The basic truth that served as the foundation for the mountain of lies known as vaccinations was the observation that mammals who recover from infection with microorganisms acquire natural immunity from further infections. Whenever T cells (the little packman cells which kill viruses, bacteria, and cancer cells, thus conferring cellular immunity) and B cells (antibody producing cells which confer humoral immunity) 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 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 the respiratory tract of ALL mammals (since animals are just as devastated by these inoculations with disease as are humans) contain secretory IgA (an antibody which initiates the natural God given immune response) within the respiratory tract mucosa. Bypassing this mucosal aspect of the immune system by directly injecting organisms into the bloodstream leads to a corruption in the immune system itself. As a result, the pathogenic viruses or bacteria cannot be eliminated by the immune system and remain in the body, where they will further grow and/or mutate as the individual is exposed to ever more antigens and toxins in the environment which continue to assault the immune system.
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. Thus, when one is stimulated, the other is inhibited. Since vaccines activate the B cells to secrete antibody, the T cells are subsequently suppressed. This suppression of the cell mediated response is 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; they actually prevent the disease from ever being resolved. The organisms continue circulating through the body, mutating and transforming into other organisms (as demonstrated by the work of Professor Antoine Bechamp), depending on the acidity and toxicity of the internal terrain of the body. Note that Bechamp proved that Louis Pasteur’s “germ theory” of disease was incorrect due to this ability of organisms to transform and mutate based on the body’s internal terrain (as Pasteur admitted on his deathbed). Thus, treatment of infection with antibiotics as well as “prevention” of disease with vaccines are both just examples of cutting off the branches of dis-ease, when the root of the cause is a toxic internal environment. However, since Pasteur’s germ theory was conducive to the profits of the burgeoning pharmaceutical companies who only manage dis-ease, no mention of the work of Professor Bechamp has been 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 heavy 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 pathologic 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 hyperactivity of the humoral (antibody producing) pole of the immune system is, in this author’s opinion, the sole cause of all autoimmune diseases. The only thing which determines which autoimmune disease you develop is which tissues in your 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, the allergic response producing constriction of the bronchioles is called asthma. 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 attacked, you develop “leaky skin” syndrome, where contact antigens which could not otherwise traverse the skin are allowed in, leading to skin allergies to contact antigens. 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 potential 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). And on, and on, and on.