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What in the world are these COVID-19 shots? They’re mRNA instructions to your body to make from your own genes, supposedly, spike proteins. Spike glycoproteins, which also happens to be cobra venom factor. Please, medical professional scientists around the world, go look at these people’s research. They’re the one that created the weapon. Maybe you can help understand the mystery here of why so many people are dying having neurological side effects that are permanent, semi-permanent.

In 2009, go look at their studies. 2009, 2011, 2012 being funded by Anthony Fauci’s department, they disclose that in order to cleave, which means to cut, RNA or DNA, they used 2 substances. They list that they use in their research to do mRNA gene therapy, a substance called snake venom phosphodiesterase. They use snake venom to do mRNA research. Why is no one looking at the possibility snake venom might be in these shots causing every side effect of venom you’re seeing reported as COVID-19 injection injuries?

The other component that it lists in these studies, every single study, is a substance called RNase. It says in every one of their studies that RNase 1, RNase 2, and snake venom phosphodiesterase are used to cleave or cut RNA or DNA to get the mRNA they want into your cells to do what they call genetic engineering, generating something your body doesn’t normally make. RNase is a component of snake venom. RNase, DNase, and phosphodiesterase are all components of venom. And it’s what they’ve been using in their research.

If you go look at Katalin Kariko’s interview in April of 2020, she’s interviewed by the university in Europe she attended in her undergrad. They ask her, “Where did you start using mRNA?” And she goes, “In 1978, right here at this university.” And what did you guys accomplish? She goes, “Well, we thought we could use mRNA to help beat viral illnesses.” But the mRNA wouldn’t work until we found out at the same university with a researcher she was working with that if you took a lipid nanoparticle hydrogel and wrapped it around the mRNA that the LNP, lipid nanoparticle hydrogel, actually was the thing that was creating an immune reaction with RNase. She says it out loud in the interview. We used LNP, lipid nanoparticle hydrogel, with mRNA and RNase to create our mRNA antiviral technology. RNase is snake venom. It’s a component of snake venom. They’ve been looking at this research since 1978 and working with it.

So why in the world does Robert Malone say he doesn’t want to talk about snake venom peptides? He either doesn’t know a damn thing about them at all because he never invented these in the first place, or he absolutely knows that venom peptides are used in research just like Judy Mikovits has admitted to as a scientist and as a chemist working in labs for the NIH for decades. She knew. She knew right away. Right when Bryan Ardis came out with the information, she knew it. She’s like, “Of course they use venom in viral research.” Well, why doesn’t anyone talk about it? RNase and phosphodiesterase, these components of venoms, cause every single neurological damage in the human body that you’re seeing as a reaction to the mRNA injections.

Snake venom destroys cell membranes. Phosphodiesterases shred the membranes of cells. Then what’s exposed is genetic material like the nucleus, where the RNA and DNA exist. They’re saying they actually can use venom components to cleave or cut DNA and RNA to insert mRNA. It is not that clear cut and dry. Are you seeing only benefits from the mRNA injections, and everyone’s healthier than they were before? Are you seeing that? No. You’re seeing detrimental side effects being reported at a massive scale than what you’ve ever seen. Guess what else creates massive side effects at a global scale if you decided to envenomate everybody, or give them instructions to do it.

Drug makers no longer want to make drugs, have factories to make tablets, make liquids, and then have to ship them. Because it’s very expensive. So they’re doing what’s called genetic engineering to see if they can get your human body to make the drug so they don’t have to. One of the biggest sources of drug research and drug manufacturing is the isolation of components of venoms. Because they’re extremely biologically active. They have a massive influence on our human body and all mammals’ bodies. They lower your blood pressure, because you’ll be weak and lethargic and you can’t run away. Then the snake comes and kills you. They cause you blood clotting. They cause you to be paralyzed so you can’t run so they can eat you. This is the whole reason of venoms.

Dr. Bryan Ardis is a tireless researcher, always seeking to weed out deception in health and medicine, and seeking and provide truth through his personal research and product formulations. Dr. Ardis deserves a Nobel Peace Prize in our opinion. Dr. Ardis gives his very well researched expertise backed by official data on how COVID-19 was accomplished. He reveals the conotoxins and snake venom and poisons inside ALL the current vaccines. The only truthful answer behind this sinister substance that was added to our water and vaccines is that there is massive depopulation operation and agenda being conducted on a global scale. The symptoms and deaths were simply due to venom within the tap water and vaccines. Nicotine stops the "COVID virus" and vaccine injuries dead in its tracks? Now you know exactly why the agenda against NICOTINE has gone into overdrive. The VENOM attacks NICOTINE RECEPTOR SITES.

The development of technology has taken a scary turn. For quite some time now, the elites have been secretly inventing bioweapons and have been unleashing them in our environment. Their inventions can now change human DNA and can even manipulate the environment that we live in. This agenda is BIG. However, we can protect ourselves by staying informed with true and unbiased information backed by scientific studies and by being prepared and vigilant.

Since like 1904, the research to isolate, manufacture, and instruct human beings how to make spike proteins, this type of technology, they have been working out and constructing since 1904, but really ramped up in the 1940s. That’s when it really started. There’s enough evidence there. This is how Ralph Baric or anybody else in trying to create a bioweapon using spike proteins, they got all this information from the research of Stanley Cohen.

Paul F. Reid got a patent in 2010 for the spike protein identical to be used as a large scale antiviral vaccine, and he was paid for by our United States government from 1993 to 1996 in Fort Dietrich, Maryland. His job was to isolate the spike protein, find out how to mass produce it synthetically in bacteria and yeast systems for the intent to be delivered to humans in a vaccine form for a viral infection. That is what he was awarded in 2010 for a patent for his work he was paid for with grants from our government, our tax dollars to do this in a mass scale from 1993 to 1996. And yes, they have been manufacturing spike proteins for a long time. They have also already determined for decades, this is way before Baric. They’ve known this for decades. They know how to get bacteria, yeast, baculovirus, and mammal cell lines to synthetically manufacture spike proteins. So, this has been a long time coming.

They know everything about this technology. The entire technology of spike proteins and the mRNA technology to get the human body, mammal cells, to make spike proteins is nothing more, it is nothing more than 100% everything they know how to do and how to create snake venom peptides, and get those microorganisms to make it. mRNA technology, spike protein technology, all of it is simply snake venom research and technology. Every way in which the spike proteins hurt the human body are identical to every single toxic component of snake venoms or any venoms, scorpion venoms, bee venoms, spider venoms, snake venoms.

All of them have the same toxic effects, and they’re 3-fold. All the injuries from the vaccines have 3 ways they’re going to hurt you, the same 3 ways all venoms hurt a human also. That is hemotoxic, meaning it’s going to injure your blood vessels, hurt your red blood cells, your platelets, cause blood clotting, cause strokes, cause hemorrhaging. That is a venom side effect to the blood. They call this the clot shot for a reason because it’s causing blood clots.

In snake venom, there’s a specific component . It’s called a procoagulating Factor Va protein in venom. That is exactly what scientists have known for years causes blood clotting without needing the human body’s blood clotting factors to initiate the blood clots. It’s totally independent of the human’s body’s ability to make blood clotting. This is why, when you see elevated D-dimer test in vaccinated patients, which they’re finding in over 60% of people getting these shots, look at medscape.com right now, it says all medical doctors, to interpret elevated D-dimers all you need to do is look for snake venom poisoning because it causes blood clotting, and you’ll see elevated D-dimers as a result.

So, everyone should be looking for venom, and the people that created these shots, they use snake venom in their gene editing therapy research to do mRNA injections. Katalin Karikó herself, at the University of Pennsylvania, who created the mRNA technology for COVID-19 shots, says since 1978, they’ve been taking components of snake venom, wrapping it in lipid nanoparticle hydrogel to protect the mRNA from degradation or being destroyed by RNase.

RNase they also use in their vaccines. RNase is a component of all snake venoms. It’s what destroys RNA and DNA, and they somehow need to get their mRNA into your nucleus. So, they are suggesting the use, and have been for decades, to use snake venom components that we know shred membranes. That’s what they’re using, the technology of venom. How do you use that to carry out their nefarious agenda? There’s 3 ways these spike protein shots will hurt you. You’re either going to have blood toxicity effects called hemotoxic effects or you’re going to have neurological effects. These are called neurotoxins. How many neurological problems are we seeing after COVID-19 injections or with COVID-19 infection?

When you look at what doctors have put together for treatment protocols. The first thing to look for is are mitochondrial nutrients being prescribed, or being recommended? Are they a part of the treatment plan? Almost never do you see that they’re actually a part of a treatment plan. When you put together a treatment plan for a patient and the mitochondrial nutrients aren’t there, you aren’t paying attention to energy production. You aren’t paying attention to the foundation of the healing response in the body. So now, you’re going to get this hit or miss response happening all the time.

The average allopathic doctor, a white coat MD, the average one gets 19.6 hours of nutrition over their entire education, which typically spans about 6,000 hours. What that equates to is a weekend workshop. There is no way that you can be effective working with a patient when you have a weekend workshop of nutrition that’s neutered and watered down, even during a weekend workshop. The curricula at all of these major medical schools is missing the most important ingredient, a focus on mitochondria. That’s the difference when you get into other forms of education, real medicine, like naturopathic medicine.

If we put our focus on mitochondria and trusting that when the body at the cell level produces ATP, we will get a very positive, very beneficial result, much more often than not, because we’re working with the body and this basic understanding that the body at the cellular level is designed to heal. It’s not a belief. It’s a fact. It’s a fact that we have to start expressing, it’s a fact that we have to start embracing. The whole notion of hypervitaminosis is a joke. It’s a lie. It’s a lie that the medical-pharmaceutical killing machine tells, because they want you to be scared of the things that actually work.

If the spike protein on COVID is what was causing the most disease of 28 different tissues in the human body, which is what Salk Institute said, now they’re injecting people with millions, maybe billions of spike proteins into the human body with the Johnson & Johnson, AstraZeneca, and Novavax shots. It’s just the spike protein. They’re injecting those inside of you. They’re telling you worldwide that the COVID-19 spike protein on COVID is so deadly, you can’t even stand within 6 feet of another person, but you should inject the spike proteins inside of you?

In 2022, during the lockdown, researchers were actually doing experiments injecting animals with conotoxins and cobratoxins, the spike protein of C0VID. And they found that it will cross the blood-brain barrier within 72 hours. It targets the alpha-7 nicotine receptors on glioma C6 cells. Within 72 hours, they confirmed a glioblastoma was being formed by the venoms' attachments to those nicotine receptors.

After 72 hours of watching the brain tumor grow, these scientists injected the animals with two different doses of nicotine and they show the results at 1 microliter per milliliter of blood. When they introduced nicotine within 72 hours, the glioblastoma was dissolved by half the size just with nicotine. They then suspended the study at the end of 72 hours. Wouldn't you as a researcher be shocked to see such an amazing result of a brain tumor being dissolved by half in 72 hours with something as simple as nicotine? Why would you terminate the study at hour 72? Why wouldn't you continue to see how long it will take for nicotine to completely dissolve that tumor? They don't want you to know that nicotine can completely reverse cancerous tumors in any part of your body.

At the same time, they were testing to see if the venoms found in every C0VID-19 patient caused brain tumors called glioblastomas and that they can reverse it in less than 72 hours with nicotine. At the same time, they were investigating the same venoms injected into animals to see if they create Parkinson's animals, seriously, in less than 72 hours. Can they create Type 1 diabetics in less than 24 hours? And can they create myocarditis in a mammal? All of these four conditions are considered irreversible in humans. Do you know that in every single case during the pandemic while we were being locked down, researchers around the world were injecting the same venoms they found in C0VID-19 patients, the exact same ones found to be the spike proteins of C0VID? They're injecting them into animal models, which by the way, science calls us animals.

They are injecting all of these animals with these venoms and creating four different supposed irreversible human diseases. And in every single scenario, all they did was supply strict nicotine to these animals and reverse glioblastomas and type 1 diabetes, which supposedly is irreversible. They reversed Parkinson's in 72 hours. And they reversed myocarditis after treating the animals with nicotine for only 72 hours. By day 14 after treatment, the myocarditis was reversed.

Why is no one talking about that? Why is this a marine drug study? Not a joke, it's the name Marine Drug Medical Journal. Why aren't those being shared with oncologists? Every single individual right now being diagnosed with glioblastoma tumors in their brain, not a single one, has ever recommended nicotine administration. Not a single one is addressing that. They're only gonna offer what? Chemotherapy, radiation, and surgery. And you should ask yourself why?

With these post inoculation severe injuries, the spike glycoprotein is playing an instrumental role because it does not break down. It does not degrade easily or readily. We have to understand the mechanisms of action. The spike glycoprotein creates a number of problems. The spike glycoprotein is going to be a wrecking ball within the cell structure.

Within the cell we have organelles, mitochondria that produce energy, microtubules that help with the communication system, the smooth endoplasmic reticulum where enzymes are made and detoxification happens. Within each cell they’re all interdependent and they work in harmony. If you take a wrecking ball into that, you are going to destroy structures. And when you destroy structures, you throw off the entire function in the cell. And if the cell can’t maintain life following that, the cell is going to die. And if that happens in a number of cells, you’re going to have tissues that die. So that’s how this works at the cell level.

The spike glycoprotein is a wrecking ball to mitochondria. Mitochondria produce energy, therefore it’s going to lead to incredible fatigue in the body, but especially within the cell. Every single known biologic function in the body is energy dependent, like osmosis and passive transport. Everything in the body depends on energy. So if there is a molecule in the cell that is breaking down the energy producing factories of the cell, there’s going to be severe consequences. And that’s one of the things that the spike glycoprotein does. It also inhibits the formation of nitric oxide. And we’ve known this since early on and they knew this long before, because this is by design.

The mRNA sequences that are injected into people can reverse transcribe in as little as 6 hours and upload into the human genome. Meaning that a person can now for the first time be officially genetically modified. And that’s a huge concern. There should never be a product on the market that is mutagenic. Meaning it causes for DNA changes either as a consequence of it, or a direct intention of it. And in this case, it looks to be a direct intention of it, that they wanted people to get genetically modified. So you have to ask? Why would they want people to get genetically modified?

If you create and inject people with genetically modifying compounds, not only are they going to suffer, not only are they going to experience disease and ultimately and decline into the grave, but you also can sterilize young girls. You can also sterilize young boys. And then you kill off the older generation. You kill off the middle generation, and you ensure that the new generation coming up cannot reproduce. And that’s what we’re seeing with the spike glycoprotein. This is what it does. We found it in the gonads of young girls and young boys, in the testes and the ovaries. These are the things that they said could not happen. It could not reverse transcribe and upload in the genome.

We’ve been told a lie. We know that the spike glycoprotein outside of the cell is going to have an incredible binding affinity for the ACE2 cell receptor. What does that mean? Your body has ACE2 cell receptors all over the place. They’re like little hands on the outside of cells. And when a spike glycoprotein comes in contact, it binds strongly to that cell receptor. And the cell receptor will pull that spike glycoprotein into the cell and then you have the wrecking ball now on the inside of the cell. If you’ve been injected and genetically modified, now your cell is producing that wrecking ball inside of it. And when that spike glycoprotein gets outside of the cell, when it gets into the tissues, we know it’s going to disrupt T-cells in a great way, which is going to really just completely dysregulate how your immune system functions. That’s going to mean that there’s going to be a rise in cancers and there’s going to be a rise in illness.

It’s as if they taught the immune system how to attack itself. The first time we’ve ever seen an autoimmune condition against the immune system. Immune system fighting itself. Disease within the body will proliferate, especially cancers. And what have we seeing? An egregious rise in turbo-cancers at all ages. But that’s not even the worst thing that the spike glycoprotein does.

The spike glycoprotein is also going to lead to a phenomenon known as glycosylation. It is a sticky protein. Glycosylation is where red blood cells get coded with a sticky substance, in this case the spike glycoprotein, and that creates and causes red blood cells to stick together. So if we have two red blood cells, they’re supposed to be floating freely in the blood so that they can maximize the surface area, the surface area for binding oxygen and bringing to the cells, so the mitochondria can produce energy. Picking up carbon dioxide along the way. It’s a nice, beautiful, sacred divine exchange that occurs. Oxygen for carbon dioxide. The red blood cell is giving you oxygen that you just breathed in. You are going to turn that into energy. Then the CO2 will hitch a ride to the lungs where it can be exhaled. And then we give it to the plants, who are going to do just the opposite. It’s a beautiful symbiotic relationship that has always existed.

They’ve attacked that symbiotic relationship. Now you have a spike glycoprotein that causes these red blood cells to stick together, and when they stick together, they lose surface area. And now when they lose surface area, they can’t grab as much oxygen or carry away as much carbon dioxide. So that’s where we start seeing drops in O2 saturation rates in patients who are suffering. It’s like there’s air all around them but they can’t breathe, because their red blood cells are stuck together and can’t bind that oxygen. And what’s building up in their tissue is toxic carbon dioxide. They are suffocating with plenty of air all around.

You can intubate them and put them on a ventilator; it won’t matter. You’re now suffocating them with oxygen. Because the phenomenon of glycosylation is occurring. Well, where have we seen that before? And what disease processes? Diabetes. But it’s never been like this. And when you get enough of these red blood cells stuck together, something happens. They start to clot. And as they start to clot, the clots get longer and longer. If the enzyme isn’t activated from breaking the clot down, that enzyme is plasmin. So the spike glycoprotein does two things with the blood that are very lethal. Number one, is it causes what’s called hemagglutination or sticky blood, red blood cells get stuck together.

Number two, it prevents the enzyme plasmin from being activated to break the blood clots down. That seems like a pretty destructive combo. Nowhere else in nature does this occur. Yes, there are toxins in nature that cause red blood cells to glycosylate and stick together. And there are molecules in nature that prevent the breakdown of blood clots. But never in the same substance do we see both of those mechanisms of action happening at the same time, with the same substance.

This is the first time in human history this has occurred. This is not a result of rapid evolution, this is by design that makes it a bioweapon. The spike glycoprotein. It doesn’t matter if that is something that is injected into a person and now their body is mass producing it with no off switch in sight. The result is the same. There is a wrecking ball in the cell, there is a wrecking ball in the bloodstream, and it prevents, in the bloodstream, red blood cells from having surface area to bind oxygen and carry carbon dioxide. And it prevents also the breakdown of the blood clot.

There is a glycoprotein in snake venom called ecarin. Guess what it does? It causes red blood cells to stick together really, really strongly. Hemagglutination. And then there’s another one called textilinin. Textilinin is from a different snake. What it does is it prevents the breakdown of blood clots. So what would happen if you put both of those things together? Well, if you put both of those things together, you’d have a bioweapon. Something that not only causes hemagglutination, red blood cells to stick together, but also prevents them from breaking apart. And if you attack that sacred thing that we have been given, this gift of life where we are dependent on oxygen and getting rid of carbon dioxide, what you have done is set the body up for certain system failure, certain death.

So people say, well, how can you prove that the spike protein was engineered in a lab? Number one, how can you prove that it was not? And number two, where in nature do we see this exact series of egregious lethal mechanisms of action in one glycoprotein structure? Show me one place where there is a glycoprotein anywhere in the known world that does all of these disastrous things at the cellular level and in the bloodstream. And of course, everything in the body is dependent upon the bloodstream.

It’s why when you look at the Pfizer documents that they didn’t want to let out, that there are over 1300 known diseases associated with the shots alone. That right there tells you it’s not safe. The number of people who got the shot and got sick anyway, got hospitalized anyway, died anyway. It’s not effective. So that’s the greatest lie being told in our time right now, that these are safe and effective. They are not safe and effective. They’re bioweapons. And it makes it intentional because there’s nothing in nature that does all of these mechanisms of action in one molecule. Only the spike glycoprotein.

The patent that was granted in 2018, was originally granted in 2014, and then there have been successive patents after this that have built on this particular submittal. This patent, # 9884895 was patented by inventors, Ralph Baric, Sudhakar Agnihothram, and Boyd Yount, all associated with the University of North Carolina Chapel Hill. This particular patent actually patents the spike protein for coronaviruses. So there are methodologies for making genetically modified spike proteins for coronaviruses. It’s interesting, because both the Moderna vaccine and the Pfizer vaccine are both mRNA vaccines. And it’s odd that this patent was granted 2 years prior to any notification of the COVID-19 pandemic. And Ralph Baric, who is a principal investigator in the effort that led to this patent, this is one of the very few patents that he has. He has 6 patents altogether. And this is the only composition patent that he has of this nature. It happens to be on a coronavirus, and now 7 years after this patent has been granted, we’ve sustained this pandemic of the same type of virus.

Right now, there's over 500 million people worldwide who have some type of diabetes. Diabetes is the inability to control blood sugar levels and maintain normal blood sugar levels. All diabetics have excess blood sugar. Diabetics are the ones most prone to have E. coli bacterial infections and Candida or yeast overgrowth anywhere in their body, including in their bowels, in their kidneys and in their bladder. You'll often see this reoccurring in diabetics called a urinary tract infection. It's usually caused by E. coli bacteria or yeast. The problem for you is you are the highest risk group for now having your own mammal cells manufacture the trans-spliced alpha-cobratoxin mRNA in your body, in your own cells, but you not only have mammal cells that can engineer full venom proteins now.

You also have E. coli bacteria eating on the blood sugar in excess in your body and replicating in your body and then you yeast in your body that's replicating by feeding on the sugar in your body and those E. coli bacteria and those yeast, we've known since 1999, have been engineered to suck in plasmids with venom spike protein genes in them and manufacture relentlessly, and faster than mammal cells manufacture the venom in your body. And this is exactly how they created the COVID-19 pandemic.

We all suspected that they were putting the venom proteins that are synthetically manufactured around the world, in our water systems and we were just drinking it. No, they didn't even need a viral vector. In fact, they didn't need a viral vector at all for this entire pandemic. They have been manufacturing DNA plasmids with the spike protein genes that are venom proteins in those plasmids and they published that. They can release them in the air, they can drop them in the air, they can put them in your water systems, which they are. They also can inject it inside of our food.

“Shedding” is a real and predictable phenomenon that can be explained by known mechanisms unique to the mRNA technology. COVID-19 vaccine shedding (becoming ill from vaccinated individuals) represents the one way the unvaccinated are also at risk from the vaccines and hence still need to be directly concerned about them. In theory, shedding with the mRNA vaccines should be “impossible. Those being affected by it are in a horrible situation, particularly if everyone is gaslighting them about it and insisting it’s all in their head. It provides one of the strongest arguments to pull the mRNA vaccines from the market and prohibit the widespread deployment of mRNA technologies in the future.

When you're hearing about Bill Gates and his Gavi group, orchestrating farmlands around the world that he's buying up and he is injecting avocados, tomatoes, and lettuce with the mRNA injections. They're creating mRNA-injected food for us when they are injecting the plants with these DNA plasmids they call mRNA injections. The DNA plasmids get sucked into bacteria and yeast, I don't know if you know this, but fungus and bacteria live in the soil of all your farmlands and it gets drawn up into your plants. The plants need bacteria and fungus to grow. So, in every single one of your vegetables, every single one of your fruits, they're injecting DNA plasmids in these mRNA injections they're calling them, they're injecting them into the plants. Inside those plants, the E. coli bacteria and the yeast are going to start replicating venom proteins and then you're gonna eat them. This is how they're going to continue to get these venom-laced plasmids into your body.

And who needs to be investigated for these crimes against humanity, in my view? Fauci, NIAIDA. Collins, a former head of the NIH. Walensky of the CDC. And the leaders of the FDA and the leaders of big tech and the leaders of big pharma who put this out knowing what it was going to do to the public, and even working to hide the documentation of the early clinical trials to prevent that from becoming public so that the people would not know the truth that they already knew inside the vaccine manufacturers, that this was a deadly intervention that would kill untold numbers of innocent people. In some cases, up to 90% of patients who were put on respirators died. And yet, where did you get this idea that everybody in the hospital in the ICU unit needs to be on this respirator? The CDC.

The CDC just reported recently, there are outbreaks of E. coli bacteria on all spinach farms in America. Oh really? Really? Why do you think they want you eating E. coli bacteria on your vegetables and on your plants because they need to get E. coli bacteria into you. Why? Those E. coli and yeast have been manufactured and engineered to replicate venoms as they do what's called conjugating. They suck in the plasmid and that plasmid holds the instruction for the bacteria and yeast to manufacture venom proteins inside of you. This has been one of the biggest things we've realized.

The Nuremberg Code criminalizes forced medical experimentation, any kind of coercion without informed consent. But how can you have informed consent as a patient if you’re not informed? And so there’s no question that what’s being pushed on people today, these vaccines without proper information, without the truth being revealed to the potential users of this intervention, this is a direct violation of the Nuremberg Code.

We're actually presenting to the whole world what it is they're utilizing in the form of plasmids in engineering bacteria and yeast in our cells and what is called trans-splicing technology to get microorganisms in our body and our own cells to manufacture venoms, which will have a detrimental disease-causing turbo cancer-creating side effect which you're seeing worldwide from these shots. There are solutions, anybody who's having continuous post-COVID, long-hauler syndrome they're calling it. Anybody you know at home struggling with, still years later, numbness and tingling all over their body, tinnitus, 6 ringing in their ears since having a mild case of COVID, loss of taste and smells since having COVID? How about brain fog, motor deficits, new onset of diabetes, new onset of diagnosis of high blood pressure, insomnia? Anybody you know struggling with any of these scenarios or symptoms they call long-hauler COVID symptoms?

It was already proven by Dr. Carlo Brogna in Italy that long-hauler COVID patients, 100% of them, have in their bowels bacteria called E. coli replicating snake venom peptides, starfish venom peptides, and cone snail venom peptides in their bowels. The exact same collection of venoms confirmed in the published study October, 2021, titled Toxin-like peptides found in blood, urine and feces of every COVID-19 patient, when Carlo Brogna and his team confirmed 36 different animal venom proteins were only found in COVID-19 patients. The entire COVID-19 narrative, this post-COVID syndrome called long-hauler COVID symptoms, that isn't related to the vaccines. That's with COVID.

COVID is DNA plasmids with venom spike proteins in it and they used bacteria and yeast in our bodies to replicate the venoms and if they got enough plasmids into us, our own cells would splice them together and spit out these venom proteins that are neurotoxic leading to neurological symptoms of every kind. Venoms do that. They also affect the blood with hemotoxicity, they call it causing blood clotting or hemorrhaging, which you're seeing after the shots and after COVID. They also cause multiple organ failure with a substance called phospholipase A2 that's in every venom and they have those in the plasmids also. So, as we were exposed to the plasmids they called SARS-CoV-2 virus with the spike protein genes, we were exposed to these and then our body manufactured the venoms to lead to all these horrific outcomes we're seeing longstanding.

In the 2017 study titled “Antiviral Therapeutics from Animal Venom Peptides,” they suggest the use of scorpion venom for fever, blisters, and cold sores, which is supposedly the herpes simplex virus. They also recommend scorpion venom as a vaccine for HIV. They also recommend snake venoms for HIV. It actually reads” “snake venom molecules are homologous with HIV-1 glycoprotein.” That means HIV could have the same evolutionary origin as snake venom. They know it’s venom. They just call it a “virus.”

They know it's venom. They say it’s identical. They say it’s homologous. “Adenoviruses” and “retroviruses” is code language for “venom.” They’re just using language that doesn’t allow us to understand or interpret what they’re actually saying or meaning. The definition of homologous reads similar to, or similar evolutionary origin, meaning HIV could have the same evolutionary origin as snake venom.

They are creating E. coli infections in people everywhere, and they’re aerosolizing conotoxin, venoms, or others. You’re breathing it in. When it reaches your bloodstream, if you have E. coli in your body, E. coli generates more venom. Look at the study from Utah State University in 2018. They call it synthetic snake venom phospholipase A2 with genetic engineering. All they did was put it in the presence of E. coli, and E. coli overproduced more and more synthetic venom.

The actual people who are being targeted with this COVID-19 weapon are diabetics. If you look up who’s dying the most often, being hospitalized, dying from COVID? It’s always diabetics. It’s always been diabetics the whole time. Native Americans were the highest percentage people dying in America. Blacks and Hispanics, in that same order, are the highest percentages of diabetics by race in America.

What is it that diabetics struggle with? Managing blood sugar. When there is excess blood sugar in the body, guess what that does to yeast and E. coli? They can’t beat it because bacteria and yeast thrive on sugar.

Millions of Americans have been injecting themselves with GLP–1 drugs such as Ozempic and Wegovy. Each of these drugs is made of Gila monster lizard venom, which, outside of being as toxic as a rattlesnake bite, also has a black box warning of thyroid cancer within 12 months of use. Gila monster lizard venom was as “toxic” as “western diamondback rattlesnake” venom.

Every cell in your body has nicotine receptors including the gut, a few people, when chewing and swallowing nicotine gum get nauseous and vomit or get loose stools. This is because so much of the venom spike proteins are attached to the nicotine receptors that line your entire bowel lining, and when nicotine is present the massive amount of venom in the bowel lining gets released and you will feel like you have food poisoning. Why because venoms are poison, and god designed the human body to throw up poison and poop out loosely, all poisons.

If this happens, please switch to nicotine patches. The nicotine skips the bowels and gets absorbed into your blood stream through your skin in less than 30 seconds. This is why we do patches every day. Most people have no reaction to the gum or nicotine orally but some do, that get mitigated by using a topical nicotine patch. Many people can benefit from buying organic tobacco leaf online and boil the leaves and do a foot soak for 20-30 minutes several times a week to absorb nicotine that way.

The media giants helped cover up the truth about how Ivermectin and Quercetin and zinc and vitamin D could save lives. So, they were just pushing pharmaceutical propaganda and essentially, driving innocent people off a medical cliff to their own deaths, while the media was being paid sponsorship money by the pharmaceutical companies that were murdering humanity.

We will never lose a single soldier. We will lose nobody. Nobody that has finally investigated vaccines, recognizes how dangerous they can be, how bad the science is, can ever be won by a Sanjay Gupta or Anderson Cooper or whatever media whore it is. You will never win them back. If they attack, we win. If they leave us alone, we win. They cannot figure out what to do because every day, we win and they lose, and they’re getting more and more angry. They’re swinging more and more wildly, which means martial law attempts to control us, burning books, censoring. These are foot stomping Hitler’s, little babies that have not pulled off their agenda. These are the dying gasps of a dying regime driven by money and greed and a desire for power that is losing to people who speak the truth. And that truth flows through us from God.

Moving Beyond the COVID-19 Lies : Restoring Health & Hope for Humanity October 1, 2024 by Dr. Bryan Ardis

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