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Guilt and CMT types

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I have CMT1b. I do not feel at all guilty about my children because

I did not know that I had it when they were born (I only recently was

diagnosed). If I knew it then I think I would have tried anything

available to prevent my child from getting the gene, but even if

nothing were possible, I would still have children. Maybe it is

easier for me to say this because I had a late diagnosis and have not

been very disabled by it. I feel very, very sad when I think that

perhaps my children will have the pain and problems and I feel even

worse when I think that they may have children with it. I did not

have any known signs as a child and have not known a child with CMT

so I really do not know how hard that can be. I can very much

empathize with people who feel that it is cruel to have a child who

will be doomed with suffering. However, we never know what a child

will be born with and there are so many things that can " go wrong. "

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