Guest guest Posted April 24, 2006 Report Share Posted April 24, 2006 Welcome Tammy, Thanks for your note of introduction. Since there is CMT 1A in your family, you might want to read about Vitamin C in our files, also about Vitamin E, then ask your docs about them. Since CMT 1A is so common, more research has been completed in that field. Some of us find exercise and diet/nutrition helpful, also physical therapy, stretching, etc. We've got plenty of parents with CMT children who will jump in to welcome you and lend their expertise when they see this. Again welcome, hope you find helpful and the research informative. You might want to get the new CMT/Hereditary Neuropathy booklet from HNF-cure.org too. ~ Gretchen/Founder of and Moderator Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2006 Report Share Posted November 6, 2006 Hi Tammy, I am sorry to hear about your aunt. I hope that she recovers quickly from the cancer. What does the D stand for in CMTD? Quote Link to comment Share on other sites More sharing options...
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