How ‘One Health’ Could Become A Global One Health Disaster

How ‘One Health’ Could Become A Global One Health Disaster

ER Editor: Dr. Byram Bridle usefully walks us through standard vaccines vs. mRNA injections in the first half of his piece. Our concern here is with the second half of the article: the immediate plan to use mRNA vaccines on animals, both for the welfare of the animals themselves and for humans through our food sources. This is already starting in Australia.


How ‘One Health’ Could Become A Global One Health Disaster

A Call for a Moratorium on mRNA Vaccines for Veterinary Use

This article discloses a major new concern that I have with mRNA vaccine technology in its current form. As such, I have taken care to build the rationale for this. Please take the time to read to the end because this is an issue that could potentially affect us all and should be opened to discussion and scientific investigations.

The Elegant Concept of Vaccines

The purpose of a vaccine is to simulate infection with a pathogen so a person can mount a protective immune response without having to be exposed to the risks associated with the disease caused by the pathogen. Naturally acquired immunity represents the gold standard that vaccinologists try to achieve with their immunization technologies. Natural immunity is usually broadly reactive to minimize risk of immunoevasion, confers long-lasting protection against acquisition of the disease and prevents transmission of the causative pathogen to others. In principle, the concept is sound. In practice, we still have much to learn about natural immune responses and some vaccines come closer than others to achieving this gold standard of immunity.

Lipid Nanoparticles and mRNA Vaccine Technology

Messenger RNA is a genetic blueprint that cells use to manufacture proteins. This can only happen if the mRNA can get into cells. To facilitate this, mRNAs get packaged into tiny bubbles made of fat, called lipid nanoparticles (LNPs). When LNPs come into contact with the fat layer that surrounds cells, which is called the cell membrane, they fuse and release the mRNAs into the cell.

LNPs were originally designed with the goal of delivering drugs throughout the body, including into the brain to treat things like Alzheimer’s diseasebrain cancers, and Parkinson’s disease. They were also being tested for wide-spread delivery of genetic blueprints to try to correct genes associated with diseases; known as gene therapy. However, one of the major roadblocks to using LNPs for these purposes was that multiple administrations resulted in excessive toxicities, in part due to activation of inflammatory mechanisms of the immune system. As a consequence, companies strategically decided to try using LNP-encapsulated mRNAs as vaccines. The rationale was two-fold:

  1. The immune system needs to detect something as being dangerous before it responds to it. LNPs containing mRNAs are highly ‘reactogenic’ and, therefore, perceived as being dangerous to the body. By virtue of being reactogenic, this technology induces inflammation, which is the foundation for any immune response.
  2. According to Health Canada, “An ideal vaccine is… effective in providing lifelong protection against disease after a single dose that can be administered at birth”. For multiple reasons, including having immature immune systems, newborn babies cannot respond properly to vaccines, so my opinion is that a couple of doses would normally be required for an ideal vaccine in infants and they would have to be administered well after birth. However, for those with fully mature immune systems, it is reasonable and, therefore, correct for Health Canada to expect that a good vaccine would only require a single dose to provide “lifelong protection against disease”. They appropriately left out the last-ditch effort of ‘reducing severity of disease’ in their delineation of an ideal vaccine. As such, companies working with LNPs that are toxic when administered multiple times latched onto the concept of using LNP-encapsulated mRNAs as vaccines in adults, where they would theoretically only have to be delivered once.

Therefore, companies like Pfizer/BioNTech and Moderna made LNPs containing the mRNAs that encode the spike protein from severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), which is the causative agent of the novel coronavirus disease that was first identified (ER: or lab-created?) in 2019 (COVID-19). These products were tested to assess their potential to be used as vaccines.

mRNA ‘Vaccines’ Failed to Meet Expectations

Unfortunately, the mRNA products against COVID-19 failed miserably to live up to Health Canada’s definition of an ideal vaccine. First, they fail to protect against infection and acquisition of disease. And, on the basis of fifth doses (and beyond) now being recommended in Canada, they don’t come close to being effective with a single dose. Alarmingly, this means the entire premise of using them as vaccines to avoid multi-dose-associated toxicities has been lost. As such, Health Canada would likely be compelled to define the mRNA COVID-19 products as being as far from ideal as one can possibly get while still trying to cling to the otherwise elegant concept of a vaccine. Remarkably, in the United States, they had to change the definition of a vaccine to be able to apply this term to this technology once the aforementioned flaws were unveiled by the public rollout. At the end of the day, the public are expected to make their own informed decisions about vaccines, and their general perception matches the classical textbook definition of a vaccine, which is something that induces an immune response that protects a person from getting the disease and prevents them from transmitting the causative agent to others. As such, the public needs to be aware of how far from a benchmark vaccine the mRNA products are.

The COVID-19 ‘Vaccine’ Rollout Has Revealed Troubling Features of The Technology

Global experimentation on the public has revealed key problems with mRNA ‘vaccines’ that public health officials decided were not best studied prior their rollout. These include:

  1. Induction of immune responses that are far from protective. They cannot prevent infection, nor transmission. This means that they apply a sub-lethal immunological selection pressure against pathogens that are prone to mutation. This is a classical recipe for driving the emergence of variants that can evade the immune system. In short, it is not only probable but even likely that the mRNA products have accelerated the emergence of the new variants of SARS-CoV-2 that we keep hearing about.
  2. Identification of safety signals. Members of the public, outside of the context of the official and ongoing clinical experiments, have been used to identify an array of side-effects that were missed in the rush to get the mRNA products to market. These adverse events have the potential to be lethal. Publicly admitted ones include blood clots, myocarditis, pericarditis, and anaphylactic shock. The very mechanism of action of the mRNA products is cause for concern. Getting a person’s own cells to express the spike protein from SARS-CoV-2 means, by definition, that those cells will be killed by the ensuing immune response. The degree of this self-destruction and whether it can spill over into long-term autoimmune diseases remains understudied and actively debated within communities that still allow reasonable discussions to occur uncensored. By virtue of sole reliance during the rollout on passive monitoring systems, which substantially underestimate side-effects, additional dangers are also the subject of ongoing heated debates. Regardless, mRNA vaccines are admittedly unsafe and even lethal for at least some recipients.
  3. mRNA vaccines are injected into muscles, get distributed throughout the body seeding a wide array of organs and tissues, and these vaccines can be shed from the body. For example, it was recently demonstrated that mRNA COVID-19 ‘vaccines’ could be detected in the breastmilk of nursing mothers.

One Health: Vaccinating Animals to Protect the Health of People

The concept of ‘one health’ is that the health of people, animals, and the environment are interlinked and interdependent. The health of one can potentially impact the health of the other two. For example, the most potentially dangerous forms of the ‘flu’ occur when human influenza viruses exchange chunks of genetic material with influenza viruses that infect pigs and birds. This can result in outbreaks in the human population of swine and avian flus. There are also zoonotic pathogens that can be transmitted, unchanged, from animals to people. As such, there are growing efforts to to promote global human health by mass vaccinating animals. (ER: Surely this is a pretext for nefarious agendas!) The concept is elegant. If the animals can’t get a disease and transmit the causative agent to people, this could avoid outbreaks in the human population. (ER: Which sounds incredibly naive to us.)

One Health: Fast-Tracking of Veterinary mRNA Vaccines

Some people may be unaware that a large number of mRNA vaccines are being developed with the goal of administering these to species of veterinary interest. The first clinical testing of a mRNA vaccine was actually in cattle, preceding the rollout into people. Australia has a good example of new mRNA vaccines against Foot and Mouth Disease and Lumpy Skin Disease being fast-tracked as a way to address the economic impact of these diseases on their livestock industry. Yes, warp speed-like development of mRNA vaccines has been adopted by the veterinary industry. I encourage you to conduct a literature search, which will show that mRNA-based vaccines are being developed for a wide array of other pathogens, including influenza viruses in poultry and swine.

Why Should People Care About mRNA Vaccines for Veterinary Applications?

There are at least three reasons…

  1. If veterinary mRNA vaccines targeting pathogens that can infect people are as far from meeting Health Canada’s definition of an ideal vaccine as the COVID-19 products, then massive numbers of animals will be conferred with fare from sterilizing immunity. This, in turn, could produce massive reservoirs of animals around the world that can promote the emergence of unique and potentially immuno-evasive variants of zoonotic pathogens that could then infect people. Global regulators must insist, without compromise, veterinary mRNA immunization products for zoonotic pathogens confer sterilizing or near-sterilizing immunity, unlike the mRNA ‘vaccines’ for people. This means that animals receiving these products should not be susceptible to the target disease, nor should they be able to transmit the causative agent to others, especially humans. Unlike COVID-19 ‘vaccines’, veterinary mRNA vaccines should be required to undergo formal transmission testing as part of their approval process.
  2. COVID-19 mRNA ‘vaccines’ are injected into muscles, they distribute throughout the body and can leave the body such as via breastmilk. What if the vaccines can get into edible tissues of food animals? It would not be safe for people to consume veterinary mRNA vaccines in milk, eggs, and meat. Careful testing needs to be done to determine how long mRNAs from vaccines last in veterinary species. This would determine, in part, the ‘wash-out’ period, which is how long one needs to wait before obtaining food from agricultural species to ensure humans are not exposed to the medical product. Worse, wherever mRNA can be found, we can likely expect there to also be the protein that it encodes. This represents one of my biggest concerns about veterinary mRNA vaccines. Proteins are more durable and, therefore, longer lasting than mRNAs, and the synthetic mRNAs in vaccines last much longer than their natural counterparts. The potential problem here is the phenomenon of oral tolerance. Our immune systems are designed to interpret things that we eat as being non-dangerous. This is to avoid harmful chronic inflammation in our gastro-intestinal tract, as well as food allergies. When we eat something, even in tiny quantities, our immune system gets programmed to ignore it. Now, consider the possibility of eating or drinking key target proteins from pathogens that are dangerous to people. If our immune systems were to be trained to ignore these critical parts of pathogens, we would become more susceptible to the diseases they cause. By virtue of trying to protect ourselves by vaccinating animals, we could, theoretically and counterintuitively, render ourselves more susceptible to diseases. This could be disastrous for public health. Talk about a potential downside of ‘GMO foods’ (GMO = genetically modified organism).
  3. Concern for the well-being of the animals, especially if multiple different mRNA vaccines that require repeated dosing are used. mRNA vaccines are not entirely safe in people, especially if more than one dose is administered, and this may apply to animals as well. Care must be taken to ensure that animal welfare is preserved, along with their ability to reproduce efficiently. Research in animals represents an ideal scenario to conduct extensive and careful studies into the safety of mRNA vaccine technologies, including addressing the numerous legitimate, well-rationalized safety questions that have been raised but largely ignored during the rollout into humans.

The Precautionary Principle

In this article, have I proven risks of veterinary mRNA vaccines? No, that was not the purpose. It is possible that these concerns will one day be allayed by the careful conduct of scientific investigations; and let’s hope that is the case. However, as a medical scientist, I lean on two key principles when it comes to public health and safety…

  1. Hypotheses that are formulated with a strong scientific rationale are the legitimate starting point for discussions and investigations.
  2. The precautionary principle is that novel medical products should never be implemented into practice until very high standards of safety and efficacy have been proven. And when it comes to safety, this would include addressing all well-rationalized scientific concerns, including those that were deemed inappropriate to raise during the rollout into humans. Hopefully, a return to our scientific roots and principles will be allowed prior to veterinary mRNA vaccines being licensed for routine use.

What to Do

  1. Scholarly debate. No scientific topic should be off-limits for respectful discussions. The issues raised in this article should be critically assessed to either affirm or allay these concerns. After all, robust, uncensored scholarly debate represents the best way to ensure both the safety of the public when it comes to novel medical technologies, including making sure they are fully informed when making their own decisions.
  2. Research. Governments need to recognize the potential for mRNA vaccine technologies to not only have positive global impacts on health, but also the possibility of substantial negative outcomes. mRNA vaccines and funds for research need to be made readily available to third-party investigators to run critical experiments to address questions like, but not limited to:
  • Do veterinary mRNA vaccines induce immune responses that protect against infection?
  • Do they protect against transmission of the causative agent of the disease?
  • Do veterinary mRNA vaccines or any of their components, including the proteins they encode, get into milk, meat, eggs, and/or other food products (e.g., livers, etc.)?
  • If so, how long are they present?
  • Can consumption of proteins from zoonotic pathogens potentiate oral induction of immunological tolerance that would render a person more susceptible to the disease being targeted?

Until the concerns raised in this article are definitively addressed, it is my expert opinion that no mRNA vaccine intended for veterinary use (nor any for human use, for that matter) should be licensed by any regulatory body. This is for the sake of both human and animal health.

Overly rapid deployment of this technology anywhere in the world has the potential to cause public health problems elsewhere on the globe. After all, pathogens do not respect boundaries. Those developing mRNA vaccine technologies need to give consideration to their fellow human beings. What you do could impact the health of those around you, and not necessarily for the better.




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Is C60 And EDTA Safe? Clinical Review

Is C60 And EDTA Safe? Clinical Review

by Dr. Ariyana Love (ND)

There are some drugs being promoted by independent media and fringe Medical Doctors that are quite dangerous. The two drugs in question are C60 and EDTA. We are going to look at the clinical research that has been done to determine if these drugs are truly safe and effective treatments for COVID poisoning and if there’s a better solution.

Given what Pharma is doing to humanity now, I cannot comprehend why anybody would continuing trusting pharmaceutical drugs. Adding toxicity to poisoning is totally the wrong treatment! When poisoned, you must detox a person and then support their immune system with antioxidants and super nutrients so their body can recover and biological damage can be reversed. Pharma drugs leave a person totally exhausted and the immune system drained. Without supporting the immune system, you are not giving an effective treatment protocol.

Dr. Zev Zelenko was a perfect example of medical ingenuity using the allopathic system. He knew to prescribe drugs for his patients that effectively kill parasites, like Ivermectin but he didn’t stop there. Dr. Zelenko also provided immune support and detox supplementation, like his Z-Stack and Z-Detox. This is what Pharma educated MD’s largely fail to do. You can order from Dr. Zelenko’s website, here.

C60 is being promoted by lawyer Todd Calender as a treatment for jab injured persons and by Independent Journalist Sarah Westall, who is promoting C60 and frequency treatment for vaxx detox. These are completely wrong treatments. I have many testimonials from jab injured clients who became severely worse weeks after any kind of frequency treatment. This is because frequency activates the self-replication of the magnetic nanotechnology, as explained in the toxicology report entitled, “Toxicology of chemically modified graphene-based materials for medical application”.


EDTA and C60 are cytotoxic and neurotoxic poisons. C60 is being used now as a CHEMO drug and as a Pharma treatment for HIV. It contains metallic nanoparticles that can cross the Blood Brain Barrier (BBB). Metallic nanoparticles are toxic to living cells. Studies show that C60 also induces cancer growth. Isn’t it diabolical how Pharma always uses drugs that induce cancer when “treating” cancer?

Fullerene C60 is being marketed as a nutritional supplement when in fact C60 is an industrial lubricant. This study shows that C60 induces chronic nephrotoxicity. Mice who were injected with C60 had macroscopic lesions of the kidney(s) and this study showed that C60 failed to prolong the life span of mice. So why the hell are people using it?

C60 damages your DNA as another study shows.

“A large-scale association study for nanoparticle C60 uncovers mechanisms of nanotoxicity disrupting the native conformations of DNA/RNA C60 enables to disrupt the structure of G-quadruplex DNA, and thereby provides a possibility to activate the telomerase by facilitating its access to telomeres and in this way promotes the proliferation of tumor cells.”

Another study reveals that fullerene C60 accumulates in the body following repeated exposure and therefore increases the concern for a potential to induce detrimental health effects in the long-term. If the body cannot process the metallic nanoparticles and eliminate them then you are essentially poisoning yourself.

What’s most disturbing is that C60 has a resonant mode shape in the Terra Hz band. This would make it an ideal body control medium through phase array that can be focused on an individual or group for targeted activation. Terahertz antennas can excite the C60 nano molecules at their resonant frequency and cause the cell they are near or in to burst.


EDTA is another dangerous pharmacopeia drug that Ana Maria Mihalcea (MD) is promoting as a heavy metal chelator.

EDTA has been found to be both cytotoxic and genotoxic in laboratory animals.

“The binding of divalent and trivalent cations by EDTA can cause mineral deficiencies, which seem to be responsible for all of the known pharmacological and toxicological effects. Sensitivity to the toxic effects of EDTA is, at least in part, related to the deficiency of zinc.”

EDTA was also determined to be an environmental hazard. It’s toxic and inhibits cellular division and chlorophyll synthesis.

Lastly I wish to point out how animals were severely harmed in the testing of EDTA and C60.


There are plenty of natural medicines that will effectively detox your body of heavy metals. Nature is always more superior to synthetic, chemical drugs because they work with our body and empower our bodies to heal and restore to balance. Sea salt is the greatest chelator of all and it’s all natural without any toxic side effects.

For example, redox molecules are isolated from sea salt and redox molecules repair damaged DNA. They chelate or remove toxic metals, increasing natural endogenous production of antioxidants, enhancing protection from free radicals and promote apoptosis (death of cancerous or mutated cells). There’s plenty of research demonstrating how redox molecules effectively chelate metals so there’s never a need to use dangerous, toxic drugs such as EDTA. Redox molecules also increase endogenous glutathione by 800%.

You can read more about redox molecules here and you can order redox molecules here.

Ph Miracle Products Prime Ph supplement is a natural sodium chlorite solution that’s also derived from sea salt. It is a powerful oxidant that’s activated by our stomach acids. It chelates the body of toxic metals and binds to the bad acids through our stomach, easily expelling them from the body. Order Prime Ph here.

Blue Green Algae from Klamath Lake, Orgeon, is another natural heavy metal chelator. Blue Green Algae is the most nutrient dense food known to man, far superior to Spirulina. Blue Green Algae increases adult stem cell production and does targeted cellular repair. Read more and order here.

Borax is another effective heavy metal chelator. This natural salt derivative is a powerful treatment for autoimmune disease, reduces inflammation and treats chronic pain. Make sure you use a natural source.

Young Living’s Pine needle oil is far superior than Ivermectin at destroying parasites, especially when you combine it ideally with lemon peel oil and clove, sage, oregano or geranium. Order Young Living Essential Oils here.


Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents

Snake Venom Key Ingredient In “Covid-19 Vaccine” Patents

By Dr. Ariyana Love, ND

The world premier documentary Watch The Water aired on Red Voice Media this week. Dr. Bryan Ardis dropped a bombshell during his interview with Stew Peters about one of the greatest conspiracy truths of all time. The intentional poisoning of the world’s population through our municipal water supply using snake venom.

Please see: VenomTech company announces massive library of SNAKE VENOM peptides for pharmaceutical development; “nanocarriers” stabilize snake venom in WATER (PubMed)


Most snake venoms contain proteolytic enzymes. I found Snake venom in ten Covid-19 vaccine patents listed as “venom” and “proteolytic” (enzyme).

Snake venom is being recently touted as an “anti-HIV” drug, since January 2022. There’s six PLA2s from Snake Venoms patents “against HIV”. These synthetically derived snake venoms are marketed under the guise of being “antiviral” and as a preventive treatment for HIV infection.

The study claims snake venom works to “protect against Lentiviruses” through the “destruction of the viral membrane.” However, this is a lie because we know the Lentiviruses are a lab generated, chimeric mRNA bioweapon containing SARS, MERS, HIV 1-3 and SRV-1 (AIDS), as I documented in my article entitled, Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning.

In actuality, snake venom is being used to destroy the human cell membrane not the “viral membrane”, so that nanoparticles can enter the cell and code your genome. This PubMed study proves that HIV is being encoded into people’s cells to produce a new cell line persistently. So snake venom assists mRNA to clone your cells. The J&J patent also mentions “RNA Replicons” which are forever replicating proteins.

Our Satanic “elites” have programmed the AI to create bioweapons far more complex than humans could ever come up with and the AI came up with 40,000 of the most deadly bioweapons to date.


The ACE2 protein acts as an anti-inflammatory, keeping immune cells from inflicting damage on the body’s own cells. The ACE2 receptor helps muscles contract and acts as a messenger between nerves, muscles and cells. It’s crucial in your cell signaling processes.

The ACE2 molecule acts as a gateway, preventing toxins from entering your cells. The mainstream narrative says that SARS-CoV-2 or the “spike protein”, attaches to human cells and blocks the ACE2 receptors. Snake venoms are postsynaptic neurotoxins, meaning they block the Ace2 receptors. So, I think we’ve identified the “spike protein”.

Snake venom latches onto ACE2 proteins and they get knocked out of commission. This destroys the body’s cell signaling function and enables the nanotech weapons system to enter the cells and reach the nucleus, where the mRNA is reverse-transcribed and integrated into the human genome.

Snake venom causes paralysis, the loss of muscle function and respiratory failure. It also causes inflammation, cytokine storms and induces auto-immune illness. Studies say snake venom triggers irreversible intracellular alterations, organ failure and continued cell death.

Heart and lung cells are covered with these ACE2 surface proteins which could explain why there’s so many reports of acute Myocardial injury following “Covid-19 vaccination”. I am receiving a lot of reports from my clients of prolonged stomach pain from these lethal jabs, another causation of snake venom which affects your digestion. 

Speaking of digestion, the Food and Agriculture Organization of the US approved the use of snake venom in food last year (2021). According to the FAO/WHO the PLA2 enzyme (snake venom) complies with the General Specifications and Considerations for Enzyme Preparations Used in Food Processing. They’re using a combination of snake venom and a genetically modified Streptomyces violaceoruber bacteria (strain pChi). In other words, it will alter your genome.

Notice the conflict of interest in this safety study that declares the pChi strain is not harmful for consumption. The study does admit that this bacterial strain modifies your genome. I don’t believe that any level of genetic modification of humans is at all safe.


60% of snake venom consists of a neurotoxic substance called Crotoxin. It was the first proteinic toxin to be crystallized into protein crystallization. Once crystallized it can be used in structural biology. You can even buy Crotoxin online


Organoids are being grown a lab to mass produce snake venom. Organoids of snake glands can produce snake venom artificially, without the entire snake. 


Monoclonal antibodies were funded and developed by DARPA and Bill Gates. All monoclonal antibody patents reveal this is a mRNA “vaccine” that codes your cells with HIV-1. Just like the “Covid-19 vaccines”, monoclonal antibodies never underwent clinical safety trials. They’ve never been approved for use on humans and were passed under the Emergency Use Authorization.

In his interview with Mike Adams, Dr. Bryan Ardis mentioned a study funded by Fauci and the NIH that proved monoclonal antibodies are in fact, unsafe. They specifically target and destroy your T-cells (killer cells) through cytotoxicity. Thermo Fisher’s monoclonal antibodies actually contain snake venom (PLA2)!

Please read: Monoclonal Antibodies Is Experimental Gene Therapy – Patent Review

All monoclonal antibodies contain Hydroxychloroquine or chloroquine in “some embodiments”. This explains why some people report feeling better after using monoclonal antibodies at first and that’s enough to fool doctors but later they become extremely fatigued. The long-term effects are still unknown but they cannot be good. When your immune system is destroyed, your body cannot fight off disease.


The Oxford patent mentions “Nanobodies” and says that “antibodies have been replaced with Nanobodies”. The whole purpose of the “Covid-19 vaccines” was to invoke an “antibody response”. Now that lie too is exposed. The nanotechnology is being programmed to kill.


There are breakthrough medicines and supplements that work antidotally against all poisons, including snake venom. In the Dr. Bryan Ardis interview with Dr. Braun, he mentioned the power of redox molecules against snake poison.

A peer-reviewed study from 2018, shows that Melatonin will also protect you against snake venom: 

“Besides antibodies, molecules like melatonin are reported to underlie the antivenom effect. The study of such was established in Egyptian cobra (Naja haje) venom using a rat model; the vital organs, like kidney, liver and heart, of the rat were protected from the venomous effect.”

Contact me on Telegram for information on where you can obtain the redox molecule supplement that enables your body to remove all poisons and restores all of your body system functions.

Also, follow my Telegram channel here.

Watch my latest interview with Stew Peters at Red Voice Media, here.



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