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The Pfizer shot contains synthetic messenger RNA that stays in the body indefinitely, unable to be detoxed. It destroys toll-like receptors 3, 7, and 8, which are crucial for our immune system's defense against viruses and bacteria. This makes vaccinated individuals more susceptible to COVID-19. The spike protein from the shot enters the cell nucleus, binds to DNA, and blocks repair enzymes, potentially leading to cancer. There is evidence of an increase in cancer cases among vaccinated individuals. Multiple shots further weaken the immune system, with German data suggesting that by the end of 2022, fully vaccinated individuals over 30 may have immune suppression similar to AIDS.

Data accumulated to the point where meta-analysis studies could be done. These are very comprehensive analyses, and it virtually came back consistently that there was no benefit to risk ratio for taking a messenger RNA vaccine. In fact, it was more dangerous to take a vaccine than it was to contract COVID-19 and be hospitalized with it. This is we're now in 2022 that the status started to come out. The side effects for this essentially gene therapy were so enormous and progressive. It was difficult to fathom. And then finally, a few months ago, some of the detailed biochemistry studies started to appear in the literature. And this sudden flood of messenger RNA, it appears irrespective of what the messenger RNA insert is coding for. Just the sheer amount of number of millions of molecules of messenger RNA entering the cell is creating biochemical

The spike protein from various vaccines can bind to cancer-related genes, induce cancer pathways, and inhibit DNA repair. It can turn cells into spike factories, leading to immune system attacks and potential cancer development. Reports of increased cancers and harmful effects on organs have been observed. Military data was allegedly suppressed. This situation is seen as a crime against humanity.

A study comparing gene profiles of 800 healthy individuals to mRNA-injured individuals found severe genetic dysregulation in the latter. Seven of the injured individuals developed new-onset cancers within a year of mRNA injection, while three experienced cardiovascular or long vaccine syndrome. Gene expression comparisons revealed thousands of dysregulated gene expressions in the mRNA-injured, linked to mitochondrial failure and oncogenic activations. Cancer suppression genes were not being suppressed, and immune dysregulation was observed. The study claims to be the first to show long-term genetic disruptions in the vaccinated, indicating molecular chaos within cells. This may be the biological mechanism behind cardiovascular and carcinogenic issues seen in the vaccinated, possibly due to genomic integration of DNA plasmids from the manufacturing process. The speaker states that this is a landmark report and calls for further investigation into the effects on the population, noting that a large percentage of the global population received COVID vaccines.

These injections now, five years down the line, have been injected into over eighty percent of Americans, about seventy percent of the global population, and it has poisoned the vast majority of the world, their entire body. We actually looked at the genetic profiles of those who received mRNA injections and developed cancer or new onset adverse events, and we found that thousands of gene expressions were dysregulated, and the genes involved cancer control and cancer suppression genes. So those were being screwed up resulting in these cancers as well as immune collapse. And so, yeah, this was a biological attack on humanity.

The speaker claims SV40 in literature turns on cancer genes. They further claim the spike protein impairs tumor suppressor systems P53 and BRCA, promoting cancer and inhibiting the ability to fight it. The speaker suggests cancer rates are up, and the question is how much is due to vaccines. They state that repeated shots every six months increase the chances of getting loaded with synthetic genetic material that will cause harm, including heart disease, neurologic disease, blood clotting, immunologic problems, and cancer.

The spike protein may inhibit tumor suppressor genes like MHS 3p53 and BRCA2, potentially leading to cancer. The mRNA vaccine contains a base that allows the spike protein to be produced for longer, possibly further inhibiting tumor suppressor genes. Concerns are raised about the long-term effects of these vaccines, with a call for them to be banned for general use and reserved for gene therapy in advanced cancer cases.

COVID-19 vaccines, especially mRNA ones, may promote cancer through impairing DNA repair, inhibiting tumor suppressor systems like p53 and BRCA, and containing DNA impurities. These impurities include fragments from circular DNA used in the manufacturing process, such as SV40, a known proto-oncogene activator. The vaccines could potentially initiate or accelerate cancer growth by weakening natural tumor surveillance systems. This phenomenon is referred to as "turbo cancer."

- The mRNA on plasmids was produced, and after processing, much DNA from plasmids remained; Kevin MacKinnon found that vials were full of plasmid DNA, the whole plasmid and parts of it, and this was published. Authorities claimed it doesn’t matter and that vaccines have saved millions of lives, so why not have some DNA in them. - The DNA in the vaccine vials was packaged in lipid nanoparticles and was shown by colleagues last year (the INMODIA publication) to enter human cells in culture and remain stable in cells for days, as did the mRNA. Despite this, the message given was to poof, never mind, don’t worry, be happy. - A radical change occurred due to a discovery by Kevin MacKinnon three weeks ago: during transcription on the chromosome, byproducts are generated; some mRNA strands do not detach from the DNA where they’re formed, creating hybrids of DNA and RNA that come off together. These hybrids are dangerous. - In cells, an enzyme called RNase H takes care of these sparks and extinguishes them immediately; otherwise they can cause damage to the chromosome, potentially lighting “fires” on the chromosomes. If not extinguished, the fires can cause diverse damage depending on where they occur, potentially leading to illnesses described in medical textbooks, including tumors (neoplastic disease), autoimmune disease, developmental impairment, birth defects, or death. - The speaker asserts these hybrids and their mishandling could lead to a broad range of illnesses, and emphasizes that this situation is not limited to the COVID vaccine but applies to all Moderna RNA vaccines, including new Moderna RNA vaccines entering the market, such as a flu vaccine, and mentions veterinary RNA vaccines as well. - The claim is made that these vaccines will be heavily contaminated with deadly dangerous hybrids, and it is the duty of authorities and controlling authorities to stop proceeding and not turn away; otherwise they will face court for not fulfilling their duties. The speaker has been giving interviews and asserts this narrative is spreading worldwide, framing it as akin to attempted murder and urging physicians to refuse vaccination.

Speaker 1 reports evidence from multiple sources, including InModia lab in Germany and John Cantazaro at NEO7 Bioscience, that Pfizer and Moderna code is reverse transcribed and inserted into human DNA. According to Speaker 1, this means individuals could carry a "stamp" of Pfizer or Moderna in their genome. The speaker suggests the body may not be editing out or repressing this code, as spike protein evidence persists for years. Transmission of spike protein producing genetic code is possible, along with fragments of code for the spike protein, SV40, and other DNA fragments. Speaker 1 raises concerns about potential health issues like blood clots, heart damage, autoimmunity, and unusual tumors. John Cantazaro's research indicates a dramatically altered genetic profile in vaccinated individuals, tilting towards neoplasm or cancer. Speaker 1 shares an anecdote about a patient who developed terminal cancer after vaccination, with Cantazaro confirming the presence of Pfizer code in the patient's genome.

The speaker describes a cascade of harms from mRNA injections, asserting that different individuals experience a variety of issues because the injections initiate chaos at the transcriptomic level. A recent study is cited as proof, noting that the process regulates thousands of gene expressions that are critical for immune regulation and mitochondrial function, and it purportedly invokes cancerous activity by suppressing tumor suppressor genes p53 and BRCA. The speaker says this occurs at the transcriptomic level, and references another study from the prior week that shows proteomically that the proteins produced from the dysregulated transcription are defective, contributing to a range of issues. Moving up to the next tier in the cascade, the speaker describes biochemical changes following injection. After vaccination, there are elevated inflammatory markers such as CRP, and increases in BNP and various cardiac enzymes, which are presented as indications of cardiac damage. The implication is that these biochemical changes reflect downstream harms. At the final tier, the speaker connects these molecular and biochemical disturbances to clinical outcomes. The claimed clinical harms include myocarditis, clotting syndrome, strokes, and cancers. The overall narrative is that the mRNA injections initiate a multi-tier cascade—from transcriptomic disruptions affecting gene regulation, immune function, and mitochondrial activity, through proteomic consequences with defective proteins, to biochemical signals of inflammation and cardiac injury, culminating in a range of clinical conditions. The speaker emphasizes that the referenced studies are either recent or in progress. One study is described as having been “proved” and is on the preprint server undergoing peer review, while another study is noted as having appeared “last week,” illustrating the progression from transcriptomic changes to proteomic outcomes. The sequence of claims is structured as a tiered pathway—transcriptomic, proteomic, biochemical, and clinical—culminating in diverse harms observed in some vaccinated individuals, with the assertion that the effects vary by person due to the initial chaotic molecular changes. The clinical spectrum listed includes myocarditis, clotting syndrome, strokes, and cancers, linked to the preceding molecular and biochemical alterations.

The speaker describes the first peer-reviewed paper documenting evidence of genomic integration of mRNA vaccine genetic material in a human being. They report a case of a 31-year-old woman who developed stage four bladder cancer within a year after three mRNA shots. They say they analyzed her circulating tumor DNA and performed multiomic analysis, including transcriptomic and proteomic analysis. They report finding, “within her chromosome 19,” in the circulating tumor DNA, a 20 base pair segment matching the Pfizer DNA plasmid reference sequence. The speaker characterizes the finding as a “non human non human chimeric hybrid,” stating it transitions from human to Pfizer to human. They add that there is “about a one in a trillion chance this was just an anomaly.”

A new study indicates mRNA injections induce severe, long-lasting genetic disruption linked to cancer and chronic disease. Comparing gene profiles of mRNA-injured individuals to pre-COVID samples revealed thousands of dysregulated gene expressions linked to mitochondrial failure, suppressed cancer suppression genes, and immune dysregulation. Molecular chaos may result in cardiovascular, neurological, and carcinogenic issues, possibly due to genomic integration of DNA plasmids. A separate study showed mRNA boosters trigger dangerous immune and blood abnormalities, including increased blood clotting and immune suppression, within 48 hours in healthy young adults. Additionally, pets are being used as self-amplifying mRNA vectors via Merck's Nobivac NXT, exposing pet owners to shedding of self-amplifying RNA and toxic antigens. This could potentially cause long-term genetic dysfunction in humans, with the possibility of the synthetic particle recombining with wild viruses. Individuals should ask vets about RNA or mRNA injections for pets and refuse mRNA injections for themselves.

The speakers describe a study in which gene expression profiles are compared across several groups to assess the impact of mRNA injury. The comparison set includes a healthy control group that was observed before the COVID-19 era, individuals classified as mRNA injured, a subset of three individuals with cancer, and a smaller number of participants who exhibited neurological and cardiovascular adverse events. The central finding reported is that, in the mRNA-injured group, thousands of gene expressions become dysfunctional. The dysfunction spans several critical cellular and biological processes, notably mitochondrial function, immune function, and protein production. The speakers indicate that these alterations include the production of abnormal proteins as a consequence of the disrupted gene expression patterns. In addition to widespread dysfunction in metabolic and cellular pathways, the speakers note that genes involved in cancer surveillance are turned off in the mRNA-injured group. Specific genes named are p53, KRAS, and BRCA, with their expression or regulatory activity described as being suppressed or deactivated. The implication conveyed is that the disruption of cancer surveillance mechanisms accompanies the broader profile of gene expression changes observed in response to the mRNA injury. The overall conclusion presented by the speakers is that flooding the body with synthetic messenger RNA is associated with unleashing biochemical havoc, which they characterize as having severe consequences. The framing suggests a causal or strongly associative link between exposure to synthetic mRNA and the observed downstream effects on gene expression, including mitochondrial and immune dysfunction, abnormal protein production, and the suppression of key cancer-related surveillance genes. The narrative emphasizes the magnitude of the molecular disturbances, noting that thousands of gene expressions become dysfunctional and that critical safeguards against cancer may be compromised in the mRNA-injured group.

The spike protein found in various COVID-19 vaccines, such as J&J, AstraZeneca, Moderna, and Pfizer, is considered toxic. It binds to genes associated with cancer, like p53, BRCA1, and BRCA2. This spike protein has been linked to an increase in cancers, particularly lymphomas, leukemias, and blood cancers, as it affects the bone marrow. The mRNA in the vaccines can enter any cell in the body, turning it into a spike protein factory. This disrupts DNA repair, affects mitochondria, and depletes energy in brain, liver, and other cells. The immune system attacks these spike protein-expressing cells, causing pain and inflammation. The evidence of these harmful effects has been observed in labs and confirmed by medical professionals worldwide. The suppression of data by the Department of Defense is seen as a crime against humanity, as these vaccines harm human cells, organs, hormones, and reproductive systems.

"you were two to four times more likely to suffer serious harm from taking the COVID vaccine than you were to be hospitalized with COVID." "what is more better described as a gene therapy than as a vaccine." "$500,000,000 worth of investments in the mRNA technology for vaccines." "mega analysis of all the data." "Hundreds of studies, peer reviewed studies showing the harms of the mRNA vaccine." "the side effects of this gene therapy was so enormous and progressive, it was difficult to fathom." "The millions of molecules of mRNA entering the cell is creating biochemical havoc." "It's disrupting protein metabolism." "It's interfering with tumor suppressor genes." "In other words, it may be a risk factor for cancer." "it's highly likely that the COVID vaccines have been a factor, a significant factor in the cancer of members of the royal family."

Lipid nanoparticles, not intended for human or veterinary use, were administered to billions of people worldwide. Synthetic RNA from the vaccines persisted for months in the body. The spike protein, found in the brain, peripheral nerves, and organs, caused damage and autoimmune diseases. Spike protein accumulation was also observed in the heart, renal glands, and elastic fibers of the skin. Reproductive harms, such as placental and testicular damage, were reported. The spike protein affected the body's ability to react to other infections and weakened the immune system. It caused damage to blood vessels, including small and large vessels, and led to coronary events and abnormal protein accumulation. The immune system was blinded, leading to a decrease in tumor surveillance and tolerance to pathogens. The video also mentioned the potential impact on cancer.

A scientist reports an increase in cancer cases worldwide after the rollout of experimental injections. CDC data confirms this trend, with a significant increase in cancer cases. The spike protein in these injections binds to the p53 gene, leading to cancer pathways opening up. There are numerous harmful effects caused by the spike protein, and the scientist is concerned about the lack of long-term safety studies for these products. The lipid nanoparticles in Pfizer and Moderna vaccines, not intended for human or veterinary use, have been administered to over 5 billion people. The J&J vaccine, containing a carcinogenic substance, was quietly pulled from the market. The NIH is withholding information on cancer pathways and forced the retraction of a scientific paper. These injections also affect the immune system's ability to function properly, impacting cancer prevention. The scientist apologizes for those who received these injections without informed consent and urges action at the local level to stop further harm.

The spike and pseudouridine in the shots are changing receptor patterns on cells, suppressing the immune system's ability to fight off viruses like herpes, HPV, and RSV. Toll-like receptors, which train cells to fight cancer, are also being suppressed. These receptors are like the marines of our immune system, constantly circulating and identifying friend or foe. However, the shots are causing these marines, along with dendritic cells and macrophages, to become inactive, leaving the body defenseless against cancer cells and pathogens. It is unclear when this suppression stops or how to reverse it. While not affecting everyone, the degree to which it is happening is concerning.

The spike protein found in various COVID-19 vaccines, such as J&J, AstraZeneca, Moderna, and Pfizer, has been shown to bind to tumor suppressor genes and cancer-related genes, potentially leading to the activation of cancer pathways. This spike protein can affect the bone marrow and other cells in the body, inhibiting DNA repair and damaging mitochondria, resulting in various health issues like arthritic and muscle pain. The immune system may attack cells expressing the spike protein, causing further complications. The suppression and concealment of data by the Department of Defense regarding these effects is considered a crime against humanity. The use of these vaccines is believed to harm human cells, the body, hormones, and reproductive organs.

Speaker 1 explains cancer is usually a mutation, and the immune system surveils with 30,000,000 T cells. After vaccination there is suppression of many cell lines. The mRNA shot uses pseudouridine in a lipid nanoparticle to evade the immune system, and it can "hijack your cells, and makes your cells the spike factory." The spike "breaks off of the surface of your cell and goes into circulation." Pseudouridine can cause decrease in certain protein kinase pathways and certain retinoic acid receptor pathways, many things that are responsible for normal cell function and then can lead to mutagenesis as well. Stanford study by Doctor Woltkin et al shows "up to sixty days later, the synthetic mRNA is still in lymph nodes and spike is still circulating." Toll-like receptors downregulated: seven, eight, three, four; Dr. Fossa notes downregulation linked to multiple cancers. Micro RNA array disruption and G protein disruptions are mentioned.

The speaker believes vaccines are causing cancer, with the risk increasing exponentially with each booster, because boosters suppress T cell response, which controls cancer. Experts claim messenger RNA is safe because we are exposed to it daily and it's easily disposed of, but the speaker argues that mRNA vaccines are stabilized to prevent disposal, which is the core problem. The speaker claims that mRNA can integrate and hack your genetic code, promoting oncogenes and down-regulating suppressor genes. They state that the UK and Australia have invested heavily in mRNA technology without proper oversight. The speaker advocates for ending this culture and improving population health.

The discussion reports a comparative analysis of gene expression profiles among four groups: a healthy control group pre-COVID, individuals who were injured by mRNA, and subgroups including three individuals with cancer and a few with neurological and cardiovascular adverse events. The study found that in the mRNA injured group, thousands of gene expressions become dysfunctional, affecting mitochondrial function, immune function, and protein production, leading to the creation of abnormal proteins. It also notes that cancer surveillance genes are literally turned off, specifically mentioning p53 and KRAS, as well as BRCA. The overall claim is that flooding the body with synthetic messenger RNA unleashes biochemical havoc, with severe consequences.

Lipid nanoparticles, not intended for human or veterinary use, were administered to billions of people worldwide. Synthetic RNA and spike proteins from the vaccines were found to persist in the body for months, accumulating in the brain, peripheral nerves, liver, and other organs. Autoimmune diseases, myocarditis, renal gland damage, and reproductive harms were also observed. The spike protein affected the immune system, weakened the body's response to other infections, and caused damage to blood vessels, including the coronary vessels. It also led to the accumulation of abnormal proteins in the blood and impaired tumor surveillance. The potential impact on cancer was highlighted as a significant concern.

"What happened is that the data had accumulated to the point where meta analysis studies could be done." "And it virtually came back consistently that there was no benefit to risk ratio for taking a messenger RNA vaccine." "In fact, it was more dangerous to take a vaccine than it was to contract COVID nineteen and be hospitalized with it." "The side effects for this essentially gene therapy was so enormous and progressive, it was difficult to fathom." "Just the sheer amount of number of millions of molecules of messenger RNA entering the cell is creating biochemical havoc." "It's disrupting protein metabolism." "It's interfering with tumor suppressor genes." "It's just completely it's damaging the mitochondria, the powerhouses of the cell." "It's it had to be stopped."