CAUSING VIDS (VACCINE INDUCED DISEASES)

(AN EPIDEMIC OF GENOCIDE)

by Rebecca Carley, M.D.

Court Qualified Expert in VIDS and Legal Abuse Syndrome

Amended June 23, 2008 (New additions in RED)

“One basic truth can be used as a foundation for a mountain of lies, and if we dig down deep enough in the mountain of lies, and bring out that truth, to set it on top of the mountain of lies; the entire mountain of lies will crumble under the weight of that one truth. And there is nothing more devastating to a structure of lies than the revelation of the truth upon which the structure of lies was built, because the shock waves of the revelation of the truth reverberate, and continue to reverberate throughout the Earth for generations to follow, awakening even those people who had no desire to be awakened to the truth.” (by Delamar Duvaris as written in the preface of “Behold the Pale Horse” by William Cooper).

The basic truth that served as the foundation for the mountain of lies known as vaccinations was the observation that mammals which recover from infection with microorganisms acquire natural immunity from further infections. Whenever cytotoxic T cells (the little Pac man cells which devour and neutralize viruses, bacteria, and cancer cells, thus conferring cellular immunity and are also responsible for allograft rejection) and B cells (antibody producing cells which confer humoral immunity by circulating in the body’s fluids or “humors”, primarily serum or lymph) are activated by various substances foreign to the body called antigens, some of the T and B cells become memory cells. Thus, the next time the individual meets up with that same antigen, the immune system can be quickly triggered to demolish it. This is the process known as natural immunity.

This truth gave birth to a beLIEf that if a foreign antigen was injected into an individual, that individual would then become immune to a future infection. This beLIEf, (you see the lie in the middle), was given the name, “vaccinations”. What the promoters of vaccination failed to realize is that secretory IgA (an antibody found predominately in saliva and secretions of the gastrointestinal and respiratory tract mucosa) is the initial normal antibody response to all airborne and ingested pathogens. IgA helps protect against viral infection, agglutinate bacteria, neutralize microbial toxins, and decrease attachment of pathogens to mucosal surfaces. What this author has realized is that bypassing this mucosal aspect of the immune system by directly injecting organisms into the body leads to a corruption in the immune system itself whereby IgA is transmuted into IgE, and/or the B cells are hyperactivated to produce pathologic amounts of self-attacking antibody as well as suppression of cytotoxic T cells (as explained shortly). As a result, the pathogenic viruses or bacteria cannot be eliminated by the immune system and remain in the body, where they cause chronic disease and thus further grow and/or mutate as the individual is exposed to ever more antigens and toxins in the environment. This is especially true with pathogens grouped under the term “stealth adapted”. These are formed when vaccine viruses combine with viruses from tissues used to culture them, or when bacteria lose their cell walls when a person takes antibiotics and transform into “L forms”, leading to a lack of some critical antigens normally recognized by the cellular immune system. Another example is stealth adapted (mutated) cytomegaloviruses which arose from African green monkey (simian) kidney cells when they were used to culture polio virus for live polio virus vaccines. Thus, not only was the vaccinee inoculated with polio, but with the cytomegalovirus as well.

The mechanism by which the immune system is corrupted can best be realized when you understand that the two poles of the immune system (the cellular and humoral mechanisms) have a reciprocal relationship in that when the activity of one pole is increased, the other must decrease. Thus, when one is stimulated, the other is inhibited. Since vaccines activate the B cells to secrete antibody, the cytotoxic (killer) T cells are subsequently suppressed. (In fact, progressive vaccinia (following vaccination with smallpox) occurs in the presence of high titers of circulating antibody to the virus¹ combined with suppressed cytotoxic T cells, leading to spreading of lesions all over the body). This suppression of the cell mediated response is thus a key factor in the development of cancer and life threatening infections. In fact, the “prevention” of a disease via vaccination is, in reality, an inability to expel organisms due to the suppression of the cell-mediated response. Thus, rather than preventing disease, the disease is actually prevented from ever being resolved. The organisms continue circulating through the body, adapting to the hostile environment by transforming into other organisms depending on acidity, toxicity and other changes to the internal terrain of the body as demonstrated by the works of Professor Antoine Béchamp. He established this prior to the development of the “germ theory” of disease by Louis Pasteur. Pasteur’s “germ theory” was a plagiarist’s attempt to reshape the truth from Béchamp into his own “original” premise – the beLIEf that germs are out to “attack” us, thereby causing dis-ease. Thus, treatment of infection with antibiotics as well as “prevention” of disease with vaccines are both just corrupted attempts at cutting off the branches of dis-ease, when the root of the cause is a toxic internal environment combined with nutritional deficiency. However, since Pasteur’s germ theory was conducive to the profits of the burgeoning pharmaceutical cartels that only manage dis-ease, no mention of the work of Professor Béchamp is made in medical school curricula.

To make matters worse than the suppression of cellular immunity which occurs when vaccines are injected, adjuvants (which are substances added to vaccines to enhance the antibody response) can actually lead to serious side effects themselves. Adjuvants include oil emulsions, mineral compounds (which may contain the toxic metal aluminum), bacterial products, liposomes (which allow delayed release of substances), and squalene. The side effects of adjuvants themselves include hyperactivity of B cells leading to pathologic² levels of antibody production, as well as allergic reaction to the adjuvants themselves (as demonstrated in Gulf War I soldiers injected with vaccines containing the adjuvant squalene, to which antibodies were found in many soldiers). Note that the pathologically elevated hyperactivity of antibody production caused by adjuvants also results in a distraction from the other antigens that the immune system encounters “naturally”, which must be addressed to maintain health.

This author realized years ago that inoculations caused the transformation of IgA into IgE; however, thanks to researcher Patrick Jordan finding the NATO Life Sciences book entitled “Immunological Adjuvants and Vaccines” (6), it has now been revealed that it is the aluminum which is put into vaccines as an adjuvant which causes production of IgE…the antibody of allergy and anaphylactic shock. This shocking admission comes in this book after the statement on page 6 that aluminum “was introduced in 1926, before strict control by regulatory authorities was practiced; whether it would be allowed by regulatory authorities today is far from certain”.

On page 37 of this NATO book, it states that studies demonstrate that “aluminum causes stimulation of the production of anaphylactic antibody (IgE) in the mouse”, and that “the effect of aluminum on the IgE response in humans does not appear to have been investigated”. This is just like the statement in the package insert of all vaccines (including the Gardasil vaccine which alleges it protects against cervical cancer) that “no studies have been done to evaluate for the potential to cause carcinogenicity or genotoxicity”. However, these experiments are being carried out in children every time they are inoculated with disease…and the skyrocketing allergies, anaphylactic reactions and cancer make it self evident that the inoculations are behind it all. Thanks to the book, I now have the evidence that IgE production is due to vaccines, as well as the fact that these mad scientists know exactly what they are doing. If this is not evidence of crimes against humanity, what is?

Additionally, the overall hyperactivity of the humoral (antibody producing) pole of the immune system is, in this author’s opinion, the sole cause of all autoimmune diseases; where the auto-antibodies produced activate functioning T cells to then attack self; and both the activated B & T cells also produce cytokines (which further enhance inflammation and immunological involvement). The only thing which determines which autoimmune disease you develop is which tissues in your body are attacked by auto-antibodies³. PLEASE NOTE THAT THIS FINDING HAS NOW BEEN CONFIRMED BY DR. JEFFREY BROWNING SENIOR DIRECTOR, DEPARTMENT OF IMMUNOBIOLOGY, BIOGEN-IDEC, IN HIS SCIENTIFIC PAPER ENTITLED “B CELLS MOVE TO CENTRE STAGE: NOVEL OPPORTUNITIES FOR AUTOIMMUNE DISEASE TREATMENT” PUBLISHED IN NATURE REVIEWS DRUG DISCOVERY 5, 564-576 (JULY 2006); AVAILABLE ON THE INTERNET AT: http://www.nature.com/nrd/journal/v5/n7/full/nrd2085.html#a1 .

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:

1. 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. See the package insert from Pfizer’s Rabies vaccine from the “10^th Edition of the Compendium of Veterinary Products” published in 2007 posted on www.drcarley.com, which states “tissue origin vaccines contain extraneous protein in addition to the [rabies] antigen that can lead to autoimmune disease”. THIS IS TRUE FOR ALL VACCINES, BUT THIS IS THE FIRST TIME I HAVE SEEN IT ADMITTED BY ANY VACCINE MANUFACTURER.
2. 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).
3. 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.
4. Intentional inclusion of antigens in vaccines to cause formation of antibodies that attack specific hormones or races. It is 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 occurring due to intentional inclusion of melanin in vaccines given to people of color. Additionally, experiments done on women of childbearing age in the Philippines and probably other locations where HCG (human chorionic gonadotropin) placed into vaccines given these women resulted in antibodies against the HCG hormone, and subsequent spontaneous abortion thus occurred when the women became pregnant. The NATO book “Immunological Adjuvants and Vaccines” also describes, in the chapter entitled “The Development and Preliminary Clinical Evaluation of an Antifertility vaccine” (6) how an antifertility vaccine has been developed incorporating HCG in a vaccine with diphtheria toxoid; and that the vaccine will soon be suitable for “large scale clinical use”. The “task force” (which involves many agencies within the World Health Organization in this chapter’s references) “is in the process of developing other fertility regulating vaccines as well”. Could the escalating problems with infertility in this country be due to women having been given this vaccine without their knowledge or consent?