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Re:mito v MS diagnosis

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I was originally diagnosed with MS based on 3 MRIs. When I was told of the

diagnosis I requested a referral to the " best " neuro in the area.

The neuro examined the MRIs and took a very careful history. He then

suggested that the lesions seen on the MRIs were not truly typical of MS and the

family history pointed to a mitochondrial disorder. It was then that further

tests were run (emg, lactic acid) and a diagnosis of MELAS was made based on a

blood test.

I was very fortunate that the diagnosis was made in only a three month

period. Of course in retrospect I have had all sorts mito-related problems,

misdiagnosed and mistreated, all my life. I will have continuing problems of

all

sorts but we are at last treating them as well as we can within the knowledge

base that now exists.

a

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