Guest guest Posted May 26, 2009 Report Share Posted May 26, 2009 Hi Group, My name is Kris and I am from a small town in Texas. I was informally diagnosed with CMT in June of 2008, but due to lack of insurance and funds I have not been able to do any testing other than Nerve Conduction Studies. I have two children with only my 3 year old son showing signs of CMT. The good news is he is on Medicaid and they are paying for his genetic testing. Both my wife and I(when I am able to) work in the medical field, which has helped in understanding CMT, but as everyone knows each case is different so my hope is between this group and the CMTA we can get some of our questions answered. Kris Quote Link to comment Share on other sites More sharing options...
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