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

Research conducted by Bruce Patterson at InCelDx reveals that spike proteins can remain in the body for extended periods. In severe COVID cases, the s one segment was found in white blood cells for up to 15 months after infection. Even after vaccination, the full-length spike protein, including the s one and s two segments, was detected in white blood cells for at least 9 months. Another study from Stanford, led by Roelkern and colleagues, discovered messenger RNA, the genetic code for the spike protein, in lymph nodes for up to 2 months. These findings suggest that both messenger RNA and spike proteins can persist in the human body for several months.

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 vaccine's mRNA is identical to the RNA in our cells, which doesn't cause long-term adverse effects. The RNA in the vaccine is degraded within a week and completely gone. The lipid nanoparticles in the vaccine contain four types of fat, two of which are present in our cells and are gone within 24 to 48 hours. None of the vaccine's components remain in the body after days to a week. The mRNA doesn't integrate, affect, change, or mutate the DNA. Adverse events to vaccines mostly occur within the first six weeks, and with 15 million people already vaccinated, only rare anaphylaxis-like reactions have been observed. The chances of experiencing an unusual adverse event are less than 1 in 15 million.

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.

The vaccine contains fatty acids and messenger RNA encased in fatty acid nanoparticles for protection. Once injected, the components are taken up by cells and eventually disintegrate. Some misinformation and fears about the vaccine's contents exist, but it is important to communicate clearly about its temporary nature and immune response activation. Additionally, the vaccine has been found in various tissues throughout the body, contrary to initial beliefs about its localized effects and degradation timeline.

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.

Recent studies indicate the persistence of spike protein in the body long after the initial introduction. A Yale study detected it 709 days out, while a Patterson study found it 245 days out. This extended presence is unusual, as most proteins have a turnover rate of weeks, not years. This suggests either the spike protein is being continuously regenerated within the body or it is somehow evading destruction for extended periods in bodily reservoirs. This leads to speculation that the mRNA may be lasting longer than expected or that plasmids are still present and generating spike protein. The exact mechanism behind this phenomenon is currently unknown.

Speaker 0 lays out a numerical comparison between vaccine versus infection to determine which creates more spike proteins, according to the source material. First, the infection scenario. The unit counted is the virion (one complete virus particle). At the peak of infection, the body could be fighting off somewhere between one to 100,000,000,000 virions. Each virion has spike proteins on its surface, counted as between twenty five and fifty spikes per virion. The calculation multiplies the range of virions by the spikes per virion, giving a peak infection spike protein load of two to 10,000,000,000,000 spike proteins. Next, the vaccination scenario. The math starts with modified messenger RNA (modRNA) molecules in a vaccine dose. A single vaccine dose contains somewhere between 14 to 42,000,000,000,000 modRNA molecules. Each of these trillions of modRNA molecules can produce multiple spike proteins, ranging from 10 to 1,000 each. When the numbers are multiplied, the source calculates a potential total of up to 100,000,000,000,000,000 spike proteins (up to 10^17, i.e., up to one hundred quadrillion). Speaker 0 then contrasts the two scenarios. In a side-by-side view, the initial particles are billions of virions versus trillions of modRNA molecules. The timing differs as well: a natural infection builds up over about a week, whereas the vaccine dose is delivered all at once, in just a few seconds. The final totals are two to 10,000,000,000,000 spikes from infection versus a potential of up to one hundred quadrillion from vaccination. Visually, this difference is stark, with the infection spike protein bar being far smaller than the vaccine spike protein bar, illustrating an order-of-magnitude difference. The discussion then moves to the distribution and persistence of spike proteins. The source describes the virus's spread as more localized or comparatively narrow, while vaccine components are said to travel throughout the entire body, with accumulation in areas including major organs like the heart and the brain, and the potential to cross barriers such as the blood-brain barrier and the placental barrier. Regarding duration, spike mRNA was reportedly detected in cerebral arteries after seventeen months, and some vaccinated individuals were reportedly still spike positive for up to sixteen hundred days. The source concludes, “Your spike load is orders of magnitude higher via injection.” Speaker 0 notes that the numbers show trillions versus quadrillions and emphasizes the presented math and its implications as the core of the comparison, while acknowledging the source’s look at spike proteins’ distribution and persistence.

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

There is no question that the inclusion of DNA was not an accident, and the 1/3 DNA, 2/3 RNA ratio was intentional. The long-term effects of both DNA and RNA are influencing the ability to fight cancer. The key question is what effect the DNA has on the cell nucleus, and how to differentiate its damage from that of mRNA. mRNA is connected to ACE 2 receptors and causes damage throughout the reproductive and cardio systems. mRNA creates a spike protein flag, which the immune system attacks, leading to organ damage. The presence of DNA makes the process last longer. While mRNA would create spike for 8-12 months, DNA can influence the nucleus for years, producing mRNA near the nucleus. This extends the process from months to 8-10 years due to the decision to include DNA.

The Pfizer vaccine may contain DNA in addition to mRNA, according to a scientist who sequenced the vaccine in their lab. The DNA is a vector used in the production of the mRNA. The scientist examined vials of the vaccine from a local vaccination program and found DNA in them. This DNA could potentially be linked to rare but serious side effects, such as death from cardiac arrest. It has the ability to integrate into the genomic DNA of cells, potentially causing long-term effects. The presence of this DNA raises concerns about the regulatory process that allowed it to be included in the vaccine. There is a theoretical risk of autoimmune reactions and future cancer development. Further investigation is needed to determine the extent of these risks.

The vaccine does not contain animal products. The vial mainly contains water for injection, a strand of messenger RNA, and fatty acids that protect the RNA. The RNA is fragile and needs protection. The fatty acids form a nanoparticle that is taken up by the cell. Two of the four lipids in the lipid nanoparticles are highly toxic, completely novel, and never authorized before in any medicinal product. After being taken up, the components disintegrate and are recycled within hours to days. The therapeutic goods administration in Australia (TGA) data shows the vaccine has been found in adipose tissue, adrenal glands, bladder, bone, bone marrow, brain, eyes, heart injection site, kidneys, large intestine, liver, and lungs. There is no degradation data available, so it is unknown how quickly it goes away.

The mRNA COVID-19 vaccine delivers instructions for creating spike proteins, which then trigger an immune response. The vaccine components are said to break down and disappear from the body within days, leaving no trace and unable to affect DNA. However, some claim that data from the Therapeutic Goods Administration in Australia shows the vaccine distributes throughout the body, not just the injection site, and that there was no data on how quickly it degrades. Research indicates vaccine mRNA can be detected in some individuals for up to 14-15 days. A rare post-vaccination syndrome (PVS) is described where individuals exhibit elevated levels of spike protein for extended periods, up to 709 days, along with reactivation of dormant viruses. A hypothesis suggests that in some individuals, the vaccine mRNA may reverse transcribe and integrate into DNA, causing continuous spike protein production and potentially leading to T-cell exhaustion. The concern is raised about the long-term health consequences and potential for germline transfer if DNA is altered.

Speaker 0 describes what he claims is the strongest case report ever done on vaccine injury, specifically mRNA vaccine injury. The subject is a 51-year-old man who developed myocarditis, pulmonary embolism, neurological disturbances, and skin disturbances, constituting multisystem long vaccine syndrome. The key findings are said to be detected 3.6 years after his last shot. Exosomes circulating in his body allegedly contain Pfizer mRNA, and this mRNA is still present in those exosomes years after vaccination. The same mRNA is reportedly also found in his skin. In addition, plasmid DNA from the manufacturing process is claimed to be present in his skin, again 3.6 years after vaccination. Specifically, the plasmid DNA allegedly includes the SV40 segment, the spike expression cassette, and the open reading frame region, with all components of the plasmids in the Grover's disease–affected skin area. Microscopic analysis of the Grover’s disease area allegedly showed staining for SARS-CoV-2 spike or vaccine spike, indicating the presence of spike protein in that skin region. This staining for spike protein is reported as occurring 3.6 years after the shot. Overall, the speaker asserts that all vaccine components—mRNA, plasmid DNA with defined segments, and spike protein—remain in the body for multiple years, with findings in exosomes and skin indicating long-lasting presence. The speaker also asserts that this represents a situation in which “we were completely lied to.”

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

Residual effects from one or two COVID shots can include late blood clots and cardiac arrests years later. The mRNA and spike protein from the shots can linger in the body, causing various health issues like heart and brain damage, blood clots, and immunologic problems. A spike detox program is recommended to address these concerns.

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's new evidence suggesting shedding might be real. The mRNA vaccines were called vaccines instead of gene therapy so they wouldn't have to test for shedding on non-injected people. We're giving your body the code to make the virus' spike protein, creating immunity. The spike protein alone won't kill you, but your body learns to eliminate it. If you later get COVID, your body will recognize and attack the spike protein. However, there's no guarantee your body stops producing the spike protein. Your cells, once healthy, now make spike proteins, which your immune system attacks, even if it's your own cells. The mRNA in the vaccines is stabilized to last longer and is coated in lipid nanoparticles to protect it and cross the blood-brain barrier.

Yale researchers discovered COVID spike proteins in the blood of individuals who received mRNA vaccines, even up to two years post-vaccination, without prior COVID infection. This raises concerns that the vaccine's genetic material may have integrated with human DNA, leading to ongoing spike protein production. While the findings suggest potential long-term effects, they do not definitively prove genetic integration. The researchers plan to publish their findings on a preprint server and seek validation from an independent lab. These developments could have significant implications for mRNA vaccine safety guidelines affecting over a billion vaccinated individuals. Further details will be shared as the research progresses.

The Pfizer vaccine contains not only mRNA but also plasma DNA from the vector used in its production. I sequenced samples from two batches of the vaccine in Colombia and found this DNA, which raises concerns about potential health risks. This DNA could integrate into the genomic DNA of cells, leading to permanent changes. Such integration poses theoretical risks, including autoimmune responses and cancer, depending on where the DNA inserts itself in the genome. While these risks may be rare, they warrant investigation to understand their implications better.

The Pfizer vaccine may contain DNA in addition to mRNA, according to a researcher who sequenced the vaccine in their lab. The DNA is a vector used in the production of the mRNA. The researcher expressed concern about the potential consequences of this, including rare but serious side effects like death from cardiac arrest. The DNA could integrate into the genomic DNA of cells and become a permanent part of them, posing a risk of genome modification and autoimmune attacks. There is also a theoretical risk of future cancer depending on where the foreign DNA lands in the genome. The researcher believes further investigation is needed to determine if these risks are occurring.

The mRNA COVID vaccine gives your body instructions to create copies of spike proteins. As soon as the spike protein is made, the vaccine breaks down and disappears from your body, usually within a matter of days or even hours. The vaccine is administered into your arm muscle, where it's quickly metabolized. The vaccine is taken up at the injection site and does not diffuse throughout the body. Your cells destroy the vaccine and recycle its components. Your immune system recognizes the spike proteins and learns how to fight the virus, without you actually getting sick. After a few days, all the mRNA from the vaccine is gone and the spike proteins that your cells produced are destroyed by your immune system. The only thing that remains is the memory of how to fight COVID-19, so your immune system is ready if it encounters the virus again. There is nothing to fear from the vaccine.

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.