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Dear ERS,

Just to clarify, is a email discussion group in

which we share 'experientally' how we manage our CMT. I

realize not everyone has a CMT diagnosis, some are still

in the process, while others have had the diagnosis for

years, and yet some have been mis-diagnosed.

Many neurological diseases have similiar symptoms.

Please remember why we're here: for sharing resources,

positive living strategies and new treatment paradigms in

Charcot Marie Tooth disease.

~Gretchen/Moderator

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