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,

I think now there are about 20 types of CMT. Seems about 3 or 4 can be

diagnosed by the DNA testing. Other types I guess depend on family

history, nerve studies, EMG, etc. One of the genetics site has a

specific type for Tunisian families. That amazed me. As for

self-diagnosis, maybe a better approach is to find a good neurologist,

get ALL the neurological tests, etc. Here is the DNA lab website if you

want it (but the DNA test is done in your Dr.s office, then sent in)

http://www.athenadiagnostics.com

I have been diagnosed with CMT since 1962. Back then there weren't

'types'.Since no one in my family has it/had it, I am classified a

'spontaneous mutation'. For me, I just accept I have 'CMT' and go on

from there.

Gretchen

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Hi everyone. Just wondering. I am due to have pins removed from my toes

tomorrow. Do they numb your foot (I hope so) when they remove them, because

otherwise the pain will be hard to take. Also, can you drive and work

afterwards? If someone could let me know if they have been through this, I

would greatly appreciate. Thanks alot.

Terry Little

Littlet@...

20 types

,

I think now there are about 20 types of CMT. Seems about 3 or 4 can be

diagnosed by the DNA testing. Other types I guess depend on family

history, nerve studies, EMG, etc. One of the genetics site has a

specific type for Tunisian families. That amazed me. As for

self-diagnosis, maybe a better approach is to find a good neurologist,

get ALL the neurological tests, etc. Here is the DNA lab website if you

want it (but the DNA test is done in your Dr.s office, then sent in)

http://www.athenadiagnostics.com

I have been diagnosed with CMT since 1962. Back then there weren't

'types'.Since no one in my family has it/had it, I am classified a

'spontaneous mutation'. For me, I just accept I have 'CMT' and go on

from there.

Gretchen

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Old school buds here:

http://click.egroups.com/1/5536/10/_/616793/_/961205302/

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