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#1 | |||
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Apparently there is a new drug that is a derivative of Gilenya. They are starting phase 3 trials for up to 5 years to treat SPMS. Just thought I'd post in case anyone is interested.
http://www.nationalmssociety.org/new....aspx?nid=7954
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On Tysabri and love it. . |
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#2 | |||
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Thank you for this - I think this is something that a lot of people like me struggle with; knowing that once the announcement is made that we have made the leap from RRMS to SPMS, it's a wilderness and there is nothing out there to give us hope. I know I am dreading it and fearful of it happening.
This is super comforting ![]()
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Lyn . Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993. |
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#3 | |||
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Quote:
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On Tysabri and love it. . |
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"Thanks for this!" says: | SallyC (06-28-2013) |
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#4 | |||
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In Remembrance
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Yes, there's money to be made off of us SPMSers too!
![]() Do I sound cynical? ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#5 | |||
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Hahaha Sal
You make me laugh. Cynical? No! Realistic? Yes!
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Lyn . Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993. |
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"Thanks for this!" says: | SallyC (06-29-2013) |
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