Vaccines

Aajonus identified five basic ingredients that he said were present in every vaccine without exception. These were liquid mercury, liquid aluminum, formaldehyde, ether, and detergent. He returned to this list repeatedly across many workshops and publications, describing each ingredient individually to make clear that every one of them was a serious industrial poison on its own, and that their combination in a single injection created a toxic soup whose interactions within the body were entirely unpredictable.

Liquid mercury, referred to in ingredient lists under at least twelve different names including thimerosal, antiseptic, antibacterial, and preservative, he identified as a potent neurotoxin. He described research from the University of Alberta showing time-lapse photography of neurons growing in culture, and when a two percent solution of thimerosal was added, the neurons dissolved visibly and rapidly. He said that any vaccine, any injection containing mercury, could be counted on to destroy nerve and brain cells, and that if memories were stored in those cells, they were gone permanently.

Liquid aluminum he described as behaving in the blood the way liquid aluminum poured into an aquarium would behave, settling to the bottom and making fish unable to swim. He said it disrupted blood circulation and contributed to excessive clotting, which produced strokes, seizures, and a wide range of neurological conditions he grouped under the term vaccine-induced disease, or VID.

Formaldehyde he identified as an embalming fluid. He explained that formaldehyde coats cells so that they no longer function, no longer respire, and solidify in place. He described it as the ingredient most responsible for long-term preservation of cellular damage.

Ether he described as the substance used to put patients to sleep for surgery. He said injecting ether into the body caused certain parts of the brain to shut down and cut off, producing a form of neurological suppression that operated internally rather than externally.

Detergent he identified as the fifth ingredient, present ostensibly to keep the solution clean, and equally toxic in injection as the others.

He frequently used the illustration of a blender to make this concrete. He asked audiences to imagine taking a thermometer containing mercury, a vial of aluminum, a container of formaldehyde, a dose of ether, and some detergent, adding a rotten egg in which a disease had been grown, blending all of it together, and then offering the result to someone in a cup. He said that no one would drink it, and he asked why anyone would therefore allow it to be injected directly into the bloodstream.

Beyond the five core ingredients, Aajonus described vaccines as containing between 26 and 63 additional toxic substances, varying somewhat by vaccine type and by workshop, with figures of 41, 43, 53, 56, and 58 also cited in different passages. He was consistent that every single one of these additional ingredients was toxic on its own, that none of them qualified as a nutrient or food in any sense, and that they were labeled as inert despite being anything but.

He published a partial list in his newsletter that included aluminum hydroxide, aluminum phosphate, ammonium potassium sulfate, aluminum sulfate, amphotericin B, animal tissues from pig blood, horse blood, rabbit brain, dog kidney, monkey kidney, chick embryo, chicken egg, and duck egg, animal serum including bovine calf, caso-amino acids, dimethyl-betacyclodextrin, fetal serum, betapropiolactone, formaldehyde, formalin, gelatin, and glutaraldehyde, among others. He noted that some vaccines also contained squalene, which he said was capable of causing five different types of cancer, breaking down the liver, and destroying the kidney.

He described the word "adjuvant" as a term invented specifically to spin the concept of toxins in vaccines into a package that sounded acceptable and even helpful, and said that all adjuvants were in fact poisons regardless of what they were called.

He emphasized that the presence of any so-called disease material in this soup was quantitatively negligible compared to the toxic load. He said the biological component, whether bacterial waste products or dissolved animal tissue, amounted to at most two million particles, or perhaps 100,000, or 200,000 depending on the batch, and that all of this material could fit on a pinhead. Five white blood cells, he said, could consume that quantity of disease material in an instant through normal phagocytic activity. The idea that this quantity of biological material could generate meaningful immunity was, in his words, absurd, ludicrous, and never provable, because it simply did not work.

Aajonus described the manufacturing process used to extract the biological component of vaccines, and he found the process itself to be evidence of how far removed the final product was from anything that could legitimately produce immunity. He said that when vaccine manufacturers created the biological portion of a vaccine, they used a solvent, typically gasoline rather than kerosene, to dissolve the source tissue, which might be a raw egg, pig tissue, or monkey tissue. The so-called disease cells were then extracted from this gasoline solution and placed into the vaccine formula along with the five core ingredients and all the additional toxic compounds.

He also described the source material itself as rotten, decaying tissue. He said that eggs used to grow disease were deliberately heated to destroy defensive bacteria, then injected with a particular pathogen and allowed to decay while the pathogen replicated. This deteriorating biological material was then blended into the final formula. He noted that 99 percent of all vaccines were grown in eggs, meaning nearly all disease material in vaccines originated from avian cells, and that the viruses produced by those cells were avian in nature, adapted to a bird's cellular environment rather than a human one.

One of Aajonus's central arguments against the immunity claim was that sterilizing a disease to make it safe for injection fundamentally altered the biological entity being injected to the point where it bore no meaningful relationship to the natural disease. He said that sterilization altered the RNA, DNA, structure, and actions of diseases and viruses. When this altered entity entered the body, the body tried to analyze it but could not find the logical reason for the unnatural disease or virus, and could not find the key to identifying when the bacteria or virus would be active.

He argued that even if the body did generate some response to this sterilized material, that response would be specific to the artificial sterilized entity, not to the natural disease. The immunity produced, even by the vaccine industry's own logic, would therefore be immunity to something that did not exist in nature and posed no real threat, while providing no protection against the actual disease.

He also pointed out that even if vaccines could in theory create a targeted immune response, the biological component was so overwhelmed by the toxic component that the body's entire energy and attention would be directed toward managing the poison rather than developing any immune response. The toxic load, he said, prevented the body from entertaining the biological material in any meaningful way. The body was too busy trying to survive the mercury, aluminum, formaldehyde, ether, and detergent to notice the 200,000 dissolved animal cells sitting on a pinhead alongside them.

Aajonus taught that viruses change every 72 hours, a property he described as making every virus a retrovirus in the sense that its RNA and DNA are constantly being altered as cells produce slightly different solvents to address their changing detoxification needs. He said the body allowed itself approximately 72 hours of detoxification with a specific virus before producing a different one for different cleansing, and that what the medical community identified as viral evolution was simply this ongoing natural process of cellular solvent production.

Given this 72-hour cycle of change, he said that any vaccine developed to counter a specific virus was obsolete within 72 hours of that virus first appearing. In practice, it took a minimum of 18 months to manufacture a vaccine and bring it to market, with some vaccines taking two to three years. This meant that by the time any flu vaccine reached the public, the specific virus it had been designed to address was already extinct in its original form, having gone through hundreds of cycles of change. He said the pharmaceutical industry knew this, and that the flu vaccine business was therefore a racket based on deliberate misdirection about how viruses actually behave.

He noted that the swine flu vaccine was a particular example of this fraud. He said the only way to get swine flu was to be injected with it, because swine flu was a disease of toxic pigs and humans were not pigs. Similarly, bird flu could not transfer to humans because humans were not birds. The entire premise of cross-species viral transmission for purposes of vaccine development was, in his view, biologically preposterous.

Aajonus addressed polio specifically and at length, regarding it as the flagship example of how vaccine effectiveness statistics were falsified. He said that when the polio vaccine was introduced in 1958, the incidence of polio had already declined to approximately one percent of its peak levels. The vaccine industry released the product after the disease was nearly gone and then claimed credit for eliminating it.

He described specific statistical evidence he had examined showing the reported incidents of polio in 1958, before compulsory vaccination, and in 1959, when the law was adopted, and he said the data showed that vaccination was followed not by continued decline but by increases in certain areas. He mentioned three states in one county where the disease actually increased after the vaccine was made compulsory.

He also described Dr. William F. Koch's finding, which he cited approvingly, that the injection of any serum, vaccine, or even penicillin produced a very marked increase in the incidence of polio of at least 400 percent, and that the statistics were so conclusive no one could deny them.

He characterized the claim that Salk's vaccine eliminated polio as myth, and said the vaccine took credit for a decline that had already occurred through other means, specifically through the reduction of the industrial poisoning that he identified as the actual cause of the disease.

Aajonus taught that the 1918 influenza pandemic, popularly called the Spanish flu, was not caused by a flu virus but by the Spanish flu vaccine itself. He said that nobody died of the flu until they received that vaccine, and that the vaccine was Rockefeller's and Rothschild's first major vaccine product, pushed aggressively after three earlier failed attempts. He credited this event as the origin of the mass vaccine industry and described the 50 million deaths attributed to that pandemic as the consequence of the vaccine rather than the disease.

Aajonus described the body's response to vaccine injection in terms of where the toxic substances were ultimately stored. He said that most of the poisons injected through vaccines ended up in the stomach lining. The body, unable to dissolve heavy metals like mercury and aluminum through normal hydrochloric acid processes, and unable to easily process formaldehyde and ether through conventional detoxification pathways, would sequester these substances in the stomach lining. From there, a small amount would be dumped into the digestive tract every time the person ate anything, and would be immediately reabsorbed.

He said that when he performed autopsies on stomachs, the amounts of formaldehyde, ether, mercury, and aluminum he found in the stomach lining from vaccines were enormous. He said that people whose bodies successfully moved vaccine toxins into the stomach lining would not experience immediate severe reactions such as anaphylactic shock or acute illness, but would carry those toxins indefinitely, slowly reabsorbing them with every meal, with long-term consequences he described as worse in aggregate than the acute reactions.

Some toxic material, he said, would accumulate not in the stomach lining but in sealed pockets in other tissues. The location of those deposits determined what disease would eventually develop. If the waste from a vaccine collected in the pancreas, the pancreas would stop working and the person would become diabetic. If it collected in connective tissue, the result was multiple sclerosis or lupus. If it infected the nervous system, neurological disease followed. He described his own experience of vaccine toxicity reaching the brain and causing neurological destruction, and reaching the heart and causing heart spasms for seven years.

Aajonus provided specific quantitative details about mercury in vaccines. He said that one vaccine contained 1,236 times the toxic dose recognized by the FDA as dangerous. He described the total mercury load in a single vaccine as six million quadrillion molecules, a number he put in spatial terms by saying you could go around the planet a couple of times if you laid those molecules end to end.

He then described the difficulty of removing mercury from the body. It takes, he said, 50 to 200 fat molecules to harness one molecule of mercury safely enough to transport it out of the body without causing additional damage in transit. Working through the mathematics, he concluded that to eliminate the mercury from a single vaccine, a person would need to consume a cup of raw cream and a stick of raw butter every day for ten years. He then pointed out that children were receiving 68 to 113 vaccines by the time they were 16 or 60 years old in some states, with some states requiring up to 90 vaccines by age 16. He said that children subjected to this vaccination schedule would never be able to eliminate the accumulated contamination through any realistic dietary protocol, though controlling it was possible.

He identified mercury's primary mechanism of damage as the dissolution of neurons. He cited the Alberta University research showing neurons dissolving in real time under the addition of a two percent thimerosal solution, and said this explained why any injection containing mercury could be expected to result in the permanent loss of nerve and brain cells, along with whatever memories or functions those cells carried.

Aajonus described his own autism as having been caused directly by his third vaccination, which he received at 18 months old. He identified it specifically as a tetanus vaccine. He said the result was that he became unable to comprehend communication, unable to convert letters into words or words into concepts, describing it as like being blind in a cognitive sense. He said he could not communicate at all and that his memory had been severely damaged. It took him until age eight to develop any consistent communication by hearing the same words repeated enough times. He described the eight years from 18 months to eight years as a period of profound cognitive isolation caused entirely by the vaccine.

He attributed this damage to the neurological poisons in the vaccine reaching his brain. He also described receiving what he believed was a covert swine flu injection at some point after publicly speaking out against vaccines on a radio program, noting that he woke up nauseous with three bumps and pinholes at the injection sites.

He said that mercury dissolved neurons and that wherever vaccine waste accumulated in the brain or nervous system, the specific functions associated with those areas would be destroyed. He said that if people experienced complete memory loss for a specific thing or period, that was usually a mercury problem.

Aajonus also addressed the biological contamination present in vaccines beyond the intentional ingredients. He described a partial list of contaminants he and colleagues had identified through laboratory work. In the Rimavex measles vaccine, various chicken viruses were found. In polio vaccine, acanthamoeba, a brain-eating amoeba, was identified, along with simian cytomegalovirus. Simian foamy virus was found in the rotavirus vaccine. Bird-cancer viruses were found in the MMR vaccine. Various microorganisms were identified in the anthrax vaccine. Potentially dangerous enzyme inhibitors were found in several vaccines. Duck, dog, and rabbit viruses were found in the rubella vaccine. Avian leucosis virus was found in the flu vaccine. Pestivirus was found in the MMR vaccine.

He also noted that some polio vaccines, adenovirus vaccines, rubella and hepatitis A and measles vaccines had been manufactured using aborted human fetal tissue, and that he had found what he believed were bacterial fragments and poliovirus in these vaccines that may have originated from that fetal tissue.

He described the SV40 monkey virus entering the polio vaccine as a known historical example of this contamination process, but said this was only the most famous case among many. He pointed out that when tissue from any animal species was used to grow a vaccine, every microorganism present in that tissue was a potential contaminant in the final product, and because no one thought to test for many of these organisms, their effects on humans were entirely unknown.

He said the public believed vaccine manufacturing facilities were the cleanest places in the world, and that this belief was false. Contamination, he said, occurred routinely.

Aajonus described the historical development of the modern vaccine as beginning with Louis Pasteur's complete and consistent failure to produce a vaccine that any animal survived. He said Pasteur himself acknowledged on his deathbed that it was not the bacteria but the environment within the body that created disease, confirming what Aajonus taught as the correct framework. But before that deathbed confession, Pasteur's vaccine experiments killed every test animal through anaphylactic shock.

Aajonus described the mechanism. When the body receives that level of toxicity via injection, he said, it interprets the event as a death event and goes into anaphylactic shock, which kills the organism. The discovery that changed this was the addition of neurological poisons to the vaccine formula. When neurotoxins were included in the injection, the body's neurological signaling was disrupted enough that it no longer triggered the anaphylactic response. The animal did not immediately die. This was then presented as evidence that the vaccine was being tolerated and was working. He described this as the moment the modern vaccine industry was born, built on the realization that poisoning the nervous system enough would prevent the immediate death while concealing the ongoing damage.

Aajonus identified the vaccine industry as having been created by the Rockefeller family in the United States and the Rothschild family in Europe. He said the original intent had been to find the chemically active ingredients in foods that caused the reversal of disease, isolate them, and use them therapeutically, but that this goal was abandoned in favor of far more profitable toxin-based interventions. He estimated the global vaccine market at thirteen trillion dollars per year, and said this financial scale explained why the fraud was maintained across generations of doctors, researchers, and public health officials.

He described multiple layers of motivation for those who continued to administer vaccines: money, fear of losing employment, the desire for professional advancement, misguided idealism, unthinking habit, and institutional pressure. He said that when he was working within the vaccine establishment and raised concerns, he was told to keep quiet, that colleagues avoided him to avoid being associated with his questions, and that the institutional culture made it effectively impossible to disseminate negative findings about vaccine safety.

He also addressed the political dimension, noting that pharmaceutical companies had been given legal waivers by Congress for side effects including disease, paralysis, and death caused by their vaccines, and that this waiver removed all accountability from the industry. He described this as both immoral and ethically illegal under the Geneva Convention, which he said prohibited injecting any unproven medical substance into a human body without the pure consent of the individual and without the injecting party accepting full responsibility for any resulting damage.

Aajonus developed a practical tool for people trying to avoid mandatory vaccination in situations where it was legally required or socially pressured. He described a six-page document available through his website that listed every ingredient in the vaccine in question and required the person insisting on the vaccination to sign an acknowledgment of one million dollars of personal financial responsibility for any harm that resulted from each vaccine administered. He said that no one ever signed it. The document was designed both as a legal shield and as an educational tool, since anyone who read through it carefully would understand what they were demanding that another person's body receive.

He also cited the Geneva Convention as legal authority for refusing vaccination, noting that its provisions prevented any non-consented experimental medical injection without individual acceptance and injector liability. He said people could use this framework to refuse yellow fever vaccines required for international travel, and described the alternative as being quarantined for three to eight hours, up to 24 hours, to confirm they were not sick before being allowed to board their flight, which he considered an acceptable trade-off.

For families in the 18 states he said required childhood vaccination, he recommended moving out of those states rather than subjecting children to the vaccines for the sake of convenience.

Because the toxic load of a vaccine overwhelmed any biological immune response, Aajonus said the net effect of vaccination was not immunity but immune suppression. The body devoted all of its resources to managing the poison and had nothing left to run the normal bacterial, viral, fungal, or parasitic cleansing processes that constituted real immune function. Colds, flus, and other cleansing events were suppressed not because the body had become immune to the triggering agents but because it was too toxic and overloaded to generate a proper cleanse.

He said this created the appearance of the vaccine working. The person did not get the cold or flu. But the toxic material that would have been expelled in that cleansing process instead accumulated further in the body, contributing to the chronic degenerative conditions that appeared years or decades later. He characterized this suppression of cleansing as a long-term disaster whose full consequences would not become visible in humans until approximately the third and fourth generations of vaccinated populations, estimating that mutations would start to become exaggerated and apparent around the year 2015.

He also described vaccines as causing the very diseases they claimed to prevent. Some version of the disease was always present in the vaccine, and in some people, particularly in those whose bodies were already compromised, that disease material could establish itself and cause active infection. He described cases of hepatitis B developing after hepatitis B vaccination, and described the historical example of 63 deaths and 25,585 cases of hepatitis occurring at a single military boot camp within a six-month period as a direct result of the yellow fever vaccine, citing former Secretary of War Henry L. Stimson's report.

In other cases, the vaccine did not produce the disease it was supposed to prevent but produced a different disease entirely, such as meningitis, that went unrecognized as vaccine-caused because no one expected that connection.

For people who had already received vaccines and were dealing with the resulting toxicity, Aajonus recommended a dietary approach centered on raw fats. The specific protocol he described for vaccine-induced damage, particularly the mercury and aluminum that accumulated in blood and neurological tissue, was eating half to one cup of raw berries (raspberries, blackberries, boysenberries, or cranberries) blended with three to eight tablespoons of raw coconut cream, one to two tablespoons of unsalted raw butter, and one to two tablespoons of raw cream, eaten as the afternoon fruit meal. He said this combination helped remove mercury and aluminum, which caused blood and neurological serums to become high in sediment and caused excessive clotting resulting in strokes, seizures, and many other neurological VID conditions.

For people dealing with more recently administered vaccines, he referenced the balanced diet in his book The Recipe for Living Without Disease, pages 40 through 42. The general principle was that raw cream and raw butter, consumed in large consistent quantities over a long period, were the primary vehicles through which mercury could be harnessed and transported out of the body safely, given that each mercury molecule required 50 to 200 fat molecules to be safely bound and removed.

He also noted that the toxins from vaccines most commonly sequestered in the stomach lining, and that this storage location, while protective against acute anaphylaxis, resulted in continuous slow reabsorption of those toxins with every meal, making ongoing fat consumption consistently important rather than something that could be accomplished through a finite protocol.

Aajonus cited Pasteur's deathbed statement to his assistants repeatedly as a foundational repudiation of the germ theory upon which all vaccine science rested. He said Pasteur confessed that a poor, toxic environment within the body creates disease, and that microbes do not cause disease. He interpreted this as Pasteur ultimately confirming what Aajonus had come to through his own research and clinical observation: that the body's internal terrain, specifically the presence or absence of industrial toxins, was the determinative factor in disease development, not the presence of bacteria or viruses. Since vaccines were full of industrial toxins and contained no nutrients, they could only make the internal terrain worse, producing more disease of greater variety over longer time spans, while simultaneously suppressing the body's natural cleansing mechanisms that would otherwise have moved some of those toxins out.

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