Endless amounts of federal grant money have been spent on research claiming to hunt for elusive genes that cause Autism, Cancer, Long Covid, etc., but the answer is carefully and purposely avoided to keep the status quo, which is to supply an endless stream of new patients passing through a revolving one way door to the medical and pharmaceutical monopolies.

VACCINE-INDUCED AUTISM IS AN IMMUNE REACTION THAT DISRUPTS THE FUNCTIONING AND GROWTH OF THE BRAIN, CAUSED BY THE INJECTION OF A FOREIGN SUBSTANCE INTO A HUMAN BEING THAT RESULTS IN A RELEASE OF HISTAMINE THAT PERMEATES (MAKES SWISS CHEESE OUT OF) THE BLOOD BRAIN BARRIER AND ALLOWS UNWANTED PATHOGENS, ENZYMES, HORMONES, AND BODY WAIST PROTEINS TO ENTER THE BRAIN. VACCINATION-INDUCED INFLAMMATION IS ALSO PRESENT, AND IS CAPABLE OF REACTIVATING DORMANT PATHOGENS. THE SEVERITY OF THE "AUTISM" DEPENDS ON THE EXPOSURE TO THE PATHOGENS INVOLVED, PLUS THE QUANTITY AND LENGTH OF TIME OF THE HISTAMINE RELEASE. A VACCINE ADJUVANT IS THE CHEMICAL IN A VACCINE WHICH STIMULATES THE IMMUNE SYSTEM, AND IN THE CASE OF ALUMINUM, IT IS A TOXIN THAT THE BODY VIOLENTLY ATTEMPTS TO REJECT. ADJUVANTS CAN ALSO CAUSE NEW OR EXACERBATED FOOD AND OTHER ALLERGIES, THAT ARE THE RESULT OF THE ADJUVANT(S) OVER-SENSITIZING T-CELLS TO FOOD AND OTHER PROTEINS, AND THE POSSIBLE SUSTAINED TRIGGERING OF MAST CELLS THAT PRODUCE VARIOUS PROLONGED LEVELS OF HISTAMINE. ACCORDING TO DR. PHILLIP DEMIO, "EPSTEIN BARR VIRUS TITERS ARE OFF THE CHARTS IN MOST AUTISTIC CHILDREN."

CANCER GENESIS SIMPLIFIED: CANCER CAN BE ENCOURAGED / INDUCED BY THE SARS COV-2 "SPIKE" PROTEIN (IN THE WILD OR THROUGH "VACCINATION") CAUSING THE INACTIVATION OR INHIBITION OF THE PD-1 PROTEIN ON T-CELLS. PD-1 PROTEINS HELP REGULATE THE IMMUNE SYSTEM, AND ALLOW AN IMMUNE CELL TO RECOGNIZE AND KILL AN INFECTED CELL, INCLUDING CANCER CELLS. IT IS INTERESTING TO NOTE THAT THE EPSTEIN BARR VIRUS WILL ALSO COMPROMISE PD-1 PROTEINS.

According to Public Broadcasting Service Television's program called Frontline, which aired on July 22, 2014, the United States of America has one of the highest child poverty rates in all of the developed world. PBS Television investigators revealed that 46,000,000 Americans live in poverty, and 16,000,000 are children. 1 in 5 children in the United States lives in Poverty. Many poor Americans can't afford balanced meals and experience panic attacks. Instead of providing magnesium-rich foods to the poor, or even telling Americans that a diet low in magnesium can result in such things as panic disorder, muscle spasms, heart arrhythmias, and possible early death, the United States Government is allowing doctors to prescribe expensive addictive pharmaceutical drugs such as XANAX, in what appears to be an attempt to control and limit the population of the United States of America, and at the same time increase income for the Food and Drug Administration (FDA), who holds lucrative patents on certain drugs. At the same time, politicians such as 2008 presidential candidate, John McCain and his wife, disclosed that they owned $25,000,000.00 U.S. Dollars worth of stock in Gilead Sciences, the company that makes Tamiflu and other drugs. In addition, former Secretary of State, Donald Rumsfeld was on the Board of Directors for Gilead Sciences. The Center for Disease Control and the Food and Drug Administration are two leading government agencies responsible for the health of United States Citizens. Both of these agencies allowed Americans to needlessly suffer and die, while paying billions of dollars to pharmaceutical companies for useless $200.00 dollar per month prescription antacids that made the stomach a breeding ground for the H-Pylori Bacteria that was typically causing the ulcers. The Food and Drug Administration is the government agency that approves new drugs, and is paid directly by the same drug companies to do so. Taking antibiotics for seven days would have healed these stomach ulcers and killed the H-Pylori Bacteria. The CDC and FDA withheld this information from the American people, resulting in windfall profits for the medical profession, doctors, clinics, hospitals, and neighborhood pharmacies. These are just a couple examples of how pharmaceutical companies and the medical profession concentrate on higher profits for themselves, even if it harms or kills the Americans they claim to protect. But now pharmaceuticals have sunk to an all-time low - taking the minds and lives of countless of children worldwide through the use of defective vaccines with high profit margins. In the early 2000s, an English company called POWDERMED invented a safe vaccine, which created a huge problem for other drug companies. The POWDERMED vaccines did NOT cause autism. Pfizer pharmaceuticals bought the company in 2006, and quietly closed it down at the end of December, 2008. Pediatricians are the biggest contributors to autism and autoimmune disease. A Vaccination is similar to multiple brain concussions suffered by football players IF the blood-brain-barrier is open. The blood-brain-barrier is commonly opened by a naturally produced chemical called HISTAMINE. Histamine is released primarily by Mast Cells when a child is teething, has a cold, has asthma, or has allergies. Food allergies, especially undiagnosed food allergies, can cause the release of histamine which dilates blood vessels. Since allergies are typically genetic, one or both parents of these potentially children may also experience light-headedness or a noticeable increase in heart rate or heart pounding if they stand up suddenly from a sitting or lying position. The severity of these symptoms of Postural Orthostatic Tachycardia Syndrome (POTS) depends on their exposure to allergens and stress, minus the amount of histamine removed from their body due to the rest and sleep they had during the previous night. The worst time to vaccinate an infant or toddler is during teething. Food allergies may commonly cause diarrhea, followed by constipation. If a child is vaccinated under these conditions, the inflammation-causing vaccine adjuvant will enter the brain and cause macrophages called glial cells to become inflamed, and the brain becomes swollen (encephalitis). Glial cells surround Oligodendrocytes that produce the MYELIN that forms the insulating layers around nerves that carry electrical impulses that control thinking and muscle movement. If other pathogens are present in the body, even in a dormant state, we have observed that inflammation becomes more aggressive and debilitating, which re-confirms the 1926 findings of RAMON et al. Ironically, this inflammation triggers an additional condition called oxidative stress. Oxidative stress helps deplete the body's stores of INTRACELLULAR magnesium that is used to make about 300 enzymes each day, and stops the body from properly using Thiamine, commonly called vitamin B1. Thiamine is used by the mitochondrion of every cell in the body, and can produce symptoms of BERI BERI, especially fatigue, poor memory, and poor concentration. Autism is proportionate to the severity of the symptoms and the length of time the inflammation is allowed to continue. Poorly trained and profit motivated pediatricians say vaccines are safe, and doctor such Paul Offit, the poster child for vaccines and bad medicine, claim that 10,000 vaccines can be safely given to a child. Let's examine Doctor Paul OffitsOne standard dose of a typical vaccine is currently 0.5 milliliters of fluid. 10,000 vaccines is approximately 5 liters of fluid, or 1.3 U.S. Gallons of liquid. Americans are being blackmailed by profit motivated pediatricians and drug companies who are telling them that they will report them to social services if they do not buy their vaccines.

In a multi-year study we observed a reproducible universal cascade of events which results in autism. These events are typically initiated by prolonged trauma to the immune system which causes oxidative stress (which we observed to deplete both Vitamin D and Magnesium), and hyper-activates immune cell activity. The most common cause of prolonged trauma/hyper-activation of the immune system is the result of an intramuscular vaccination. However, serious insults to the immune system from diseases such as Shigellosis, or physical trauma, such as car crashes, may also produce a similar outcome without ever receiving a vaccination. We observed that these Autism-inducing vaccines primarily target people from Ireland, Scotland, Great Brittan, Denmark, and nearby Northern and Western European countries who carry the Human Leukocyte Antigen (HLA) gene mutation, such as the HLA DR-15 allele, which allows pathogens, such as the Epstein Barr Virus, to evade the immune system. This, together with one or more genetic mutations that result in a Cystathionine Beta-Synthase deficiency that inhibits transsulfuration, especially the CBS 699t allele, can cause debilitating and/or life-threatening cascades of events. We have observed that these events become more debilitating or deadly deadly when a dormant or active infection is present, especially those infections related to pathogens carried by ticks, mosquitoes, or similar biting insects (insect-borne vectors). We have found that diseases such as Borrelia burgdorferi, Bartonella, Babesia, Protozoa Rheumatica, and others have kept their hosts ill from months to many years. Multiple co-infections such as Mycoplasma were always found to be present. These pathogens were never found alone, but were always found in groups. Lastly we observed a Glutathione S-Transferase deficiency, which was typically attributed to a GST-M1/P1/T1/Z1 polymorphism. We observed that a prior history of mononucleosis appears to be a 100% predictor of a life-threatening vaccine reaction, especially in older children if the Gardasil HPV vaccine is involved. We believe that if an LPS Stimulated Comprehensive Cytokine Panel was used to pre-screen prospective vaccine recipients, that Autism would be greatly diminished, and if people with genetic mutations that effect the Human The result of vaccinating a child under these conditions can easily result in Autism, and we have documented the following cascade of debilitating events leading up to it, which may result in many other diseases, including Multiple Sclerosis:

NOTE-May 2014: DNA NON-B CONFORMATION mutations were found in 100% of vaccines tested in France and produced by MERCK PHARMACEUTICALS. DNA mutations were confirmed by two independent genetic labs: one located in the United States, the other in France. We can now scientifically state that vaccines can DIRECTLY cause Neurologic, Autoimmune, and Psychiatric Disorders. MERCK'S genetically modified vaccine contaminants are not just mutations, they are totally new molecules, never before seen in nature.

..."The human genetic consequences of these non-B structures are approximately 20 neurological diseases, approximately 50 genomic disorders (caused by gross deletions, inversions, duplications and translocations), and several psychiatric diseases involving polymorphisms in simple repeating sequences." .... click here for Abstract

Histamine opens the blood brain barrier, exposing the brain to pathogens and toxins in the blood, including vaccines. Toddlers are vaccinated at the worst possible time because teething produces both Histamine and Oxidative Stress.

In 2008, Stomatovic et al Curr Neuropharmacol. Sep 2008; 6(3): 179–192. doi: 10.2174/157015908785777210 discovered that Histamine, including the Histamine caused by teething, opens the blood brain barrier, which allows vaccines and their inflammation-producing adjuvants (chemical helpers that can force the immune system to become hyperactive) to cross the blood brain barrier. A vaccine can directly cause encephalitis (swelling of the brain).

Gibson et al, discovered that Oxidative Stress was associated with neurodegeneration of cells in the brain and the appearance of a Thiamine deficiency. We found signs of this Thiamine deficiency in many of the children and adults in our study.

Stress results in activation of the hypothalamic pituitary adrenal axis and can affect illnesses such as autoimmune and neuroinflammatory syndrome (Stenberg & Wilder, 1993).

Cortisol is a glucocorticoid that inhibits the activation and or uptake of vitamin D, therefore, VITAMIN D WILL ALWAYS BE LOW, and is a key symptom for the syndrome we are documenting.

We observed that administering Vitamin D to our group played a key role and appeared to help relive gut inflammation and pain, possibly by enhancing cortisol (glucocorticoid) activity, which is consistent with the findings of Zhang et al, April 9, 2013, doi:10.1074/jbc.M112.427054jbc.M112.427054.

We also found symptoms of depleted intracellular magnesium, even though serum magnesium was within limits. SEROTONIN, MELATONIN, AND MAGNESIUM DEPENDENT ENZYMES WILL ALWAYS BE DEFICIENT.

It further appears that drug companies may be attempting to discredit the usefulness of Vitamin A, which when depleted, actually causes oxidative stress, mitochondrial dysfunction, and energy deprivation through PARP-1. FASEB J. Nov 2008; 22(11): 3878–3887. doi: 10.1096/fj.08-112375

In rare cases, a pediatrician can inject a vaccine directly into a blood vessel by failing to aspirate the syringe, which may result in autism.

Virtually all of what is called Autism is the result of vaccines containing an aluminum adjuvant (especially the genetically modified and contaminated Recombinant vaccines such as MMR and Gardasil), together with current intramuscular vaccination administration methods. Intramuscular elude a strong TH2 immune response which bypass natural immune system safeguards, and places medically engineered antigens and contaminants in direct contact with hepatic pathways to the brain. Of great concern is the use of surfactants such as Polysorbate 80 (TWEEN 80), which not only keep vaccine ingredients from clumping together, but may coat proteins in the vaccine and form "bullet proteins" which may allow them to pass through the blood brain barrier, resulting in the vaccine causing inflammation (encephalitis) and producing antibodies within the brain. An allergic reaction to a vaccine component, especially the bacteria or yeast that MMR and Gardasil antigens are grown in, may result in acute stress. Acute stress may result in histamine production. TEETHING ALSO PRODUCES HISTAMINE. Histamine opens the blood brain barrier. Vaccines may also enter the the brain if the child is actively producing histamine from a cold or allergy, because histamine permeates the blood brain barrier. This characteristic was examined as a possible answer to delivering drugs into the brain. Many people are still not aware that vaccines using bacteria and viruses can cause the recipient to become contagious for 21 days or more, but some rare reports confirm contamination of sewer systems from proprietary vaccine antigens from the feces of vaccinated individual years later. The Standard Of Care in the United States is to disregard contraindications and warnings by vaccine manufacturers, especially those involving involving allergies to vaccine ingredients. Children are mass-vaccinated by pediatricians who care more about profits than they care about averting autism, which in many cases results in an encephalitic inflammatory adverse vaccine reaction that fails to self-limit.

There was a safer vaccine technology called POWDERMED, that didn't cause autism, but it was bought out by PFIZER, and was never heard from again. Vaccination typically involves injecting a small amount of a live or dead virus or bacteria or protein(s) from that virus or bacteria (RECOMBINANT VACCINE) inside the human body, mixed with a chemical that stimulates the immune system and typically contains aluminum nano-particles. This causes an acute response from the immune system. In 1926, Glenny et al discovered that mixing a diphtheria toxoid with aluminum produced large amounts of diphtheria antibodies in Guinea pigs, but it wasn't until 1932 that this technique was used for the general public.

Our study of vaccine-induced Autism has confirmed what Ramon et al had documented in the mid 1920s: Infections cause an enhanced immune response. If an infant or toddler with a dormant or active infection is vaccinated, the immune response can be life-threatening. In older children vaccinated with the Gardasil HPV vaccine, we found infections such as Mononucleosis to be virtually a 100% predictor of a life-threatening vaccine reaction, even if the person had Mono 10 years previously.

Since the majority of these vaccine-hyperactivated immune cells are located in the gut, the Gastrointestinal (GI) Tract can become inflamed and expose immune cells in the lining of the gut. Food proteins passing through the GI Tract may then come into contact with these exposed immune cells in the epithelial layer. The result can be the production of antibodies to proteins contained in the food the child ate. These antibodies are the reason why the child forms new food allergies, which typically include the gluten in bread, casein in milk, and peanut protein from peanuts and peanut butter. When these foods are eaten again, presenting cells can identify these food proteins as allergens, and mast cells produce histamine in response. This may result in a Histamine Intolerance. Since histamine dilates blood vessels, both children and adults may now complain of dizziness and or a rapid heartbeat upon standing. This condition is commonly referred to as POTS, which is short for POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME.

Our research shows that when the GI Tract becomes seriously inflamed for extended periods of time, diarrhea may result, followed by malabsorption. The next phase is constipation, in which the body attempts to squeeze and retain as many nutrients as possible passing through the GI Tract and large bowel. Sustained inflammation will now result in Oxidative Stress which will deplete intracellular magnesium and inhibit the uptake of Thiamine. When Magnesium is excreted during stress, the production of approximately 300 different enzymes will be compromised.

Mood changes and irritability are typical first signs of low magnesium. Methylation and transsulfuration cycles fail, especially when HLA and CBS gene mutations are present, especially in people of Irish ancestry and those of nearby Western and Northern European regions. Southern Italy has been identified as another hotspot for these genetic mutations, due to the Vikings influence. AXON growth, proliferation, and guidance will be compromised VIA the H3K4 Trimethylation cycle and the inhibited production of Semaphorin. Semaphorins have recently been investigated in tumor formation and suppression, and the loss of production of anti-tumor Semaphorin 3F may allow Semaphorin 5A to enhance tumor formation and proliferation until inflammation and the typical infections we observed, such as EBV and Bartonella, are brought under control. Proper nutrition pathways must quickly be re-established, typically with the aid of low-dose Naltrexone when gut sensitivities are acute.

There are at least 3 conditions that must be met for cognitive and / or motor skill impairment to take place. These typically include, but are not limited to: 1) elevated pathogen load, typically due to a Human Leukocyte Antigen gene mutation, especially the HLA DR-15 mutation which may allow the Epstein Barr Virus to go virtually undetected by the immune system; 2) failure or inhibition of transsulfuration, which typically involves a Cystathionine Beta-Synthase (CBS) deficiency, which may involve the 699t allele; 3) An impairment of Glutathione S-Transferase, typically due to a GSTM-1 or similar genetic mutation which inhibits Glutathione use. It is during this time that multiple pathogens become virulent, and cognitive and motor skills become impaired, and the longer inflammation runs rampant, the more damage is (permanently) done.

When Cystathionine Beta-Synthase (CBS) becomes deficient, Glutathione may become depleted, inflammation may also increase, and connective tissue disorders can occur. This is the result of sulfur not properly processed in the first step of transsulfuration. Sulfites may enter the brain and cause debilitating head pain. This may be the prime reason why children bang their heads. If you see head banging in young children, always suspect a defect in the TRANSSULFURATION PATHWAY.

To make matters worse, the cortisol that is produced to calm inflammation also inhibits the production of Melatonin by the pineal gland, which causes varying degrees of memory loss and insomnia in the infant, child, or adult. Until (systemic) inflammation is reduced or eliminated, the child may sleep only one or two hours at a time. Low Dose Naltrexone has been found to eventually allow the child to sleep for five or more hours in some cases.

When these serious vaccine-induced gut issues exist, we also observed that mega-doses of thiamine did nothing, but the fat-soluble form of Thiamine did work (TTFD, a.k.a. ALLITHIAMINE). It was also necessary to supplement Vitamin B12 and Vitamin B6, using the active form for each. We also noted that many children reached a plateau in their recovery, and blood panels were run. An LPS Stimulated Comprehensive was run first to determine if systemic inflammation, an infection, or a hidden pathogen was present. This was useful, as virtually all normal testing came back within gate. However, even though base counts were mostly normal, many LIPOPOLYSACCHARIDE STIMULATED CYTOKINES came back far below lower gate (limits), some as much 25% of the lower limit. It should also be noted that CD57 tests were far below acceptable limits in a significant number of children. This did not indicate that all of these had Lyme Disease, although some of them did.

Some of the most commonly found infections were from biting insect vectors, including ticks and mosquitoes, which included the newly discovered Protozoa Rheumatica, along with common tick-born pathogens, such as Bartonella, Babesia (especially in kids with "sweaty heads"), Babesia, and much more, along with elevated EBV, Mycoplasma, etc. It is interesting to note that multiple pathogens were commonly found, which often tended to skew symptoms (molecular mimicry).