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Renowned Toxicologist Issues Grave Warning Over Pfizer Vaccine DNA Integration A chilling laboratory finding has been revealed by toxicologist Dr. Lindsay Janci, and it demands immediate independent investigation. Dr. Janci highlighted an alarming in vitro study on ovarian carcinoma cells. When these cells were exposed to the Pfizer COVID-19...

36,156 Aufrufe • vor 9 Monaten •via X (Twitter)

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A toxicologist's devastating testimony on how COVID-19 mRNA vaccines could cause cancer and alter the human gene pool. This is a must-read. Dr. Lindsay Janci just laid out a harrowing case. The concern isn't just short-term side effects; it's the potential for genetic vaccines to drive cancer and be passed to future generations. Her summary is a masterclass in scientific alarm. Here are the 9+ potential pathways to cancer she detailed: 1. LNP Delivery to Stem Cells: Lipid Nanoparticles (LNPs) don't just go to muscle cells. They readily transfect hemopoietic stem cells—the origin of all our blood cells. 2. Cancer Metastasis: LNPs may cause pre-existing cancer cells to spread more easily by inducing "endothelial leakiness." 3. Inherent LNP Oncogenicity: The LNPs themselves might have cancer-causing effects, which have never been studied. 4. The SV40 Promoter: Hidden plasmid DNA in the vaccines contains the powerful SV40 promoter. If this genetic switch integrates near an oncogene, it could explosively drive cancer growth. 5. SV40 Enhancer (Nuclear Targeting): This sequence is designed to rush DNA into the cell nucleus—a key step for "insertional mutagenesis," where foreign DNA disrupts our own genes. 6. Spike Protein & p53: The spike protein itself has been shown to inhibit p53, a critical tumor suppressor protein that stops cancer from developing. 7. Insertional Mutagenesis & Frameshifts: Plasmid DNA doesn't need SV40 to get into the nucleus. Once integrated, it can cause frameshift mutations, leading to aberrant, cancer-causing proteins. 8. mRNA Reverse Transcription: The mRNA can be reverse-transcribed back into DNA and integrated into our genome, a known cancer mechanism, especially in ovaries & testes where reverse transcriptase is high. 9. Immunosuppression: The vaccines may suppress specialized T-cells that act as "guards" keeping dormant cancer clones in check. Weakening this guard can lead to a surge in cancers, similar to what we see in aging pets. But it gets worse. Dr. Janci issued a grave warning about heritable genetic damage: The DNA plasmids and reverse-transcribed DNA can potentially integrate into sperm and ova (gametes). This means the genetic payload could be passed to our children and "contaminate the gene pool." She reveals two mechanisms: - Genomic Integration: Direct insertion into the gamete's DNA, likely causing cancer in offspring rather than functional spike production. . Sperm-Mediated Gene Transfer (SMGT): A process where sperm can carry extra-chromosomal DNA and pass it on to the next generation without full genomic integration, leading to constitutive spike protein expression in children. The most chilling part? Dr. Janci states that this is "not being investigated at all." Despite reaching out to multiple labs, no one is testing sperm or ova from vaccinated individuals for these integrations. This isn't conspiracy theory. This is a credentialed toxicologist presenting a plausible, mechanistic roadmap for a public health catastrophe. The absolute lack of curiosity from health agencies is deafening. The question is no longer if there are risks, but why those in charge are refusing to look.

Camus

18,244 Aufrufe • vor 9 Monaten

Dr. Sucharit Bhakdi, a renowned microbiologist and immunologist, is issuing a dire warning to humanity about the dangers of mRNA vaccines. He claims that the integration of foreign genes into human chromosomes through these vaccines poses catastrophic risks—not only to individuals but to future generations. According to Dr. Bhakdi, the introduction of bacterial plasmids and foreign DNA into human cells via mRNA vaccines is a reckless experiment that could lead to permanent genetic alterations. "Any foreign gene integrated into your chromosome can trigger cancer immediately, cause widespread cellular dysfunction, and be passed down to your offspring," Dr. Bhakdi warns. He emphasizes that once these genetic changes occur, they are irreversible, transforming the very blueprint of human biology. Every cell altered by these foreign genes, he argues, is "doomed," setting the stage for unpredictable and potentially devastating health consequences. Dr. Bhakdi asserts that global health authorities like the WHO, CDC, and FDA are pushing these vaccines without fully acknowledging their risks. He points to the presence of bacterial-derived plasmids in mRNA vaccines, which he claims can infiltrate human cells and wreak havoc on genetic stability. This, he says, is not a theoretical concern but a reality already unfolding with the rollout of these vaccines worldwide. This is not a message of fear but a call to awareness. Dr. Bhakdi urges people to question the narrative, demand transparency, and protect their health and future generations from what he describes as a dangerous overreach by global health institutions. "We are at a crossroads," he declares. "The genetic integrity of humanity is at stake."

Camus

56,578 Aufrufe • vor 1 Jahr

A bombshell scientific publication confirms a critical danger in the Pfizer/BioNTech COVID-19 vaccine, and the implications are as severe as they are alarming. The core issue is plasmid DNA contamination. New research confirms this contaminating DNA is not just present in the vial; it is capable of entering human cells. This fact alone is concerning, but the true danger lies in what this DNA contains. Scientists have identified the presence of an SV40 viral promoter/enhancer sequence within Pfizer's plasmid DNA. For decades, SV40 has been known to be a potent tool for driving gene expression and is associated with potential genomic integration risks. Here is why this is a catastrophic failure in regulatory disclosure and vaccine design: 1. Nuclear Entry & Genomic Integration: The SV40 promoter is functionally active in human cells. Its presence means the contaminating plasmid DNA has a non-zero chance of entering the nucleus of a human cell. Once inside the nucleus, it runs a tangible risk of integrating into the human genome. 2. Uncontrolled, Long-Term Gene Expression: If integration occurs, it could effectively turn the vaccine into an unintended and uncontrolled gene therapy. This could force the body to produce the SARS-CoV-2 spike protein indefinitely—for months, years, or permanently, with unknown health consequences. 3. A Deliberate Omission? Most damningly, Pfizer never disclosed the presence of this known biohazard, the SV40 sequence, to regulatory bodies during the approval process. There was no functional reason for its inclusion, as Moderna's production process utilized a standard bacterial plasmid without such dangerous components. The authors of this pivotal study are now calling for the immediate suspension of these mRNA vaccines until a full understanding of their long-term genomic risks is achieved. They further state that Pfizer and BioNTech must be held accountable for exposing the global population to a risk this significant without informed consent. This is no longer speculation. This is published, peer-reviewed science confirming a pathway for potential permanent alteration of the human genome. The demand for transparency and accountability has never been more urgent.

Camus

205,889 Aufrufe • vor 9 Monaten

A discussion between Dr. Brian Hooker and Dr. Ryan Cole exposes a catastrophic oversight in COVID-19 mRNA vaccine science. The implications for cancer and heritable genetic damage are no longer theoretical—they are a present danger. A critical study on a liver cell line revealed something we were told was impossible: portions of the vaccine's mRNA can reverse-transcribe and integrate into the human genome. This isn't just about a temporary shot; it's about permanent, unpredictable genetic alteration. Why is this a game-changer? 1. Mutagenesis & Cancer: These insertions are like random typos in the source code of life. They disrupt the reading frame of DNA, leading to malformed proteins. When these random insertions occur near critical cell cycle genes, tumor suppressor genes (like p53), or oncogenes, it is a direct step toward mutagenesis and cancer formation. 2. Germline Mutation Threat: The lipid nanoparticle (LNP) delivery system is not contained. Biodistribution studies show it travels throughout the body, accumulating in the liver, spleen, bone marrow, brain, and critically—the ovaries and testes. This means the potential for genetic damage isn't limited to one person; it raises the terrifying prospect of permanent, heritable germline mutations. 3. Disarming Our Defenses: Dr. Cole highlights peer-reviewed evidence that the spike protein itself binds to and disrupts p53, the "guardian of the genome," and BRCA genes, crucial for suppressing breast and ovarian cancers. We are injecting a substance that actively disarms our most critical cellular defense systems. The scientific establishment's failure to act is deafening. As Dr. Cole states, the NIH should be urgently funding studies on every cell line to answer the essential questions: - Is this intercalating into neural tissue? - Is it causing germline mutations? The era of claiming "it stays in the arm" or "it doesn't affect DNA" is over. The evidence is here, and it points to a profound and permanent manipulation of human genetics with unknown consequences for generations.

Camus

14,188 Aufrufe • vor 9 Monaten

Professor Emeritus Yasufumi Murakami of Tokyo University of Science: "It is almost certain that vaccines are contaminated with DNA. mRNA vaccines containing the DNA causes turbo cancers." Professor Murakami explains the mechanism of turbo cancers: The covid vaccines are expected to contain only mRNA. However, it has been proven that the vaccines contain considerable amounts of DNA and other substances that should not be present. There is no doubt about it now. DNA can enter human cells very easily, regardless of length, and can get into cells everywhere. When DNA gets in the center of an important gene, the important gene will stop functioning. One problem is that the mRNA vaccine of Pfizer contains a promoter sequence of the cancer virus called SV40. This sequence could enter the human genome, and awakens and activates dormant carcinogenic genes. As a result, the risk of developing cancer increases. mRNA vaccines increase the risk of developing cancer while suppressing the immunity. Vaccination increases the risk of developing cancer dramatically compared to the unvaccinated state. The more people get vaccinated, the more people will probably get cancer. Vaccines appear to increase the risk of all types of cancers. There is credible information that the number of leukemia cases is on the rise. Vaccination causes the promoter sequence of the cancer virus to enter white blood cells and attach to red blood cells everywhere. As a result, more and more leukemia cases are reported. A lot of spikes of mRNA are produced. The spikes would be most protected from destruction. Possibly, long spike genes remain intact. So, if the long spike genes remain there, gene expression will continue to take place all the time. That is, spikes are generated forever. Once the DNA gets into the stem cells, the DNA will keep creating more and more spikes. As a result, IgG4 antibodies are induced. The number of spike-producing cells will not decrease, and it becomes impossible to get rid of spike-producing cells. As a results, It becomes normal for spikes to be present in cells. The produced spikes then flow into the bloodstream and cause a variety of health problems. So, any vaccine that induces IgG4 is deemed as a defective vaccine, and should no longer be produced. Normally, cancer cells are born and grow slowly. However, the vaccine suppresses the immunity, which makes it easier for cancer cells to grow. The vaccines cause turbo cancers. Suppression of the immunity is a major factor of turbo cancers. The increase in IgG4 antibodies results in suppression of cancer immunity. The more DNA the vaccine contains, the more intense the inflammation caused by the vaccine becomes. DNA is a foreign substance to the cells. So, DNA causes a severe reaction and kills the immune system of the cells. The more DNA the vaccine contains, the more severe the side effects caused by the vaccine become. Vaccines could contain many different impurities, but one possibility could be DNA. In the first place, DNA is something that should not be put into cells of your body.

You

574,563 Aufrufe • vor 2 Jahren

A molecular biologist's devastating critique of mRNA COVID-19 vaccines, outlining why they must be stopped. According to Dr. Janci Chunn Lindsey, a PhD molecular biologist and toxicologist, the public has been misled about the fundamental nature of COVID-19 mRNA vaccines. She identifies them not as traditional vaccines, but as gene therapies—a claim she states was falsely denied from the outset. The core mechanism is this: your cells are instructed to produce a foreign viral protein (the spike protein), which your body is then triggered to attack. The critical issue? The genetic material doesn't stay in the arm as promised. It travels systemically, reaching the brain, bone marrow, ovaries, and testes. This widespread distribution means your own cells, in vital organs, become targets for your immune system. Dr. Lindsey links this to an explosion in autoimmunity and severe reproductive issues, citing a concerning similarity between the spike protein and syncytin proteins, which are essential for placental formation and fertility. Perhaps most alarmingly, she raises a specter from 30 years of gene therapy research: the risk of creating transgenic humans. With the genetic material confirmed in ovaries and testes, no studies have investigated if sperm or ova are transfected, potentially passing this genetic code to partners or children. She states plummeting birth rates and increased miscarriages are consistent with this risk. The initial assurances of mRNA's brief stability are also labeled a lie. Modifications make the RNA both highly stable and toxic to mitochondria. Studies have found mRNA in lymph nodes after 60 days and spike protein in the brain after 9 months. Furthermore, claims that the material would not interfere with DNA are challenged. Dr. Lindsey cites studies showing the genetic material does enter the nucleus, impairs DNA repair proteins, and can be reverse-transcribed into the human genome, posing a mutagenic risk that aligns with the observed increase in cancers. In conclusion, she states that past vaccines were pulled for far fewer casualties. Now, with children suffering heart attacks and strokes, regulatory bodies are absent. Her urgent call: to protect our children and our future, these shots must be stopped.

Camus

178,794 Aufrufe • vor 9 Monaten

🚨🚨🚨 Dutch Cancer Researcher and Erasmus Medical Centre Assc Prof Maarten Fornerod discusses DNA contamination in COVID Vaccines. ---------------------------- ...for last 35 years or so I've been working uh in the areas of molecular biology, gene expression, biology, cancer biology and recently in the last years, maybe last 10 years in the context of big data and computational biology... ...when we use genetic vaccines what we do essentially is we're making a complex intervention in a very complex system. It's impossible to predict what happens if you combine these two complex systems, and you get unpredictable effects. .. And the only way to go about this is to do genotoxic research, when you want to introduce a genetic medicine into a human being and that genetotic research has to be independent, it has to be double blind, has to be long lasting. AND ALL THESE HAVE NOT BEEN DONE WITH THE GENETIC CORONA VACCINES! if there's a vaccine, there's a little bit of DNA in there upon injection that is very, very rapidly degraded by the human body. However if it's protected and in a lipid nanoarticle it can very efficiently be transduced in the cell... I've been doing this this many, many times. This is called lipofection and it's a very efficient way to introduce DNA into a cell. ...Many people think that this is not possible. But I've been working in nuclear transport for many years, I think more than 10 years. So I've been exposed to a lot of molecular cell biology of nuclear cytoplasmic transport. And it's clear that the DNA can enter the nucleus. Now to make things worse, the mRNA vaccine doesn't stay in the arm but it's detected in , in all different organs including the reproductive system. And so partly this is based on animal models, of course we know from Michael Morz that he has detected uh the spike protein in brain, in the heart and it's for sure it's detected in the blood and even in breast milk. ..So there's NO DOUBT that this mRNA vaccine spreads widely in the human body. ..Now from a genetic point of view, there are possible consequences uh of this and the consequences could be a 1. long term disruption of cellular processes that could lead to disease. 2. there's a risk of insertional mutageenesis in somatic cells that can lead to cancer. 3. the insertion mutogenesis takes place in a germ cell which would be a hereditary burden uh on the human population. 4. And you could also think that these um DNAs, could transfect the microbiome and it could possibly lead to bacterial resistance. So these are all possible..the consequences of these genetic vaccines in my view, the shortcomings in this rollout of these vaccines were there was no genotoxic research performed at all. There was no safety studies, on carcinogenic potential of these vaccines. My personal opinion is that it's now not a question of whether, it will integrate in recipient's DNA, but how often it occurs... It's just a numbers game. If you do this in many cells, many persons it will no doubt integrate in cells in human recipients. So the question does it affect the human genome? I would say it probably, I think it most certainly does. And you see Kevin McKernan here and he represented ah a preliminary data where he detected a possible Pfizer DNA in colon cancer biopsy one year after vaccination.

aussie17

126,273 Aufrufe • vor 1 Jahr

Dr. Sucharit Bhakdi: A chilling revelation about the COVID-19 mRNA vaccines. According to Dr. Bhakdi, the experimental nature of the COVID-19 vaccinations was intentional from the very beginning. He cites a Robert Koch Institute protocol which allegedly stated that multiple vaccines would be developed and tested in a rapid process, indicating everything was pre-planned. He asserts that proper pre-market testing was impossible, pointing out that BioNTech does not even possess an experimental animal facility to conduct mandatory safety and efficacy studies. The clinical trials were therefore fundamentally inadequate. The damning proof, he notes, is in the official documents themselves: "Relevant data will only be raised post-marketing." This seven-word sentence admits that the global population was to be the test subject for collecting crucial safety data. Dr. Bhakdi highlights a peer-reviewed publication from the lab of MWGFD, revealing the vaccines are contaminated with bacterial DNA. This DNA is packaged alongside the mRNA and is efficiently absorbed into human cells. Within hours, our cells are hijacked to produce the foreign spike protein, and this production continues for days, potentially months. The uptake of this functioning foreign gene is, by definition, a genetic modification of the cell. His conclusion is stark: "The vaccinated have become genetically modified organisms." This unauthorized genetic alteration, conducted without informed consent on a global scale, is not just negligent. Dr. Bhakdi states unequivocally: "That's criminal. That's a capital crime." This was not a vaccination program. It was an unprecedented genetic experiment.

Camus

104,791 Aufrufe • vor 10 Monaten

It Wasn't Supposed To Be There, Let Alone Replicate: Bombshell Analysis of a Cancer Biopsy Reveals 'Shocking' Levels of Pfizer's Vaccine Sequence, Suggesting a Mechanism Far Different Than What Was Promised. In an interview with Sharyl Attkisson, Dr. Kevin McKernan, a seasoned expert in genomics, revealed a discovery concerning COVID-19 mRNA vaccines that warrants immediate and serious investigation. The Finding: Researchers analyzed tissue from a patient who developed an aggressive colon cancer and died just 30 days after diagnosis. This individual had received four doses of the Pfizer vaccine. Using advanced genomic sequencing, they went looking for a trace of the vaccine in the cancerous tissue. The Shock: Not only was the Pfizer vaccine sequence present, but the quantity was described as "a lot of it." As Dr. McKernan states, this was "not expected." The volume of genetic material suggests it did not just passively reside there; the data indicates it may have gotten into the cells and started replicating. The Critical Concern: While a direct causal link to cancer cannot be definitively established from this single case, the presence of replicating vaccine sequences in a tumor is profoundly concerning. Dr. McKernan explains that there are known biological mechanisms where this could play a role in oncogenesis (the formation of cancer). The Call to Action: This is where public awareness becomes crucial. Dr. McKernan's urgent message is that evidence is being lost. "Too many of these tumor biopsies are getting thrown away." If a family member develops an unexplained cancer, it is imperative to: 1. Get a pathologist involved. 2. Ensure a slide or tissue sample is preserved and retained for potential future study. This is not about spreading fear, but about preserving data. To understand if this is an isolated tragedy or a wider pattern, the scientific community needs samples to investigate. The answers lie in the tissue, and we must not let that evidence disappear.

Camus

112,276 Aufrufe • vor 9 Monaten

New Research Deep Dive: The "Shedding" Conversation Just Got More Serious A new in-vitro study (using human cells in a lab) on the Pfizer mRNA vaccine has revealed critical findings that can no longer be ignored. Let's break it down. The researchers confirmed two major things: 1️⃣ Spike Protein Production: The cells successfully took up the mRNA and began producing the SARS-CoV-2 spike protein, displaying it on their surface. This was expected. 2️⃣ Spike Protein "Shedding" via Exosomes: Here's the crucial part. The cells didn't just keep the spike protein to themselves. They packaged it into exosomes—tiny extracellular vesicles cells use to communicate—and excreted them into the environment. Why does this matter? This provides a potential mechanistic blueprint for how spike protein could travel systemically throughout the body after vaccination. These spike-laden exosomes can enter the bloodstream and, theoretically, deliver their cargo to distant organs and other cells. But the most alarming part? The authors note a profound lack of safety data. They explicitly state: We have no scientific studies to determine if this exosome-mediated spread of spike protein is toxic to other human cells. Even more concerning, they observed "pathological changes" and toxicity within the cells producing the spike. And these weren't weak cells—they were robust, immortalized embryonic kidney cells, chosen for their resilience. If these cells showed adverse effects, what is the impact on our more delicate primary cells? The authors themselves caution that proper toxicology studies on normal human cell lines are urgently needed... and are currently unavailable. This isn't conspiracy theory. This is cell biology. The conversation must evolve from if spike protein can travel, to what are the systemic consequences when it does. The call for rigorous, independent safety science has never been louder.

Camus

48,219 Aufrufe • vor 7 Monaten