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There is a new mRNA COVID-19 vaccine, but there is no evidence to support its effectiveness or safety in human trials. Additionally, several studies from different countries suggest that these vaccines may actually increase the risk of contracting COVID-19 over time. This is concerning and not a typical outcome.

Speaker says, "it's a festering wound for people" and, "we cannot sweep it under the rug." They urge action, noting, "the new administration to step up and do something" because "the next you know, they have 500 mRNA shots in the pipeline." They warn, "33 of those are self amplifying, which is just really terrifying." They ask, "What does that mean? Meaning, like, they're designed to continue to replicate indefinitely." They add, "I mean, already the ones we have, we don't have an off switch, and this is like no off switch on steroids." They claim, "They have them in Japan and India and The EU already." They conclude, "They're the one that I think is in the pipeline in The US is for the h one n one."

The USDA approved self-amplifying mRNA injections for rabies and other diseases in cats and dogs. These injections are authorized, widely available for online purchase, and administered by veterinarians. The speaker claims that these injections can possibly shed onto humans. The platform, Nobivac NXT developed by Merck, is available for purchase online. According to the speaker, if pets receive Nobivac NXT, they might shed self-amplifying RNA or antigens onto owners through bodily fluids. The speaker asserts that this was not tested and was authorized regardless. The effects are currently unknown.

Technology is being rapidly advanced and implemented in humans, particularly messenger RNA vaccines. These advancements are being fast-tracked, and it's important to acknowledge that our food species will also be affected by these vaccines.

mRNA and DNA injections are deemed unnecessary, ineffective, and unsafe in this symposium. The idea of injecting foreign proteins into the body without control over their production is considered insane. There is no control over which cells produce the protein or in what quantity, which varies greatly among individuals. The immune system attacks cells coerced to produce and present the foreign protein, leading to inflammation and potential organ damage. Additionally, the choice to use toxic spike proteins, package mRNA in toxic lipid nanoparticles, and grant emergency use authorization is seen as the height of insanity.

These injections now, five years down the line, have been injected into over eighty percent of Americans, about seventy percent of the global population, and it has poisoned the vast majority of the world, their entire body. We actually looked at the genetic profiles of those who received mRNA injections and developed cancer or new onset adverse events, and we found that thousands of gene expressions were dysregulated, and the genes involved cancer control and cancer suppression genes. So those were being screwed up resulting in these cancers as well as immune collapse. And so, yeah, this was a biological attack on humanity.

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 mRNA in vaccines can replicate, including the replication engine, leading to potential spread from person to person. Concerns exist about the inability to stop this replication, with unknown consequences for humanity. The spike protein in these vaccines can be toxic, affecting various tissues. Deployment of this technology in vaccines for humans is already happening, with over 4,000 people injected in Japan.

The current vaccines contain harmful monkey virus sequences and toxic lipid nanoparticles, which are not meant for human use. Many people have already experienced injuries and deaths from these products, but the full effects may take years to manifest. Research shows that these gene therapies can create abnormal proteins, potentially leading to autoimmune diseases. The idea of using this technology for cancer treatment raises concerns, as it disrupts natural immune functions. Health and wellness cannot be achieved through injections or pills; they come from a healthy lifestyle. Questions arise about why some countries, like China, do not administer these genetic injections to their military. Informed consent is crucial, but many patients are unaware of the risks and that these products are not fully approved. The technology remains as unsafe as it was in the past.

Self-amplifying RNA (saRNA) is being fast-tracked in the US after approval in Japan and Europe. SaRNA is similar to mRNA but replicates itself like a virus. Concerns are raised about its biodistribution and persistence, suggesting it could act as an STD. A white paper calls for a halt on saRNA vaccine deployment until comprehensive safety studies address contagious risks. It is argued that Moderna and Pfizer shots already shed and act as STDs, transmitting spike protein infections. SaRNA is designed to replicate and remain strong, potentially causing a contagious cancer-like disease. COVID shots may contain cancer-causing viruses like SV40, possibly with SV40 promoters to enhance their effectiveness. mRNA degrades over time, but saRNA is designed to make more of itself. There are ways to detox from mRNA, but not a self-replicator. Ultramethylene Blue is promoted for cell health, available at the Alex Jones store.

The FDA is fast tracking self-amplifying RNA (saRNA) vaccine platforms, a technology similar to COVID-era mRNA injections, potentially creating transmissible biological agents. Arcturus Therapeutics received FDA fast track designation for its saRNA vaccine candidate for pandemic influenza A virus H5N1, funded by BARDA and the Gates Foundation. Unlike traditional mRNA, saRNA replicates within cells, increasing toxicity, extending persistence, and raising transmissibility concerns. Attorney Tom Renz expresses alarm, stating clinical trials are dangerous and saRNA vaccines could mutate and become transmissible. Yale studies show mRNA persisting in the system for over 700 days post-vaccination, raising concerns about saRNA lasting indefinitely. Renz cites potential SV40 contamination and recombination with wild-type viruses as risks. There are three mechanisms by which saRNA could become transmissible: recombination, contamination, and hyper-stability. Renz criticizes AI's biased assessment of vaccine safety, noting the need to argue extensively with AI systems to reveal potential issues. He warns against AI-driven personalized cancer drugs without long-term safety tests.

FDA, I don't know why, just approved a new Moderna COVID vaccine. Here is the package insert. It's called MN Spike. It's a vaccine indicated for active immunization to prevent coronavirus disease. This product can cause myocarditis and pericarditis, usually within the first week following vaccination. Ingredients include polyethylene glycol, antifreeze. And it codes for the spike glycoprotein. This is the first time in human history that we have injected a product into the body that have forced our ribosomes, protein manufacturing machinery, to produce a nonhuman protein. This product has not been evaluated for the potential for it to cause cancer. not a single, not one randomized controlled trial against a placebo. What do they compare it to? The earlier version of their vaccine. In my opinion, all COVID vaccines should be pulled from the market immediately and a thorough investigation be launched.

A new study indicates mRNA injections induce severe, long-lasting genetic disruption linked to cancer and chronic disease. Comparing gene profiles of mRNA-injured individuals to pre-COVID samples revealed thousands of dysregulated gene expressions linked to mitochondrial failure, suppressed cancer suppression genes, and immune dysregulation. Molecular chaos may result in cardiovascular, neurological, and carcinogenic issues, possibly due to genomic integration of DNA plasmids. A separate study showed mRNA boosters trigger dangerous immune and blood abnormalities, including increased blood clotting and immune suppression, within 48 hours in healthy young adults. Additionally, pets are being used as self-amplifying mRNA vectors via Merck's Nobivac NXT, exposing pet owners to shedding of self-amplifying RNA and toxic antigens. This could potentially cause long-term genetic dysfunction in humans, with the possibility of the synthetic particle recombining with wild viruses. Individuals should ask vets about RNA or mRNA injections for pets and refuse mRNA injections for themselves.

The USDA last year approved self amplifying mRNA injections for our cats and our dogs for rabies and a few other things. And these are authorized and they're widely available for online purchase. And so veterinarians across the country are currently injecting self amplifying mRNA into our pets. If you look up Nobivac Nex NXT, it's the platform developed by Merck. You will find it online, and you can even buy it. It's possible if their dogs or cats receive the Nobivac NXT self self amplifying RNA particles. It's possible they are either shedding the self amplifying RNA or the antigen products that the dogs or cats are now producing onto the owners through bodily fluids. And so, none of this was tested by the way. They just authorized it anyways because they don't care.

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

Self amplifying mRNA vaccine, which got fast track FDA approval a few months ago for the h five n one influenza. "That's even worse, quote, self replicating. We know Pfizer admits that their COVID shot is self replicating, thus sheds. This is officially sheds." "But now, when these self amplifying mRNA vaccines shed, they are shedding machinery that if you take it into your body, will start producing more mRNA." "There are women who miscarried when they were exposed to the Pfizer vaccine or Moderna vaccine." "Pfizer told their officials that they had to report in the trial if any pregnant woman was exposed to anyone who was vaccinated." So shedding was a problem. So many people, like, didn't take it, but their spouse did. They got sick.

The transcript discusses self-amplifying replicon mRNA injections and asserts that they are being deployed for both humans and animals globally. It states that the UK approved Arcturus Therapeutics’ self-amplifying COVID-19 vaccine for adults over 18, and that the European Union previously approved the same inoculation for adults, placing it in both the EU and the UK. It also claims that Japan approved it in 2023, and that India has approved these replicon injections as well, indicating a global rollout. It highlights that in the United States, the USDA approved the self-amplifying mRNA particle injections for pets, specifically mentioning Merck’s Novavax NXT for dogs and cats, and asserts that this is being injected into pets and that shedding onto human owners across the US is possible. It notes that the FDA has fast-tracked an H5N1 bird flu replicon injection trial, emphasizing concern about these developments. The speaker outlines purported dangers of these replicating genetic materials, including the possibility of shedding from humans to humans or from pets to humans, and the potential for recombination with wild viruses to create chimeric mutants. It emphasizes the claimed approval of Arcturus Therapeutics’ injection “everywhere in the clinical trials” and then provides adverse event statistics: eighty-five percent suffered systemic adverse events, and fifteen percent required medical attention. A Uganda study is cited, claiming that the replicon injections induced severe blood abnormalities in ninety-three percent of recipients, with thrombocytopenia, lymphopenia, and neutropenia reported, implying degraded immune systems and increased risks of internal bleeding in a majority of participants. The Uganda study is also described as showing eighty-five percent experiencing vomiting, high fevers, and feeling absolutely terrible. The speaker concludes with a strong stance against these injections, calling them a “self amplifying assault on humanity” and arguing that they should be pulled off the market and banned for human use. The overall message is a warning about global deployment, potential shedding and recombination risks, significant adverse event rates, and a call to ban self-amplifying mRNA injections for humans. The named entities include Arcturus Therapeutics, Merck, Novavax NXT, and references to regulatory actions in the UK, EU, Japan, India, and the US.

Speaker 0: They argue that because the vaccine is classified as such, they don’t have to worry about being sued. They claim immunity from liability is dependent on there being no fraud, and there clearly was fraud. Speaker 1: They say there is fraud. They note that immunity from liability depends on fraud, and in light of that, it matters. They explain that there was fraud. Speaker 0: Expresses surprise and asks for caveats about fraud. Acknowledges there were caveats. Speaker 1: Confirms there is fraud and says it makes the situation more interesting. Speaker 0: Asks how fraud is defined, noting that drugs were sold with multiple studies and only one was good. Speaker 1: Responds with a point about safety testing for the mRNA vaccines. States that the insufficient safety testing was done before release, and that the product injected into billions of people involved DNA plasmids. There is massive contamination in the shots actually delivered, including the SV40 promoter from simian virus 40. The point is that safety testing for one drug was completed, but people were injected with something different that had other components that were not tested, which is described as fraudulent. Speaker 0: Requests an explanation of the SV40 issue for the audience. Speaker 1: Describes production techniques used to generate the product. Explains that a plasmid, a circular piece of DNA, was used to produce the product in vats, with bacteria performing the production, later coated in lipid nanoparticle. There is a requirement to purify DNA and set standards for DNA contamination, with limits that cannot be exceeded. In this case, the problem isn’t only poor quality control but that there was a more painstaking way to produce the same product that did not involve DNA plasmids at all. Consequently, leftover material in vials injected into people contained DNA contamination across the board. Kevin McKernan tested vials, finding DNA contamination in the samples. Speaker 1: Explains that the DNA left over includes the SV40 promoter, a genetic trigger from simian virus 40, which is known to be carcinogenic. Since this promoter is left in the vials from injections given to people, it challenges the claim that the mRNA shots could not integrate into the genome. While acknowledging that there are cellular processes such as reverse transcription, the speaker asserts that even the claim of “no DNA” is false because there is DNA in the vials, specifically DNA with the SV40 promoter, a genetic engineering tool with carcinogenic potential. The speaker concludes that this appears to be fraud: injecting a different product into the public on the basis of safety testing that was conducted with a product produced by a different process. Speaker 0: Reiterates the conclusion: you can’t inject a different product into the public on the basis of safety testing that was done with something produced by a different process.

A peer-reviewed paper confirms Pfizer's mRNA vaccine is contaminated with dangerous DNA and SV40 enhancers. During production, bacterial plasmid DNA led to contamination with spike protein genes, antibiotic resistance markers, and SV40 enhancers. Researchers found four to five times more DNA than the safe limit; these DNA fragments could integrate into the human genome due to the SV40 enhancer. Experiments showed the vaccines were toxic to cells, causing pathological changes and spike protein production, potentially spreading body-wide via exosomes. The DNA contamination, tucked into lipid nanoparticles, could lead to unintended gene therapy. The SV40 enhancer, deliberately added but removed from regulatory paperwork, raises questions about Pfizer's intentions. Experts theorize this contamination could be linked to an increase in "turbo cancers," coinciding with Pfizer's acquisition of a cancer drugmaker. An epidemiologist noted the study found DNA from the manufacturing process way over regulatory limits, including the cancer-promoting SV40 promoter enhancer and spike-producing DNA. A separate study found vaccine spike protein expressed in cerebral arteries of stroke patients for up to seventeen months, potentially contributing to autoimmune responses. There are now 11 independent reports that have found, DNA contamination within these shots of up to 60000% above regulatory limits.

The speaker claims that "The USDA last year approved self amplifying mRNA injections for our cats and our dogs for rabies and a few other things. And these are authorized and they're widely available for online purchase." They say "veterinarians across the country are currently injecting self amplifying mRNA into our pets." They warn that "This can probably shut on to humans and this this has to be stopped" and ask, "Has it started yet?" "Yes." They cite "Nobivac Nex NXT, it's the platform developed by Merck" and that "you will find it online, and you can even buy it." They claim it is "possible... they are either shedding the self amplifying RNA or the antigen products that the dogs or cats are now producing onto the owners through bodily fluids." They add that "none of this was tested" and "they just authorized it anyways because they don't care," and that "it's completely unknown really at this point."

The speaker believes mRNA shots are a "festering wound" impacting everyone that cannot be ignored. The speaker urges the new administration to address the issue, citing 500 mRNA shots in the pipeline, 33 of which are self-amplifying. Self-amplifying means they are designed to replicate indefinitely, which the speaker finds "terrifying" because current mRNA shots already lack an "off switch." The speaker claims these self-amplifying shots are already in use in Japan, India, and the EU. The speaker believes the one in the US pipeline is for H1N1, so it may not be used unless there is an issue, but they are still experimenting with it.

The Pfizer vaccine is contaminated with plasma DNA, not just mRNA. This DNA is the DNA vector used as the template for the in vitro transcription reaction. This was discovered by sequencing vials of Pfizer vaccine from Colombia. It's surprising that there's any DNA in there. The speaker is alarmed about the possible consequences of this, including rare but serious side effects like death from cardiac arrest. Mixing DNA with a lipid complex allows it to enter cells and become a permanent fixture. This is a real hazard for genome modification of long-lived somatic cells, like stem cells, and could cause a sustained autoimmune attack. There is also a very real theoretical risk of future cancer in some people. The risk is not zero and it may be high enough that we ought to figure out if this is happening or not.

The discussion centers on pets being used as self-amplifying mRNA vectors. The USDA quietly approved Merck's self-amplifying RNA shots called Novavac NXT for cats and dogs with no real safety testing. It says it gives a small dose of RNA particles delivered in the Novavac NXT vaccine. RNA copies exponentially in the cells, and the copies are transcripted into large amounts of the desired antigen. The antigen stimulates a more robust humular and cellular immune response. All sounds good in theory. However, these injections may shed messenger RNA and synthetic antigens to human owners through breath, saliva, or fluids may cause long term genetic damage similar to that seen in humans may recombine with wild viruses creating dangerous new pathogens. This rollout puts both pets and their owners into an uncontrolled genetic experiment without consent. “So says Nicholas Holcher, Miles per hour. So masters in public health. We don't know. Nobody tested it. Nobody did any studies. We don't have long term studies. We don't have short term studies. We just don't know. I'm a little scared. I really don't want to be a part of this.” And by the way, they're actually talking about spraying messenger RNA on our crops. How are we affecting our I feel like this is the everybody remember the book Brave New World by Aldous Huxley. I think I had to read it in high school. Was one of those required readings. Or what was the other book? 1984? Like, I feel like we're living in this dystopian universe where we just experiment with all these genetic things and we just throw it into the environment and throw it into our pets and throw it into people, and we don't know what the outcome is until we see. Are we all gonna go the way the dinosaurs? I don't know. Now I really sound like a conspiracy theorist. Are we all gonna like, is somebody gonna come along in a few thousand years and find fossil remains and try to figure out why we all died? I don't know. It's fine. It's fine. It's just a little nervous.” One speaker says they homestead: they raise their own chickens. They’re not treated with chemicals. Their dogs and cats don't get vaccinated with things that might shed into the environment, and they’re growing all their own organic fruits and vegetables. “Yep, I'm I'm I'm going that way. Y'all y'all do what you need to do. It's a little scary. I don't recommend that particular vaccine for your dogs. I I guess that's the bottom line. I don't know. Be careful what you eat.”

Speaker asserts that extremely dangerous self-amplifying replicon mRNA injections are currently being deployed for humans and animals worldwide. A few days ago, the UK approved Arcturus Therapeutics’ self-amplifying COVID-19 injection for adults over 18, and previously the European Union approved the same replicon injection for adults, so it is in the EU and the UK. Japan approved it in 2023, and India has approved these replicon injections as well, indicating rollout across the globe. In the United States, it is claimed that the USDA approved the self-amplifying mRNA particle injections for dogs and cats, specifically Novavax NXT by Merck, suggesting active injection into pets and potential shedding onto human owners in the US. The speaker states that the FDA fast-tracked an H5N1 bird flu replicon injection trial, raising concern given the alleged dangers of these products. The speaker emphasizes the potential for shedding of replicating genetic material from humans or from pets to humans, and the possibility that these replicating constructs could recombine with wild viruses to create chimeric mutants. They highlight a high rate of adverse events associated with the Arcturus Therapeutics injection, claiming that eighty-five percent suffered systemic adverse events and fifteen percent required medical attention. A recent study in Uganda is cited, alleged to have induced severe blood abnormalities in ninety-three percent of recipients, including thrombocytopenia, lymphopenia, and neutropenia, with immune systems degraded and increased risks of internal bleeding in a majority of participants. The report also claims that eighty-five percent experienced vomiting and high fevers, and felt absolutely terrible. The speaker concludes that this self-amplifying assault on humanity needs to end, calling for these injections to be pulled from the market and banned for human use.

Speaker 0 says they found “information like this,” such as vaccine insert paper, with “nothing printed on it,” which they call disheartening and disgusting. They add that it “just keeps happening” and claim the CDC redacts “every single word” of a 148-page study on a myocarditis after COVID vaccination. Speaker 0 says they asked someone to print the study, and that the entire 148 pages are redacted. They ask what a study does if “there’s nothing there,” and they ask what might have been there that required redaction. Speaker 1 says they are “witnessing an active cover up” involving “a colossal consumer product safety debacle” affecting the entire world. They claim that in the United States, the CDC, National Institutes of Health, and FDA are actively involved in a cover up, and that similar cover ups are occurring in the UK with the MHRA, in Europe with European medicine agencies, and in Australia with the Therapeutic Goods Administration. Speaker 1 states that each company that puts out a product has an obligation to produce “ninety days of safety monitoring” after the product comes out, describing it as a regulatory dossier. They claim that if someone has a problem and reports it to a company like Pfizer, Pfizer must report, write down what happened, collate it into a report, and make it publicly available. Speaker 1 says that when the ninety days elapsed for Pfizer’s first vaccine approved on 12/10/2020, Pfizer “didn’t produce a report.” They add that people asked what was happening with the vaccine, and Pfizer allegedly would not disclose what happened, leading to a court case. Speaker 1 says the lawyer for the FDA stepped in to say they did not want to release Pfizer’s dossier for fifty-five years. Speaker 1 then says that after the plaintiff pushed, the Pfizer dossier “slowly” came out. They claim Pfizer recorded one thousand two hundred and twenty-three deaths with their product within ninety days of release, and they say people called Pfizer in desperation watching family members die after taking the vaccine. Speaker 1 also claims Pfizer recorded “over twelve hundred” new adverse events and refers to “doctor Boden” discussing problems they say they have been grappling with. They conclude by claiming the FDA worked to cover this up and should have been regulating the company with at least monthly meetings and full disclosure about novel vaccines, described by Speaker 1 as a genetic transfer technology platform and as the first time human beings were injected with foreign genetic material in world history, after which “they were getting it full on.” Speaker 1 ends by saying “Two thirds of the world’s population took”