“Bypassing the mucosal aspect of the immune system by directly injecting organisms into the body leads to a corruption in the immune system itself where IgA (Immunoglobulin A) is transmitted into IgE (Immunoglobulin E), and/or the B cells are hyperactivated to produce pathological amounts of self-tracking antibody as well as suppression of cytotoxic T cells ‘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 them into ‘L forms,’ leading to a lack of some critical antigens normally recognized by the cellular 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 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 secret antibody, the cytotoxic (killer) T cells are subsequently suppressed. 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. 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 can develop leaky gut syndrome. Crohn’s disease and colitis are also caused by auto-antibody attack 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 unable to traverse the lining of the respiratory tract, causing the creation of antibodies against those antigens (usually dust, mold, pet or pollen antigens). If the components of the articular surface of the joints are attacked by auto-antibodies, you develop rheumatoid (or juvenile) arthritis. If the kidney tissue is attacked by auto-antibodies, you develop one of the many types of nephritis.
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). And on and on and on.
The brain and spinal chord can also be attacked with auto-antibodies (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, Guillain-Barré, and seizure disorders.”
— Rebecca Carley, MD