Check out this great article on the NY Times site: Voices of CMT
And you can listen to their stories here: Listen
I want to say thank you to all of them for speaking about their lives with CMT.
So many parts of what they said resonate with me...the more awareness we can create, the bigger chances that hopefully one day everyone will know what this disease is and that they will find the cure for CMT in our lifetime :)
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My life with CMT and trying to deal with constant chronic pain with a positive attitude...
Saturday, April 9, 2011
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About Me
- Michele
- CT, United States
- I'm a girl with hopes and dreams who has Charcot-Marie-Tooth (I know! You've never heard of it!). In this blog, I talk about my journey with this invisible disease and 2 reconstructive foot surgeries (and a 3rd minor surgery) I've gone through in the last 18 months. And I try to do it all with a positive attitude and a smile on my face :)
Highlights of My Journey
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