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Lydia-- This sounds REALLY interesting. I always said my sister a's

MS was SO different than most others. She progressed so rapidly and did

end up totally immobile and blind. And I had a cousin that died within

10yrs of dx, also totally immobile, couldn't talk, could only blink her

eyes before she died. If this NMO is genetic at all, I think I better

get myself tested if that testing is available. Looks like the only

place doing anything with it is the Mayo Clinic. S---, I don't know if

I'm up for the road trip!

But I am grateful to you for finding this reference. I had never heard

of it. Thanks. Beverly

>

> Has anybody heard of this? NMO antibody test at Mayo clinic. My

> neurologist said I might have a disease that closely mimics MS but is

> not the same thing and drugs for MS don't work. My blood has to be

> sent to Mayo Clinic because they are the only ones that does this

test.

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