Guest guest Posted July 14, 2006 Report Posted July 14, 2006 Briget: Glad to hear from you. You are not alone in frustration with neurologists in general. They are the techno-geeks of medicine. I went through the same diagnosis trip that you did, but I had ALS thrown into the mix. My sister has MS so I had a ten year view into what living with MS might offer, a walk in the park when looking at ALS. He even asked if AIDS might be in my past. The local neurologist finally referred me to a specialist who took all of 5 minutes to say I have classic symptoms and leg architecture of CMT. My thought was if the presenting symptoms were so classic, why didn't the local Bozo see them? The best care I have received came through the local Muscular Dystrophy Association clinics. As much as I hate " La Grande Jerry " , the MDA here has given me great support. In Western Virginia, there is a cluster of CMT patients and the local MDA has a real interest in serving them. Call your local MDA and see what they have to offer. As to leg cramps, 500 milligrams/day of Magnesium has solved my cramps. I hope your supplements include magnesium. -- Larry Quote
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