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A cardiologist provides an update on the Pfizer and Moderna vaccines, highlighting concerning findings. Studies on heart muscle cells from rats showed abnormal contractions and electrical activity within 48 hours of exposure to the vaccines. Messenger RNA from the vaccines was found in the human heart and circulating in the blood for up to 28 days. Circulating spike protein, produced by the messenger RNA, was detected in half of vaccinated individuals for up to 6 months. The spike protein is known to be harmful to cells and organs. The messenger RNA used in the vaccines has been modified and has numerous patents. Autopsy studies suggest that a significant number of deaths may be attributed to the vaccines. A case of a basketball player who suffered cardiac arrest after vaccination is highlighted as a cause for concern.

First, the mRNA is injected within lipid nanoparticles in your arm. It travels through every organ system, including the heart. There are two papers, one by Baumeyer and colleagues, one by Crosson and colleagues. 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. You can only detect it with a microscope, which is very disturbing. 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. Then when you go exercise, we found there's two triggers either during exercise or sports when there's exertion or during the morning waking hours of sleep. In these two periods of time, there's a surge in catecholamines including dopamine, norepinephrine, and epinephrine. And so during these times when you have this cardiac damage, you have this scarring, that's the trigger you do that leads to this vaccine induced cardiac arrest. And that's why we saw a lot of sudden deaths among athletes back in 2021.

Speaker 1 discusses the progression of understanding around heart damage associated with this product, emphasizing key studies and their implications. He recalls that in 2022 German scientists tested and reported that heart damage seen in myocarditis patients corresponds to vaccine-triggered autoimmune reactions. They examined endomyocardial biopsies and observed that the cardiac detection of the spike protein and CD4+ T cell–dominated inflammation suggested a vaccine-triggered autoimmune process. He notes headlines that infections could cause more myocarditis than vaccination and cites a large Israeli population study from that year finding no increase in myocarditis or pericarditis among unvaccinated individuals, challenging the notion that vaccination is the sole driver. Speaker 1 then highlights a new study published in the American Heart Association journal Circulation, framing it as a major development not from fringe sources but from a prestigious, mainstream journal. He asserts that this study goes beyond epidemiology by demonstrating a mechanism. In an experimental model, mice were used to induce myocarditis-like cardiac damage; researchers then compared these findings to humans who had similar heart damage post-vaccination. They found that T cells from patients with acute myopericarditis recognize vaccine-encoded spike epitopes that are homologous to cardiac self proteins, indicating cross-reactivity where the immune system targets both the spike protein and cardiac proteins. Speaker 1 explains that the study measured functional responses to potassium channels (KV) and observed an expanded pattern of cytokine production in patients with mild pericarditis after mRNA vaccination, but not in patients with COVID-19 without vaccination. This expanded cytokine response mirrored what was seen in AMP (myopericarditis) mice and in autoimmune myocarditis, linking the clinical data with the animal model. He paraphrases the study’s plain-language takeaway: post-mRNA vaccine myopericarditis is driven by molecular mimicry, with the immune system failing to distinguish self from non-self in susceptible patients. The study further notes that vaccine distribution contributes to susceptibility; the widespread distribution of the vaccine allows the heart to be targeted, leading to cardiac-selective autoimmunity by “heart-homing imprinting.” Speaker 1 emphasizes the significance of the source, stating that the journal is not fringe: it is the Circulation journal, ranked third in its field with a cardiovascular-focused impact in the 99th percentile. The overall conclusion presented is that these findings provide a clear mechanism for post-vaccination myopericarditis and establish a direct link between vaccine-encoded spike epitopes and cardiac autoimmunity.

The discussion centers on new evidence regarding myocarditis and pericarditis in the context of mRNA vaccination. It cites earlier 2022 German research showing that heart damage seen in myocarditis cases after vaccination may be a vaccine-triggered autoimmune reaction. The study analyzed endomyocardial biopsy samples and found that the cardiac tissue’s spike protein detection and CD4+ T cell–dominated inflammation suggested an autoimmune mechanism linking the vaccine to heart damage. This was contrasted with an Israel-based population study of hundreds of thousands of unvaccinated individuals that reported no increase in myocarditis or pericarditis incidence, highlighting a discrepancy with the vaccine-triggered autoimmune hypothesis. The center of the new claim is a study published in Circulation by the American Heart Association. The speakers emphasize the credibility of Circulation as a top cardiovascular journal. The study used an experimental mouse model to induce cardiac damage and then examined humans with similar heart damage after vaccination to see if the same mechanism applied. They report that T cells from patients with acute myopericarditis recognize vaccine-encoded spike epitopes that are homologous to cardiac self-proteins. In other words, the immune cells targeting the spike protein may also attack cardiac proteins due to molecular similarity. Further details from the study indicate that, in patients with mild pericarditis after mRNA vaccination (but not in those with COVID-19), there was an expanded pattern of cytokine production similar to that observed in myopericarditis–affected mice and in autoimmune myocarditis. The takeaway provided in plain language is that post-mRNA vaccine myopericarditis is driven by molecular mimicry, causing the immune system to fail to distinguish self from non-self in susceptible patients. The susceptibility is described as being influenced by the widespread distribution of the vaccine, which purportedly leads to heart-homing imprinting and a heart-targeted autoimmune response. The speakers stress that this journal is not fringe and highlight its high impact in cardiovascular medicine. They conclude that the data collectively suggest a mechanism by which the vaccine could provoke cardiac autoimmunity, with implications for clinical communication and understanding of post-vaccination myocarditis.

A recent study suggests a potential link between mRNA COVID-19 vaccines and sudden cardiac deaths. Researchers found that when Pfizer and Moderna vaccines were applied directly to heart muscle cells, abnormal function and electrical currents occurred within 48 hours, indicating cardiac toxicity. Another study showed that mRNA was physically stuck in the hearts of individuals who died after vaccination. Additionally, a large study found abnormal heart scans in those who received the vaccine, with virtually everyone showing abnormal results. Even individuals with inflammation or higher mRNA doses had worse cardiac findings. This suggests the possibility of cardiac dysfunction or arrest without myocarditis. The information challenges the official narrative and raises concerns.

The discussion centers on evidence linking myocarditis and pericarditis to mRNA vaccination and the proposed mechanism behind it. It references a 2022 German study reporting that endomyocardial biopsy data from people with myocarditis showed cardiac detection of the spike protein and CD4+ T cell–dominated inflammation, suggesting a vaccine-triggered autoimmune reaction. The presenters note headlines at the time comparing myocarditis risk to infection, with claims that infection causes more myocarditis, and remind that vaccines were said not to stop transmission. They then cite a large Israeli population study from the same year involving subjects not vaccinated against SARS-CoV-2, which found no increase in the incidence of myocarditis or pericarditis, implying no observed vaccine-related signal in that cohort. Attention shifts to a more recent study published in Circulation by the American Heart Association, described as a high-impact, non-fringe journal, indicating a clearer mechanism has been demonstrated. The study described used an experimental mouse model to induce cardiac damage and then compared it to human cases with heart damage following vaccination. It states that T cells from patients with acute myocarditis or myopericarditis recognize vaccine-encoded spike epitopes that are homologous to cardiac self proteins, meaning the immune response to the spike protein can cross-react with heart tissues. The researchers further report that functional responses to potassium channels in patients with mild pericarditis after mRNA vaccination, but not in patients with COVID-19, showed an expanded pattern of cytokine production similar to that observed in myopericarditis mice and in autoimmune myocarditis. In plain terms, the summary of their takeaway is that post-mRNA vaccine myopericarditis is driven by molecular mimicry: the immune system cannot distinguish self from non-self, leading to an autoimmune attack on heart tissue in susceptible patients. The distribution of the vaccine (its widespread dissemination) is cited as a factor that makes patients susceptible by promoting heart-homing imprinting, effectively creating an anti-heart autoimmune response. The speakers emphasize that this Circulation article is a top-tier source, underscoring that the mechanism has been demonstrated with both animal models and human pathology, supporting the claim that the phenomenon has a defined immunological basis.

The speaker discusses a significant increase in myocarditis cases post-vaccination, with studies showing abnormal cardiac scans in vaccinated individuals. They suggest a potential link between mRNA vaccines and heart inflammation, emphasizing the need for long-term monitoring. Research indicates that mRNA and spike proteins can cause myocarditis, posing a concern for all mRNA products. The heart appears to be a vulnerable target due to various factors.

There is a causal link between vaccination and both myocarditis and pericarditis. The reason for this is still unclear. It may be that the SARS CoV-2 spike protein mimics a protein found on heart muscle cells. If that's the case, when you create an immune response to the SARS CoV-2 spike protein, you could also inadvertently create an immune response to your own heart muscle.

Heart inflammation, indicated by blue arrows, occurs after receiving a shot due to the presence of ACE2 receptors in the heart. This inflammation is caused by spike proteins from the shot, leading to the immune system attacking the heart tissues. The pericardium, the heart's surrounding sac, also experiences inflammation, as shown by the red arrows. Unfortunately, the heart cannot heal itself once damaged. The presence of blue dots signifies inflammation, while the gray area in the middle represents early scarring.

The speaker confirms that earlier discussions on COVID vaccines mentioned that the nanoparticles remained near the injection site before leaving the body. However, documents released in court revealed that Pfizer knew that lipid nanoparticles not only collected at the injection site but also in various organs such as the adrenal glands, ovaries, liver, kidneys, and brain. The speaker clarifies that the studies showed the presence of a fluorescent label, not necessarily the lipid nanoparticles themselves.

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.

Since the pandemic began, I have aimed to provide objective scientific insights as a publicly funded servant. Regarding concerns about heart inflammation linked to COVID-19 vaccines, I acknowledge the potential connection based on extensive scientific literature and reports from Pfizer to regulatory agencies. Traditional vaccine technology suggests that vaccines remain at the injection site, but this does not apply to mRNA vaccines, which disperse throughout the body. Research shows that only about 25% of the vaccine dose stays in the shoulder. Polyethylene glycol, a component of the vaccine, enhances this distribution, allowing lipid nanoparticles to evade immune cells that would normally capture the antigen for immune activation.

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.

In a deceased patient, spike protein was found in the heart but not nucleocapsid protein. The autopsy revealed bronchopneumonia, Parkinson's disease, necrotic encephalitis, and myocarditis. The author suggests that the spike protein in affected tissues was likely from gene-based COVID-19 vaccines, not a SARS CoV-2 infection, as nucleocapsid protein was absent. Spike protein was found in areas with brain and heart inflammation, possibly contributing to the disease.

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.

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

"Unfortunately, the mRNA platform, though it is brilliant in its conception, is fatally flawed." "the myocarditis and pericarditis that showed up as a result of COVID vaccinations are inherent to the platform, not to the messenger RNA that was delivered inside these shots." "the design of this platform is to induce your own cells to make a foreign protein which gets displayed on the surface of those cells." "there's no targeting mechanism to lead it to happen only in certain tissues, it can happen haphazardly around the body, including in places like your heart." "And what that triggers is your own immune system to see those foreign proteins and conclude the only thing they can, which is that those cells have been virally infected." "the right response, the response, the natural response of the body is to take virally infected cells and destroy them."

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.

"So here we see the syringe needle going in and the lipid nanoparticles coming out." "Probably three to 6,000 per injection." "These are completely new to the human body, and they circulate around in the blood." "They're supposed to stay in the deltoid muscle, but they don't." "They circulate everywhere around the body." "Then when they come to a cell, they'll go inside the cell, this process called endocytosis." "Any contaminating DNA will be carried very, very efficiently by the lipid nanoparticles into cells, coming into contact with the walls of the vascular endothelium, the lining of the blood vessels." "If the lipid nanoparticles are 80 nanometers each, it would be 87 of them to fit across the diameter of a red blood cell." "So 5,000,000,000 of these red blood cells in one milliliter of blood, and yet this is the size of the lipid nanoparticles." "Until these problems are resolved there should be a moratorium on mRNA vaccines." "In my view let me know what you think."

According to Pfizer documents, one month after the vaccine rollout in November 2020, Pfizer knew the vaccines didn't stop COVID and identified vaccine failure. Internal documents showed COVID was the third most common side effect. Within months, Pfizer hired 2,400 staffers to process adverse event reports. By May 2021, Pfizer and the FDA knew the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The CDC initially claimed the injection materials stayed in the injection site, but Pfizer knew the materials biodistribute throughout the body within 48 hours, settling in the brain, liver, adrenals, and spleen. In women, they accumulate in the ovaries, and there's no known mechanism for the body to eliminate the lipid nanoparticles from the ovaries.

There is concerning evidence of cardiac arrests in people who have received the vaccine. A study by Nakahara found that positron emission tomography scans showed changes in heart metabolism in almost everyone who took the shot for at least 6 months. This is worrisome, as we don't fully understand the implications. Harvard researchers discovered messenger RNA stuck in the hearts of deceased individuals. Additionally, Schreckener from Germany revealed that Pfizer and Moderna vaccines may be directly toxic to heart muscle cells. Based on this information, there is a strong suggestion that these vaccines should be removed from the market.

The safety of messenger RNA (mRNA) vaccines, such as Pfizer and Moderna, is being questioned. Studies have shown that mRNA can be toxic to heart muscle cells and can remain in the human heart, bloodstream, lymph nodes, and injection site for extended periods. This raises concerns about the safety of mRNA technology for vaccines, as it may make flu shots and other vaccines more dangerous. Some argue for a ban on mRNA development due to the COVID-19 vaccine controversy.

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.

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.

Pfizer did not use the actual spike mRNA; a luciferase reporter mRNA in the same lipid nanoparticles tracked biodistribution in rodents. After injection, most mRNA remained at the injection site, but notable levels were detected in the liver; limitations may underestimate low-level distributions, yet components are not confined to the injection site. Moderna did not perform a dedicated biodistribution study with the COVID mRNA; data came from a surrogate CMV mRNA (mRNA-sixteen 47) in the same lipid nanoparticle. In rats, high levels at the injection site and in draining lymph nodes, spleen, eye, and liver; lower levels in heart, lungs, testes, and brain, with the mRNA crossing the blood brain barrier. In humans, vaccine mRNA and its spike protein have been detected across blood, lymph nodes, heart, and brain, with persistence lasting weeks to months and reportedly seven zero six days post vaccination.