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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.

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.

Some people may find the concept of self-assembling nanoparticles crazy, but evidence from Pfizer's mRNA Science Day presentation supports it. The presentation discusses lipid components, RNA, and ionizable kinetonic lipid in lipid nanoparticles for COVID vaccines. Additionally, collaborations between Pfizer, CureVac, and DARPA suggest military connections. Moderna's patent mentions stealth nanoparticles with various materials like polyurethane and nylon. Bill Gates and Fauci have also mentioned self-assembling nanoparticles. This information highlights the importance of understanding these technologies.

The mRNA in the jab was encapsulated in a lipid nanoparticle designed to cross the blood-brain barrier to deliver drugs to brain cancer patients. This lipid nanoparticle, designed by Acuitas and invested in by Justin Trudeau, had no market from 2011 to 2019 because it killed every lab animal it was tested on. When testing lipid nanoparticles on humans, protocols dictated it could only be administered to individuals with five months or less to live. These patients agreed to the testing, believing they were contributing to the development of a brain-specific drug delivery system. The lipid nanoparticle was never approved for healthy humans due to its toxicity.

"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 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.

Aluminium adjuvants in vaccines at the injection site are ingested by macrophages, a type of white blood cell. These macrophages can become completely filled with aluminium without immediate damage. These cells can then travel throughout the body, including to the lymph nodes, potentially aiding the intended immune response. However, they can also migrate to other areas, such as brain tissue. Research by Roman Girardi's group in rats demonstrated the movement of these cells from the injection site to the brain. This suggests a mechanism for aluminium to accumulate in brain tissue via these macrophages.

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.

Before the emergency use authorization of the vaccines, significant concerns were already known. The Pfizer technical document revealed that these vaccines caused widespread distribution of the encoded protein in major tissues and were associated with inflammatory reactions due to lipid nanoparticles. It was understood that these nanoparticles could deliver RNA and DNA into cells, and the use of pseudo uridine was intended to enhance the immune response and prolong the product's effectiveness. However, critical investigations regarding potential shedding, reproductive toxicity, and the presence of contaminants were not conducted. These omissions are concerning, especially considering previous FDA regulations that recognized the risks of genotoxicity related to manufacturing processes.

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.

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.

Moderna's patents reveal the use of modified polynucleotides and lipid nanoparticles in their mRNA vaccines. These nanoparticles, with sizes between 80 and 160 nanometers, contain modified mRNA encoding a polypeptide. The term "lipid" is used to refer to nanotechnology, as these lipids possess positive electromagnetic fields. The patents also mention self-assembled and programmable nanoparticles that can receive external programs. Microsoft has explored the concept of biological computers operating inside living cells, using DNA as a programmable material. One specific patent, U.S. 9539210B2, discusses vaccine nanotechnology capable of delivering molecules, including toxins from chemical weapons or agents of biowarfare. This information is crucial for all American citizens.

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

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.

mRNA was found in the milk of 4 out of 40 women in one study, only in the week following injection. Another study found mRNA free and encapsulated in extracellular vesicles (exosomes) in milk 2 days after injection, with most mRNA in vesicles. Vaccine mRNA is encapsulated in artificial lipid nanoparticles (LNPs) that mimic natural exosomes, which are generated by cells and involved in intercellular communication. LNPs and natural extracellular vesicles fuse with cell membranes and release their contents into the cell. Natural vesicles are more efficient than artificial nanoparticles at transporting molecules to cells, and their cargo is protected from gastric juice. These factors are important if mRNA is found in milk.

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."

mRNA has been found in the milk of women after receiving injections. In one study, mRNA was detected in the milk of 4 out of 40 women, mainly in the week following the injection. Another study found mRNA in extracellular vesicles called exosomes, which are natural carriers of molecules. These vesicles contained mRNA for 2 days after injection, with a higher concentration in the exosomes. It is worth noting that the majority of mRNA was found in these natural vesicles rather than in its naked form. Artificial lipid nanoparticles (LNP) used in vaccines aim to mimic these natural exosomes. Natural vesicles are more effective in delivering molecules to cells and are protected from digestion in the digestive tract.

Nicholas Holcher, an epidemiologist and foundation administrator at the McCullough Foundation, appears on the WiderWake Media Podcast to discuss what he calls harms from the mRNA COVID vaccines and to critique mainstream approaches to the pandemic and public health policy. - Vaccine definitions and mRNA technology - Pre-2000 definition: a vaccine is an injectable or oral product that introduces a killed part of a virus or an inactivated form to the body so that encountering a wild-type version would not infect or would cause a less severe illness. - He asserts that mRNA injections are not vaccines: they are a gene transfer platform using modified messenger RNA with long persistence in the body (via N1-methylpseudouridine), delivered in lipid nanoparticles. He claims these bubbles distribute systemically, including to the brain, heart, bone marrow, and reproductive system, and that they instruct cells to produce a spike protein, effectively turning organs into “toxic spike protein production factories.” He says this leads to autoimmune attack on those tissues and contributes to adverse events, including myocarditis, strokes, immune destruction, and “turbo cancers.” - History and purpose of mRNA in vaccines - According to Holcher, work on this technology existed for decades but animals testing showed high mortality or sterilization in ferrets and mice, preventing approval except under a declared global emergency. He contends the COVID-19 crisis enabled emergency use authorization across Western countries, with ulterior aims to inject the globe with mRNA technology. - Global impact and uptake - He estimates about 70% of the global population received at least one COVID-19 injection (mRNA or viral vector). He notes Eastern countries used non-mRNA platforms (e.g., AstraZeneca/J&J in some places; Sinovac elsewhere) but that uptake in the West was high. - Harms and evidence - Excess deaths: cites a study by Dennis Brancourt et al. estimating around 17 million deaths worldwide as a result of COVID injections (as of September 2023); he claims US deaths could be in the hundreds of thousands to millions. - Turbo cancers: cites multiple studies in 2023 showing increased risk of seven cancer types (colorectal, bladder, breast, thyroid, prostate, etc.) in vaccinated groups; cites a major cancer journal, OncoTarget, reporting hundreds of turbo cancer cases across 27 countries, with Pfizer contributing most cases. Holcher also mentions his own group’s work with Neo7 Bioscience documenting genomic integration of vaccine-derived mRNA in a stage IV bladder cancer patient (31-year-old woman) with a segment of mRNA found in circulating tumor DNA on chromosome 19; another study reported thousands of dysregulated genes in post-vaccine cancers, including p53, KRAS, and BRCA. - Definition of turbo cancer: per Merrick et al., rapid, aggressive tumor progression with sudden onset and early metastasis, often in younger individuals, and resistant to treatment. - Fertility, pregnancy, and autism - Fertility: cites studies suggesting fertility impacts, including Karaman et al. finding depletion of primordial follicles in rats after mRNA vaccination; Manichi et al. reporting 33% lower conception rates in vaccinated women in Denmark; a study indicating a ~20% drop in sperm concentration and motility with no recovery over five months. - Autism: asserts a large body of evidence linking vaccines to neurodevelopmental disorders, citing a 136-study review with 107 studies finding positive associations between vaccines and neurodevelopmental issues, including autism, attributed to toxicity and immune system disruption, particularly in children with high vaccine exposure and reduced detox capacity (CYP450 impairment). - Other topics tied to vaccines and public response - The COVID-19 period and vaccine skepticism: claims the pandemic catalyzed a large anti-vaccine movement because people were compelled to take an experimental gene therapy product. - Sam Altman and gene editing: discusses Altman’s Preventive venture with the aim to reduce heritable diseases via in utero gene editing but warns of the path to designer babies and the potential for harm in early-iteration edits, citing prior CRISPR experiments on human embryos that produced deformed offspring or nonviable results. - AI, workers, and future society: predicts two-tier society with implanted or enhanced individuals and a replacement of human labor by robots and AI systems; discusses military and surveillance ambitions in gene editing and AI augmentation. - Mental health and digital life: references a randomized trial showing that turning off mobile Internet improved depression scores and well-being to an extent comparable to or greater than antidepressants. - World Health Organization (WHO): notes the US has pulled out of the WHO, arguing this is good for the US but potentially harmful for others still in the organization; expresses concerns about the pandemic treaty and ongoing global health governance, including vaccine passport-style surveillance. - FDA and public health policy: acknowledges some shifts (e.g., cutting doses from the childhood schedule) but argues the FDA remains compromised and too aligned with vaccine industry interests; criticizes the removal of a potential black box warning for vaccines and calls for more accountability. - Resources and contact - Holcher invites listeners to follow him on X (Twitter) at @nichulsher and to read their work on focalpoints.com and through McCullough’s network. Note: The transcript presents Holcher’s claims and interpretations about vaccines, turbo cancers, autism, fertility, and policy changes. The summary reproduces these points without endorsement or evaluation.

In a 2016 interview, the CEO of Moderna emphasized the importance of using lipid nanoparticles to deliver RNA molecules effectively. However, repeated doses of these nanoparticles can lead to dangerous side effects, as seen in past abandoned technologies by big companies like Merck and Novartis. The difficulty of getting RNA into cells without causing harmful side effects was also highlighted.

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.