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"The mRNA vaccines, you know, from COVID don't work against upper respiratory infections." "There are two problems with them." "One is they target a single protein, which drives what what's called an antigenic shift." "If it drives the virus to mutate, and it actually can prolong the pandemic." "We saw that during COVID, people took shots, mRNA shots for the original COVID variant and immediately, mutated into the Omicron virus to which the vaccine was ineffective, and that's what it does." "And the other issue is, that it the way that distributes in the body, the way that it migrates in the body, there's no control over and no predictability." "So it goes to every organ." "It turns your body into a an antigen factory where you're manufacturing antigens, and different people need different loads of antigens." "And we've seen now these epidemics of myocarditis and pericarditis, particularly in kids."

The speaker discusses the presence of spike protein in an antibody test after being symptomatic for over a year. They explain that the absence of nucleocapsid protein indicates that the individual had the vaccine-induced spike protein injury rather than a COVID infection. The speaker mentions that the spike protein antibody levels were significantly higher than expected, potentially thousands of times higher, even two years after vaccination. They express sympathy for the individual's suffering and emphasize the importance of sharing their experience despite pressure from the pharmaceutical industry and government. The individual shares their struggle and highlights the support they receive. The speaker acknowledges the wide range of symptoms experienced by the individual and notes that their story will resonate with others.

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.

I was fired after 31 years as an ER doctor for questioning the need for vaccination in those with natural immunity. Pfizer's hidden biodistribution studies reveal the vaccines spread throughout the body, causing various side effects due to the spike protein reaching all organs.

A study in Cleveland on 51,000 healthcare workers showed a direct correlation between COVID vaccinations and infection rates. Unvaccinated individuals had lower infection rates compared to those with one, two, three doses, or a bivalent booster. The study found that the more shots received, the higher the likelihood of getting and spreading COVID.

I got the vaccine. Did you really? Yeah, even the fourth one. Were you pressured into it? Kind of. I went to the doctor for blood work, and we noticed some unusual particles. I asked what they were, and the doctor revealed they were related to the vaccine. I was shocked. This is why some people experience severe issues, like having numerous white blood clots in their blood.

Speaker 0/J: The discussion centers on a study with dramatic implications, including claims that publishing such data could be career-ending, and questions about why the data would be so catastrophic. Speaker 2: The study involved eighteen thousand four hundred sixty eight subjects, of which one thousand nine hundred fifty seven were fully unvaccinated. When comparing the health outcomes of the vaccinated versus the unvaccinated, they found an increased risk in the vaccinated of several chronic health conditions. The vaccinated subjects were over four times more likely to have an asthma diagnosis—specifically four point two nine times in the adjusted analysis—and they note there are studies showing a range from three point two six to five point six five. Speaker 1: They also found three times the risk for atopic diseases. Speaker 2: Atopic diseases are described as a subset of allergic diseases. Speaker 1: They found an almost six times risk for autoimmune disease. Speaker 3: The autoimmune diseases this paper looked at include thrombocytopenic purpura, rheumatoid arthritis, SLE, systemic lupus erythematosus, MS, multiple sclerosis, and Guillain Barre syndrome. They mention there are over 80 different autoimmune diseases, and their data showed for autoimmunity a six times increase in those who got vaccines when compared to the unvaccinated. Speaker 2: This is presented as staggering because autoimmune disorders represent significant morbidity and health costs and suffering accrued over a lifetime. Neurodevelopmental disorders are also discussed. Speaker 0: What kind numbers we talked about? Do you remember? Speaker 1: Five and a half times risk for neurodevelopmental disorders. Speaker 2: They state the immune system is intimately connected with both brain development and brain functioning, and so when the immune system gets triggered by illness, potentially by vaccination, you can get neuropsychiatric symptoms presumably related to brain inflammation and immune processes in the brain. Speaker 0: Two point nine two times the amount of motor disabilities, four point four seven times the amount of speech disorders in the vaccinated compared to the unvaccinated, Speaker 3: Three times the rate of developmental delay. They found the same patterns as with allergy and autoimmunity. Also, six times more acute and chronic ear infections. Speaker 2: Interestingly, there were several health conditions where they couldn't even do this analysis because there were none in the unvaccinated group. The mathematical formulas require non-zero counts in both groups to compare risk. Speaker 1: For example, there were two sixty two children who had ADHD in the vaccinated group. Amongst the unvaccinated group, there were zero cases of ADHD. Speaker 3: These results are described as mind boggling. Conditions were not found at all in almost two thousand unvaccinated kids: zero brain dysfunction, zero diabetes, zero behavioral problems, zero learning disabilities, zero intellectual disabilities, zero tics, and zero other psychological disabilities in the unvaccinated.

People tested at Quest have an upper antibody limit of 25,000. Unvaccinated individuals typically test under 1,000. Vaccinated individuals often test over 25,000, averaging ten times higher than the unvaccinated, even four years post-vaccination. These high antibody levels are alarming, suggesting persistent spike protein presence and potential health issues. COVID is no longer a major illness concern, but elevated antibody levels remain a concern.

Speaker 0 expresses that publishing the material would effectively end his career. Speaker 1 questions what in the data could make the outcomes catastrophic for his career. Speaker 2 notes the study as a “bombshell.” The study included 18,468 subjects, of whom 1,957 were fully unvaccinated. When comparing vaccinated to unvaccinated groups, there was an increased risk of several chronic health conditions in the vaccinated group. Specifically, the vaccinated were over four times more likely to have an asthma diagnosis, with an adjusted figure of 4.29 times (range 3.26 to 5.65 across analyses). Speaker 4 adds that the study also found a threefold increase in atopic diseases, which are a subset of allergic diseases. The researchers reported almost a sixfold risk for autoimmune disease, listing autoimmune conditions such as thrombocytopenic purpura, rheumatoid arthritis, SLE (systemic lupus erythematosus), multiple sclerosis, and Guillain–Barré syndrome. They note there are over 80 different autoimmune diseases, and the data showed a sixfold increase in autoimmunity among the vaccinated compared to the unvaccinated. Speaker 3 highlights neurodevelopmental disorders, noting a five-and-a-half times increased risk. The discussion emphasizes that the immune system is intimately connected with brain development and functioning, suggesting that when the immune system is triggered by illness or vaccination, neuropsychiatric symptoms may arise due to brain inflammation and immune processes in the brain. Speaker 2 reports two point nine two times the amount of motor disabilities and four point four seven times the amount of speech disorders in the vaccinated group versus the unvaccinated, along with a threefold rate of developmental delay. The data also show, consistent with allergy and autoimmunity findings, six times more acute and chronic ear infections in the vaccinated group. Speaker 3 notes that in several health conditions, analysis could not be performed because there were none in the unvaccinated group, and the methods required nonzero counts in both groups. For example, there were two hundred sixty-two children who had ADHD in the vaccinated group, while the unvaccinated group had zero cases of ADHD. The same pattern is described for other conditions: zero cases of brain dysfunction, diabetes, behavioral problems, learning disabilities, intellectual disabilities, ticks, and other psychological disabilities in the unvaccinated group.

In my practice, we have administered around three to four thousand vaccinations. Initially, we didn't see many side effects, but they gradually increased throughout the year. More and more people started experiencing post-vaccination symptoms such as heart rhythm disorders, extreme fatigue, persistent muscle pain, and nerve inflammation. We formed groups of doctors who also administer vaccines, and they observed the same issues in their patients. However, discussing these concerns was difficult, as it was dismissed as a psychological overreaction. It was shocking to find that scientific discourse on the matter was not allowed. The increasing number of patients created an internal conflict for me and many other doctors who genuinely want the best for their patients. One case that stood out was a sixteen-year-old boy who developed nausea and chest pain forty-eight hours after the second dose. His EKG showed significant abnormalities, and he was diagnosed with severe myocarditis and heart swelling. Thankfully, he recovered, but this made me pause and reflect, especially when other people, including parents, expressed uncertainty and entrusted their lives to us. This trust carries a tremendous responsibility to be honest. Whether we have seen a particular case once or ten times, the connection to the vaccine remains uncertain. Until proven otherwise, we must inform people about what we observe and the experiences we have. This right belongs to individuals when they decide to undergo any form of physical intervention, no matter how small. It became an internal conflict for me because there was immense societal pressure to vaccinate as many people as possible across all age groups, while my personal experience as a doctor showed that it is not without side effects. That was the moment when I realized I couldn't continue vaccinating because I had to stay true to the truth and honor that trust. We have had around three to four hundred people come to us with post-vaccination symptoms. I have seen approximately sixty to eighty EKGs that showed clear abnormalities or rhythm disorders in previously young and healthy individuals. I have also seen a similar number of imaging results.

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 speaker claims the spike protein antibody test from LabCorp correlates with vaccination status, unlike other tests. They state that unvaccinated individuals typically score under 1,000, while vaccinated individuals often exceed 25,000, even four years post-vaccination. The speaker expresses alarm at these high antibody levels, suggesting persistent spike protein production. They reference a study indicating spike protein production up to 700 days post-vaccination, but question its validity due to low antibody levels reported in the study. The speaker also notes that they continue to see new vaccine-injured patients, seeing six new patients in the past week.

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.

Finished with a patient today. He is in research. We're using a lab in Germany. We have detectable Pfizer messenger RNA in his body now three point two years after the shots. For sure. So people who took these shots, they've got it at least long term now. And I've testified in the House last year and I said, I think we've got five to fifteen years of concern here. This is very long acting genetic material. And I think we should assume that all messenger RNA coming forward is going to be very long acting in the body and we need to be prepared for it.

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.

The authors discuss the unusual presence of IgG4 antibodies in mRNA vaccinated individuals, which is not typically seen post-virus infection. IgG4 antibodies are usually associated with parasite infections, allergens, autoimmune diseases, and cancer. The immune system's recognition of repeated antigens can induce IgG4 production, potentially leading to t cell exhaustion and autoimmunity. Scientists are cautious about the implications of IgG4 antibodies and suggest further research comparing outcomes among vaccinated and unvaccinated individuals. This data analysis may reveal any potential clinical impacts over time.

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.

I got vaccinated, but never boosted. The sickest I've been in 15 years was after the vaccine. Since then, I've had COVID five times, but the worst bout was just a sinus infection. I was in bed for two days after the vaccine with my heart racing. It's concerning we can't even discuss these reactions openly. Many people I know felt extremely ill after their second shot. These side effects aren't discussed enough. Plus, we're dealing with companies known for lying and criminal fines, yet they're exempt from vaccine side effect liability.

The speaker states: "We found circulating Pfizer mRNA in his exosomes three point six years after his last shot, and we also found plasmid DNA from the manufacturing process SV40 ORI segments, as well as the spike expression segments in his skin, in his Grover's disease area. He developed this skin disease after the shots." They add: "We also found vaccine spike protein and no nucleocapsid in this skin area as well." The speaker emphasizes timing: "Three point six years after his last shot, he suffered from myocarditis, pulmonary embolism, multisystem vaccination syndrome, neurological adverse events as well." They conclude: "And so the fact that we are finding this material forty three months after the last shot means we were lied to completely." The speaker claims: "We were told it would stay in the arm, it would degrade within weeks, that was wrong and we expect lawsuits to begin to flood in."

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.”

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.

The spike protein from the COVID-19 virus circulates in the body and can land in multiple organs, causing various diseases. Lab studies have shown that even without the virus, just injecting the spike protein can induce the same lung, vascular, heart, and brain diseases as COVID-19. The spike protein is considered the toxin responsible for causing the disease. This raises questions about why we are injecting something that is essentially a toxin into the human body, as it is not a traditional vaccine.

When you get a COVID infection, antibodies form to the spike on the virus. Giving a booster shot causes antibodies to form to the top, bottom, and side of the spike antigen. This creates a strain theory where the antibodies bind to different parts of the spike. The strain theory is also seen in half of the vaccines on Earth, where long strands of antibodies form a meshwork that can trap platelets. This can lead to personality changes, including autism, if the network forms in a blood vessel going to the amygdala. Children receive 20 booster vaccines before the age of 4, and 10 of them can replicate this scenario.

In a study, it was found that the risk of contracting COVID-19 increased with the number of vaccine doses received. Compared to those who were not vaccinated, individuals who received one dose were 1.7 times more likely to test positive for COVID-19. The risk increased to 2.6 times for those who received two doses, 3.1 times for those with three doses, and 3.8 times for those with more than three doses. The study showed a clear correlation between the number of vaccines received and the risk of testing positive for COVID-19. The results were highly significant, with a P value of 0.001, indicating a 99% likelihood of being a genuine result.

I did this myself. And lo and behold, I discovered a bunch of DNA pieces, in the mRNA vaccines. The public deserves to know what they're taking. If it's a vaccine or anything else, the public deserves to know what's in it. Molecular biology tools can do this for you. But we can quantify down to the molecule number. We did an experiment to prove it. And it's the exact same frequency that I predicted about a year ago, about one in a thousand to one in ten thousand cells have taken up different pieces of this vaccine and it's a permanent fixture of their genomes now. This proves that it happens with this contaminating DNA, which is why I was so weirded out about this stuff when I first discovered it.