[1] Most of the flu vaccines given to millions of children and adults each year contain this neurotoxin and are much responsible for the massive allergy epidemics afflicting the immunized population.

Flu vaccines can do more than just cause autoimmune diseases. The flu vaccine may even pose an immediate risk to your cardiovascular system. One 2007 study published in the Annals of Medicine, concluded that:“Abnormalities in arterial function and LDL oxidation may persist for at least two weeks after a slight inflammatory reaction induced by influenza vaccination. These could explain in part the earlier reported increase in cardiovascular risk during the first weeks after an acute inflammatory disorder.”

How many people die from a heart attack after receiving a flu shot? I don’t think we’ll ever find out. However, we now know for certain that the true risks of vaccination have been deliberately kept from us by those agencies that are responsible for public health.

CDC Caught Deliberately Falsifying Vaccine Research

The Centers for Disease Control and Prevention (CDC) have for many years denied a possible link between mercury in vaccines and autism. However, in October 2011, the CDC has been caught deliberately fudging data to try to cover up evidence linking mercury in vaccines with autism.[2]

To conceal any incriminating vaccine data the CDC had handed its massive database of vaccine records over to a private company, effectively pronouncing it off-limits to researchers and preventing dissemination of the data through the Freedom of Information Act (FOIA).

However, this didn’t stop the Coalition for Mercury-Free Drugs (CoMeD). During an enquiry through FOIA it was discovered, as suspected, that the same original Danish study which the CDC referred to as ‘definitive evidence’ that Thimerosal does not increase a child’s chances of developing autism, actually revealed the exact opposite to be true. The Danish research is irrefutably clear about the findings: Thimerosal in vaccines increases a person’s chances of developing autism and other neurological diseases.

In the United States, at least one in every 100 vaccinated children is afflicted with autism, while only 1 in every 2,000 non-vaccinated children has the disease. In European countries like Iceland, where children receive just one third the number of vaccines shots, only 1 in 30,000 children have autism. One doesn’t need to be a scientist to make sense of this man-made tragedy.

The cover-up by the CDC has let those responsible for the huge autism epidemic, which began ever since mercury and adjuvants were first added to vaccines, off the hook. Without this elaborate conspiracy against the people, libel lawsuits resulting from permanent vaccine injuries in children would have bankrupted numerous governments, including the United States and Great Britain, and almost the entire pharmaceutical industry.

All vaccines significantly alter the immune system and, therefore, play a major role in triggering autoimmune diseases and numerous other health conditions. In a 2005 epidemiological study covering over 151 previously conducted studies, researchers from the Department of Health Care and Epidemiology, University of British Columbia found an inverse association between acute infections and cancer development.[3] The study found that suppressing childhood infections with vaccines significantly increases one’s risk of developing cancer later in life.

Chronic diseases were extremely rare over 100 years ago when few vaccines were given to the population. The more vaccines are administered, the more compromised the immune system becomes.[4] Most diseases back then used to be acute infections resulting from poor hygiene and nutrition, contaminated drinking water and overcrowded cities. Even the CDC admits on their web site that clean water is more effective in preventing infectious diseases than vaccines. The only problem with using clean water as the preferred medicine is that, unlike with mass vaccination, one cannot make the same billions of dollars of profit year after year by installing some simple water purification devices in affected communities, or by educating the people that drinking clean non-fluoridated water is what keeps the body healthy and the immune system strong.

Science is beginning to recognize that damaging the intestinal lining through harsh, erosive chemicals, dehydration and poor nutrition is causing for more diseases than previously thought. Recently, researchers at UT Southwestern Medical Center in Dallas, Texas, discovered that that a once mysterious cell population which lurks in the intestinal lining is essential for preventing normally beneficial bacteria from invading into deeper tissue where they can cause debilitating conditions like inflammatory bowel disease (IBD).[5]

According to the research findings, people suffering from the disease frequently have more bacteria that adhere to, or invade, their gut lining. When their immune system mounts an attack on these microbial invaders, they can develop painful ulcers and bloody diarrhea.

The researchers also found that a specialized T cell normally present on body surfaces such as the skin and the gastrointestinal tract patrols intestinal borders, sensing when microorganisms have invaded the epithelial cells lining the intestine. “When this happens, these T cells swing into action, making antibiotic proteins that kill the rogue bacteria and prevent their entry into deeper tissue.” said Dr. Hooper, who is also an investigator for the Howard Hughes Medical Institute at UT Southwestern. This action lasts for several hours until other immune cells can be recruited as backup. However, there are consequences when the intestinal tract becomes a constant battleground.

A battleground is recognized by its devastated environment. Overexposure to toxins, food additives, trans fatty acids (as found in fast foods, such as hamburgers and French fries), medical drugs, alcohol, undigested putrefied foods, denatured proteins, and more, can easily cause what is known as “leaky gut”, a condition where bacteria and toxins enter the intestinal tissues, blood and lymph. An initially limited and localized immune reaction may then escalate and spread to other areas in the body. T cells are only supposed to deal with foreign invaders, but they will need to be activated against the body’s own tissues when toxins (antigens) begin to accumulate there.

The encounter with the antigens raises the level of antigen/antibody complexes in the blood and upsets the fine balance that exists between the immune reaction and its suppression. Autoimmune diseases, which indicate an extremely high level of toxicity in the body, directly result from a disturbance of this balance. If antibody production is continually high in synovial joints, inflammation becomes chronic, leading to gradually increasing deformity, pain, and loss of function.

The overuse of the immune system leads to self-destruction in the body. If this form of self-destruction occurs, for example, in the fatty myelin sheath of nerve tissue, it is called Multiple Sclerosis. However, we know that fat tissue is capable of absorbing a large amount of toxins and harmful heavy metals, thereby keeping them from doing direct harm.

Naturally, toxins migrate toward fatty tissue. A fatty liver is a merely a survival attempt by the body to deal with the load of toxins the liver can longer break down and remove because of chronic congestion of its bile ducts. Yet, seen from a deeper perspective, what appears to be the body’s act of self-destruction is but a final attempt at self-preservation. The body only “attacks” itself if the toxicity has increased to such a degree that it could cause more damage than an autoimmune response would.

The body certainly has no intention of committing suicide, although the term “autoimmune disease” implies just that. When the body’s cell membranes are clogged with foreign, harmful chemicals, foreign protein fragments and toxic particles like trans fatty acids, it is an absolutely normal response by the immune system to attack these contaminants. The resulting inflammation provides it with the opportunity to ‘wash out’ and remove at least some of the toxins. To call this survival response a disease makes no sense, is unscientific and reflects a lack of knowledge of the true nature of the body.

Gallstones inhibit the body’s ability to keep itself nourished and clean, which makes them a leading cause of toxicity. They prevent the liver from adequately taking noxious substances out of the bloodstream. If the liver cannot filter out toxins from the blood, they end up being dumped into the extracellular fluid. The more toxins accumulate in the extracellular fluid, the more severely that cell membranes become clogged with injurious materials. An autoimmune response may be necessary to destroy the most contaminated cells and thereby save the rest of the body, at least for a while. When all gallstones are removed from the liver and gallbladder, the immune system does not have to take recourse to such extreme measures of defending the body on the cellular level.

A healthy, balanced diet can, of course, greatly support the body in maintaining a balanced immune system. For example, research conducted at the University of Cambridge and published in the journal Cell in October 2011 revealed that compounds found in cruciferous vegetables, such as broccoli, kale, bok choy, and many varieties of leafy greens act as chemical signals necessary for a fully functioning immune system.[6]

With my best wishes,

Andreas

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