In article <woody-3112950101100001 at culver_pm2_26.netvoyage.net>, woody at netvoyage.net (Mark Woodrow Hall) says:
>>I am a 29 year old male that was diagnosed with charcot-marie-tooth
>approximately 4 years ago. At birth I had intestinal atresia and at 13
>was diagnosed with hyperglycemia. I believe these to be related but three
>neurologists so far, who have decided on instinct, have decided that CMT
>is the cause of my atrophy. If anyone has information about who I can see
>that may take the time to examine medical history or who is on the cutting
>edge of research, please email me.
>>Mark W. Hall
>>woody at netvoyage.net
The National Ataxia Foundation provides support to those with C-M-T or
other types of ataxia.
See the National Ataxia Foundation home page at:
http://126.96.36.199 or http://www.ataxia.org
Also the Usenet Newsgroup: alt.support.ataxia
Email the NAF at: naf at mr.net
They are located in Minnesota and have the latest information on
research into most forms of ataxia.