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Welcome ,

Sorry you have the health problems that will probably make you

feel very at home here, but glad you found us. Welcome aboard.

Your story sounds sadly familiar.

Pray your muscle biopsy shows something helpful to your

getting answers and treatment. How blessed that you made

contact with other limbs on your family tree to help point you in a

genetic direction.

This wonderful mito community is a of great knowledgeable and

compassionate mito patients and caretakers. Many of our group

are at the mito conference (umdf) in Pittsburgh this weekend, so

I'm sure you will get many more welcomes when people arrive

back home next week.

I haven't had a chance to read other posts before responding to

yours, so in case you don't already know about it and someone

else hasn't told you about the www.umdf.org site, there's a

wealth of info there.

If you have questions, or just need some support, there are lots

of people here to help make your path a bit easier.

Best Wishes,

Anita in PA

(Lyme Disease and Thiamine-responsive PDH)

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