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Hello all,
I'm a semi-retired husband with SPMS. I was Dx'ed in '01 after a looong and tiring battle. I have all the usual symptoms, fatigue, spasticity, bladder, etc. I am putting a lot of faith in this newer CCVSI, am I being too optimistic?
Hi Todd, welcome to TIMS. As far as CCSVI goes, I would say be cautiously optimistic. From the sounds of the Buffalo testing, I think we can say at this stage you likely would find some evidence of CCSVI on testing. I don't imagine we can say whether your particular scenario will be easily treated. If you have not already done so, you can read about the experiences of other SPMS-ers post surgery, on the CCSVI tracking project 'sticky'. http://www.thisisms.com/ftopic-8346-0-d ... -spms.html
HTH!
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Hi Toddh, I saw your posting and wanted to let you know that I am also from Nova Scotia, Cape Breton actually. Have had MS for 14 years, just joined today and looking for information on CCSVI.
HI Todd....
another bluenoser here.... live in Yar. CO........
diagnosed since 05......
i visit the halifax clinic as you do to i am sure....
i am hopeful for this new finding as well.....
i am one of 4 in my family with MS.....