Guest guest Posted December 12, 2011 Report Share Posted December 12, 2011 Three levels of TOXICOLOGY Deniers of thimerosal harm are those that either believe in Paracelsus that the dose makes the poison or if better informed that of toxicology of the lowest effect level. Today, these ideas for toxic harm are completely out of date. Looking at the lethal level for mercury it would seem thimerosal is about as toxic as common salt. The ability of mercury to provide a swift death for an adult is very limited compared to its more sinister toxic ability at EXTREMELY low levels. For children with unformed brain barriers and especially if already PARTLY toxified by mercury the harm is acute and more so for boys. Evidence now KNOWN. Hence the reason more boys die from SIDS in the first 6 months of life and usually nearer to the birth date than the 6 month date. And very near the VACCINE dates. Those that believe Paracelsus are those happy to kill an infant as they get protected as adults. A despicable attitude with little interest in the real reason a million children have died and using explanations that a change in sleeping position is the difference between death or life., Quite preposterous and blaming the family for the recent genocide. Educated people hold to the EPA idea that you need to take care not for immediate death from thimerosal but from its first observed toxic effect. The EPA lead the world in this respect and place a reference level of 0.1 micrograms ot thimerosal exposure for each kilogram of the mass of the person. Again simple in that it fails to recognise that babies are not just little children and thimerosal targets little babies and especially little baby boys more so than adults. Hence the multi-millions of girls that survive where boys succumb. And those clever adults shouting look the thimerosal jab hasn't killed me. But what if they were ten times lighter or had ten times the dose of vaccine. What if they had an immune system compromised so there was no blood-brain barrier. Just like in effect what we put our babies through with their unformed blood- brain barrier and often super light weight if premature where SIDS et al is vastly much HIGHER. If girls don't die in the wrong sleeping ^position as facts prove then that is making a mockery out of the sleeping idea. Making a mockery even of the EPA who know of great harm at sub-lethal levels. They argue: The EPA level is a reference and if you have a 50 fold OVEREXPOSURE you just need to wait long enough until the toxic level becomes less than that specified by the EPA. There is a snag. Baby Harry for example died withing six hours of a toxic thimerosal injection at more than the reference level of the EPA. There are big faults with such a simplistic theory. But those that inject potent NEUROTOXINS or are happy for SIDS and autism to continue are not listening to reason. Your government, your Big Pharma, your doctor would NEVER risk your life, your health. Try to get recompense if the worst happens. I would like people to realise that these people can change from GUARANTING no harm to witnessing that the survivor (mom, dad, carer) go to prison for the harm that the vaccine has done. But TODAY all these simplistic TOXIC ideas DO NOT PROTECT us. The idea of multiple exposures has been known to the educated for generations. Mercury pollution comes from vaccines but also a host of other exposures. It takes one drop to over expose a dangerously toxic person. The multiple exposure need not be mercury. Other chemicals are neurotoxic and lead for some chemical pathways is more toxic than mercury. The least normal action is ADDITIVE but sometimes the TOXIC effects increase out of all reason considering the tiny amounts in us. But mercury does have a bigger toxic effect than other elements simply because of its effects below the lowest effect level even of the EPA. It is toxic at the MOLECULAR level. Just because most apparently survive such low levels is NO reason to inject all our babies with the stuff. New research adding to our old body of toxicology tells us of this harm at the molecular level. Thimerosal contains not one molecule, nor millions but trillions of molecules. Each one capable of acting ADVERSELY at any level above ZERO. For microglia, the experimenters find that even at micromolar amounts that cells are killed, at sub micromolar amounts the cells are killing themselves in response to harm caused. But at the molecular level the cells are being turned from their normal correct functions. Levels of ions carefully controlled are sent haywire. Perhaps allowing too much ion into the cell or too little. The control has been LOST. Diabetes is just one such control that is being increasingly LOST. Sodium levels mysteriously become out of control in some babies. We have direct EXPERIMENTAL evidence of this loss of control from levels of thimerosal below that level of reference. And often to add insult the loss of control is because some normal and SAFE chemical in us in now not being used. This builds up perhaps in some ANAPHYLACTIC way. Killed or harmed by chemicals we absolutely NEED but now are being turned away by some bully of a mercury ion blocking it from its task. We are not playing life or death though a million babies are suddenly dead over the years. We are not making children with disorganised brain cells though there are now tens of millions suffering. The use of thimerosal already at levels which can kill or make us ill are causing harm that is NOT evident now, maybe never will be but is compromising the normal health and well being that we would have if thimerosal vaccines were truly STOPPED as promised more than TEN YEARS AGO. 1 Toxins sometimes not much KILLS 2 Toxins at lower levels makes us ILL 3 Toxins at the molecular level are altering the normal functioning of our bodies and often not realised or blamed on abuse which is correct but the abusers are ESCAPING JUSTICE. They can in addition recruit good molecules to harm us in tandem. Three levels of TOXICOLOGY Quote Link to comment Share on other sites More sharing options...
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