database—not because anyone suppressed it, but because no system was built to see a sequence, only to count events.

The fever → antibiotic trap is the most common lighter effect, and it drives a lot of hidden antibiotic overuse. Baby gets routine vaccines → 24-72 hours of fever, fussiness, runny nose, crying, poor sleep. Parents go to urgent care/ER. Doctor, not wanting to miss an ear infection, prescribes amoxicillin “just in case” for otitis media or upper respiratory symptoms that are actually inflammatory responses.

It’s not recorded as vaccine-related; it’s recorded as “otitis media” or “URI.”That matters because unnecessary antibiotics disrupt the infant microbiome when immune memory is forming. An AAP study of 560 children found early antibiotic exposure was associated with lower antibody levels to multiple childhood vaccines in the first 2 years. Low responders then got more otitis, more sinusitis, more flu, more pneumonia. A Hong Kong territory-wide cohort found antibiotic use before COVID vaccination was associated with a higher risk of breakthrough infection and severe outcomes.

So: vaccine → fever → antibiotics → dysbiosis → lower vaccine response → more infections → more antibiotics.



Dr. Harold E. Buttram wrote years ago about a little-known letter-to-the-editor in the New England Journal of Medicine in 1984 about an interesting German study. In the study, researchers found a significant but temporary drop in T-helper lymphocytes in 11 healthy adults after routine tetanus booster vaccinations. “Special concern rests in the fact that, in 4 of the subjects, the T-helper lymphocytes fell to levels seen in active AIDS patients. The implications of this study are enormous.

Concerning this German study, if this was the result of a single vaccine in healthy adults, it is sobering to think of the possible consequences of multiple vaccines (18 vaccines within the first six months of life at latest count) given to infants with their immature and vulnerable immune systems,” wrote Buttram.

The New England Journal of Medicine study showed that tetanus vaccines cause T-cell ratios to drop below normal, with the greatest decrease after two weeks. Though the altered ratios were found to be similar to those found in people with AIDS, the important information from this study has never seen the light of day. “I consider it one of the most flagrant examples of negligence in the area of safety testing in childhood vaccines, the fact that this study has never been repeated,” wrote Buttram.

Reported Vaccine Reactions

All the vaccine reactions below are officially recognized effects of vaccines, as recognized by the Pharmaceutical companies that make them. Notice death by injection is not mentioned, even though we know vaccines do kill children and the government pays up on those deaths via the Federal Vaccine Court.

This extensive list sustains the assertion that widespread reactions more subtle than death and Autism exist and are not rare. Babies’ bodies do not enjoy vaccines, especially when multiple vaccines are administered at the same time. A case can easily be made that vaccines are not nearly as safe as health officials and doctors insist and are more effective at creating problems for children and their families than they alleviate.

And though politicians, medical and health officials will deny it to their dying breath, vaccines could be the cause of Shaken Baby Death Syndrome and SIDS, Sudden Infant Death Syndrome, bringing the death count from the childhood immunization schedule to a totally unacceptable level.

According to a 2009 New York Times article on swine-flu vaccines, “As soon as swine flu vaccinations start next month, some people getting them will drop dead of heart attacks or strokes.” The article added that children would suffer seizures and pregnant women would miscarry, while immediately arguing that the vaccine would not necessarily have caused these events.

There lies the central problem: serious illness or death following vaccination is recorded, but coincidence is often presumed even as cases accumulate into an undeniable safety signal. Although officials have recognized certain vaccine-associated injuries, the sweeping assurance that “vaccines are safe” almost always eclipses the individual victims whose reports eventually force those acknowledgments.

This was not always the official posture. Earlier vaccination campaigns were suspended or products withdrawn after comparatively small safety signals appeared. With the mRNA vaccines, however, regulators acknowledged an increased risk of myocarditis and pericarditis—while admitting that the possible long-term consequences remain unknown—and responded primarily by changing labels rather than withdrawing the products.

The FDA’s updated warning confirms both the increased risk and the remaining uncertainty. We cannot honestly state as established fact that millions have died from these vaccines, but that is probably an honest assessment when you look at the increase in sudden death statistics. Still, millions of injuries and deaths could apparently be alleged, reported, or suspected, which is the case, without bringing the campaign to an end. At this point, one is left wondering whether anything short of an alien invasion would persuade authorities to pull them from the market.

COVID-19 Vaccines Are Not Totally Safe And Effective

Common local reactions: injection-site pain, tenderness, redness, swelling, warmth, itching, induration, bruising, and enlarged lymph nodes.
Common general reactions: fatigue, headache, muscle pain, joint pain, chills, fever, nausea, vomiting, diarrhea, malaise, dizziness, and reduced appetite.
mRNA vaccines: severe allergic reactions including anaphylaxis; myocarditis and pericarditis; fainting; lymph-node swelling; rash, hives, itching, and facial swelling.
mRNA postmarketing reports: paresthesia or reduced sensation, tinnitus, erythema multiforme, facial paralysis, febrile seizures, menstrual bleeding changes, and injection-site reactions occurring later than the usual vaccination period.
Protein-based vaccine: injection-site reactions, fatigue, headache, muscle or joint pain, malaise, nausea or vomiting, fever, chills, lymph-node swelling, severe allergy, myocarditis, and pericarditis.
Adenovirus vector vaccines: injection-site reactions, headache, fatigue, muscle pain, fever, chills, nausea, and joint pain.
Adenovirus vector serious warnings and reports: thrombosis with thrombocytopenia syndrome, immune thrombocytopenia, Guillain-Barré syndrome, capillary-leak syndrome, venous thromboembolism, transverse myelitis, tinnitus, anaphylaxis, and myocarditis or pericarditis.

Other Vaccines

Common reactions and important warnings or reported events by vaccine family

Adenovirus: injection-site pain, headache, fatigue, fever, muscle pain, vomiting or diarrhea; shedding and transmission of live virus; severe allergy.

Measles, mumps, rubella: fever, rash, injection-site reactions, swollen glands, joint pain; febrile seizures, thrombocytopenia, severe allergy, encephalitis or encephalopathy, and inclusion-body encephalitis in immune deficiency.

Anthrax: injection-site pain, redness, swelling, itching, or lump; fatigue, headache, muscle pain, fever, nausea; severe allergy.

MMRV: fever, rash, injection-site pain; febrile seizures, thrombocytopenia, severe allergy, encephalitis, and vaccine-strain infection in susceptible or immune-deficient people.

BCG tuberculosis: local ulcer, scarring, abscess, lymph-node inflammation; osteitis or osteomyelitis; disseminated BCG infection, especially in immune-deficient people.

Meningococcal: injection-site pain, headache, fatigue, muscle pain, fever, nausea; severe allergy, fainting, seizures, Guillain-Barré syndrome, and neurologic reports.

Chikungunya: injection-site pain, headache, fatigue, muscle or joint pain, fever, nausea; prolonged chikungunya-like reactions; serious neurologic or cardiac events reported.

Pneumococcal: injection-site pain, redness or swelling, fatigue, headache, muscle pain, fever, chills, reduced appetite, irritability, or drowsiness; reports of severe allergy, seizures, and thrombocytopenia.

Cholera: tiredness, headache, abdominal pain, nausea or vomiting, reduced appetite, diarrhea; shedding of live vaccine organism; severe allergy.

Polio: injection-site reactions and fever; severe allergy; with live oral vaccine, vaccine-associated paralytic poliomyelitis and circulating vaccine-derived poliovirus.

Dengue: injection-site pain, headache, malaise, muscle pain, fever; allergic reactions; increased risk of severe dengue in people without prior dengue infection.

Rabies: injection-site pain, redness, swelling or itching; headache, nausea, abdominal or muscle pain, dizziness; severe allergy, serum-sickness-like illness, and neurologic reports.

DTaP, Tdap, Td: pain, redness, or swelling; fever; fussiness; fatigue; headache; stomach symptoms; extensive limb swelling; fainting; seizures; brachial neuritis; Guillain-Barré syndrome; severe allergy.

Rotavirus: irritability, vomiting, diarrhea, fever; intussusception; severe allergy; vaccine-virus shedding and infection in immune-deficient contacts.

Ebola: injection-site pain, headache, fatigue, muscle or joint pain, fever, nausea, rash; arthritis or joint symptoms; severe allergy.

RSV: injection-site pain, fatigue, headache, muscle or joint pain, nausea; severe allergy; Guillain-Barré syndrome and other neurologic events under monitoring; preterm birth signal for maternal vaccination.

Haemophilus influenzae type b: pain, redness, or swelling; fever; irritability; drowsiness; reduced appetite; severe allergy; seizures; thrombocytopenia; and Guillain-Barré reports.

Smallpox mpox JYNNEOS: injection-site pain, redness, swelling, itching or lump, fatigue, headache, muscle pain, nausea; severe allergy; myocarditis and pericarditis monitored as potential risks.

Hepatitis A: injection-site pain or redness, headache, fatigue, fever, nausea, reduced appetite; severe allergy; neurologic and blood-disorder reports.

Smallpox ACAM2000: inoculation-site reactions, fever, fatigue, headache, muscle pain, lymph-node swelling; myocarditis, pericarditis, encephalitis, eczema vaccinatum, progressive vaccinia, generalized vaccinia, ocular vaccinia, and fetal vaccinia.

Hepatitis B and combination A B: injection-site pain, headache, fatigue, fever, dizziness, nausea; severe allergy, thrombocytopenia, Guillain-Barré syndrome, demyelinating and other neurologic reports.

Tick-borne encephalitis: injection-site pain or tenderness, headache, fatigue, muscle pain, fever, restlessness in children; severe allergy and neurologic reports.

Human papillomavirus: injection-site pain, swelling or redness, headache, fever, nausea, dizziness, fainting; severe allergy; blood clots and neurologic reports without established causation.

Typhoid: injection-site pain, tenderness, redness or swelling, headache, fever, malaise, nausea; with oral live vaccine, abdominal symptoms and shedding; severe allergy.

Influenza injected: injection-site pain or swelling, headache, fatigue, muscle aches, fever, nausea; severe allergy, Guillain-Barré syndrome, febrile seizures, vasculitis, and thrombocytopenia reports.

Varicella: injection-site pain, redness or swelling, fever, varicella-like rash; febrile seizures, thrombocytopenia, encephalitis, pneumonia, hepatitis, shingles, and transmission of vaccine virus.

Influenza nasal live: runny or blocked nose, sore throat, cough, headache, fever, reduced appetite, wheezing; severe allergy and Guillain-Barré reports; vaccine-virus shedding.

Yellow fever: injection-site pain, headache, muscle pain, fever, malaise; severe allergy, vaccine-associated neurologic disease, and vaccine-associated viscerotropic disease.

Japanese encephalitis: injection-site pain or tenderness, headache, muscle pain, fatigue, fever; severe allergy and neurologic reports.

Zoster shingles: injection-site pain, redness or swelling, fatigue, muscle pain, headache, chills, fever, stomach symptoms; severe allergy, Guillain-Barré syndrome, and shingles-like rash reports.

Source basis: official vaccine prescribing information and package inserts. This list condenses label language; product-specific labels control.

Dating back to the 1930s, pharmaceuticals have added thimerosal (made up of ethyl mercury) to many of the vaccines given to children. However, it was not until 1999 in America that a Congressional mandate compelled the FDA to disclose the amount of mercury in the vaccines. Many became gravely concerned when it was learned that, for many years, infants had routinely received 25 to 50 or more times the amount of mercury in a given day than was considered safe under U.S. Environmental Protection Agency standards. For centuries, mercury has been known as one of the most toxic heavy metals, but pediatricians had no problem injecting it into babies on their first day of life and many times after.

Very recently, an animal study has revealed a possible mechanism for this toxicity in which mercury exposures resulted in retrograde degeneration of neuronal (brain) membranes, producing molecular lesions similar to those seen in the brains of patients dying with Alzheimer’s disease.

The incidence of childhood asthma, diabetes, and
autoimmune diseases has doubled during the past 20 years;
Attention Deficit Disorder has tripled; Autism has increased 600%.
What part have vaccines played?
Dr. Stanley Monteith, M.D.

Though vaccine reactions are official, no one really wants to answer this question. It is not human nature to admit wrongness, ignorance, or arrogance. The price the human race pays for this is off the Richter scale. So, as far as I am concerned, health officials are some of the sickest, most demented people on the planet.

Dr.Sircus is a reader-supported publication."

Dr. Mark Sircus
AC., OMD, DM (P)
Professor of Natural Oncology, Da Vinci Institute of Holistic Medicine
Doctor of Oriental and Pastoral Medicine
Founder of Natural Allopathic Medicine

[ExomatrixTV]

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[ExomatrixTV]

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Pfizer DNA found in heart tumor of a healthy 35-year-old man who developed an extremely rare and deadly heart cancer shortly after his COVID-19 vaccinations — that is the shocking conclusion of a new case study published this month. The findings align with a growing body of signals raising serious questions about the long-term safety of mRNA vaccine platforms.

• A rare cancer of unexplained age

The patient had one of the rarest malignant conditions known to science. In an analysis of more than seven million registered cancer cases, only 0.008 percent involved a malignant primary heart tumor. All the more remarkable is the case of this otherwise healthy young man with no personal or family history of cancer, no hereditary predisposition, no history of radiation, and no demonstrable SARS-CoV-2 infection. His first symptoms—headache, dizziness, and nausea—occurred 161 days after his first Pfizer injection. Less than a week later, he was in the hospital with a heart tumor of nearly ten centimeters and metastases.

• Vaccination DNA found in the tumor itself

The most disturbing aspect of this study is not the diagnosis itself, but what researchers found in the preserved tumor tissue four years later: DNA originating from the Pfizer vaccine. Research by Kevin McKernan and colleagues had previously shown that plasmid DNA was present in multiple analyzed vaccine vials in amounts exceeding the FDA and World Health Organization's permitted safety threshold by a factor of 36 to more than 600. For the Pfizer product this man received, the exceedance was 36 to 153 times the standard. This DNA is delivered directly into human cells via lipid nanoparticles — the same delivery mechanism as the mRNA itself.

• Tumor growth that seems to defy the laws of biology

What also raises the alarm among the researchers are the tumor's growth rates. Based on repeated brain scans, they were able to calculate that the tumor had a doubling time of approximately ten days. A tumor of this size — almost as big as a baseball — would normally take between 900 and 1,000 days to grow this large. However, only 170 days elapsed between the first vaccination and the diagnosis. The most logical explanation is not that the vaccine created the cancer out of thin air, but that a pre-existing, dormant tumor suddenly began to grow rapidly.

• Scientific context: not the first signal

The study is not an isolated case. Earlier, Hulscher and colleagues showed that vaccine mRNA was still detectable in circulating exosomes up to 1,284 days after the last dose, while plasmid DNA was still present in body tissue on day 1,364 after vaccination. A large-scale South Korean cohort study involving more than 8.4 million people found increased risks of multiple types of cancer in the year following COVID-19 vaccination. And a systematic review documented 333 patients in 27 countries who developed cancer after vaccination or infection.

• No alternative explanation found

The researchers point out that in this case, all usual risk factors are absent. Nucleocapsid protein — a marker for SARS-CoV-2 infection — was not found in the tumor. The detected DNA fragments are synthetic in nature and could originate exclusively from the vaccine.

• Call for immediate investigation

Epidemiologist Nicolas Hulscher, one of the authors, described the findings unequivocally as proof that turbo cancer really exists: the suspect's DNA was found at the crime scene. “This is the smoking gun.” He and his co-authors are calling for large-scale follow-up research. The question that is being asked ever more loudly is: how much longer will these kinds of signals be brushed aside?

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