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The talk discusses a 58-page document from Australia's therapeutic goods administration, revealing widespread distribution of lipid nanoparticles from the Pfizer vaccine. The nanoparticles were found in various organs, including the liver, ovaries, and bone marrow. Despite concerns about potential inflammatory reactions, the expression of spike protein was not studied. The document questions why the vaccine was approved without this crucial information. The data was available before vaccine authorization, raising doubts about the decision-making process.

it's modified mRNA, and it's designed not to degrade, and there are studies that show it sticks around the body. We don't know how long. The lipid nanoparticle was designed to permeate difficult to permeate barriers, like the blood brain, like placenta barrier. Did you believe when Fauci told us that the mRNA shot would stay in the arm? In rats, it biodistributed all over the body, accumulated in the adrenal glands, in the ovaries. This encapsulated lipid nanoparticle distributes all over the body, and when it attaches to a cell, it unloads its mRNA into the cell and turns the cell into a manufacturing cell of a protein that is toxic to it. They're turning cells like a heart cell into a manufacturing site for the spike protein, which is toxic, the body attacks it. The designers of the injection knew it. And Anthony Fauci knew it, and he lied. DNA contamination ... McKernan study ... 36 to 627 times. The allowed amount is ten nanograms per dose. That saves three point two million lives. No. It didn't. It's impossible. That's entirely possible.

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus a month after rollout in November 2020. They allege Pfizer knew the third most common side effect was COVID. Within months, Pfizer supposedly needed to hire 2,400 staffers to process adverse event reports. The speaker asserts Pfizer and the FDA knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The speaker states the CDC initially claimed the injection materials stayed at the injection site, but Pfizer knew they biodistributed throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

"it's modified mRNA, and it's designed not to degrade. And there are studies that show it sticks around the body." "The lipid nanoparticle. Do you realize that it was designed to permeate difficult to permeate barriers? Like the blood brain, like placenta barrier." "Japanese FOIA of the study that was conducted about distribution where in rats, biodistributed all over the body, accumulated in the adrenal glands, in the ovaries." "it's messenger RNA, modified RNA, this encapsulated lipid nanoparticle that distributes all over the body." "when it attaches to a cell, it unloads its mRNA into the cell and turns the cell into a manufacturing cell of a protein that is toxic to it." "Are you aware of that? I mean, just yeah. Yes or no? I mean, do you know that or not? Because I talk to a lot of doctors, don't have a clue."

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus one month after rollout in November 2020, and that "vaccine failure" was identified internally. They allege Pfizer knew they needed to hire 2,400 staffers to process adverse event reports shortly after rollout. The speaker further claims Pfizer knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but the government didn't inform parents of the elevated risk until August 2021. They state that contrary to CDC claims, the vaccine materials (lipid nanoparticles, mRNA, polyethylene glycol-coated industrial fat, and spike protein) do not stay in the injection site, but biodistribute throughout the body within 48 hours, accumulating in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries.

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.

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.

According to the speaker, Pfizer documents reveal that one month after the vaccine rollout in November 2020, Pfizer knew the vaccines didn't stop COVID and identified vaccine failure. Within months, the company allegedly needed to hire 2,400 staffers to process adverse event reports. The speaker claims Pfizer knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this information wasn't shared with parents until August 2021. The speaker alleges that the CDC initially stated the injection materials stayed in the injection site, but Pfizer knew these materials biodistribute throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. The speaker asserts that there is no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

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 speaker believes the accumulation of lipid nanoparticles in the ovaries following mRNA product administration was intentional, not accidental. mRNA products from Moderna and Pfizer BioNTech are encapsulated in lipid nanoparticles for structure and slow release. However, these nanoparticles are known to accumulate in the ovaries of every species tested. The speaker claims this formulation was chosen with the full knowledge that it would accumulate in the ovaries of girls and women, and that this has happened to every female administered the material.

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

The speaker clarifies they are injured by an mRNA therapeutic, not a vaccine, and highlights issues with lipid nanoparticles and synthetic mRNA, which can persist for hundreds of days. They claim that instructing cells to produce a protein that presents on the cell surface can trigger autoimmune disorders. The speaker states that the spike protein itself is biologically active, causing cells to grow and divide inappropriately, and was known to damage the placenta and lungs. They assert they knew early on that the shot didn't stay in the arm. They cite 2005 research showing the SARS-CoV-1 spike protein alone could harm animals. The speaker references 2015 gain-of-function research at UNC, NIH, and Wuhan labs, where a more lethal and transmissible SARS virus was created. A traditional vaccine attempt for this virus caused harm and lethality in animals, with pathology slides showing similar vascular lung damage seen with SARS-CoV-2. The speaker concludes that "they" knew about these risks but still rolled out the vaccine, profiting from it while falsely claiming it was safe and effective.

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."

In this video, the speaker discusses a study on the biodistribution of lipid nanoparticles used in mRNA injections. They mention that these nanoparticles tend to concentrate in the ovaries, which are biologically active organs. The speaker also mentions that the Pfizer paperwork states a 16% decrease in fertility in rats. Overall, the video raises concerns about the potential effects of these nanoparticles on fertility.

Speaker 0: This is kind of dark, and I'm sorry. I gotta go there. It's kind of impossible that they didn't know all this shit. We didn't need the foyer requested pharmacokinetic data from Japan, although thank God for Byron Bridal for getting which that to shows clearly in Wistar rats that the lipid nanoparticles in this Pfizer context traffic everywhere in the body and bioaccumulate, including into the ovaries and the adrenals, etcetera. There was a paper published in 2012 that demonstrated exactly this in Wistar Rats, same model, same lipid nanoparticles, they use different kinds of nanoparticles, but it showed the same thing very clearly that one of the main places that these lipid nanoparticles traffic to were the ovaries. And the reason why we use Wistar rat models and mice models before we go to humans is because we're very similar biologically. That's the whole reason. So if something happens in a mouse or a rat, you gotta be careful because it might happen in a human too. Wink, wink. So another thing I wanna throw in here is that we there's this drug pardon me. There's this drug called ONPATTRO, which is utilizing the exact same kinds of lipid nanoparticles, which act as like in the same way that chylomicrons do. It's like these things that we inherently have for fat metabolism that have, proteins absorbed, which is on the surface of the lipid nanoparticle, that traffic these guys, these lipid nanoparticles with their silencing RNA, cargo to the liver via APOE because there are these APOE receptors in the liver in high quantity or they're expressed at high levels. And so these genius biotech guys have discovered and I'm not being sarcastic. They are geniuses for doing this. This shit shouldn't be being used in humans. This stuff traffics directly to the liver. This is all known. They've been studying lipid nanoparticles and trying to make them not toxic for freaking two decades, people. But the thing is that's very suspicious to me and I have no answers to these questions so far is how is it possible that in 2020 or whenever it was they did this, Moderna and Pfizer simultaneously solved the toxicity problem of lipid nanoparticles by coming up with this ionizable cationic lipid? What the hell is that? Speaker 1: It was Operation Warp Speed, because you wave a magic wand from the executive office of the President of The United States and everything, all the checks and balances downstream go away. He's very proud of the fact Speaker 0: that

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

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."

The speaker claims that contrary to official statements, materials from the injections do not stay in the injection site, but biodistribute throughout the body, accumulating in organs like the liver, adrenals, spleen, lymphatic system, and ovaries, and crossing the blood-brain barrier. They assert there is no known mechanism for these materials to leave the body. A study from Hong Kong allegedly showed systemic damage in rats after the first injection and heart engorgement and multi-organ system failure after the second. The speaker states that a CDC document prepared in 2020-2021 outlined a plan for six shots. The speaker concludes that more shots increase the likelihood of disability, death, or sterilization, and "they" are aware of this.

The speaker discusses a document from the therapeutic goods administration in Australia that reveals the distribution of lipid nanoparticles from COVID-19 vaccines in various organs. The nanoparticles were found in organs such as the liver, brain, eyes, heart, kidneys, and more. The speaker expresses concern about the potential implications of this distribution. They also mention other topics such as mask bans, vaccine policy, and the alleged suppression of alternative treatments. The speaker concludes by promoting a website for purchasing various products.

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.

The speaker discusses the potential harms of lipid nanoparticles and synthetic RNA used in vaccines. They mention that the nanoparticles can accumulate in various organs, including the ovaries, bone marrow, spleen, and liver. The synthetic RNA can persist in the body for months. The spike protein, found in vaccines, is said to cause harm and can accumulate in the brain, peripheral nerves, and organs like the liver and heart. It can also lead to autoimmune diseases and reproductive issues. Studies have shown abnormal findings in PET scans and decreased sperm counts after vaccination. The speaker suggests that these potential harms should have been known before administering the vaccines.

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.