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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 an agreement on the topic.

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 an agreement on the topic.

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 transcript argues that deflating the parasitic system is necessary because oversized states and corporations cause decay, corruption, and injustice, harming the people, workers, creators, and those harmed by elite interests. It cites examples such as Tanks for Kidney’s RT Documentary, Organ Harvesting, Black Market Transplants, and Crimes Against Humanity. It presents a quantified claim: extrapolating estimates for 2022 to 2023 plus half of 2024 yields total excess deaths of thirty-six million since the Covid Vax rollout, and adding nine million from Covid “killing protocols” in 2020 brings the total to forty-five million for four and a half years of Covid killing protocols. It describes SARS-CoV-2, the virus and vaccine bioweapons, as part of a narrative that depopulation and genocide are not taboo due to mass propaganda, corrupted science, lack of truthful science, and censorship in mainstream media and on tech platforms. It asserts that elites and many people still think SARS-CoV-2 is naturally evolved, but truthful science allegedly proves beyond doubt that SARS-CoV-2 was designed and made by humans in a bio lab. The transcript claims the genetic code of SARS-CoV-2 contains several lab-made inserts, such as PRRA and HIVGP120, which are described as too large and too numerous and only appearing in other natural viruses that are genetically very different from SARS-CoV-2, making natural mutation or recombination quasi zero. It also references a substantial trail of documents and testimonies years before and after the release of SARS-CoV-2 about these genetic codes, the existing biochemical technology to insert them, financing of the research, scientific documents, and patents. It then asserts that GenTech Covid vaccines cause human cells to produce, for months up to years, huge amounts of the toxic spike protein of SARS-CoV-2 in all organs and tissues, much greater than the mucosal infection from the virus itself in healthy unvaccinated people, which supposedly causes mild illness. The claim continues that these GenTech Covid vaccines are, in fact, bioweapons and much worse than the virus itself. It adds that not only the produced toxic spike protein but also other components and contaminations of these vaccines cause serious health damage. The source cited for these claims is Source2mia.org, with a request to like and follow.

When mRNA vaccines are injected, the amount of protein produced is not directly controlled by the dose of RNA given. Factors like metabolism and cell activity influence protein output. Doses vary between Moderna and Pfizer vaccines, but the key is the spike protein produced in the body. Studies show some individuals may not produce enough spike protein for immunity, while others may have excess leading to side effects or toxicity. In vitro experiments may not accurately predict in vivo outcomes due to individual differences.

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.

Speaker: Humanity was hit with dual biological weapons. When I say dual, I mean by the manufactured SARS CoV two virus that was manufactured in collaboration with UNC Chapel Hill and Wuhan. So we have that that has exposed basically the entire population to the spike protein. But then we also had the second biological weapon, was the mRNA injections, which installed about 7x more spike into people and those who received it per injection. And now we do understand that this can indeed shed onto others, particularly when you're freshly vaccinated and you're producing high levels of spike protein. We do believe this can shed via what's called exosomes, either through your breath or through your bodily fluids. So, yes, humanity has been hit by these weapons.

"Now, when these genes, packages, enter the cells, then the cells will start making this damn virus protein which is called the spike." "This is going to happen to any mRNA or gene based vaccine." "Those packages are going to cause your cells in the blood vessels to create this protein and this protein is going to be a foreign non self protein that is going to be recognised by any antibodies that you have and these antibodies are going to be there after the first injection." "If any of these vessels is clogged because of a thrombus or because it's injured, the cells that are being supplied by oxygen are going to die." "So if these tiny vessels in the brain or the heart are damaged, you are damaged for life. You will never be the same again."

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.

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

The spike protein, according to research in South Africa, induces fibrin from fibrinogen, forming the backbone of clotting in a way not previously seen. Unlike normal fibrin clots that are easily broken down, clots formed from COVID or the spike protein from the vaccine are difficult to break down, causing issues for many people. A cardiologist stated that in their decades of practice, they have never treated as many blood clots as in the last five years. These blood clots occur after the virus infection and the vaccine because the spike protein causes blood clots. Therefore, it is reckless to continue vaccinating people and loading the body with spike protein, causing more blood clots. According to a paper in Cell (July 2021), the nucleoprotein, not the spike protein, supplied broad and durable immunity for the prevention of infection. The speaker questions why the vaccine wasn't changed to target the nucleoprotein once this information came to light.

Source tomia.org April 2024. Why deflate the parasitic system? Because the parasitic destructiveness oversized states and corporations always leads to decay, corruption, injustice to the destruction of its many hosts, the people, the working and creative people, the maimed and dying slaves of the elites. See examples below. Tanks for Kidneys RT Documentary, Organ Harvesting, Black Market Transplants, Crimes Against Humanity. If I extrapolate my estimate for 2022 to 2023 plus half of 2024 I get in total thirty six million excess deaths since the Covid Vax rollout. Adding the nine million from the Covid killing protocols in 2020 gives a total of forty five million for four point five years of Covid killing protocols. SARS CoV-two virus and vaccine bio weapons Considering the estimated forty five million extra deaths and estimated one point nine billion serious adverse effects for four point five years of Covid killing protocols and deployed SARS CoV-two virus and vaccine bio weapons the words bio weaponized, propagandized, lured, coerced and mandated depopulation and genocide should not be taboo because of the mass propaganda corrupted science lack of truthful science and censorship in the mainstream media and on tech platforms thus the elites many people still think SARS CoV-two is a naturally evolved virus. Truthful science though proves beyond any doubt SARS CoV-two is designed and made by humans in a bio lab. After all and first of all, science shows the genetic code of SARS CoV-two contains several lab made inserts, not natural mutations or recombinations of natural viruses. Because these inserted codes, PRRA, HIVGP120 are much too large and too many and because these genetic codes only appear in other natural viruses that are genetically much too different from SARS CoV-two the probability that SARS CoV-two has naturally mutated or recombined from other natural viruses is quasi zero. Furthermore there exists a substantial trail of documents and testimonies years before and after the release of SARS CoV-two about these genetic codes and the existing biochemical technology needed to insert them, financing of the research, scientific documents, patents. Since the GenTech covid vaccines make the human body cells produce during months up to years huge amounts of the toxic spike protein of SARS CoV-two. In fact in all organs and tissues much greater amounts than the average, dominantly only mucosal, infection with SARS CoV-two itself which for the majority of healthy unvaccinated people causes hardly any illness just cold like symptoms. These Gentech covid vaccines are of course themselves bio weapons and much worse than the virus itself. Furthermore not only the produced toxic spike protein but also other components and contaminations of these vaccines are cause of serious health damage. Source2mia.org, please like and follow.

The upper limit of the test is 25,000. And and people that have not gotten the COVID shots, I'd say it ranges it's usually under a thousand. And then people that have gotten the shots, I mean, it's a lot of them are off the chart. They're over 25,000. But on average, they're probably 10 times higher than the people who have not gotten a shot. And this is people who were you know, they were vaccinated four years ago. It wasn't like they just got the shot. But four years later, you should not have sky high antibody levels. And that's what I'm seeing. And that is alarming. It just suggests that there is a lot of spike protein still in the body causing problems.

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.

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 an agreement on the topic.

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

"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 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.

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.

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.

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 an agreement on the topic.

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.