What Can I Do To Avoid and Stop Government Mandated Swine Flu Vaccine - Part IV

by Dr. Robert O. Young

* Thimerosal (mercury) - a neurotoxin linked to psychological, neurological, & immunological problems--especially autism. Nervous system damage (such as sub-acute sclerosing panencephalitis (SSPE), brachial plexitis, post-vaccinal encephalitis, transverse myelitis and peripheral neuropathies), kidney disease, birth defects, dental problems, mood swings, mental changes, hallucinations, memory loss, and inability to concentrate can occur. Symptoms also include tremors, loss of dermal sensitivity, slurred speech, and--in rare cases--even death and paralysis. This additive alone was the catalyst for another recent Class Action Lawsuit organized by mothers of children born with autism & the many related behavioral disorders associated with it. Autism is now occurring at levels never seen before in history; depending on the state, its rate is now 1 in 67 to 1 in 150. The autism rates used to be 1 in 20,000. Mercury may also be associated with the significantly increased rates of senility and Alzheimer's, which is associated with five or more successive flu vaccinations. Although most mercury (thimerosal) has been removed from children's vaccines, it is still in all flu vaccines at toxic doses.
* Tri(n)butylphosphate,
* VERO cells, a continuous line of monkey kidney cells - linked to the SV-40 virus known to cause leukemia
* Washed sheep red blood cells

THESE ADDITIVES ARE GIVEN TO OUR CHILDREN WITHOUT PUBLIC KNOWLEDGE OR CONSENT.

What's the problem with this horrendous looking list? The problem is two-fold: (1) the adjuvants are added to increase inflammation and immune response in the system, and (2) the adjuvants are significantly detrimental to the overall welfare of the organisms, according to the neurosurgeon Russell Blaylock, M.D., an expert in this field. His research suggests the vaccinations may cause brain swelling and inflammation for up to two years. This alone would be enough to significantly disrupt the immune and endocrine systems, as well as increase senility, activate Alzheimer's, and other brain dysfunctions. For example, Hugh Fudenberg, MD, Founder and Director of the Neuro lmmuno Therapeutic Research Foundation, reported at the NVIC International Vaccine Conference in Arlington, Virginia in September 1997, that five consecutive seasonal (yearly) flu shots increases the risk of Alzheimer's disease ten fold. Other devastating side effects of vaccines involve neurological damage, including encephalitis, transverse myelitis, peripheral nerve damage, autism, seizures, mental retardation, language delays, behavioral problems, multiple sclerosis, and SSPE (sub-acute sclerosing panencephalitis). There is also significant animal research that supports Blaylock's findings.

The veterinary research has shown that vaccines can cause a wide range of brain and nervous system damage. In the Merck Manual it states, in regard to its own product, that vaccines can cause encephalitis: brain inflammation and damage. Merck states, "Examples are the encephalitis following measles, chicken pox, rubella, small pox, vaccinia, and many other less well-defined viral infections."

Although dog and cat research doesn't necessarily mean it will be the same for humans, it is highly probable this animal research is revealing what is really happening with human vaccines. Because of this, there is much to learn by looking at the animal vaccine research. The following is a summary of some of this research.

In the Canine Health Concerns (CHC) study, reports show that 73.1% of the dogs developed short attention spans within three months of being vaccinated. 72% of the dogs were considered to be nervous and worrying within three months post vaccination. It is interesting that dogs can develop paralyzed rear legs and death shortly after a vaccine shot and that paresis is listed as a symptom of encephalitis in the Merck Manual. The Science of Vaccine Damage by Catherine O'Driscoll outlines results from several animal studies regarding the effects of vaccinations on dogs and cats as collaborated by a team at Purdue University School of Veterinary Medicine.

Vaccinated dogs in the produced study developed autoantibodies to their own bio-chemical protein structures, which included antibodies against fibronectin, laminin, DNA, albumin, cytochrome C, cardiolipin, and collagen. The fibronectin is involved in tissue repair, cell multiplication and growth, and the differentiation between tissues and organs. The vaccinated dogs also developed autoantibodies to laminin affecting adhesion, differentiation, spreading, and proliferation and moving of cells. What the vaccines are doing is disrupting the natural intelligence of the cells. The vaccinated dogs also developed autoantibodies to their own collagen, which is about one quarter of all the protein in the body and thus, in the CHC 1997 study of 4,000 dogs there was a much higher number of dogs developing mobility problems shortly after they were vaccinated. The dogs also developed autoantibodies to their own DNA.

The AVMA (American Veterinary Medical Association) Vaccine-Associated Feline Sarcoma Task Force conducted several studies to determine why 160,000 cats each year in the USA developed terminal cancer at their injection sites. Veterinarians around the world, as well as the British Government, have acknowledged the fact that cats do get vaccine-induced cancer. In August 2003 the Journal of Veterinary Medicine reported an Italian study that showed dogs also developed vaccine-induced cancer at their injection sites. It is no coincidence that vaccine-site cancer is a possible sequel to human vaccines. For example, Dr. Berniece Eddy, a microbiologist at the National Institutes of Health (NIH), has proven that both dead and live vaccines carry a monkey retrovirus (SV-40) that produces an inheritable cancer in experimental animals. It is unfortunate to note that this monkey retrovirus (SV-40), which is spread from human to human and from mother to child, also appears frequently in human cancer sites. In 1987, Dr. Hilleman, head of all vaccine production of Merck Pharmaceuticals, stunned the world with his public admissions that mass vaccination campaigns of the 1950s and '60s likely caused thousands of cancer deaths each year. This was due to the presence of SV-40. Doctors estimate that the virus was injected into tens of millions during the vaccination campaigns, including several million in Canada. It is also widely acknowledged that vaccines can cause a fast acting, usually fatal, disease called autoimmune haemolytic anaemia (AIHA). People may die from this in days. In the Merck Manual of Diagnosis and Therapy, even though Merck is a multinational vaccine manufacturer, it states that AIHA may be caused by modified live virus vaccines (MLV). The British Government's Working Group also acknowledged this.

The veterinary research also showed a connection between vaccine events and arthritis. Again, it is no accident that the New England Journal of Medicine reported it is possible to isolate the rubella virus from affected joints in children vaccinated against rubella. It also reported isolating viruses from the blood of women with prolonged arthritis following vaccination. In 2000, the CHC's 1997 findings indicated that polyarthritis and other diseases like amyloidosis, which affects organs in dogs, were linked to the combined vaccines given to dogs. The dog research also confirms our explanation of human autoimmune responses to vaccination because they also found that dogs produced antibodies against their own DNA and their own tissues, such as found in heart cells. When we look at this picture from a broader perspective, it is not too hard to show scientifically that vaccines can put people into an allergic state, which may range from mild to anaphylactic shock and death. There are also some individuals who have an inherited faulty B and T cell functioning and therefore are very susceptible to abnormal immune reactions to vaccinations. The Merck Manual warns that patients with or from families with genetically altered B and or T cell immune cell deficiency history should not receive live virus vaccines due to the severe rate and risk of infection. How is this going to work when vaccinations are mandated with no medical or religious exceptions? In other words, some of these B and T cells will manifest as food allergies, neurological deterioration, eczema and heart disease. A deranged immune response may lead to inflammatory conditions such as arthritis, colitis, pancreatitis, and a number of autoimmune diseases as well as cancer and leukemia. The more serious meaning of this is that people with these conditions can die if they receive these live virus vaccinations because their immune systems are not strong enough to handle viral assault from modified live virus vaccinations. Some veterinarians have actually said, "I think that vaccines... are leading killers of dogs and cats in America today."

For the rest of this message select: Part V - What Can I Do To Avoid and Stop Government Mandated Swine Flu Vaccine

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