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If a genetic sequence is injected that causes the body to manufacture a foreign protein, the body recognizes it as an invasion and launches an attack on cells. This autoimmune reaction can occur anywhere the injection lands, potentially causing myocarditis or a heart attack if it lands in the heart, stroke or neurological conditions if in the brain, blindness if in the eyes, or sterilization if in the ovaries. The body is being made to manufacture something that does not belong in it. The speaker believes the so-called vaccines encode spike proteins, which are acutely toxic to blood cells, prompting blood clots, and to nerve cells, causing them to malfunction. The body is forced to make something directly toxic, intentionally. The injectables are wrapped in lipid nanoparticles.

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.

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.

it's modified mRNA, and it's designed not to degrade, and there are studies that show it sticks around the body. We don't know how long. The lipid nanoparticle was designed to permeate difficult to permeate barriers, like the blood brain, like placenta barrier. Did you believe when Fauci told us that the mRNA shot would stay in the arm? In rats, it biodistributed all over the body, accumulated in the adrenal glands, in the ovaries. This encapsulated lipid nanoparticle distributes all over the body, and when it attaches to a cell, it unloads its mRNA into the cell and turns the cell into a manufacturing cell of a protein that is toxic to it. They're turning cells like a heart cell into a manufacturing site for the spike protein, which is toxic, the body attacks it. The designers of the injection knew it. And Anthony Fauci knew it, and he lied. DNA contamination ... McKernan study ... 36 to 627 times. The allowed amount is ten nanograms per dose. That saves three point two million lives. No. It didn't. It's impossible. That's entirely possible.

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.

The lipid nanoparticle in vaccines poses significant issues, particularly regarding cancer risks. While the spike protein is inflammatory, the real concern lies with the lipid nanoparticle's distribution. Instead of remaining localized at the injection site, these nanoparticles enter the bloodstream and spread throughout the body, leading to various health problems, including cardiac, neurological, and autoimmune issues. They can cross the blood-brain barrier and the placenta, causing complications in pregnant women and aggressive cancers in young adults, such as cholangiocarcinomas and breast cancers. The systemic distribution of these nanoparticles contributes to the delivery of genetic material to inappropriate sites in the body, exacerbating cancer risks and impacting the immune system.

The speaker claims mRNA injections have caused a "catastrophic" level of damage, citing excess deaths, permanent disabilities, and injuries. Worldwide deaths are estimated at around 17 million as of September 2023. In America, estimations for the first year of mRNA injection deaths range between 480,000 and 600,000, based on extrapolations from a recent preprint and VAERS data. The speaker asserts the shots are cardiotoxic and neurotoxic, linking them to myocarditis, cardiac arrests, coronary artery disease, and 86 neuropsychiatric adverse events. Vaccine spike protein has allegedly been found in the brains of stroke patients 17 months post-vaccination. The speaker states the shots induce blood clotting and damage the kidneys and gastrointestinal system. Furthermore, the speaker believes the shots are carcinogenic, with over 100 studies indicating 17 distinct mechanisms by which they may cause 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.

Before the emergency use authorization of the vaccines, significant concerns were already known. The Pfizer technical document revealed that these vaccines caused widespread distribution of the encoded protein in major tissues and were associated with inflammatory reactions due to lipid nanoparticles. It was understood that these nanoparticles could deliver RNA and DNA into cells, and the use of pseudo uridine was intended to enhance the immune response and prolong the product's effectiveness. However, critical investigations regarding potential shedding, reproductive toxicity, and the presence of contaminants were not conducted. These omissions are concerning, especially considering previous FDA regulations that recognized the risks of genotoxicity related to manufacturing processes.

We compared gene expression profiles across several groups: a healthy control group pre COVID, individuals described as mRNA injured, a group with cancer, and a few individuals who had neurological and cardiovascular adverse events. The analysis showed that in the mRNA injured group, thousands of gene expressions become dysfunctional in several key cellular pathways. Specifically, dysfunction was noted in mitochondrial function, immune function, and protein production. The changes included the production of abnormal proteins as a result of these altered gene expressions. In addition, the analysis reported that cancer surveillance genes were literally turned off in the mRNA injured group. The genes mentioned as turned off include p53, KRAS, and BRCA. This observation is presented as part of the overall pattern of molecular disruption associated with the mRNA injury state. Overall, the findings are described as indicating that flooding the body with synthetic messenger RNA unleashes biochemical havoc. The speaker emphasizes that this biochemical havoc has severe consequences, as evidenced by the observed widespread gene expression dysfunction and the suppression of critical cancer surveillance genes, alongside the production of abnormal proteins and impairments in mitochondrial, immune, and protein production pathways.

A cardiologist provides an update on the Pfizer and Moderna vaccines. Studies have shown that the vaccines can cause direct harm to heart muscle cells, abnormal heart contractions, and abnormal electrical activity. Messenger RNA from the vaccines has been found in the human heart and circulating in the blood for up to 28 days. The spike protein produced by the messenger RNA has also been detected in the blood for up to 6 months. The spike protein is dangerous to cells, tissues, and organs in the body. The messenger RNA used in the vaccines has been modified and is synthetic. Autopsy studies have shown that the vaccine can cause myocarditis and cardiac damage. A basketball player who received the vaccine suffered a cardiac arrest and died two years later.

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.

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.

Studies show that more people who received the injections are ending up in the hospital and dying. Repeat injections can lead to tolerance issues by the immune system, preventing an effective immune response. The speaker is concerned about the damages caused by these products and believes that the voices of the injured have been silenced. They suggest that the potential cytotoxicity of the spike protein should have been considered before proceeding. The exclusion criteria in the original trials excluded people with preexisting autoimmune conditions, which may be related to hyper inflammation. The speaker believes that the adverse events reported are a result of systemic damage caused by the spike protein. They also mention that the contents of the injection were expected to remain at the injection site, but evidence suggests that lipid nanoparticles can travel to the ovaries. The speaker suspects that there is information being withheld from the public.

The speaker clarifies they are injured by an mRNA therapeutic, not a vaccine, and highlights issues with lipid nanoparticles and synthetic mRNA, which can persist for hundreds of days. They claim that instructing cells to produce a protein that presents on the cell surface can trigger autoimmune disorders. The speaker states that the spike protein itself is biologically active, causing cells to grow and divide inappropriately, and was known to damage the placenta and lungs. They assert they knew early on that the shot didn't stay in the arm. They cite 2005 research showing the SARS-CoV-1 spike protein alone could harm animals. The speaker references 2015 gain-of-function research at UNC, NIH, and Wuhan labs, where a more lethal and transmissible SARS virus was created. A traditional vaccine attempt for this virus caused harm and lethality in animals, with pathology slides showing similar vascular lung damage seen with SARS-CoV-2. The speaker concludes that "they" knew about these risks but still rolled out the vaccine, profiting from it while falsely claiming it was safe and effective.

Technology was proven unsafe long before 2021. The COVID-19 vaccines contain lipid nanoparticles that carry synthetic DNA into various organs, risking genomic instability, cancers, autoimmune diseases, and hereditary disorders. Contamination levels are far above permissible limits, and we're seeing evidence in patients. Cancer-free patients are relapsing with aggressive cancers post-vaccination, including unusual and rapid tumor growth. There's a rise in blood cancers too. The vaccines also contained endotoxin, which causes shock and can lead to death. The lab-leak possibility was dismissed without investigation, leading to devastating lockdowns. The "safe and effective" mantra was a lie; these injections have caused unprecedented harm. Ethical principles were ignored, and informed consent was violated. These mRNA gene therapies shouldn't have been used on anyone. We must halt distribution, monitor cancer trends, develop testing, and research vaccine-related conditions.

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.

Speaker 0: I was fired after thirty one years as an emergency room physician with not one single patient complaint against me in those thirty one years. I was fired for saying that somebody who had natural immunity didn't need to be vaccinated against the disease to which they were already immune. Fortunately, I still had my medical license even though I lost a significant part, at least 50% of my income and I couldn't work as an emergency room doctor anymore, I still had my private practice. So when I discovered from the the biodistribution studies that Pfizer had hidden, that we knew that these vaccines go around your entire body, they do not just stay in your arm. Pfizer's biodistribution studies on the lipid nanoparticles show that they literally take those messenger RNA strands into every part of your body that go into your brain and your lungs and your heart and your liver and your reproductive organs and your bone marrow and everywhere, which is, by the way, why these COVID shots have caused a a greater array of side effects than any other medical treatment in history because this toxic spike protein ends up in literally every every

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.

Spike protein and multi-organ inflammation were detected in vaccinees, associated with severe illness. The discovery of contaminating plasmid DNA in the vaccines provides a possible explanation. Kevin McKernan found that the crucial step of removing plasmid DNA had not been properly done, and his work has been replicated. Cell uptake of plasmids alters DNA instructions, equating to genome alteration. Foreign DNA can become encased with chromosomes in newly formed nuclei. Continued production of non-self protein provokes long-term inflammation and organ damage, including heart damage and neurological/psychiatric issues. Vaccine-induced heart disease is increasingly common. Autoimmune diseases can develop in different organs simultaneously. Vaccines accumulate in reproductive organs, potentially impairing fertility. Placental damage may enable genes to enter fetal circulation. Stem cells in umbilical cord blood are reduced and impaired following vaccination. Breastfeeding may result in direct passage of vaccines into the baby's blood. Packaged DNA fragments found as vaccine contaminants can insert into chromosomal DNA, potentially leading to cancer, developmental defects, and inheritable mutations. Contamination of RNA vaccines with plasmid DNA must be expected.

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.

The speaker discusses the potential harms of lipid nanoparticles and synthetic RNA used in vaccines. They mention that the nanoparticles can accumulate in various organs, including the ovaries, bone marrow, spleen, and liver. The synthetic RNA can persist in the body for months. The spike protein, found in vaccines, is said to cause harm and can accumulate in the brain, peripheral nerves, and organs like the liver and heart. It can also lead to autoimmune diseases and reproductive issues. Studies have shown abnormal findings in PET scans and decreased sperm counts after vaccination. The speaker suggests that these potential harms should have been known before administering the vaccines.

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.

Pfizer knew a month into the rollout, November 2020, that this vaccine did not work to stop COVID. Everything that followed—the mandates, the lost jobs, the closures, children not allowed back to school if they didn’t take the shot, the armed forces compelled to take it, pilots compelled—was built on a lie of vaccine efficacy. The most common side effect of getting vaccinated is COVID, and Pfizer understood that the vaccine’s efficacy and vaccine failure showed it did not stop COVID. They also knew the injection did not stay in the deltoid. Europeans through the EMA and public health entities described side effects as chills, fever, fatigue, needing to lie down, but Pfizer knew that was a lie. In Pfizer documents, charts show that the materials—the spike protein, the mRNA, the lipid nanoparticles, and polyethylene glycol—biodistribute within forty-eight hours and leave the injection site to biodistribute to major organs throughout the body, crossing the blood-brain barrier. This may have contributed to personality changes in some loved ones who took the injection. They also accumulate in the liver, the adrenals, the spleen, the lymphatic system, and in women, the ovaries. The first injection accumulates in ovaries; the second injection more so. Experts could not find any mechanism whereby this material left the body in either gender. By the first booster, surgeries on vaccinated women reported fully blocked ovaries, among other damage. Pfizer knew that. They also hired 2,400 full-time staff to process reports of serious adverse events, starting to receive them during the 2020-2021 period. In Pfizer documents, over forty-two thousand serious adverse events were tallied from November 2020 to February 2021, with many individuals experiencing multiple events. The top documented side effects included myalgia (muscle pain), followed by joint pain, then COVID itself, and then a catastrophic tally of serious side effects including heart damage (myocarditis, pericarditis), problems with the aorta, thrombotic events (blood clots in various locations), neurological events (tremors, Guillain-Barré, dementia, epilepsy-like seizures), autoimmune disorders, and eye damage including blindness. Reproductive damage was noted: miscarriages and other issues. Twelve hundred deaths in three months were recorded as not statistically random; they were old with prior conditions, yet doctors noted causality concerns and recorded them. Pfizer knew by April 2021 that minors were injured by the vaccine, specifically myocarditis and pericarditis. Minors sustained heart damage, with thirty-five minors affected. The Israeli Ministry of Health warned the CDC and the Biden administration about minor heart damage, but FOIA requests later showed active conversations up to the White House regarding myocarditis in minors. Instead of withdrawing or advising parents, a 17-page document was produced as a script to persuade parents to vaccinate their minors, supplemented by a TikTok influencer campaign encouraging young people to get injected. These communications indicated that kids would sustain deadly heart damage, and still proceeded. Senator Ron Johnson is using the work to unredact those documents and hold hearings about the cover-up. Pfizer knew all of these things.