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Coping With Charcot-Marie-Tooth Disease

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My dear son’s incurable disease


by: Mjm on Wed, May 02 2007

Hi! my son has been diagnosed with CMT1 four years ago. He is now 8 years old and I thank God because he is attending to a normal school here in Japan. His foot has miraculously develop stronger, although his hands/grips are quite weak. I try to let him deal his life in a normal way just as how normal kids does because he doesn’t experience any pain at all yet. It is a great thing to share and know a lot of things about this disease as I didn’t have access before (computer).

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May 2007

  • charcot marie toothe disease - by Danny - (Mon, May 28 2007)
    I was diagnosed with CMT when I was 42yr. and this was after I had open heart surgery. This disease has been very life altering for me as I can no longer work, and am now permanently disabled. [more..]
  • Confused - by A K - (Mon, May 28 2007)
    Hi, My husdand has suffered from CMT since mid teens. Over the years we have tried to gain info in relation to the inherant risk to our three (now adult children). However we have only managed to become more and more confused. [more..]
  • Sometimes we have it easier - by Heather - (Tue, May 08 2007)
    I was diagnosed with CMT around the age fourteen. I am now twenty three and have trouble with walking and vague sensation in my hands. [more..]
  • My dear son’s incurable disease - by Mjm - (Wed, May 02 2007)
    Hi! my son has been diagnosed with CMT1 four years ago. He is now 8 years old and I thank God because he is attending to a normal school here in Japan. [more..]
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