While the USDA had previously given the green light for salmon to be vaccinated with the latest mRNA (modRNA) chemicals, this newest scheme is even worse in that it allows even more questionable pharmaceutical chemicals to be administered to animals that people consume as food.

“… the deadly mRNA poison vaccines weren’t enough for the Biden Harris administration,” Renz notes. “They and their big pharma partners are now licensing DNA vaccines for use in our foods.”

Renz shared screenshots from two documents showing that these DNA vaccines not only exist – and the world was not told about them until now – but are already licensed and being used in the U.S. food supply, unbeknownst to most of the country.

“Our food supply is simply NOT safe,” Renz warns.

BREAKING: The USDA is now licensing DNA vaccines in our food!@catsscareme2021 is correct they are vaccinating salmon but what you may not know is that the deadly mRNA poison vaccines weren’t enough for the Biden Harris administration. They and their big pharma partners are now… https://t.co/xF252nZPD5 pic.twitter.com/uvndKC9nBw

— Tom Renz (@RenzTom) October 29, 2024

Check out the following video to see what the salmon industry is already doing to the sea-based food supply:

Would you like some Salmon with your vaccines? I'll pass. pic.twitter.com/t49MA2nkum

— Jessica Rojas (@catsscareme2021) October 28, 2024

(Related: Be sure to also check out our earlier report about how RNA and DNA contamination of the food supply is already much worse than most people realize.)

Beware GMO salmon

Renz’s bombshell so upset Rainmaking CEO Kim Greenhouse (@Rainmaking) that she called on X / Twitter for the USDA to be “charged with crimes, including the FDA.”

“GOD HELP US,” she added in desperation.

Another echoed the sentiment that the USDA – or at least the people running the thing – needs to be taken down as soon as possible because “this is our last chance” to save the country.

“RFK Jr. can’t come on board fast enough as Food Health Czar,” wrote another, desperate for Donald Trump to win reelection and appoint Robert F. Kennedy Jr. as the lead guy for cleaning up the nation’s food supply.

The same person who celebrated RFK Jr.’s potential recalled how during a recent trip to the grocery store, she noticed what she described as “an unusually large supply of salmon on sale.”

“Typically it’s so high priced the store doesn’t stock much,” she continued. “Now I know why mass quantities are available at affordable prices.”

It is clear, wrote another, that the powers that be (TPTB) really want to lower the average lifespan to keep their human herd in check.

“It’s time to raise our own food,” wrote another about a possible solution to America’s highly polluted food supply. “Either alone or in communities.”

“I’m not eating poison or having it put in my body by a vax. I’ll raise my own thank you. Or support small organic local farms. Anything but swallow whatever the global elites want us to swallow. Don’t go along. Demand testing of our food. Raise your own. Go to small farms or on line small co-ops. Anything but taking the govt poison.”

Another agreed, noting that this is why TPTB are starting to go so aggressively against small farmers “so that we do not have a choice.”

“They are even passing laws for backyard chickens to be vaccinated,” this person added. “Some places are making it illegal to sell local products to people.”

More related news about how Big Pharma is deliberately poisoning America’s food supply with all sorts of experimental chemical concoctions can be found at Frankenfood.news.

Sources for this article include:

• X.com
• NaturalNews.com

Plasmids, which are used in the manufacturing process for vaccines, carry genetic material that can inadvertently enter the human body through vaccination. Plasmids can disrupt cellular functions or contribute to the development of antibiotic resistance. These fragments have the potential to integrate into the DNA of vaccinated individuals, potentially disrupting the function of oncogenes and tumor suppressor genes. One troubling aspect is the inclusion of sequences from the SV40 virus, known for its cancer-causing properties. The implications of such contamination are dire, with experts warning of the potential for permanent genetic changes in vaccine recipients.

This serious safety concern necessitates that ALL recombinant vaccines be investigated for DNA contamination. The current findings on DNA contamination across the vaccine supply are startling, and warrant an audit into the manufacturing processes of vaccines, including investigations into the role adjuvants and lipid nanoparticles play in facilitating the DNA contamination of human cells.

Australia taking DNA contamination of COVID vaccines seriously now

The Port Hedland council in Australia recently passed a motion recognizing “unacceptable levels of plasmid DNA contamination” in mRNA COVID vaccines. The motion, which also mandated the dissemination of this information to health practitioners and vaccine recipients, represents a significant shift in how vaccine safety concerns are addressed. Given Port Hedland’s economic significance in Australia, this council’s decision is likely to have far-reaching implications. For the first time, health practitioners are being formally alerted to the dangers posed by plasmid contamination — a topic that has been heavily suppressed since the #plasmidgate controversy surfaced in early 2023.

Adjuvants in Gardasil vaccine may facilitate plasmids into teenagers

Compounding the controversy is a recent exposé written by investigative journalist Maryanne Demasi. The exposé reveals similar issues with the Gardasil HPV vaccine. The report highlights the FDA’s awareness of residual plasmid DNA in Gardasil, a contamination concern that dates back to 2011. This is an issue that has been blacklisted from vaccine safety discussions in the media and between government regulators.

This DNA contamination is made more dangerous due to the use of adjuvants in vaccines. The adjuvant is added to vaccines to enhance the immune response. One of the most common adjuvants – aluminum salts – technically act as a transfection agent, allowing foreign DNA to enter the cytoplasm of human immune cells, which then circulate throughout the body. The implications of this toxic facilitation are profound; the introduction of lab-derived plasmids into the human body poses significant risks, including the potential for cancer and other genetic diseases.

Antigen levels and body weight/blood volume of vaccine recipient are important factors

COVID-19 vaccines use lipid nanoparticles which facilitate the entry of plasmid DNA into human cells. The Novavax vaccine contains a saponin adjuvant that has similar risks as the lipid nanoparticles. A Hepatitis B vaccine (Engerix-B), used in newborn babies, contains both aluminum hydroxide and polysorbate 20. These ingredients act as transfection agents, potentially facilitating plasmids into the baby and setting the stage for childhood cancer.

Moreover, a greater quantity of antigen has a greater chance of introducing plasmids into human cells. Conversely, the DNA contamination could have more pronounced effects on babies with a lower blood volume and body weight. The Engerix vaccine (injected into babies) contains 20 micrograms of antigen, whereas the Gardasil HPV vaccine (injected into teenagers) contains 270 micrograms. The dosage of the antigen is important, as well as the blood volume and weight of the person being injected.

The HPV vaccine contains 13 times more foreign proteins and DNA than the Hep B vaccines. Essentially, the HPV vaccines is equivalent to 13 injections of the Hep vaccine, in terms of antigen quantity. Still, the Hep B vaccine is given to infants, not teenagers, and therefore introduces a disproportionate level of contamination to a baby with lower blood volume and body weight. Both vaccines pose serious DNA contamination risks on two different ends of the exposure spectrum.

All vaccines utilize a risky transfection process using adjuvants

Essential to the function of a vaccine is the term “transfection.” This process allows foreign genetic material to enter human cells — a mechanism that typically doesn’t occur naturally. Human cells possess protective barriers that prevent the uptake of foreign nucleic acids. However, laboratory techniques have been developed to bypass these defenses. The main methods of transfection include:

• Mechanical Disruption: Physically puncturing the cell membrane to allow DNA entry
• Chemical Facilitation: Utilizing chemicals that mimic essential cellular components, acting like a Trojan horse to transport DNA into the cell
• Electroporation: Applying an electric field to create temporary pores in the cell membrane, though this method is less practical for widespread human use

Among these, chemical agents are the most viable for introducing nucleic acids into cells. Commonly used transfection agents include cationic particles, which are positively charged and attract the negatively charged components of cell membranes. Detergents can also disrupt membranes, enabling the entry of nucleic acids. The concern surrounding the use of lab-reagent plasmids is significant. These plasmids can contain nucleotides that may lead to severe genetic consequences, including cancer, if transferred into human cells. When a transfection agent is present, the likelihood of this transfer increases substantially.

While many are familiar with standard transfection agents like lipids (lipofectamine, lipid nanoparticles) and calcium phosphate, a broader range of substances can act as transfection agents. Here are some less commonly recognized ones:

• Polysorbate: A surfactant/emulsifier that can enhance transfection
• Metallic Cations: Elements such as aluminum, zirconium, and cerium, known for their positive charge and transfection efficiency
• Saponins: Soaps used as adjuvants in certain vaccines, promoting transfection
• Histidine: A positively charged amino acid that can aid in the transfection process

Understanding the toxicity potential of these transfection agents is crucial, especially in light of their implications for causing cancer in children, teenagers, and adults.

Sources include:

• NaturalNews.com
• ArkMedic.info [1]
• ArkMedic.info [2]
• Blog.MaryAnneDemasi.substack.com
• Public4PageFreezer.com

Confidential Pfizer documents leaked by Project Veritas show that Big Pharma had “evidence that suggests patients who received a (COVID-19) vaccine are at an increased risk of myocarditis.”

Meanwhile, heavily redacted CDC documents obtained by the Children’s Health Defense (CHD) via a Freedom of Information Act (FOIA) request indicate that the agency provided an undercounted figure of post-COVID-19 vaccination myocarditis cases to Israel’s Ministry of Health in early 2021.

The latest revelations come as Germany, Japan and other governments are raising questions about the significant numbers of severe adverse events recorded in individuals following the administration of the vaccines.

“This study clearly shows that Pfizer’s COVID-19 vaccine provides almost no benefit to children and adolescents, but does increase their risk of myocarditis and pericarditis,” said Dr. Brian Hooker, CHD’s chief scientific officer. “It begs the question: Why does the CDC continue to recommend these unlicensed shots for kids? Where is the data they use to support their statement that the benefits of these vaccines outweigh the risks?”

The Pfizer vaccine provided children and teens in England with only about 14 to 15 weeks of protection against the virus, as per a preprint study of over 1.7 million children ages five to 15.

Moreover, researchers investigating the safety and effectiveness of Pfizer’s vaccine in fully vaccinated, partially vaccinated, and unvaccinated children and teens, also found cases of myocarditis and pericarditis only in vaccinated children. The study found that vaccinated children required slightly fewer emergency room visits and hospital stays, but that those outcomes were extremely rare in children and teens across all groups.

COVID-19 vaccine provides almost no benefit to children, study reveals

Public health agencies in the United Kingdom and the U.S. granted authorization to the Pfizer vaccines based on clinical trials that measured immunogenicity and efficacy against infection.

Their research confirmed that even in 2021, when the vaccine was first authorized for children and teens, that age group did not face a high risk for COVID-19-related serious outcomes, including death or the need for emergency care, hospitalization or critical care.

The researchers tested the effectiveness of the first vaccine dose versus no vaccine and of two doses versus a single dose. They matched each vaccinated child with an unvaccinated one, and participants were matched by age, sex, region, prior COVID-19 testing and childhood vaccination status.

Of the 1,262,784 children in the adolescent part of the study, vaccinated and unvaccinated, there were only 72 emergency room visits, 90 COVID-19 hospitalizations and no deaths. There were nine cases of pericarditis and three cases of myocarditis, all in the vaccinated group.

Among all of the children in the vaccinated versus unvaccinated group, there were no emergency visits, only six hospitalizations and no deaths related to COVID-19. There were three cases of pericarditis, all in vaccinated children.

The researchers concluded that in adolescents, the vaccine reduced the rate of hospitalization more than it increased the risk for myocarditis and pericarditis, but for children, the increased risk of pericarditis was higher than the reduction of risk for hospitalization.

Visit VaccineInjury.news for similar stories. Watch this video featuring a discussion on COVID accountability. This video is from the Sanivan channel on Brighteon.com.

Sources include:

• ChildrensHealthDefense.org
• Brighteon.com

According to TMZ:

Taylor’s husband didn’t provide a cause of death, but noted the plan is for her organs to be donated. He signed off by saying they weren’t able to financially prepare for the hardship that would come with her passing — linking to a GoFundMe for fans who are able to help.

Back in August, Taylor addressed the medical issues she had been facing — telling her followers she felt like she’s been “fighting for my life every day” … saying she was going through indescribable pain, sometimes wishing she was dead.

Deaths such as these have become more common since the rollout of the Covid-19 injections. While there is no way to know if she was “vaccinated” or if the jabs contributed to her death, it’s a question that is always worth asking. Corporate media certainly never asks.