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Myocarditis, or heart damage, is more common than previously thought. Studies in the US military and Thailand show that around 20% of people who receive the COVID vaccine develop myocarditis, as confirmed by echocardiograms and other tests. This means that out of every 1 million vaccinated individuals, 200,000 will experience heart damage. Unfortunately, 50% of those with myocarditis will die within 5 years. This alarming increase in myocarditis cases is due to the cardiotoxic nature of the vaccine. This information comes from Dr. Cressel and Shoemaker in Toronto, Canada.

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.

Some batches of the vaccine may have serious side effects or be degraded. The batch number can be checked to see what to expect. Documentation shows that certain batches have more serious adverse effects. Even the best batches from Pfizer and Moderna had a high rate of serious adverse events in the short term, around 1800.

A recent study from Switzerland found that 1 in 35 people who received the Moderna booster shot experienced heart injury. Researchers hypothesized that many cases went unnoticed due to lack of symptoms. They tested for heart injury by measuring levels of cardiac troponin t in the blood, which indicates heart damage. This study aimed to uncover the true prevalence of vaccine-associated heart injury post mRNA booster vaccination.

The speaker discusses the individual and collective risks associated with a specific case of blindness after vaccination. While it cannot be ruled out that the vaccine may have played a role in the individual's blindness, there is no conclusive evidence to support this. However, when examining similar cases of temporary blindness associated with Moderna vaccinations, there were 78 cases, with 45 showing visual disturbances within 24-48 hours after vaccination, accompanied by fever, migraines, and headaches. The remaining cases involved temporary vision loss, but many had other risk factors that could contribute to these issues, making it difficult to establish a direct link to the vaccine. These observations are still being monitored, but currently, there is limited evidence to suggest a definitive connection between the vaccine and these cases.

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.

For biodistribution, Pfizer did not use the actual spike mRNA product in their studies. Instead, they substituted in a luciferase reporter mRNA packaged in the same lipid nanoparticles. This approach allowed them to track where the mRNA traveled in rodents. The studies showed that following intramuscular injection, most of the mRNA remained at the site of injection, but there was also notable levels detected in the liver. Despite the limitations of this approach, which can underestimate low level or transient distributions to other tissues, it nevertheless showed that the vaccine components do not remain confined to the injection site. Next slide. For Moderna, no dedicated biodistribution study was performed with the COVID mRNA itself. Instead, data was provided from a surrogate product, a CMV mRNA, mRNA-sixteen 47, which used the same lipid nanoparticle formulation. In their rat study, after intramuscular injections, high levels of the mRNA were detected at the injection site, but also in multiple organs such as the draining lymph nodes, spleen, eye, and liver. Lower levels were also found across a wide range of tissues, including the heart, lungs, testes, and brain. Importantly, this study clearly showed that the mRNA can cross the blood brain barrier. Next slide. Consistent with what is seen in animal studies, the vaccine mRNA and its spike protein have been detected in humans across multiple tissues, including blood, lymph nodes, the heart, and even the brain. These findings make it clear that the mRNA does not remain confined to the injection site. Importantly, persistence has been documented well beyond the initial hours or days, lasting weeks in some tissues, and in certain studies detectable for many months. Next slide. To summarize the biodistribution data, it's important to note that neither Moderna nor Pfizer used their actual commercial mRNA vaccine products in the preclinical biodistribution studies. Instead, they relied on surrogate construct packaged in same or similar lipid nanoparticles. Second, the results of those studies show that the mRNA and lipid nanoparticles were not confined to the injection site. Systemic distribution was observed with evidence that the mRNA can cross the blood brain barrier. Consistent with these findings, studies in humans have confirmed that vaccine mRNA can be detected in multiple tissues, including lymph nodes, the heart, the central nervous system, and blood. Finally, persistence is not just short term. In some reports, mRNA has been detected for weeks to months, and in certain cases as long as seven zero six days post vaccination. Taken together, these data highlight that biodistribution is broad and persistence is longer than initially expected, raising important questions and concerns for ongoing research and safety monitoring.

Pfizer's vaccine assessment showed biodistribution beyond the injection site, challenging claims it remains in the arm. A study using single-cell precision nanocarrier identification found LNP accumulation in mice heart tissue. This accumulation was associated with adverse proteomic changes in immune and vascular proteins. These findings raise concerns about cardiac complications, aligning with observations of COVID-19 vaccine myocarditis.

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 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.

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.

We tested different vaccines on blood slides to observe their effects. Pfizer caused immediate cell clearing, J&J led to cell clumping, and the cells became nonfunctional. The changes were rapid and significant, raising questions about the vaccines' impact on blood cells. More research is needed to understand these findings.

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.

mRNA vaccinated rats experienced a 60% reduction in primordial follicles, which are essential for life and do not regenerate. mRNA shots are allegedly getting into the ovaries, instructing them to produce toxic spike protein. The body attacks this protein, resulting in tissue damage and egg destruction. This follicle damage allegedly leads to 33% lower birth rates in vaccinated women, as seen in human data. This combination of factors is considered worrisome and demands attention from regulators. It is claimed that humanity's fertility is being run off a cliff.

Speaker 0: A brand new peer reviewed study from Switzerland reports that a staggering one in thirty five recipients of the Moderna booster shot experienced vaccine associated heart injury. One in thirty five people who took the shot experienced damage to the heart. The study unpacked the details starting with the hypothesis the researchers were trying to investigate. Going into the study, the researchers, quote, posited that the incidence of vaccine associated heart injury was more prevalent than previously thought following mRNA booster vaccination because of a lack of symptoms or mild symptoms. Essentially, their hypothesis going into the study was that after getting an mRNA booster shot, a lot more people were experiencing vaccine related heart damage than previously thought. And the reason for this was because people's hearts were getting damaged in a way where either there were no symptoms on the surface or the symptoms were mild enough for people to ignore. Meaning that the heart was actually injured, but the recipient of the booster shot was simply unaware. What these researchers did was that instead of just asking people how they felt after vaccination, they actually went in and they tested their blood. In terms of what they were testing for, quote, the researchers defined heart injury as a sharp increase in high sensitivity cardiac treponin T on the third day after vaccination without evidence of an alternative cause. The levels of cardiac treponin had to hit the upper limit of normal, 8.9 nanograms per liter in women and 15.5 nanograms per liter in men. The reason that these researchers decided to use what's known as a treponin test is because it is a very good indicator of whether or not there was damage to the heart. If a person has more of this protein called treponin T in the bloodstream, it means that recently they've experienced damage to the heart.

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.

Alden and colleagues found that Pfizer's genetic code can be integrated into the human genome within an hour in a cancerous cell line. This suggests that Pfizer and Moderna's genetic material might become a permanent part of human DNA. There is no study confirming or denying this possibility. The concern is that if eggs or sperm incorporate this genetic code, it could be passed on to future generations. This lack of research is seen as reckless and worrisome.

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.

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.

First, the mRNA is injected within lipid nanoparticles in your arm. It travels through every organ system, including the heart. Crosson found mRNA directly in the heart of deceased mRNA recipients. So we know it reaches the heart. Baumeyer found the spike protein directly in the heart in biopsies of patients with vaccine induced myocarditis. So we know the vaccine mRNA and lipid nanoparticles get into the heart, translate into spike proteins, so your cardiomyocytes begin to produce a toxic non human protein and your own body attacks the heart resulting in inflammation and cardiac scarring including micro scars which are undetectable with imaging. And so once you have this scarring, you're going to have cardiac electrical abnormalities, electrical conduction abnormalities, and your heart's not going to beat properly. And that's why we saw a lot of sudden deaths among athletes back in 2021.

Approximately 15% of people are injured by COVID-19 vaccines, with around 2.5% experiencing heart damage. The pharmaceutical industry suggests that not all vaccine vials are the same. It has been discovered that 80% of deaths from Pfizer vaccines come from 30% of the lots, while 80% of deaths from Moderna vaccines come from 20% of the lots. These lots may have varying concentrations of genetic material and contaminants, affecting their quality. This issue is currently receiving significant attention.

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.

COVID nineteen mRNA injections actually destroy eight point four percent of nonrenewable eye cells in just seventy five days. This was of sixty four healthy young adults who did receive Pfizer's mRNA injection, and they did find irreversible structural damage to the eye's corneal endothelium. The study found that endothelial cell density decreased by 8.4%. Cell size variation increased by 7.7%, which does indicate cell stress. Hexagonality, which means normal shaped cells, actually decreased by about 2% indicating structural distortions, and central corneal thickness increased by 2.8% indicating swelling and fluid imbalance. We have to remember that injury to this base layer of nonrenewable cells can lead to blurred vision, chronic swelling, and even blindness in severe cases. The harms of these shots just keep piling up.