[CUFI]

Mitochondrial Dysfunction and Vaccines
People have varied genetic makeup and individual responses so there isn’t a way to tell if a given vaccine will provide the benefit of immunity, cause the illness it’s meant to prevent, or cause mild and/or serious neurologic illness or other “adverse events” (including death) following vaccination in some individuals.

Vaccines are known to be problematic for a segment of the population with a specific mitochondrial genetic mutation which may affect up to 4,000 babies a year. Some of those with a particular form of this dysfunction are unable to detoxify the poisons such as aluminum or mercury that are in the vaccine. This inability to detoxify the metals causes damage to multiple organ systems with sometimes devastating results.

In his 2004 testimony to Congress, Dr. Rashid Buttar [iv] (former vice chair of the American Board of Clinical Metal Toxicology and scientist at North Carolina State University) said that children with autism suffer from acute mercury toxicity which results in many imbalances, including systemic candidiastis, immune-suppression, immune dysfunctions, and gastrointestinal dysbiosis. He calls these conditions fires which resulted from one spark: mercury, including (and exacerbated by) the mercury in trace amounts still in childhood vaccines.

Inadequate Testing of Vaccines
The problems associated with vaccines should lead manufacturers to conduct stringent testing. However, quite the opposite is true. In vaccine testing there is:

No cumulative safety testing done prior to licensing
No placebo standard safety testing done
No carcinogenic or mutagenic capacity testing done (even though vaccines contain animal DNA and carcinogens)
No route of exposure research to determine effective safe limits of ingredients
Safety or toxicity of vaccines is studied for short term rather than long-term. Many studies are limited to just a few weeks. When a vaccine is tested, it is given to healthy people and they are only given that one injection (not multiple injections at once, like a baby). The current CDC recommended schedule with a number of vaccines injected on a given day has never been tested. In essence, the current schedule is an experiment.

Vaccines Introduced 1985-1991 Were Not Studied For Autism



Chronic health conditions in children began growing rapidly at the same time that new vaccines were introduced 1985-1991, now impacting 1 in 2 adolescents. Autism, ADHD, food allergies, bowel diseases, and other conditions began growing exponentially in the late 1980s.

The Hib vaccine was introduced in 1985, and replaced by the Hib conjugate vaccine in 1988, to avoid a death rate of 1 per 106,000 persons. The Hepatitis B vaccine was introduced for newborns in 1991 to avoid the risk of transmission from the mother which can occur in 1 in 480 births. HepB is a blood-borne illness not transmitted by casual contact, so an infant is not at risk unless the mother is HepB-positive. Learn more by reading the report created by Foundation for Pediatric Health.

https://www.stopmandatoryvaccination...ccine-dangers/