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my introduction

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I am new to this group, but not to CMT. I just joined a few weeks ago, I

think. I live in a small town, fishing village, where I teach 5th and 6th

grades; during the summers I do some PT work in our town Library and also

volunteer to help with our festival - somewhere around July 4. My husband

is a fisherman. We are recently married, just about 10 months now.

CMT affects my feet to terrible burning pain; at work and all I am able to sit

and move about to change my pace. Sometimes it is as if my feet 'fall asleep'

it seems, to where I can't feel them. At this point I can no longer use ice

or heat and My Dr. encourages me to move about as I can and I also take

medication that helps this type of pain. My husband helps care for my feet

by his great foot massage, so I consider myself lucky.

I found about this group from a friend at the Neuropathy Trust. When I saw

the description, I thought I'd join because of the positive aspect. It is nice

to see this group is here.

Lesley

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