Shut up and eat your mRNA

...because we know what's best for you.

I used to think that the easiest way to spread a bioweapon was to convince people to willingly inject it, thinking it would provide them some protection. Now, I think the easiest way will be to put it in the food supply and have people eat it.

Man-made delivery mechanisms that contain mRNA are bioweapons, and always will be. The reason is because mRNA contains a message to make proteins that are bioactive. Bioactive means they will attach to receptors on tissue cells, and when they do, the immune system will attempt to destroy those cells. Depending on the number of cells affected, and their locations, pathology can result. We’ve already seen this happen with covid-19 mRNA shots because the spike proteins will attach to receptors on blood vessel walls and along the cells that line heart tissue. This results in weakening of vessel walls, aneurysms, internal hemorrhages, and myocarditis to varying degrees. When the spike proteins get outside the vascular system and into other organ tissues, we start to see neurological abnormalities and other organ dysfunction.

To put this in perspective, it’s important to know that our cells are making proteins, secreting proteins, and taking in proteins all the time. When we eat proteins, for example, they are broken down by gastrointestinal enzymes into smaller proteins called peptides, and even further broken down into the basic molecules that make proteins…amino acids. These peptides and amino acids are absorbed or taken into our cells to be used for other cellular functions, or to make new proteins that our body can use. Do you see the difference? The proteins we eat do not attach to cellular receptors which will create an immune response. They are broken down and absorbed without an immune response.

Livestock have been injected with mRNA that induces their cells to make bioactive proteins since 2018. Those bioactive proteins got into the muscles and organs of those animals, and we consumed them. Some of us pride ourselves to eat meat that was from animals raised without antibiotics and roamed freely. We really had no way to know if those animals had been injected with something called a vaccine unless we knew the activities of the farm or ranch firsthand. That’s a problem. Further, a withdrawal period is supposed to be honored before the animal is slaughtered, giving time for the medication or any residual substance to be eliminated or metabolized by the animal. Since protein production from mRNA shots varies between animals, tissue samples would need to be taken on each animal to rule out the presence of shot induced proteins before slaughter. Obviously, that is not being done.

So, many of us ate meat that had foreign bioactive proteins from injections all through it. Don’t freak out yet. What happened when we ate it? The normal enzymatic breakdown of those proteins into smaller peptides and amino acids most likely occurred. They were either absorbed by our cells to make normal proteins or eliminated in waste. However, there are some proteins that can avoid normal enzymatic breakdown. Prion-like or misfolded proteins are in that category. Depending on the genetic sequence of the mRNA in the shot that tells the cells of the animal what protein to make, prion-like misfolding of proteins can occur. If healthy people consume meat with misfolded or prion-like proteins that avoid enzymatic breakdown, they will most likely be eliminated in waste. However, in some people with “leaky gut” syndrome, where the epithelial layer of the intestinal tract is weak, these undigested proteins can get into the blood or lymphatic system. If that happens, the potential of the prion-like proteins to misfold proteins in the body does exist. This can result in a rare brain disease called variant Creutzfeldt-Jakob disease (vCJD). Symptoms of vCJD can take years to develop and may include neurological changes such as depression, anxiety, memory loss, and difficulty speaking or walking. As the disease progresses, it can lead to severe disability and eventually death.

That’s scary enough, but the danger is not in eating bioactive proteins. The real danger is eating the ability to MAKE the bioactive proteins. The ability to make bioactive proteins is in the mRNA. So, what happens if we eat mRNA? Eating pure mRNA or residuals that are in the meat is unlikely to have any effect because the mRNA molecule would be rapidly broken down by digestive enzymes. Ok, that’s good, but what if we eat the lipid nanoparticles that contain and protect the mRNA? Well…

Lipid nanoparticles (LNPs) are called delivery mechanisms because they are designed to protect the mRNA molecule and help it enter cells. In fact, LNPs will bind with and deliver the mRNA to just about any cell in your body because LNPs are lipid bilayers, the same as your cell membranes, including cells of the gut lining. If you were to ingest a lot of LNPs, a few of them might be able to make it past digestive juices, bind with epithelial cells of the small intestine, deliver the mRNA into those cells, and have your body start to make bioactive proteins right there. Some of those proteins will start circulating in your blood and lymph and attach to receptors along vessel walls and other tissues. Ok, NOW you can freak out.

Could an injected animal still have circulating LNPs when it gets slaughtered, and could those LNPs make it to the dinner table in a viable form, still able to deliver the mRNA to the cells of your gut lining? Not likely unless the meat is eaten raw with blood and lymph still present. Cooking the meat will destroy the viability of the LNPs.

Will the real people in control try to find a way to get viable mRNA delivery mechanisms into our food supply? You bet. I had a little chat with artificial intelligence about that.

Me: Is it possible that mRNA delivery systems can be incorporated into certain foods?

ChatGPT: Yes, it is theoretically possible to incorporate mRNA delivery systems into certain foods. The concept of using food as a vehicle for delivering therapeutic agents, including mRNA, is an area of active research and holds promise for various applications. Edible vaccines are one example of using food as a delivery system. In this approach, plant-based systems are used to produce vaccine antigens, which are then consumed orally, triggering an immune response. While this concept primarily focuses on protein-based vaccines, it is plausible to explore the use of mRNA-based vaccines or therapies in a similar manner. Incorporating mRNA delivery systems into food could offer several advantages, such as ease of administration, improved patient compliance, and potentially reduced costs compared to traditional delivery methods. However, it's important to consider factors such as stability, bioavailability, safety, and ethical considerations when developing and evaluating such systems.

Let’s explore ten possible edible mRNA delivery systems that are being investigated right now, so we can be proactive and stop them before they get to your local supermarket or restaurant. Again, swallowing foods with spike proteins or mRNA in them will most likely not have any substantial effect on you, but swallowing a delivery mechanism to have your body make foreign proteins will.

1.      Stronger lipid nanoparticles. Researchers are exploring various oral formulations, such as encapsulating mRNA within reformulated lipid nanoparticles (LNPs) or other delivery vehicles. These formulations are designed to protect the mRNA from degradation in the harsh environment of the gastrointestinal tract and facilitate its absorption through the intestinal lining.

2.     Enteric coatings: Enteric coatings are designed to protect the mRNA payload from degradation in the acidic environment of the stomach. The coating remains intact until it reaches the small intestine, where the pH is more favorable for mRNA stability. Once in the small intestine, the coating dissolves, allowing for mRNA release and absorption.

3.      Microneedle Pills: Microneedle pills are ingestible devices that contain tiny projections or microneedles made of biocompatible materials. These microneedles are designed to penetrate the intestinal lining and deliver mRNA directly into the underlying tissue, where it can be taken up by target cells.

4.      Robotic pills. Recently, a team led by Professors Traverso and Langer, pioneers and leaders in the field of drug delivery and biomedical devices, reported the design and use of robotic pills for gastrointestinal-tract-targeted oral mRNA delivery, opening up a new avenue for the oral mRNA medicines. The robotic pill is called a Self-Orienting Millimeter-Scale Applicator (SOMA). https://www.sciencedirect.com/science/article/pii/S2590238522000595

5.      Bacterial-Based Delivery: Some researchers are exploring the use of genetically engineered bacteria as delivery vehicles for mRNA. These bacteria can be designed to carry mRNA payloads and survive the gastrointestinal tract to release the mRNA in the intestine. The mRNA can then be taken up by intestinal cells for expression of proteins that create an immune response.

6.      Protease Inhibitors: Protease inhibitors (they stop enzymes that break down proteins) can be used in combination with oral mRNA formulations to prevent degradation by enzymes in the gastrointestinal tract. By inhibiting proteases, the mRNA can have an increased chance of reaching the target cells intact.

7.      Milk exosomes. Scientists figured out a way to get mRNA into tiny emulsified particles called milk exosomes made from cow’s milk. When given to mice, antibodies against the protein made by the mRNA showed up in their bloodstreams, proving the concept of delivering the message to make bioactive proteins in food will work. https://www.biorxiv.org/content/10.1101/2022.12.19.517879v1

8.      Dendrimers. To increase patient compliance with prescribed treatment, delivery of drugs orally is often preferred to other routes of drug administration. However oral bioavailability of many drugs tends to be very low. Dendrimers can be used to increase the solubility and stability of orally administered drugs and increase drug penetration through the intestinal membrane. Current research is being performed to find ways to use dendrimers to traffic genes into cells without damaging or deactivating the DNA. To maintain the activity of DNA during dehydration, the dendrimer/DNA complexes were encapsulated in a water-soluble polymer, and then deposited on or sandwiched in functional polymer films with a fast degradation rate to mediate gene transfection. Transfection is the process of deliberately introducing naked or purified genetic sequences into human tissue cells. https://pubmed.ncbi.nlm.nih.gov/18816481/

9.      Clathrin-mimetic nanoparticles. Clathrin-mediated endocytosis plays a crucial role in cellular uptake processes, allowing the cell to internalize various molecules, such as nutrients, signaling molecules, and certain pathogens. Researchers have been exploring the use of synthetic nanoparticles that mimic the properties of clathrin-coated vesicles to improve drug delivery systems. These synthetic nanoparticles, often referred to as clathrin-mimetic nanoparticles, aim to replicate the mechanisms of clathrin-mediated endocytosis to enhance cellular uptake and targeted delivery of therapeutic payloads. Clathrin-mimetic nanoparticles are typically designed to have a size and surface chemistry that mimic the natural clathrin-coated vesicles, allowing them to interact with clathrin-associated receptors on the cell membrane and trigger endocytosis. These synthetic nanoparticles hold promise in the field of drug delivery, as they can potentially improve the efficiency and specificity of cellular uptake of therapeutic agents, including mRNA.

10. Silica nanoparticles. Silica nanoparticles are primarily composed of silica (silicon dioxide) or other silica-based materials. They have a solid core made of inorganic material much more durable than lipid nanoparticles. Silica nanoparticles can be engineered with porous structures or internal voids that allow for the encapsulation of mRNA molecules. The mRNA can be loaded onto or into the nanoparticles through various methods, such as electrostatic interactions, physical adsorption, or chemical conjugation. Pulsed 18 gigahertz frequencies in 5G signals can be used to push the silica nanoparticles through cell membranes so the payload in the nanoparticles can be released. Scientists are experimenting with GUVs (Giant Unilamellar Vesicles) that mimic human cell membranes to prove this concept. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041541/

Your government and Big Pharma think consuming mRNA delivery systems is going to be good for you. Why? Because inducing your body to make foreign proteins will stimulate antibody production that will protect you and those around you from severe disease. They are wrong, and unfortunately it may take billions of injured human subjects before people wake up to this.

As mentioned earlier, the proteins produced by these mRNA delivery systems will be bioactive, meaning they will attach to receptors on cell membranes, resulting in destruction of those cells and varying degrees of pathology. That’s only the beginning. Antibodies will be produced, and they can be dangerous if too numerous or in the wrong forms.

The antibodies produced against the proteins will be focused on those mRNA coded proteins only, not the entire bacteria or virus the proteins reside on. In a natural infection, the bacteria or virus comes through the epithelial barrier in a natural way so that the immune cells that guard the barrier can experience the entire pathogen and remember all parts of it and protect you from another infection for the rest of your life. The experience of symptoms with a natural infection can range from none, to mild, to severe depending on the overall health of the immune system and how quickly it can bring you into homeostasis. One beautiful thing about a natural infection is that IgA antibodies are secreted back out into the mucous. These special antibodies will neutralize that pathogen the next time you contact it, so you never get infected again. Mucosal IgA antibodies are not secreted after injecting something called a vaccine into the body because the epithelial barrier is bypassed.

I predict injections called vaccines will go away for that very reason. Science knows that the infection must come through the epithelial barrier either by inhalation or ingestion to get mucosal protection of infection. They will prefer breathing or swallowing the delivery systems, striving for mucosal protection. It won’t work. They will find out that crossing the epithelial barrier with something that is genetically modified or incomplete will not provide the protections they attempt to achieve. The only way to get complete protection is to experience a natural infection of the entire bacteria, virus, or toxin. Don’t be afraid of natural viral infections. A virus never killed anyone. It’s the inflammatory response in immunosuppressed people that destroys lung tissue resulting in pneumonia, irritates vessel walls resulting in cardiovascular problems, or affects nerve tissue that is deadly, and that inflammation can be controlled.

Another beautiful thing about natural infections is the deployment of long-lasting memory cytotoxic T-cells that reside near the epithelial barrier. These cells can detect protein parts of viruses INSIDE of the epithelial cells before they get released into the blood or lymph. If the cytotoxic T-cells recognize any of those proteins they have memory for, the epithelial cells that contain them will be sent a signal to destroy themselves in a noninflammatory way called apoptosis. This is true protection of infection. In fact, your amazing body is constantly removing and replacing about a million cells per second by this noninflammatory apoptotic process for various reasons including infections, cellular aging, and cancers. This is completely different than the inflammatory destruction of cells that have bioactive proteins attached to them because of mRNA transfections. Transfection is the process of deliberately introducing RNA or DNA into cells to make a foreign protein, and that’s exactly what mRNA delivery systems do, whether you inject them, inhale them, or swallow them.

Vaccine manufacturers boast about the ability of their products to not only stimulate antibody production, but the ability to stimulate T-cell recognition. That sounds good, but when you follow the science, you will see that the T-cell recognition from mRNA coded proteins becomes too specific. The T-cells get trained to look for just one protein on the virus, and when that protein gets mutated, the T-cells will no longer recognize the virus when it is inside the epithelial cells. So, the epithelial cells will replicate the virus, release it into the blood and lymph, and you are infected again. Worse, the antibodies in your blood and lymph that were created from the mRNA injection (or ingestion) are also targeting a protein that doesn’t exist on the pathogen in the form that it was before mutations. They are now suboptimal antibodies that will bind to the protein on the pathogen in a way that enhances its ability to infect other cells. This is called Antibody Dependent Enhancement of Infection. They can also bind to the pathogen in a way that starts the highly inflammatory and destructive complement cascade that makes the symptoms of the infection much worse. This is called Antibody Dependent Enhancement of Disease, or a cytokine storm.

In a natural infection, B-cells that make the antibodies will communicate with T-cells to make certain that the antibodies created do not attack normal body proteins. With mRNA transfections, the cells of the body can produce an overabundance of proteins. This causes B-cells to autoactivate without T-cell involvement and create suboptimal antibodies that can attack normal body proteins. This is called Pathogenic Priming, coined by Dr. James Lyons-Weiler, and results in autoimmune conditions.

The chances of experiencing Antibody Dependent Enhancement of Infection, Antibody Dependent Enhancement of Disease, and Pathogenic Priming will increase with repeated exposure to more proteins being produced. So, each time you get a booster shot or swallow something that crosses the epithelial lining, delivering mRNA to tissue cells, you will make more proteins that will call the suboptimal antibodies into action all over again.

The idiots behind this scheme will try to convince you that the more antibodies you have, the better off you are going to be, so they want everyone to have these antibodies. They will try to accomplish this goal by putting mRNA delivery systems into the food chain. Follow the science. Be aware.