Mercury is not the cause of Autism!

Dr. Rebecca Carley has lost both her medical license and her son but she continues to assert that the cause of autism isn’t mercury and that the revelation of what is really responsible for the escalating numbers of brain injured children should bring big pharma to its knees.

We face an escalating autism epidemic that is claiming 1 in 150 or even 1 in 100 of our highly vaccinated children and we still do not know with any scientific certainty the full extent of what injecting children 48 doses of 14 vaccines by age six does to individual and public health.

Rather than just singling out mercury, Carley says that VIDS ( vaccine induced diseases) such as autism, diabetes and other autoimmune diseases and cancer result from the corruption of the immune system caused by the inoculation of viruses contained in the excessive number of vaccines given to young children.

Mercury is in some of the routinely given vaccinations but Carley maintains that it is the overall assault on the immune system rather than any individual ingredient which is the root of all these vaccine induced diseases including autism. The fact that many researchers put the blame for autism on mercury she says is distracting the public from the bigger lie that has never been told: Inoculations are the true weapons of mass destruction.

The corruption of the immune system happens when viruses are directly injected into the body, bypassing secretory IgA ( an antibody in the upper gastro-intestinal and respiratory tracts.) This antibody is critical for the processing of the germ by the immune system and for natural immunity to occur.

The devastating disease called Autism is actually a non-fatal case of subacute sclerosing panencephalitis caused by demyelination following vaccine induced encephalitis. The term subacute sclerosing panencephalitis was changed to the more commonly known one of autism to hide this fact. Thus directing attention away from the true cause of the autistic syndrome, i.e. vaccinations.

To explain why vaccinations themselves are the real cause of autism and that mercury in and of itself is not to blame, we need to understand how mercury acts on the brain neurons. Carley informs her readers that Mercury causes the death of the nerve’s axon and that this is a key feature of alzheimer’s disease, not autism. Autism is actually subacute sclerosing panencephalitis caused by the measles virus and is due to demyelination, as is MS, Guillian Barre syndrome, Lou Gehrig's disease and other diseases. The only thing that determines the symptoms is where the nervous system is damaged.

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 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, as Dr Carley goes to great lengths to explain: it is self-evident that the removal of mercury will not make vaccines "safe." She says that this is why mercury is the only causation that is mentioned because when the people 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 in regard to the true nature of vaccinations and big pharma will not want that to happen.

Indeed when you consider:

The combined profits for the ten drug companies in the Fortune 500 ($35.9 billion) were more than the profits for all the other 490 businesses put together ($33.7 billion). Over the past two decades the pharmaceutical industry has moved very far from its original high purpose of discovering and producing useful new drugs. Now primarily a marketing machine to sell drugs of dubious benefit, this industry uses its wealth and power to co-opt every institution that might stand in its way, including the US Congress, the FDA, academic medical centers, and the medical profession itself."

Dr. Marcia Angell, former editor in chief of the New England Journal of Medicine

The basic idea of vaccination originated due to the belief that if a foreign antigen was injected into an individual, then that individual would become immune to a future infection. 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 antibody response to all airborne and ingested pathogens. IgA helps protect against viral infection and bypassing this mucosal aspect of the immune system by directly injecting organisms into the body 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 cause chronic disease and thus further grow and/or mutate as the individual is exposed to ever more antigens and toxins in the environment.

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. 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 secretory antibody IgA changes into IgE leading to allergic reactions and this overall hyperactivity of the humoral (antibody producing) pole of the immune system is, in this Carley’s opinion, the sole cause of all autoimmune diseases; where the auto-antibodies produced activate functioning T cells to then attack self.

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 asthma. This process is also responsible for the hypersensitivity reaction known as anaphylaxis. If the components of the articular surface of the joints are attacked by auto-antibodies, you develop rheumatoid (or juvenile) arthritis. Your autoimmune disease then has you seeking the products of big pharma to treat your vaccine derived ill health.

Dr. James R. Shannon, former director of the National Institute of Health reported in December, 2003 that "the only safe vaccine is one that is never used".

Last word from Rebecca Carley Wake up, America-it's getting very late, it is time for the mountain of lies to crumble. Please spread the word to everyone you know we can make it happen.

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