Antibodies

The central mechanism Aajonus described regarding antibodies concerns what he called mutant antibodies, which are produced specifically in response to vaccines and by extension to antibiotics such as penicillin and tetracycline. His argument runs as follows: when the body encounters a natural disease or virus, it can find the logical reason for the process and understand the time frame of the activity. When a disease or virus is injected artificially through a vaccine, the body cannot find this logical reason, nor can it determine how long the bacteria or virus will remain active. Unable to orient the response properly, the body creates mutant antibodies. These mutant antibodies do not go dormant when the disease or virus becomes inactive, and they can remain active for up to decades.

The damage these mutant antibodies cause is specific and severe. They eat sub-particles from the inside of amino acids, that is, proteins circulating in the blood. This action renders those proteins unstable. Because amino acids are the primary building blocks of cells, the consequence is cellular malnutrition throughout the body. In all animals, this malnutrition produces gradual genetic mutations that result in weaknesses, diseases, malfunctions, and deformities. Aajonus referenced Christopher Bird's book "The Persecution and Trial of Gaston Naessens" as the source explaining the nature of the sub-particles eaten from proteins in this process.

The life span of these mutant antibodies varies depending on the agent that triggered their creation. Penicillin-induced mutant antibodies persist for at least one year. Polio-vaccine-induced mutant antibodies can persist for up to 50 years. Each additional vaccine multiplies the total number of mutant antibodies in the body, which compounds the cellular malnutrition and results in proportionally greater weaknesses, diseases, malfunctions, and deformities. Aajonus was explicit that the body responds to antibiotics such as penicillin and tetracycline exactly as it does to vaccines, meaning mutant antibodies are created by antibiotic exposure as well.

Conventional medicine holds that vaccines work by stimulating the immune system to create antibodies, which then offer protection against future disease. Aajonus addressed this claim directly and dismissed it on multiple grounds. His first objection is that the immune system is far larger and more involved than antibodies and their related killer cells. The entire body and mind together constitute what could be called the immune system, which means the concept of antibody-based protection is reductive to the point of uselessness.

His second objection concerns the quantities involved. A vaccine contains, at most, a small quantity of diseased cellular material. He stated that 200,000 dissolved animal cells fit onto a pinhead, and that five white blood cells could wipe that out in an instant through phagocytosis. The idea that this infinitesimally small quantity of antigen material generates meaningful immunity he called absurd, ridiculous, and the most absurd thing he had ever heard. When he studied at the Sorbonne Institute in Paris between 1993 and 1996, with a translator accompanying him through the technical French literature, he concluded that not one animal ever survived Pasteur's vaccines; they all went into anaphylactic shock and died. The reason they did not die in subsequent iterations of vaccine development was that neurological poisons were added to the formula, which suppressed the anaphylactic response, not because the vaccine itself became safe or effective.

His third objection concerns viral change. The body alters the solvents it produces to dissolve tissue, which are what he considered viruses to be, every 72 hours. Every 72 hours there is a change in the virus, meaning a flu vaccine manufactured 18 months earlier, which is the minimum manufacturing time, bears no relationship to the virus present in the body at the time of injection. The vaccine is already obsolete. He described the entire premise of stopping a flu with a vaccine as "not only inane, it is outright stupid" when one understands the chemistry.

Aajonus repeatedly situated the language of antibodies and immune system within what he saw as deliberate pharmaceutical obfuscation. He described the immune system as a "spacey, mysterious thing that the pharmaceutical companies come up with to help confuse you about how your body works." When the medical profession discusses the immune system, it emerges, in his description, as an "ethereal little thing that you can't see and you really can't put your finger on," invoked to sell medications and treatments. There is no ghost immune system. There is a lymphatic system, and there is E. coli in the bowel.

He was precise about what he considered the actual substrate of what medicine loosely calls immunity. E. coli in the bowel and the lymphatic system are, in his words, "basically everything you need to back up the system on anything." If any part of the body were to be identified as the immune system, it should be E. coli in the bowel and the lymphatic system. The lymph system feeds every cell in the body, removes all waste products, neutralizes toxins, and dissolves what cannot otherwise be eliminated. The body does not need to defend itself in natural environments. The only things genuinely toxic in the environment are industrial pollutants, and the lymphatic system is the mechanism designed to handle that cleansing when natural or unnatural toxic substances interfere with function.

He stated plainly that there is no such thing as a definable immune system, and that pharma and medicine "are all over the place about it, making stuff up as they go." The body does not need to defend itself against nature. Antibody-based immunity, in this framing, is a manufactured idea of the medical community, constructed to create fear and dependency on pharmaceutical products.

One specific clinical scenario in which Aajonus addressed antibody formation outside the vaccine context involved thyroid antibodies. When asked about the body producing antibodies against thyroid tissue, a phenomenon measured in conditions such as Hashimoto's thyroiditis, he gave a specific mechanistic explanation. If thyroid tissue begins to dissolve or decompose, it creates fluids that react like a foreign substance in the body. The body then creates an antibody against that decomposing tissue because it is not used to encountering that kind of tissue in the blood in that form. He confirmed that the tissue is then treated as a foreign substance, which is why antibody production occurs. This is the body responding to its own decomposing tissue presenting as unfamiliar, not the body attacking healthy tissue irrationally as the autoimmune framework suggests.

Aajonus engaged with a question about Cyrex Laboratories testing that revealed specific immunoglobulins showing up after exposure to eggs and dairy, with the conclusion that the person was allergic to those foods. The testing was presented as newer and more accurate than past allergy testing, with immunoglobulins identified as markers of reactivity to specific antigens. Aajonus's consistent response to such testing was framed by his broader position that all medical tests are purposely constructed to convince people they are deficient in something or reactive to something that can be corrected with supplements or medication, and that only proper raw foods produce homeostasis. He did not validate immunoglobulin-based allergy tests as meaningful guides to dietary choices within his framework.

A person reported that an immunologist found their immunoglobulin G at 770 against a normal range of 694 to 1618, considered low, and simultaneously reported an RNAA test result of 536 against a normal of less than 50, which the immunologist described as revealing a virus or immune system fighting something. A positive antibody to CMV IgG was also present, indicating past Epstein-Barr exposure that the immunologist considered well contained and not threatening. Aajonus's framework would treat all of these findings with the same skepticism he applied to immunological testing generally, viewing them through his lens of lymphatic congestion, toxic accumulation, and the absence of any true "immune system" that these numbers are presumed to measure. He also noted that there is no immune system per se, only the lymphatic system, when addressing the same person's question about whether the specialist was right that the immune system was very weak.

Rather than antibodies, Aajonus described the body's protective capacity as residing in specific biological systems. White blood cells, specifically phagocytes, eat dead red blood cells and contamination in the blood to keep the blood clean. When pus is present, 95 to 98 percent of it is white blood cells, which are the protection, not something yucky or bad. The lymphatic system neutralizes toxins, breaks down waste, and delivers it to the skin for elimination, with 90 percent of all toxins meant to leave through the skin. E. coli is responsible for synthesizing B vitamins and amino acids and functions as a backup for the entire system.

Venom and toxic substances from bites can be neutralized by the body sending them to the stomach, where hydrochloric acid, which is strong enough to dissolve bone without dissolving the stomach lining itself, can help neutralize some industrial poisons. The body also stores certain toxic substances, including vaccine residues such as formaldehyde, ether, mercury, and aluminum, in the stomach lining. Aajonus found these substances present in all 32 autopsies he performed on cadavers, with 30 of the 32 showing dense concentrations of vaccine toxicity. The people whose bodies stored these toxins in the stomach lining showed fewer short-term negative effects from vaccines because they did not go into anaphylactic shock, but they would carry those stored toxins long-term.

Aajonus attributed a wide range of diseases directly to the mutant antibody mechanism and the toxic contents of vaccines more broadly. When vaccine waste collects in the pancreas, the pancreas stops working and diabetes results. When it collects in the connective tissue, MS or lupus results. When it affects the nervous system, neurological conditions result. He stated that 70 percent of all diseases today are caused by vaccines, with about 90 percent of all diseases treated by the pharmaceutical industry. Impetigo in children he described as a result of vaccines. MS and lupus in every patient he treated were associated with the inability to perspire, which meant toxins stored in connective tissue could not exit through the skin. The most severe lupus case he saw was a tennis player who could not perspire despite intense physical activity, and all the toxins from muscular activity and sun exposure stored in his connective tissue until at age 38 he suddenly developed the full condition.

The glandular system, including the endocrine glands, can be damaged by mercury from vaccines stored there, producing conditions involving chronic fatigue and fibromyalgia. Every case of fibromyalgia and most cases of chronic fatigue he saw involved a congested lymphatic system. In some cases, the endocrine gland system was also damaged by mercury from vaccines or medications stored in the glands, compounding the lymphatic congestion.

For people who received vaccines or were abducted and injected without consent, Aajonus recommended specific foods to support the body's elimination of the toxic contents. He recommended eating lots of cheese, butter, a butter and honey mixture, cilantro leaves and cilantro juice, plenty of eggs, meats, milk, and berries with cream. The cheese was emphasized for its role in absorbing and binding toxins, drawing them out of tissues. Baths were also referenced as essential for helping discharge vaccine toxins through the skin. He described his own experience after being injected with what he believed was the swine flu vaccine during an assault, and said he did everything possible to ensure the toxins discharged through the skin rather than through the bowels, urinary tract, or mucous membranes, because those internal routes could have caused the tissues to be eaten away. He experienced discharge through one nostril daily, with crusty crystallized yellow to amber fluid, discharging approximately two ounces per day.