Guest guest Posted November 25, 2006 Report Share Posted November 25, 2006 , My name is Pam, I live in the Chicago area. I have CMT2 with MPZ. I received my genetic test last month. Pam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 25, 2006 Report Share Posted November 25, 2006 and Pam, I have CMT 2, confirmed by EMG/NCV, but have not been DNA tested. ~ Gretchen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2007 Report Share Posted September 17, 2007 Hi Emine, Yes, I seem to have CMT 2. I was diagnosed as a child when I was 10 years old. I am now 55. I don't use AFOs. I have custom orthotics in my shoes, to support my feet. And good shoes. Both are wonderful. Yes, there is more research starting to show now for CMT 2 and all the subtypes, so far all I have read is the genetics research. There is an excellent researcher nearby in Los Angeles working on mitochondria's impact on cells in CMT 2. I have just finished reading all the papers that were presented at the CMT Consortium this summer. As I read, I made some notes, and once I organize my notes, will try to post some insights. ~ Gretchen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 17, 2007 Report Share Posted September 17, 2007 Gretchen, I don't know how you do it. This newsletter is so wonderful. All the reading you do and digest for us is extraordinary. A mere 'thanks' seems so inadequate, but thanks. Elinor Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.