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525 hogs were given a live mRNA vaccine, resulting in 25 deaths, 55 near-death anorexic cases, lameness in 20, loss of condition in 12, and near-death symptoms in 25 more. Autopsies revealed remnants of the vaccine in the meat. This poses risks for consumers and producers, affecting both health and business. The concern is the presence of live virus in meat for consumption and the impact on animal health and business sustainability. Share thoughts in the comments and spread awareness. Support local and American products.

We are making this dream a reality with this announcement. The COVID vaccine has proven to be highly effective, although its logistics were complex due to the new technology.

The Pfizer vaccine has undergone standard clinical trials and received provisional authorization in New Zealand. It is not considered to be in a trial period anymore. With hundreds of millions of doses administered worldwide, there have been no alarming or unexpected findings. The evidence gathered from these vaccinations aligns with what was observed during the clinical trials and in other countries.

Speaker 0 asked for the impossible: to develop a vaccine in 8 months instead of 10 years without cutting corners. They emphasized safety. Speaker 1 questioned Pfizer's transparency in mutating COVID viruses. Speaker 0 stressed the importance of vaccination for public health. Pfizer's CEO discussed vaccine production and effectiveness. They thanked the US government for support. The CEO highlighted the vaccine's 95.6% efficacy. The conversation ended with a call for public vaccination.

Vaccines are seen as magical but expectations should be tempered. Pfizer's vaccine is 95% effective, but efficacy drops over time. Boosters may be needed annually. Moderna is working on a combined flu and COVID vaccine. The future is uncertain, but we must adapt.

Speaker 0: This is Prevenar, made by Pfizer. There are several products on the market, but the concept is the same. This is one of the studies that brought this product to market. Here’s what I want to show you. You’ll notice up here, this is the number of patients in the placebo group. This where my finger is is the control group that was treated, and then this is the placebo group. Notice how many there are. What it says is you need to treat forty two thousand two hundred forty patients with the vaccine Prevenar in order to prevent forty one cases of pneumonia. And they all get the benefits of the potential side effects of the drug. Let’s look at that quickly. Section 6.2 in the package insert, lymphadenopathy cyanosis in the pediatric population, anaphylaxis, hypotonia, reduced tone in kids that get this vaccine, skin and subcutaneous disorders, vascular disorders, etcetera. In this vaccine is polysorbate 80 and aluminum as an adjuvant. Aluminum neurotoxin. Of course, there’s section 13.1. The product has not been evaluated to see if it causes cancer or interferes with reproductive health. Pretty important information to know.

The Gates Foundation and Difida have partnered on various projects, including their work on livestock. They aim to improve animal survival through vaccines and better genetics, resulting in increased productivity. This has had a significant impact in Ethiopia, where chickens are laying more eggs, providing better nutrition, and even contributing to small savings in households. Edinburgh is a hub for top-notch research in this field, which is why Dipit and the Gates Foundation are funding scientists there.

Medicines we know from the COVID vaccine. Very effective, very welcome. The logistics around that vaccine were not straightforward because of the new technologies. We're talking about countries here that do not have advanced

We are taking precautions to protect our team members from COVID-19 to avoid any interruptions or wastage of vaccine doses. To ensure this, we are considering providing an additional batch of vaccines to our collaboration partners and team members. Regarding the vaccine mandate, Pfizer imported our Vaxa vaccine specifically for our employee vaccination program. This was done to ensure that no vaccines were taken from the European contingent.

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.

We achieved over 90% efficacy with our vaccine, providing protection against all identified variants, including the challenging South African variant. Studies in South Africa showed 100% efficacy. While two doses offer limited protection against Omicron, three doses are effective against hospitalizations and deaths. A fourth booster may be needed. The Pfizer COVID vaccine was not tested for stopping transmission before market release. No serious adverse events were found in our data analysis. Lawsuits have been filed against Pfizer for alleged misrepresentation of vaccine effectiveness and safety concerns. The success of our vaccine is a significant scientific breakthrough.

In 2022, the first mRNA vaccine for pigs was approved, developed by Zoetis (formerly part of Pfizer), but meat labeling isn't required. Consumers eating pork may unknowingly consume meat from mRNA-vaccinated animals. The vaccine targets porcine epidemic diarrhea virus (PEDV), common in confined pigs on industrial farms. Pasture-raised pigs, with fresh air, space, and natural disease resistance, don't typically have this issue. mRNA technology is approved for pigs but is still being researched for cattle and poultry, so long-term risks in livestock and humans are not fully understood. To avoid mRNA in pork, consumers should know their farmer and choose pasture-raised options. No vaccines or mRNA vaccines are used in nourished pork production.

I spoke with Pfizer's CEO, Albert Bourla, about the approval process. We discussed vaccine safety and serious side effects. Many companies and institutions are embracing the COVID vaccine due to its effectiveness. Logistics are crucial in this process. Translation (if needed): I talked to Pfizer's CEO, Albert Bourla, about the approval process. We talked about vaccine safety and serious side effects. Many companies and institutions are adopting the COVID vaccine because it works well. Logistics are important in this situation.

Vaccination is presented as one of the most important advancements for farming livestock in the modern age, and the greatest leap forward in fish farming welfare since its mass adoption in recent decades. The transcript notes that most livestock in The UK are vaccinated, and fish are no exception, though they present unique challenges in vaccination. A specific example is shown: Atlantic salmon smolts being vaccinated at Scotland’s Inchmore facility, described as one of the country’s most advanced freshwater facilities. The process begins with an anesthetizing bath to knock the fish out, avoiding flopping during precision treatment. Once anesthetized, juveniles are oriented upright and forward. A “fish flippers” machine is mentioned as part of the setup, reflecting a real piece of automation. Each fish is imaged, and the automated vaccinator positions every fish in line with its injector. The system administers a cocktail of vital vaccines as quickly as possible. The machine has eight injectors and can vaccinate up to 18,000 fish an hour. Throughout the process, highly trained technicians monitor the operation. The transcript notes that this process used to be done by hand, and at many farms it still is, which takes vets and techs weeks. The current system streamlines the process, with vaccinated fish returning to hatchery tanks to recover and resume a normal feeding schedule. The broad question addressed is: why are farmers vaccinating their fish? The explanation is that bacterial and viral diseases aren’t typically an issue in hatcheries, which are biosecure facilities with little environmental interaction. The real exposure occurs when fish are at sea in ocean pens, where they’re exposed to the surrounding environment and pathogens. Salmon are transferred from freshwater hatcheries to seawater pens once they reach a certain size, following a migratory pattern akin to the wild. The environment of ocean pens makes them more susceptible to pathogens, so vaccinating fish against more than a dozen common salmon diseases helps maintain a significantly higher standard of welfare by reducing the impact of infections when they occur. Vaccinations are also credited with the near elimination of antibiotic use in salmon farming. With broad adoption of vaccines and improvements in vaccines, antibiotics have disappeared relative to years past as more fish get vaccinated. The transcript frames this as one of the many protective measures undertaken here in Scottish salmon farming by vets and biologists to improve practices. And it concludes that vaccinating fish is safe for the fish and for people.

Speaker 0 notes that vaccines are entering the food chain in several species. He mentions that currently, all farmed shrimp are being vaccinated with mRNA, and that pork is an unknown amount being vaccinated with mRNA. He references Merck, described as one of the originators of ivermectin, and asks why they didn’t make a big fuss about the money they lost during COVID because of the inability to sell ivermectin into the whole thing, suggesting they could have been a kingpin in this, and they were silent. He says this is because they own a lot of mRNA companies. He notes that some of the companies state on their advertising, “we put the right gene in your livestock vaccine.” He states there are vaccines going into the swine industry, but there is no data on how much is being sold, where, and who the buyers are, so the volume remains speculative. The technology is described as customized vaccines where, on a farm, they take samples of the diseases on the farm, then go into the lab, and a few days later, they produce an mRNA vaccine customized to the farm’s diseases. He emphasizes that there’s no testing, no research, nothing. They have a general understanding of the mRNA aspect of it on a general standpoint, but for each of these antigens, there is known no understanding.

A study involving 525 hogs injected with a live mRNA vaccine revealed concerning outcomes. After 21 days, 25 hogs died, 55 became severely anorexic, 20 experienced lameness, and 12 showed loss of condition. Overall, 30% of the animals either died or exhibited near-death symptoms. Autopsies revealed remnants of the live virus vaccine in the meat of deceased hogs, raising consumer health concerns regarding the presence of a live virus in meat products. For producers, this situation poses risks to animal health, herd viability, and business sustainability. It’s important to spread awareness about these findings and support local American products.

Vaccinations are crucial for livestock and have significantly improved fish farming welfare. In the UK, most livestock are vaccinated, including fish, which face unique challenges. At the Inchmore facility in Scotland, Atlantic salmon smolts are first anesthetized to ensure a smooth vaccination process. They are then positioned in an automated vaccinator that can immunize up to 18,000 fish per hour, a significant improvement over the manual method that used to take weeks. Salmon are vaccinated to protect against bacterial and viral diseases encountered in seawater pens after leaving bio-secure hatcheries. This proactive approach enhances fish welfare and has led to a dramatic reduction in antibiotic use in salmon farming. Overall, vaccination is a safe and effective measure for both fish and consumers.

We ensure there is enough capacity and competition for vaccines, leading to lower prices and the development of new vaccines. This includes vaccines for TB, malaria, HIV, and even COVID-19. To improve vaccines, we aim for longer duration and broader coverage, and plan to replace needles with patches. The pandemic has shown that we have not invested enough in these innovations. Our partners in India play a crucial role in achieving these breakthrough products.

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.

Medsafe has approved the Pfizer BioNTech COVID-19 vaccine for use in New Zealand. This provisional approval was agreed to and gazetted today by Medsafe. This marks the start of a new chapter in New Zealand's COVID-19 response and is a significant milestone. The most important things under consideration have been the safety, effectiveness, and quality of production of the vaccine. Medsafe's assessment process is extremely robust. Medsafe has completed its work with its advisory committee, looking at the data from clinical trials to advise on using the Pfizer vaccine in New Zealand. Even as the vaccine is rolled out, New Zealand's elimination strategy is still the way the country is dealing with the virus. Medsafe's process is meant to reassure New Zealanders that this vaccine and others that come after it are safe, effective, and the right thing to use in New Zealand.

Speaker 0: Extremely dangerous self amplifying replicon mRNA injections are currently being deployed for humans and animals across the globe. A few days ago, The UK approved Arcturus Therapeutics self amplifying COVID nineteen injection for adults over 18. Previously, the European Union approved the same Arcturus Therapeutics replicon injection for adults. So it's in The EU. It's in The UK. Japan approved it in 2023. So it's being injected into Japanese citizens as well as India. India has approved these replicon injections as well. And so it is being rolled out across the globe and here in The US is very worrisome. The USDA approved the self amplifying mRNA particle injections for our dogs and cats. This is Novavac NXT by Merck. And so that's actively being injected into our, our pets and probably shedding onto human owners across The United States as well in The US. Our FDA fast tracked an h five n one bird flu replicon injection trial, and we have to remember just how dangerous these are. So not only can they likely shed this replicating genetic material can shed onto other humans or from our pets to humans to the human owners, but they can also recombine with wild viruses and and create these chimeric mutants. But what's most important is this Arcturus Therapeutics injection being approved everywhere in the in the clinical trials for them. Eighty five percent suffered systemic adverse events, fifteen percent required medical attention. And then a recent study in Uganda, it induced severe blood abnormalities in ninety three percent of the recipients. They suffered from thrombocytopenia, lymphopenia, neutropenia. So their immune systems were being degraded, and they were suffering inter increased risks of internal bleeding in a majority of participants. And eighty five percent of them were vomiting, had high fevers, and felt absolutely terrible. So this self amplifying assault on humanity needs to come to an end. We have to pull these off of the market and ban them for human use.

Vaccines generate significant profits for companies. Adding just one vaccine to the infant child schedule can result in $1 billion in annual sales. The widespread COVID-19 vaccination has been highly lucrative for Pfizer, earning them $54 billion in 1.5 years. Moderna, on the other hand, made $56 billion, while Moderna made $34 billion during the same period.

Excitement surrounds the discussion of Pfizer's top-selling drugs as of 2019, which includes four medications and one vaccine. The clinical trials for these drugs involved long-term safety follow-ups, often lasting several years with placebo control groups to assess various health impacts. In contrast, the vaccine Prevnar had only a six-month safety review, using another vaccine as a control rather than a true placebo. This raises concerns about the thoroughness of safety evaluations for childhood vaccines, which are administered multiple times in the first six months of life. The disparity in study lengths suggests that economic interests may drive pharmaceutical companies to minimize safety testing to expedite market entry, raising questions about regulatory oversight.

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.