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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.

The injections target the immune system, causing damage and acting as multi-warheads designed to injure or kill people immediately, intermittently, or in the long run, potentially causing cancer. Turbo cancer occurs in people who already had cancer. The injections destroy the immune system, allowing existing cancers to progress rapidly. It takes a long time for cancer to progress and do damage because the immune system eliminates many aneuploidy cells. Cancers cannot develop quickly unless in cell culture with SV40 and no immune system. The speaker suspected, and it turned out to be true, that the injections were destroying the immune system, revealing undiagnosed cancers. Most people getting cancer suddenly and dying likely already had it. Severely disabling the immune system allows these pre-existing conditions to proliferate.

The speaker describes a nationwide study conducted in South Korea, stating that every resident was included in the research. The study compared individuals who received the vaccine to those who did not, and the analysis was stratified by dose number (one dose, two doses, three doses, and four or more doses). A central claim of the speaker is that this study provides the strongest signal to date supporting vaccine acquired immunodeficiency syndrome, referred to as VADES. According to the speaker, as each dose was administered, the immune function of individuals declined. By the time of the fourth dose, the speaker asserts there was a significant increase in the risk of other infections, quantified as about a 550% increase, including infections such as the common cold, tuberculosis, and upper respiratory tract infections. The speaker notes that the effect was most pronounced in young people, specifically ages zero to nineteen, who reportedly had the highest risks of these other infections. The implication presented is that the injections are causing immune collapse and exhausting T cells, leading to immune dysregulation described as IgG4 class switching. The immune system is said to become dysfunctional as a result. Additionally, the speaker mentions that, consistent with other studies they reference, genes related to immune function are claimed to become shut down. The overall assertion is that these findings point to a troubling pattern of immune impairment associated with multiple vaccine doses, culminating in the claimed immune dysfunction and increased susceptibility to other infections. The speaker emphasizes the magnitude and reliability of the sample size, stating that having an entire country’s population as the study cohort constitutes the strongest possible sample size. The summary of the presented claims centers on dose-dependent immune decline, a marked increase in non-target infections after the fourth dose, greater impact on children, evidence of immune system exhaustion and dysregulation, and purported genetic downregulation of immune pathways, all described as arising from the vaccination regimen in this nationwide South Korean study.

Kevin McKernan recently discovered that there is contamination in the mRNA shots with cDNA, including a cancer-promoting segment called SV40. SV40 turns on cancer genes in the human body and impairs tumor suppressor systems. This means that the shots not only promote cancer through SV40 but also inhibit our ability to fight cancer. The increase in cancer rates is undeniable, but the question remains: how much of this is due to the vaccines?

The speaker discusses how the spike protein in vaccines can lead to clotting issues, immune suppression, and reactivation of latent viruses like mono. This can also weaken the body's ability to fight off other viruses and cancers. An increase in cancer cases post-vaccination is noted anecdotally. The speaker attributes these effects to the spike protein in the vaccines.

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.

We all carry dormant cancers and tumors to varying degrees. The innate immune system's destruction allows these dormant tumors to become active. Once the immune system is compromised, existing weak cancer cells can proliferate unchecked, similar to antibiotic-resistant bacteria. Each cancer cell is unique, and in a weakened immune environment, those that can survive will thrive rapidly. The immune system's complexity is immense, and its overall functionality is being diminished. Notably, IgG4 levels have surged significantly in those exposed to certain injections, which may suppress the immune response to cancer cells. While the details are complex, the general principles indicate that these changes could hinder the immune system's ability to combat cancer effectively.

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 Pfizer vaccine uses synthetic messenger RNA that replicates indefinitely in cells, making it impossible to detoxify from it. This mRNA damages toll-like receptors 3, 7, and 8, which are crucial for the innate immune response, increasing susceptibility to infections like COVID. Consequently, vaccinated individuals are more likely to become ill and face higher hospitalization rates. The spike protein can bind to DNA, potentially leading to abnormal cell growth and cancer, which explains the rise in various cancers among vaccinated individuals. Recent data indicates that vaccinated people are significantly more likely to contract omicron, and ongoing vaccinations may lead to severe immune suppression, comparable to AIDS, particularly in those over 30.

The speakers discuss how initial kidney cells from monkeys used to make vaccines inadvertently gave people simian virus 40, which can lead to rapid cancer. One speaker says that this is one of the cancer-causing issues with the shots, explaining that it's supposed to stay out of the nucleus but can get in. One speaker says the initial claim was that the shot would stay local, in the arm, and dissipate quickly, but "they know that's not true." The other speaker mentions pseudouridine, a replacement nucleotide that is hard to break down, and that there's no study showing that it can be cleared from the body. This could be why some people have high antibody levels years later.

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.

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.

There are concerns that the COVID-19 vaccines may have a potential link to cancer. The spike protein in the vaccines could inhibit tumor suppressor systems in the body. Additionally, the vaccines may impair natural DNA repair mechanisms, increasing the risk of DNA damage. Contamination has also been found in Pfizer vials, which could lead to a direct DNA injection and activation of cancer-related genes. This multi-hit hypothesis suggests that repeated vaccination could promote cancer development. There have been clinical observations of rapid cancer progression and reactivation of cancers in remission after vaccination. However, no agency has confirmed a direct link between vaccines and cancer.

Many people have received COVID shots for various reasons, but there are significant concerns regarding their safety. Reports indicate rising cases of autoimmune diseases, heart inflammation, and neurological issues, including cancer. The lipid nanoparticle mRNA technology used in these vaccines has not proven to be safe long-term. Studies show these shots can suppress the immune system, particularly affecting T cells, which are crucial for fighting infections and cancer. This immune suppression may contribute to the emergence of more aggressive cancers, termed "turbo cancers," as observed by pathologists. Data from insurance and disability datasets reveal alarming increases in cancer cases following the vaccine rollout, raising serious concerns about public health.

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 Pfizer shot contains synthetic messenger RNA that stays in the body and cannot 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 getting COVID-19. The spike protein from the shot enters the cell nucleus, binds to DNA, and can cause abnormal cell replication leading to cancer. People who have received the shot are experiencing an increase in various types of cancer. Recent data shows that those who are vaccinated are 8.12 times more likely to be infected with the Omicron variant. The more shots received, the more the immune system is suppressed, potentially leading to vaccine-induced immune suppressed AIDS. This information is based on government data from Germany.

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.

People who have received the shots are experiencing immune deficiency problems. It's not HIV-induced AIDS, but rather a result of the shot damaging their immune system. This leads to a spike in cancers, autoimmune diseases, opportunistic infections, blood clots, heart attacks, strokes, myocarditis, miscarriages, ovarian and testicular dysfunction, likely infertility, and antibody-dependent enhancement.

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.

The first vaccine decreases white blood cell production by 50%. The second dose, given eight weeks later, decreases saline while increasing harmful ingredients, further attacking white blood cell production by another 25%, leaving only 25% functionality. The booster contains 81 strands of foreign bacteria that the body can't fight effectively due to the reduced white blood cell production, leading to chronic inflammation in areas of predisposition, such as gut health, respiratory issues, or pre-existing conditions. This puts the body in a constant state of fight or flight with low immunity. The second booster contains eight strands of HIV, which shuts off the ability to make white blood cells, mirroring the effects of the disease itself. People are left with no immune system, foreign bacteria, HIV strains, and other harmful ingredients.

The speaker explains that the messenger RNA in the shots is contaminated with cDNA, including a cancer-promoting segment called s v 40. They mention that s v 40 turns on cancer genes in the human body and that the spike protein in the shots impairs tumor suppressor systems. The speaker suggests that the shots promote cancer through s v 40 and inhibit our ability to fight cancer. They also mention that cancer rates are increasing. The speaker raises the question of how much of this is due to the vaccines.