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mitochondrial myopathy

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A couple weeks ago Mike went for a second opinion and saw a new

neurologist at West Va University Hospital. He had a good physical,

and medical history done. He took the special blood test again,and is

now scheduled for an EMG and muscle biopsy in October.His meds for

the diabetes has stopped working and he has been placed back on

insulin. We are hoping that a new more complete diagnosis is found so

we know what we are dealing with.It seems that the only direction the

doctors give us is to treat the symptoms or side effects and learn

how to live and adjust to this disease.Mike has the very strong

feeling the doctors do not care for chat rooms or chat help, but

where can you get better advice or help other than from people who

are experiencing the same things? Will keep an update posted as

things get completed and we find out more.Thanks for all the good

words of wisdom and hope we read in the posted messages.

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