Our government has the responsibility to prove the safety of any vaccination being recommended for broad public health, as part of an overall vaccine program. Our current knowledge of science, the immune system, and the brain would make it unlikely that broad vaccine programs could ever be approved for use today if they hadn't being going on for so long.
Our government is not only grossly negligent on the vaccine issue itself, but on numerous other true public health issues that pose a significant risk for brain inflammation in fetuses and children. The CDC, the EPA, and the FDA all play large roles in creating huge autism risk for our population.
Space in this article only allows a few examples; there are many. Environmental pollution that is fat soluble can cross the placenta, exists in mother's milk, or occurs in the general food supply fed to small children. Fat soluble toxins cross the blood-brain barrier and induce nerve inflammation.
Huge public health risks include widespread contamination of our food supply with fat soluble PCB toxins, a problem that would cost at least 50 billion dollars to clean up. Another example of broad exposure is the neurotoxic pesticides used on food (originally Nazi nerve gas agents). Another example is the military's poisoning of our water supply with perchlorate, a contaminant now found in breast milk of mothers across the country. This interferes with thyroid function in the baby, resulting in a serious risk for faulty brain development.
Another example is iron fortification of baby formulas, which encourages the growth of hostile bacteria and Candida Albicans in the child's digestive tract; organisms that produce neurotoxic waste products. Another example is the use of antibiotics before age 1, which also encourages the growth of the very same hostile bacteria and Candida. C-Section deliveries also increased the risk for a hostile digestive terrain in the baby. Candida itself directly communicates to and promotes inflammation in the human immune system causing it to malfunction.
Yet another example is the widespread use of antidepressants by pregnant and nursing mothers, which drastically disturbs the evolving function of nerves and overall health of the fetus or baby. And then there is the vaccine preservative thimerosal (different than an adjuvant), which is a neuro-inflammatory in and of itself. And this is the short list.
All of these issues play a role as a percentage of the problem that induces friction in the developing nervous system of a fetus, baby, or young child and primes the nerves to hyper-react to vaccines. Each of these problems is a true public health problem because they are caused by industry and are allowed to continue by various vested interests. Each one will take tens of billions of dollars to fix. However, that is actually the responsibility of government – to fix costly and broad public health problems – not to make them worse.
The Genetic Red-Herring
The case of Hannah Poling has forced our government to show its hand – and a very weak hand it is. They will continue to bluff and confuse the public with scientific gibberish in an effort to misdirect. Their defense in the Poling case, even though they conceded the case, is that the child had genetic mitochondrial dysfunction.
Mitochondria are the car engines in your cells that produce energy (ATP). ATP is the energy currency in your body, much like money in your wallet. You spend ATP, as needed, to do anything. Inflammation uses up ATP by causing your body to go into a hyper mode (like a 911 phone call). If ATP production is compromised then inflammation can run wild – contributing to the brain fire called autism.
True mitochondrial gene mutations are too rare to explain autism, so the government is trying to blame this mechanism in the Poling case to deflect the idea that vaccines are a risk for the majority.
What the government isn't saying is that, independent of a true genetic issue, mitochondria can be taxed into a state of stress that predisposes any child to autism risk. You don't need to have a gene mutation; that is simply a diversion and cover-up attempt.
Furthermore, the glial cells in your brain use ATP to communicate, a separate function than energy currency. This means that any time you run low in overall body energy, brain function is compromised and tilted into a pro-inflammatory mode. This is why stress makes you tired and causes you to feel physical wear and tear. It is also why any time you exercise, which conditions your body to make ATP more efficiently, your head feels better. When glial cells run low on ATP they enter a low grade chronic inflammatory mode – a condition that seriously predisposes to vaccine injury.
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