Although Dr. Browning's research is intended to stimulate the pharma cartels to produce drugs to modulate B cell function in autoimmune disease; this document makes it SELF EVIDENT that the way to stop autoimmune disease from developing in the first place is to stop inoculating people and pets with disease, which is what causes the corruption of the immune system leading to autoimmune disease in the first place! Dr. Browning's article discusses many of the following autoimmune diseases; in fact, he proves that even "neuropsychiatric disorders" can be produced by autoantibodies to N-methyl-D-aspartate (NMDA) receptors; thus explaining why even clients with "mental disease" respond to the Hippocrates protocol developed by Dr. Carley to detoxify vaccine viruses (and other toxins) using homeopathic nosodes! Thus, the autoimmune disease you develop is determined by which tissues in the body are attacked by auto antibodies. If the inside lining of the gastrointestinal tract (the mucosa) is attacked by auto-antibodies you develop leaky gut syndrome (which leads to food allergies when partially digested food particles are released into the bloodstream, are recognized as antigens foreign to the body, and elicit an antibody response against those food particles that becomes heightened every time that same food is eaten and released into the bloodstream partially digested again). Crohn's disease and colitis are also caused by auto-antibody attack on the mucosa of the GI tract itself. If the islet (insulin producing) cells of the pancreas are attacked by auto-antibodies, you develop insulin dependent (juvenile) diabetes. If the respiratory mucosa is attacked by auto-antibodies, you develop "leaky lung" syndrome where, just as with leaky gut, antigens recognized as foreign to the body which are inhaled are able to traverse the lining of the respiratory tract, causing the creation of antibodies against those antigens (usually dust, mold, pet or pollen antigens). When these substances are inhaled again, IgE (the pathologic form of IgA created after corruption of the immune system due to inoculation rather than inhalation of disease) acts as a reagin4 and sensitizes mast and basophil cells, causing release of their histamine and slow reacting substance granules on contact with the allergen to produce constriction of the bronchioles leading to asthma. This process is also responsible for the immediate hypersensitivity reaction known as anaphylaxis, which is a potential side effect noted in the Physician's Desk Reference for every vaccine; as well as the wheal and flare reaction of the skin known as hives. If the components of the articular surface of the joints are attacked by auto-antibodies, you develop rheumatoid (or juvenile) arthritis. If the skin is compromised on a chronic basis, you develop "leaky skin" syndrome, where contact antigens which could not otherwise traverse the skin lead to skin allergies to contact antigens (a delayed hypersensitivity reaction where inflammation occurs due to release of soluble factors). Additionally, depending on which level of the skin is attacked by auto-antibodies, (i.e., the epidermis or dermis), you develop eczema, psoriasis or scleroderma. If the kidney tissue is attacked by auto-antibodies, you develop one of the many types of nephritis, depending on which component of renal tissue is attacked (for example, with glomerulonephritis, the basement membrane of the glomerular apparatus within the kidney (which filters blood to form urine) is attacked by auto-antibodies, thus allowing protein to escape from the serum into the urine). If you develop auto-antibodies against thyroid gland tissue, you develop Grave's disease. If you develop auto-antibodies against the tissue of the thymus gland (which is crucial in T cell production and function), you develop myasthenia gravis. If you develop auto-antibodies against the very DNA in the nucleus of all cells, you develop systemic Lupus (thus, the autoimmune potential of DNA vaccines being developed now is self evident; worse yet, DNA components from these vaccines can be incorporated into your DNA, leading to actual genetic changes which could cause extinction of all (vaccinated) life on the Earth, as will be discussed shortly). And on, and on, and on. The brain and spinal cord can also be attacked with auto-antibodies (which this author refers to as vaccine induced encephalitis), leading to a variety of neurological diseases. The most severe of these, leading to death, are sudden infant death syndrome (SIDS) and most cases of "shaken baby syndrome". If components of the myelin sheath (the insulating covering of nerve fibers which allows proper nerve conduction) or the actual neurofilaments themselves are attacked by auto-antibodies, the resultant condition is determined solely by the location of the damage done. Such neurological conditions include but are not limited to minimal brain dysfunction, ADD/ADHD, learning disabilities, mental retardation, criminal behavior, the spectrum of pervasive developmental disorders (including autism), multiple sclerosis, Parkinson's disease, Lou Gehrig's disease, Guillen Barre', seizure disorders, etc., etc. etc. (Please note that other factors are also sometimes involved, such as: the spirochete which causes Lymes disease, aspartame and mercury in cases of MS; aspartame in seizures; or pesticides in cases of Parkinson's). Thus, when detoxing to reverse these diseases, these other substances must also be removed to obtain a full recovery. However, the corruption of the immune system caused by the injection of vaccines is a key component in these disease states leading to immune malfunction, and is the reason why an autistic child may also have leaky gut or eczema, etc. Note that myelin production, for the most part, does not begin until after birth. Most myelin is apparently laid down by age 5 years and usually completed by age 10 years, judging by the level of success at various ages in reversing autistic and other neurological VIDS symptoms that this author has observed in hundreds of children by detoxing the viruses with homeopathic nosodes5, and repairing the immune corruption by simultaneous administration of bovine colostrum (i.e., after 10 years of age, the ability to stop and repair auto-antibody induced damage in the myelin sheath and neurofilaments themselves is dramatically decreased). In summary, the hyperactivity of the humoral arm of the immune system in autoimmune disease is caused by adjuvants added just for that purpose. However, the damage caused by the autoimmunity itself (i.e., antibody against self) has several mechanisms, including the following: The antigens present in the culture media itself cannot be completely filtered and separated from the organisms cultured thereon. Thus, any antibodies formed against antigens from the culture cells themselves (for example myelin basic protein from chick embryos or the 13 vaccines which now contain aborted human fetal cells) can cross-react to form an autoimmune reaction against the myelin basic protein in your myelin sheath, etc. Molecular mimicry is due to similarity of proteins contained in organisms and mammals. (For example, the measles virus is made up of proteins similar to myelin basic protein; thus, antibodies formed against the measles virus antigens subsequently also cause an auto-antibody attack against myelin basic protein in the myelin sheath due to cross reactivity of these antibodies). Formation of immune complexes occur as antigens and antibodies interlock into clusters which can then become trapped in various tissues, especially the kidneys, lung, skin, joints, or blood vessels. Once trapped, these complexes then set off an inflammatory reaction which lead to further tissue damage. Intentional inclusion of antigens in vaccines to cause formation of antibodies that attack specific hormones or races (for example, experiments done on women of childbearing age in the Philippines and probably other locations where HCG (human chorionic gonadotropin)6 placed into vaccines given these women resulted in antibodies against the HCG hormone, and subsequent spontaneous abortion thus occurred when the women became pregnant. It is also this author's hypothesis that the epidemic of vitiligo in people of color (hypo pigmentation of skin caused by auto-antibody attack on melanocytes7) is also occurring due to intentional inclusion of melanin in vaccines given to people of color. Another heinous (and obviously genocidal) creation of the Anti-Hippocratics is the DNA vaccines now being developed. These vaccines contain plasmids, which are closed rings of recombinant DNA that make their way into the nucleus of a cell and instruct the cell to synthesize encoded antigenic proteins8. Thus, the very genetic makeup of the individual, plant or animal will be altered to produce a never ending supply of antigens to distract the immune system. These genetic changes will remain as cell division occurs, and will be transmissible to offspring. This is the TRUE "mark of the beast" , and could lead to extinction and/or modification (including behavioral) of any group inoculated. In addition to the above phenomena which lead to simultaneous depression of cellular immune function and hyperactivity of humoral immune function, vaccines also contain other toxic substances which can cause serious side effects themselves. The following ingredients are actually listed on the CDC website with this introductory statement: "Many things in today's world, including food and medicines, have chemicals added to them to prevent the growth of germs and reduce spoilage." Translation: you're already toxic, so what's the big deal with adding more poison? This author's answer to that question is that any immunotoxin can end up being the "straw that breaks the immune system's back" in that individual, leading to dis-ease. This is where genetics is key; i.e., not that what disease you develop is actually caused by some "gene" in most cases; but rather that your genes determine the strength of your immune system (i.e., how many assaults your immune system can take before it reaches critical mass, and you develop a dis-ease). Some additional ingredients in vaccines (as listed by the CDC on their website) include antibiotics, aluminum gels, formaldehyde, monosodium glutamate (MSG), egg protein, and sulfites. Thus, we have antibiotics (which you could be allergic to); aluminum (which when combined with silicon deficiency, results in the neurofibrillary tangles seen in Alzheimer's disease); formaldehyde (a toxic carcinogenic substance used to preserve dead people); MSG ( a potent excitotoxin9 which, like aspartame, can cause seizures, brain tumors, etc.); egg protein (to which you could have a life threatening anaphylactic reaction); and sulfites (another toxin which we are advised not to consume much of orally, but in vaccines, it is injected directly into the body). Is this not a veritable witch's brew of chemicals, organisms, and animal parts? What the CDC does NOT list is that 13 vaccines at present (and more are in the works) are actually cultured on aborted human fetal tissues (go to www.cogforlife.org for more info). THIS IS CANNIBALISM. Note in this list that they also fail to mention the ethyl-mercury containing preservative thimerosol, which has been the only dangerous substance in vaccines to receive mainstream media attention (albeit most of that being disinformation) after the explosion in the rate of occurrence of autism in the last generation became self-evident proof that vaccines are the causative factor. For, although the scientists working for the medical mafia continue to use statistics to twist and spin their data to make us beLIEve that vaccines are not the cause, too many thousands of parents have watched their children enter the downward spiral into autism after their children received the vaccine which was the straw that broke the back of their child's immune system. No matter what the "white coats" tell these parents, they know the truth! Mercury (also in dental amalgam fillings) is a highly toxic heavy metal, has been documented to cause cancer, and can be absorbed through the digestive track, skin, and respiratory track. Mercury is 1,000 times more toxic than lead, and is second only to uranium as the most toxic metal. If children receive all recommended vaccines, they will receive many times the "allowable safe limit" for mercury in the first two years of life (as if there is such a thing as a "safe" amount of a toxic poison). Yet, even after Congressional hearings instigated by Congressman Dan Burton (whose own grandchild became autistic after receiving vaccines) resulted in the FDA requesting (not ordering) vaccine manufacturers to remove this toxic heavy metal from their products, mercury is still present in many vaccines. Although the symptoms of mercury poisoning have been described as identical to the symptoms of autism, it should be noted that most children who descend into the hellish state known as autism do so after the MMR vaccine. The MMR vaccine is one of the few vaccines that do not contain mercury; in fact, it has NEVER contained mercury. Thus, it is self-evident that the removal of mercury will not make vaccines "safe". (This is why the mercury is the only thing being addressed at all; because when the people reading this paper realize that the very mechanism by which vaccines corrupt the immune system means that NO vaccine is safe and effective; there will be an evolution of consciousness where the structure of lies telling us vaccines are safe and effective disintegrates.)
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