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The rest of the BigTen has multiple versions of your fight song David ... maybe you'd enjoy them more as it relates to CCSVI ... though I don't think the school and state of CCSVI are intertwined.
Sorry, just expressing my frustration with the lack of treatment in Michigan.
BTW I did contact U of M's medical school and asked if they were studying CCSVI and if they would treat me for it. Their answer was a flat no! Maybe that was more like "no way!!!"
I have the Novi address too but it doesn't help until they open their doors for business. Also I talked to them several months ago before they were involved with Hubbard. At that time they said they were thinking about doing the examination only and not the procedure. So it's possible that their balloon might turn green instead of red. Hopefully they'll do both though.
David1949 wrote:I have the Novi address too but it doesn't help until they open their doors for business. Also I talked to them several months ago before they were involved with Hubbard. At that time they said they were thinking about doing the examination only and not the procedure. So it's possible that their balloon might turn green instead of red. Hopefully they'll do both though.
David and all Michiganders-
My daughter wants to fire her neurologist. He's that loveable anti-ccsvi guy from Wayne State. Any recommendations for a Michigan neuro?
Brian - my neuro did the typical office exams (not MRI) and was impressed that I had improved since a year ago. He then asked me what I was doing differently. At that point, I told him about my angio for CCSVI. He had "heard of it but really doesn't know much". By the end of my visit he asked me if I would mind if he gave out my name & phone # to another patient!! I wasn't too impressed with this neuro prior to now. The bad news?...he's in Marquette.