lyme disease on coast to coast

i wish i had heard this show:

http://www.coasttocoastam.com/show/2011/09/14


Lyme Disease
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Medical researcher Tom Grier (email: donatebrain@gmail.com
) talked about his battle with Lyme disease as well as the medical misconceptions and difficulties treating this pernicious ailment. Grier theorized that he'd originally contracted the ailment, which is spread via a tick bite, when he was a graduate student and would often go for long runs in the Minnesota wilderness. However, he said, the symptoms of Lyme disease did not emerge until over a decade later, when he began feeling extremely tired and depressed as well as experiencing fuzzy thinking, numbness in his hands and feet, visual disturbances, and other troubling conditions. After being misdiagnosed as having multiple sclerosis, the true nature of Grier's ailment was only determined after an alert doctor suggested checking for Lyme disease.

In looking at the myriad of problems associated with diagnosing the sickness, Grier proclaimed that "there's no disease on this planet that's more controversial at this point." He traced the issues back to the original description of Lyme disease in 1975, where Grier claimed that doctors "got a lot of things wrong with this new disease." Going forward, he said, the medical establishment has merely "built up on this mythology that they had started" and, even in modern times, testing for Lyme disease is only about 25% accurate. Additionally, Grier explained that Lyme disease is called "the great imitator," since it often has symptoms which look like other ailments and that the true number of those afflicted with the sickness may be 10 to 20 times greater than CDC estimates.

"They call it the 'practice' of medicine, but nowadays medicine is a fascist state," Grier lamented about the lack of options for Lyme disease victims. He observed that the scarcity of doctors who are adept in treating the sickness has created a situation where, once their specialty becomes known, they get overwhelmed with patients who are desperate for help. Alongside that problem is the lack of funding for research into the disease. Believing that a key aspect in understanding the sickness lies in its affect on the human brain, Grier said that he's been trying for over a decade to get funding from the NIH and CDC for such studies and has been continuously rebuffed. He surmised that this lack of support is because of trepidation from the medical community that his research would "prove them all wrong" about the true nature of the disease.

http://www.mdjunction.com/forums/lyme-disease-support-forums/studies-research...


http://www.canlyme.com/