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Re: neuromas

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-Gwen-Thanks for the info related to the neuroma. I hope I'm as lucky. I did

some online research last night and I learned a lot. I see that it's called a

morton's neuroma. I was curious about if they have been prevalent among people

with CMT. I COULDN'T FIND THAT OUT YET. STILL INTERESTED TO HEAR IF OTHERS HAVE

HAD THEM.

DENI GILLESPIE

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