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Zoological viruses are being put in vaccines, specifically in the cell lines. These viruses have been present for a long time but are often overlooked in papers. The speaker suggests that this is a race and gender-specific attack, as certain groups are targeted. The goal is to change our DNA and establish a one-world order. The vaccines contain various viruses, including those found in polio vaccines. The speaker claims that those who are already immune will die from the shots due to antibody-dependent enhancement. The speaker advises against taking any vaccines, including the Pfizer vaccine, as they believe all vaccines are synthetic poisons. They claim to have evidence that the Omicron variant was present in humans in 2000. The ultimate objective is to ensure everyone is injected because other aspects of the environment, such as food and particulates, also pose a risk.

mRNA technology, used in COVID vaccines, raises ethical concerns about potential control. Multiple genes and regulatory elements can be inserted, allowing for different vaccinations and antigens to be regulated. This could lead to unknown protein expression when consuming certain foods. S. Matthew Liao, a philosopher, suggests using human engineering to address global issues like meat consumption. By making people intolerant to certain proteins, it could reduce meat consumption and benefit the planet. Doctor Christina Parkes expresses ethical concerns about the regulation of genetic information through hormones, airborne substances, and the food supply. These discussions highlight the potential dangers and ethical implications of mRNA technology and human engineering.

Kevin McKernan recently discovered that there is contamination in the mRNA shots with cDNA, including a cancer-promoting segment called SV40. SV40 turns on cancer genes in the human body and impairs tumor suppressor systems. This means that the shots not only promote cancer through SV40 but also inhibit our ability to fight cancer. The increase in cancer rates is undeniable, but the question remains: how much of this is due to the vaccines?

The speaker discusses a conspiracy theory about the UN using food as a weapon and banning humans from eating meat. They claim that vaccines contain a bovine protein that causes an autoimmune response, making people allergic to beef. They argue that this is part of a plan to weaponize the food supply. The speaker also mentions the use of glyphosate in GMOs and its negative effects. They connect this to the tick-borne alpha gal syndrome, which causes an allergy to red meat. They suggest that the protein found in ticks is also present in vaccines. The speaker warns that the globalists are preprogramming people to stop eating meat and urges viewers to share the information.

The speaker questions the presence of SB40 sequences in vaccines, suggesting they could lead to cancer through insertional mutagenesis. They advocate for alternative treatments like hydroxychloroquine and ivermectin, claiming they are safe and effective. The speaker criticizes the FDA for redacting data on vaccine contamination, questioning their transparency.

This is not conspiracy theory. This has been published in the BMJ by Retzaf Levy, and they go through this process: one where they ran these vaccines in the trial and how they changed that when they decided to go and inject the rest of the world. This is traditionally a mortal sin in vaccine manufacturing or in any sort of biologic manufacturing. The process is the product. You change the process, you have to go through trials again. And the EMA even asked them to do that, although they failed to. They asked for another trial of 250 people once they changed the process and that data was never delivered. So this bait and switch is very important for you to understand why the trial data is of absolute zero consequence to what we're actually seeing in the field. Those numbers are a caricature of what they're actually doing with these injections. They know something. Pfizer very early on they had the data on this from their trial, they knew this was going to happen and they quickly went out and acquired cancer companies. They put $43,000,000,000 into the acquisition of C Gen and they put $2,260,000,000 to acquire Trillium Therapeutics. Trillium was focused on blood cancers that have a CD one forty seven marker on them. Okay? That is one of the markers that is known to be involved in COVID. So, they have a very interesting window on those malignancies and, they're buying up the cancer companies that are probably gonna play the biggest role in benefiting from the mess that they've created. So, in summary, the Pfizer vaccines on the market are not the same formulation as what was tested in the clinical trials. This is a big bait and switch and it's a fraud. So you can't believe anything they're saying about the vaccine efficiency, which we have seen even those numbers decay over time. This is probably why. They're not really what they trialed. They gave you something different. There is significant DNA contamination that's found. Like, 10 out of 11 studies have found this, and the ones that haven't found it have some financial conflicts. So, I think the consensus is out. 10 out of 10 out of 10 of the real studies, are finding this. Several are through peer review, which have not been easy to get through peer review. The peer review journals do not like these papers. They get beat around in peer review for months to years, but they're making their way out now. There is also significant DNA contamination now found in five peer reviewed studies that were not looking at this. They were looking at people's blood and tissue and it was accidentally in there. Other people had to go sleuth it out. We've got cancer on the rise and there's several papers that report cancer post vaccination. Like, right at the site of injection, they'll see neoplasms. Alright? There is there's something going on here. This can't be ignored saying it's a coincidence anymore. Now this is these are liability free and they're often mandated. Okay? This may be the largest carcinogenic hit ever to the human population. And we have these on childhood schedules. We're giving these to pregnant women. This has gone absolutely off the rails.

The speaker claims SV40 in literature turns on cancer genes. They further claim the spike protein impairs tumor suppressor systems P53 and BRCA, promoting cancer and inhibiting the ability to fight it. The speaker suggests cancer rates are up, and the question is how much is due to vaccines. They state that repeated shots every six months increase the chances of getting loaded with synthetic genetic material that will cause harm, including heart disease, neurologic disease, blood clotting, immunologic problems, and cancer.

The speaker claims that this is not conspiracy theory and cites a BMJ publication by Retzaf Levy, which describes a process in vaccine development: vaccines were trialed under one formulation, but when the decision was made to deploy them globally, the process was changed and the product injected to the rest of the world. The speaker asserts that changing the process requires new trials, yet the EMA asked for an additional trial of 250 people after the process change, and that data was never delivered. This is described as a “bait and switch,” asserted as crucial for understanding why trial data is of zero consequence to what’s seen in the field, implying that real-world outcomes do not match trial data and that the numbers from trials are a caricature of field performance. The speaker claims Pfizer had early data indicating what would happen and acted on that by acquiring cancer companies: $43,000,000,000 into the acquisition of C Gen and $2,260,000,000 to acquire Trillium Therapeutics. Trillium is described as focused on blood cancers with the CD147 marker (CD Adaptor 147) on them, a marker claimed to be known to be involved in COVID. The implication is that Pfizer is building an investment portfolio in cancer companies that would benefit from the consequences the speaker alleges they caused. In summary, the vaccines on the market are said to be not the same formulation as what was tested in clinical trials, labeling this a “bait and switch” and a fraud, and asserting that vaccine effectiveness numbers are not reliable because the products differ from trial formulations and because those numbers decay over time. The speaker alleges significant DNA contamination, stating that 10 out of 11 studies have found this, with the remaining studies allegedly constrained by financial conflicts. The claim is that consensus among real studies supports DNA contamination, with several studies through peer review, which the speaker notes is difficult for those papers to pass through peer review. It is claimed that five peer-reviewed studies not originally examining contamination found DNA in blood and tissue upon sleuthing. The speaker asserts that cancer is on the rise and that several papers report cancer post-vaccination, including neoplasms at the site of injection. The claim is that this situation cannot be dismissed as coincidence and is described as “liability free” and often mandated. The speaker posits that this may be the largest carcinogenic hit to the human population, with vaccines on childhood schedules and given to pregnant women, stating that “this has gone absolutely off the rails.”

The speaker discusses the issue of DNA contamination in mRNA COVID-19 vaccines and questions the FDA's handling of the situation. They explain that normally rigorous tests are required to ensure safety, but in this case, the FDA ignored those tests. The speaker also mentions that Moderna's own patent acknowledges concerns about DNA and insertional immunogenesis. They reveal that DNA fragments, including an antibiotic resistance gene and sequences from simian virus 40, were found in the vaccines. The speaker expresses shock at the FDA's lack of transparency and highlights the potential risks associated with DNA damage, such as cancer and birth defects.

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.

Speaker 0 posits that every time you consume natural flavorings, you could be eating something developed by human fetal cells. They claim that major food companies, including Pepsi, Nestle, and Kraft, have used a biotech company called Cinomics to create flavor enhancers. The disturbing part, they say, is that these artificial flavors were originally tested using HEK293, a cell line derived from aborted fetal tissue, and that due to legal loopholes they don’t have to tell consumers. They insist: natural flavors don’t necessarily come from nature; they can be chemically engineered in a lab using biotech derived from human cells. The explanation provided is that the food industry knows processed food loses its flavor, so instead of relying on real ingredients, they turn to biotech companies to develop flavor enhancers. Ceramics reportedly found that HEK293 cells, originally from fetal tissue, react to flavors like human taste buds, and by testing these flavors on cells, additives were created to make processed food better, allegedly addicting millions of people worldwide. These chemical compounds were then rebranded as natural flavors. Speaker 0 asserts the why behind it: the food industry is described as one giant deceptive machine that uses loopholes to keep consumers in the dark. They claim that today, even natural flavors can contain over 100 synthetic compounds developed using biotech processes that consumers aren’t told about. The overarching claim is that the motive is profit, not health, and that people are the experiment. If this has been hidden for decades, then they ask what else might be hidden, urging listeners to wake up, check labels, and demand transparency. They warn not to trust food giants that profit from deception, arguing that if manipulation of what people eat is possible, it could extend to manipulating how they think and feel. They conclude by stating that the truth is out and invite viewers to share whether they’ve been fooled by natural flavors in the comments.

In this video, the speakers discuss new information about the mRNA vaccines and the presence of DNA in them. Researchers have found that some mRNA vaccines contain DNA fragments, which can cause issues with gene expression and potentially increase the risk of cancer. The presence of DNA in the vaccines is a manufacturing problem, and it is unclear why it was included. The DNA can enter cells and interfere with important genes, leading to various health problems. The speakers emphasize the need to investigate the extent of DNA contamination in the vaccines and consider stopping their production until the issue is resolved.

The speaker alleges that after receiving FDA Emergency Use Authorization for a vaccine produced via "process one," manufacturers switched to "process two." This new process allegedly introduced contaminants, including foreign DNA and SV40, a cancer-causing substance. The speaker connects this alleged change to a reported increase in aggressive cancers, particularly among young people. Referencing an NIH paper, the speaker claims SV40 is a known oncogenic DNA virus that induces cancers in laboratory animals. The speaker asserts Pfizer knew they were putting a carcinogen in process two. They speculate that this is the reason Pfizer redacted 800 pages of the manufacturing process, citing trade secrets.

The speaker explains that there is contamination in the messenger RNA, including fragments of DNA called cDNA, with one of them being s v 40, a known cancer-promoting segment. The other speaker mentions that mainstream news reports estimate that millions of Americans had cancer due to SV 40 contamination in the past. The first speaker confirms that SV 40 turns on cancer genes and that the spike protein in the shots impairs tumor suppressor systems. They conclude that the shots promote cancer through SV 40 and suppress our ability to fight cancer. The speaker acknowledges that cancer rates are increasing, but the extent to which vaccines contribute to this is still uncertain.

The speaker raises concerns about the contamination of current vaccines with DNA and the unknown consequences of this contamination. They argue that efforts should be made to eliminate DNA contamination, even if it increases production costs. The speaker mentions a researcher from MIT who accidentally discovered that mRNA vaccines were contaminated with DNA. They criticize Pfizer for testing vaccines from one process and then vaccinating billions of people with vaccines from another process, which were contaminated with DNA. The presence of DNA in the vaccines raises risks, including potential cancer development. The speaker believes it is misleading to claim that the vaccines have undergone clinical trials when they have not been properly studied. They call for more rigorous research before commercializing vaccines.

The speaker expresses concern about the presence of SV40 sequences in vaccines, suggesting that their integration into certain genetic areas could potentially cause cancer. They mention the risk of insertional mutagenesis and the delay in bringing gene therapies to market due to this concern. The speaker also advocates for the use of alternative treatments like hydroxychloroquine and ivermectin, stating that they are safe drugs. They question the transparency of the FDA in redacting data and holding clinical data for 75 years. The speaker urges the protection of citizens and calls for one state to take the lead in doing the right thing. No questions are asked.

The speaker asserts that every time people consume natural flavorings, they may be eating something developed by human fetal cells. They claim that some of the biggest food companies, including Pepsi, Nestle, and Kraft, have used a biotech company called Cinomics to create flavor enhancers. The speaker emphasizes that these artificial flavors were originally tested using HEK293, a cell line derived from aborted fetal tissue, and that due to legal loopholes, companies do not have to disclose this information. They repeat that natural flavors do not necessarily come from nature; they can be chemically engineered in a lab using biotech derived from human cells. The explanation continues with a description of how the process works: the food industry knows that processed food loses flavor, so rather than using real ingredients, biotech companies are brought in to develop flavor enhancers. Ceramics (likely a misspoken or misnamed term) is cited as identifying that HEK293 cells, derived from fetal tissue, react to flavors like human taste buds. By testing flavors on these cells, additives were created to improve the flavor of processed food, allegedly addicting millions of people worldwide. The speaker claims that these chemical compounds were rebranded as natural flavors. The broader assertion is that the food industry operates as a large deceptive machine, using loopholes to keep consumers uninformed. The message is that even natural flavors can contain over 100 synthetic compounds developed via biotech processes that consumers are not told about. The speaker claims the issues are driven by profit rather than health, and that people are the experiment. They ask what else has been hidden if this has been kept secret for decades, urging listeners to wake up, check labels, and demand transparency. The speaker warns against trusting food giants that profit from deception, arguing that if they can manipulate what people eat, they can manipulate how people think and feel. The speaker ends by declaring that the truth is out and invites the audience to share whether they have been fooled by natural flavors in the comments.

The speaker raises concerns about the contamination of current vaccines with DNA and the unknown consequences of this contamination. They argue that efforts should be made to eliminate DNA contamination, even if it means higher production costs. The speaker mentions a researcher from MIT who discovered that mRNA vaccines were contaminated with DNA, despite DNA not being listed as a component. They criticize the authorities for testing vaccines without DNA contamination on a small group of people, but then vaccinating billions of people with contaminated vaccines. The speaker highlights the potential risks of DNA contamination, including the possibility of cancer. They conclude by stating that vaccines from the second process should undergo more rigorous studies before being commercialized.

The speaker discusses the presence of contamination in vaccines, specifically cDNA fragments and s p 40, which is a cancer-promoting segment of DNA. They mention that s v 40, a related virus, caused cancer in millions of Americans in the past. The speaker explains that s p 40 turns on cancer genes and that the spike protein in the vaccines impairs tumor suppressor systems. They conclude that the vaccines promote cancer and hinder our ability to fight it. The speaker acknowledges that cancer rates are increasing but questions how much of it is due to the vaccines.

The discussion centers on the role of parasites in food and their potential link to cancer. It suggests that cancer may be a parasitic infection, a view not widely recognized in mainstream medicine. The conversation critiques mRNA technology and vaccines, proposing that they may weaken the immune system, allowing latent parasites to proliferate, leading to multiple cancers. It also raises concerns about synthetic parasites created through advanced technology, which could be linked to the COVID-19 outbreak. The importance of antiparasitic treatments is emphasized, along with the need for a paradigm shift in understanding diseases as toxic reactions rather than infections. The speakers argue that current health crises may stem from engineered biological agents rather than traditional viruses.

The speaker discusses the issue of DNA contamination in mRNA COVID-19 vaccines and questions the FDA's handling of the situation. They explain that normally rigorous tests are required for genotoxicity and immunogenesis, but the FDA seemed to ignore these requirements. The speaker also mentions that Moderna's own patent acknowledges the concerns related to DNA and insertional immunogenesis. They reveal that DNA fragments, including an antibiotic resistance gene and sequences from simian virus 40, were found in the vaccines. The speaker expresses concern about the potential risks associated with DNA damage, such as cancer and birth defects. They criticize the FDA for downplaying the issue and emphasize the importance of transparency.

We stumbled upon articles revealing we're consuming human cell lines. Under an electron microscope, immortal cells resemble "The Thing," gobbling others—scientists describe it as "the blob." This factory food is sickening, like eating cancer. If these cell lines can be engineered, what else can be added? We worry about foreign DNAs assimilating into our cells from DNA vaccines, but creating entire cell lines means manipulating their DNA. Factory-made fake meat is essentially cancer, grown rapidly in a growth medium. It's like throwing a blob into sugar water and watching it grow, devouring other cells. Who knows what this immortal cell line does? This may be from Henrietta Lax's cells or other sources. They add beef blood and other genetic material to engineer a new substance. We must ask, are we trusting organizations like the USDA and FDA enough?

The speaker claims mRNA is in the food supply. Merck has been injecting mRNA into pigs since 2018 with a product called Sequebiti. They claim to be able to make transmissible mRNA, meaning they can put it in an animal so that it transmits to whoever is ingesting it, effectively vaccinating them. The speaker suggests this could be engineered into plants and animals. Without informed consent laws, people who refused mRNA vaccines may get them through their food.

Speaker 1 expresses concern about the presence of SV40 sequences in vaccines, suggesting it is not accidental and could lead to cancer due to insertional mutagenesis. They argue that gene therapies were delayed due to the risk of cancer from insertional mutagenesis. The speaker believes that alternative treatments like hydroxychloroquine and ivermectin are safe and questions why the FDA redacted data on endotoxin levels for 75 years. They emphasize the unusual nature of the current situation and urge the protection of citizens by not administering experimental products to pregnant women and babies. The speaker pleads for one state to take a stand and set an example for others. No questions are asked.

The speaker explains that the messenger RNA in the shots is contaminated with cDNA, including a cancer-promoting segment called s v 40. They mention that s v 40 turns on cancer genes in the human body and that the spike protein in the shots impairs tumor suppressor systems. The speaker suggests that the shots promote cancer through s v 40 and inhibit our ability to fight cancer. They also mention that cancer rates are increasing. The speaker raises the question of how much of this is due to the vaccines.