Guest guest Posted January 15, 2002 Report Share Posted January 15, 2002 I first heard about CMT but it was referred to as HMSN back in 98 but it was immediately ruled out. Then via the internet in Jan 2000 my husband downloaded pictures of feet and legs that exactly matched mine. I was shocked, horrified because my feet and legs have always looked the same right from birth and no one had picked up on it. But by the time I found out about it I'd been in a wheelchair for nearly a year without knowing why. But I'm glad to say my story rarely happens. As things stand at the moment I still don't have a diagnosis of CMT (whatever type) but no one has yet come up with an explanation as to why I show all the signs of the most commonly inherited neuromuscular disease and haven't got it. Love Sue The important thing is never to stop questioning. Website www.horder-mason.freeserve.co.uk Freelance Writer and CMTer " I Thank God for my handicaps, for through them, I have found myself, my work, and my God. " - Helen Keller Quote Link to comment Share on other sites More sharing options...
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