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Re: Future of Mito Kids

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I wish I could give you a definite answer, but I don't think anyone can. Mitochondrial disease is so unknown as of now. Every doctor I have talked to about it, admit they don't know practically anything about this disease. But to help, yes some of these kids do live pretty normal lives. My daughter Grace is 19 months and has mito. Yes, she has issues that will be with her forever, but I think she will live a pretty normal life. I think for her anymore this is normal. She has a g tube to help give all the medicine, and she even helps push the medicine in. She seems to actually enjoy going to the doctors anymore, they are practically family at this point. Who knows what the future potentially holds, but today is great. I know this is morbid, but nobody really knows what can happen tomorrow. I live on the fact that they do not think she will die from this disease, so we can handle what happens next. Hopefully your son will not have this disease, but if he does try to learn what can happen and be prepared for it. This is always a great place to vent, or to share happy stories. Everybody here can relate to almost all of the problems, and emotions with this disease. Best of luck to you and your family.

mom to 4 wonderful kids, and a new munchkin coming in Sept.

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AReckling@... wrote:

He told us that

a number of mito disorders show up simply as myopathies (which is mostly

what my son has, although he has GI issues as well).

What are myopathies?

Thanks!

Lynne

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AReckling@... wrote:

He told us that

a number of mito disorders show up simply as myopathies (which is mostly

what my son has, although he has GI issues as well).

What are myopathies?

Thanks!

Lynne

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