Guest guest Posted September 7, 2007 Report Share Posted September 7, 2007 Welcome Emine, please don't worry about the English. We understand. There is no one 'treatment' to benefit all. Our CMT is all different, depending on our genetics. Some of us, myself included, believe in the power of good nutrition, exercise and a positive attitude. I also take 1000 IU of Vitamin E everyday and drink Artesian water that gives me good concentrates in dissolved solids of Silica, Magnesium and Calcium. ~ Gretchen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 8, 2007 Report Share Posted September 8, 2007 Hi Emine, Glad you joined the ..this is a very nice group, I know you are going to like it. I live in Minnesota on a small farm, my partner is also disabled.We are very busy with everything here. I have always had CMT but when I was younger the doctors didn't know what it was...said I had Polio but I wondered how that could be as my dad and all his family had the same thing.Life has been a struggle for me with CMT but I'm glad I still here ...My CMT has gotten worse but life is still good do get depressed some days but that to, passes with time. Have trouble with my CMT losses and the way people can be at times... I can still paint something I love doing. Blessings Geri Quote Link to comment Share on other sites More sharing options...
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