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after researching and learning much from many wise and kind souls,

including many in this group, it seems that the best way for me to get

a diagnosis is to look for a caring doctor who is familiar with mito

and does fresh muscle biopsies and then knows what tests to do. does

anyone have any recommendation for a specialist who will listen to me

and work with me? it would also be great if this doctor was somewhere

close to me in illinois. thanks.

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