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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.

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 viewer asks if the proteins from the vaccine enter the bloodstream. The speaker explains that the mRNA blueprint for the protein is given, which is then translated into the protein in the muscle cells. The protein may enter the tissue and possibly trace amounts may enter the blood, but it is not measurable. The reaction occurs in the muscle, the corresponding defense cells, lymph nodes, and minimally in the blood. The speaker concludes that they have reached the desired agreement.

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 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 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.

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.

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.

In 2017, Moderna published a paper on an influenza vaccine using lipid nanoparticles. The study showed that in animals tested, the lipid nanoparticle vaccine spread into the brain, bone marrow, liver, spleen, and the muscle site where it was injected.

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.

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: 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."

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.

The mRNA COVID-19 vaccine delivers instructions for creating spike proteins, which then triggers an immune response. The vaccine and spike protein are said to break down and disappear within days, leaving no trace and not affecting DNA. The vaccine is taken up at the injection site and quickly metabolized. However, an Australian Therapeutic Goods Administration document indicates the vaccine distributes throughout the body, including adipose tissue, adrenal glands, and the brain. There was allegedly no data on how quickly the mRNA degrades. Research indicates vaccine mRNA can be detected up to 14-15 days post-vaccination in some individuals. A rare post-vaccination syndrome (PVS) is associated with chronic conditions and elevated spike protein levels up to 709 days post-vaccination, even without detectable SARS-CoV-2 infection. One hypothesis suggests that the mRNA may reverse transcribe and integrate into DNA, causing continuous spike protein production and potentially leading to T cell exhaustion. The possibility of germline transfer and long-term health consequences is raised.

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.

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.

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.

First, the mRNA is injected within lipid nanoparticles in your arm. It travels through every organ system, including the heart. Crosson found mRNA directly in the heart of deceased mRNA recipients. So we know it reaches the heart. Baumeyer found the spike protein directly in the heart in biopsies of patients with vaccine induced myocarditis. So we know the vaccine mRNA and lipid nanoparticles get into the heart, translate into spike proteins, so your cardiomyocytes begin to produce a toxic non human protein and your own body attacks the heart resulting in inflammation and cardiac scarring including micro scars which are undetectable with imaging. And so once you have this scarring, you're going to have cardiac electrical abnormalities, electrical conduction abnormalities, and your heart's not going to beat properly. And that's why we saw a lot of sudden deaths among athletes back in 2021.

Lipid nanoparticles, not intended for human or veterinary use, were administered to billions of people worldwide. Synthetic RNA and spike proteins from the vaccines were found to persist in the body for months, accumulating in the brain, peripheral nerves, liver, and other organs. Autoimmune diseases, myocarditis, renal gland damage, and reproductive harms were also observed. The spike protein affected the immune system, weakened the body's response to other infections, and caused damage to blood vessels, including the coronary vessels. It also led to the accumulation of abnormal proteins in the blood and impaired tumor surveillance. The potential impact on cancer was highlighted as a significant concern.