Guest guest Posted June 3, 2008 Report Share Posted June 3, 2008 Hello Everyone, I'm Jen. I love this group and am learning so much. We just found out that my daughter and my husband have CMT. I felt very lost at first, but am so grateful for all of the helpful information on the web, especially here. Thank you all for your efforts to share what you learn with others. We have an appointment next week at a Muscular Dystrophy clinic. I may have questions after that. My husband's family all have the typical CMT feet. They just never knew why until recently. My brother-in-law's are quite bad. He has had doctors tell him that they can't believe he can walk on feet like his. His reply is, " Well, no one ever told me that, so I just have always walked. " This inspires me as I look to the future for my daughter. I am happy that we have options for her and I have hope that together we will find a way through her challenges and that she can still have a very wonderful life. Quote Link to comment Share on other sites More sharing options...
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