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Member
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Join Date: Jan 2008
Location: Kansas
Posts: 971
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Member
Join Date: Jan 2008
Location: Kansas
Posts: 971
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Quote:
Originally Posted by Dejibo
. . . It's scary to ride bareback through the MS world. not sure if I am ready for that.
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I don't have an lot of answers for you, Dej, but I'd be scared, too. Beta was not effective for me, so the other interferons would also likely not be.
I've had a lot of BAD site reactions with Copaxone, and was relieved when my MS Specialists allowed me to decrease my frequency and number of sites used, because I was also worried about what other options might be, if Copaxone didn't work out.
I do know, though, that she mentioned some drugs that are currently being studied as options at one point. I wasn't real interested in those, because of the possibility of being on a placebo, and getting nothing at all.
However, if the ABCR's were not an option, (and, I agree, I'm also afraid of Ty), I'd probably look into a med that's being researched.
~ Faith
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aka MamaBug
Symptoms since 01/2002; Dx with MS: 10/2003; Back in limbo, then re-dx w/ MS: 07/2008
Betaseron 11/2003-08/2008; Copaxone 09/2008-present
Began receiving SSDI 11/2008
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