Guest guest Posted March 15, 2008 Report Share Posted March 15, 2008 No proof autism and vaccines are linked, but what about mitochondria? Maybe you are right, this makes more sense than does a man named Kanner that coined the phrase autism; because of a child's actions and symptoms that he thought fit the child's label. Now after all these years, NIH funding was finally used for a productive study and now we know the mechanism that caused the depletion of our child’s glutathione. It was as we thought, this statement is from a few minutes of searching on Google; in this you will see the ingredients in children’s vaccine's. "Vaccinations contain at least four neuro-toxins: mercury, formaldehyde, MSG and aluminum hydroxide. Researchers at the University of British Columbia have been looking at the possible effects of the fourth item in this list. They injected mice with anthrax vaccine containing aluminum hydroxide. After 20 weeks studying the mice, the team found statistically significant increases in anxiety (38 percent); memory deficits (41 times more errors than the sample group); and allergic skin reaction (20 percent). On autopsy, brain tissue samples showed that 35 percent of the cells were in the process of destroying themselves. According to Shaw, lead researcher for the project, his research shows a link between aluminum hydroxide and symptoms of Parkinson's, Alzheimer's and Lou Gehrig's disease. "No one in my lab wants to get vaccinated," he said. "This totally creeped us out. We weren't out there to poke holes in vaccines. But all of a sudden, oh my God--we've got neuron death!" (www.straight.com/content/cfm?id=16717). According to Shaw; lead researcher, his research shows a link between aluminum hydroxide and symptoms of Parkinson's, Alzheimer's and Lou Gehrig's disease. "No one in my lab wants to get vaccinated. Just a thought, we could learn from this statement. From scientist’s that know, and not just those spouting CDC propaganda as most are. Who try to defend putting toxic chemicals in our children’s vaccines. The public should know that there is a challenge and you will be paid to take in your body the amount of mercury, aluminum, MSG, and Formaldehyde, that these children received in the 90's. So far there are no takers. The apologist’s get quiet when we ask, if they are so sure of the safety of the ingredients AKA "poisons" or "neurotoxins," why not? those who would suggest this is safe for our kid's, seem to not want this to be injected into their own selves. These seem to be the kind of people who when a ship is sinking would push women and children out of the way to get in the life boat. It is clear they can't seem to understand the simplicity of the new science coming out on mitochondria that explains why most of these children have depleted glutathione. The following information is from a one minute search on Google. Mitochondrial Damage “One major mechanism for metals toxicity appears to be direct and indirect damage to mitochondria via depletion of glutathione, an endogenous thiol-containing (SH-) antioxidant, which results in excessive free radical generation and mitochondrial damage. 28 Anecdotally, Dr Neustadt, in his clinic, frequently observes an elevation of urinary pyroglutamate, an organic acid that is a specific marker for glutathione depletion in patients with confirmed mercury toxicity. 29 Not surprisingly, these patients also complain of fatigue, a hallmark symptom of mitochondrial damage. Mercury can accumulate in mitochondria and causes granular inclusions, which are visible with a scanning electron micrograph. 30 Oxidative stress occurs in vitro and in vivo from both organic and inorganic mercury via their high affinity for binding thiols (sulfur-containing molecules) and the depletion of mitochondrial glutathione. 27 The central nervous system is particularly sensitive to damage by MeHg-induced glutathione depletion. In one study, ex vivo human neurons, astrocytes, and neuroblastoma cells were exposed for 24 hours to various levels of MeHg. The LC 50 (concentration at which 50% of the cells Died)” (http://montanaim.com/pubs/Heavy_Metals_Article.PDF.Heavy-Metal Toxicity—With Emphasis on Mercury. Neustadt, ND, and Steve Pieczenik, MD, PhD) Just a thought, Ethyl-mercury which is found in thimerosal, was found to be two and a half times more toxic than Methyl-mercury. The reason? Ethyl-mercury metabolizes into inorganic mercury, which keeps it from ever excreting itself from the child’s brain. "ALUMINUM" This neurotoxin is the same as in children’s multi dose vaccines. We will now learn what he meant by neuron death, that is the same as APOPTOSIS this is the word, when I called the mitochondrial foundation that they use when defining mitochondrial dysfunction. Now we will add "ETHYL-MERCURY" the main ingredient in thimerosal 49 % by weight mercury, here is what a NIH study says: Burbacher and his colleagues found ethyl mercury’s fast breakdown leaves higher levels of so-called "inorganic" mercury in the brain. Inorganic mercury lingers in the brain for a year or more, potentially altering certain cells. A previous study has shown such damaged cells are also found in children with autism. Could this be the mutated cells they’re finding? When you research thimerosal you find it is mutagenic. It seems another study may have just found the damage done by the neurotoxin’s effects. Using monkeys, Burbacher found the brains of thimerosal-exposed infants had twice as much inorganic mercury as methyl mercury-exposed infants. It seems this NIH paid for study puts the myth the CDC created that this is a “friendlier” “gentler” and “kinder” mercury AKA "poison" or "neurotoxin." To rest The Food and Drug Administration has never required testing of thimerosal's safety or of its safe exposure levels for newborns and children. In a congressional hearing FDA officer DR. Egan was asked, Why there hasn’t been any research done since 1929. The only research done was on 22 people dying of meningitis. Congressman Burton said that they all died and we do not know if it is safe or not. This man freaked out, because on his watch, a generation of children was lost at a estimated cost of 200 to 400 billion a year. In the next ten years, the Iraq war for all the time we have been there has cost I believe 550 to 600 Billion dollars that equates to a little over half to three quarters of the war so far, but this will be for the rest of these kid’s lives every year. You would think, the CDC would stop turning out these kids at 3.2 to 5 million each getting back to DR. Egan he almost could not talk, they had two women from HHS on both sides of him walking arm and arm he looked like he was in shock. He actually looked like a deer caught in head lights. Thats when I personally got angry, that these people don’t take vaccine safety serious. Our vaccine damaged kids are just collateral damage and the cost of doing business, here is how serious they take safety this is from the IOM meeting: Dr. Stratton: "We said this before you got here, and I think we said this yesterday, the point of no return, the line we will not cross in public policy is to pull the vaccine, change the schedule. We could say it is time to revisit this but we will never recommend that level. Even recommending research is recommendations for policy. We wouldn't say compensate, we wouldn't say pull the vaccine, we wouldn't say stop the program." Similarly, Dr. McCormick, at page 97 in discussing whether autism could be associated with vaccines, stated that "we are not ever going to come down that it is a true side effect," despite the fact that the committee had not yet considered any evidence on this issue. Just a thought, what if we are hurting children,? and we are. In New jersey the autism rate, I mean mitochondria dysfunction is 1 in 96 children and 1 in 50 boys. DR.Stratton said it best "we will never recommend that level" Some children that have a DX. for autism also have high testosterone from depletion of glutathione. It's sort of like a car with the accelerator stuck open making testosterone and cannot stop. In New Haven, Conn. a Yale School of Medicine study shows for the first time that a high level of testosterone, such as that caused by the use of steroids to increase muscle mass or for replacement therapy, can lead to a catastrophic loss of brain cells. AKA apoptosis. Quote Link to comment Share on other sites More sharing options...
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