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02-01-2009, 01:15 AM
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Legzz --
I have that problem (aching for 3 days, Ibuprofen every 3-6 hrs to get me through it) with arms, legs and hips. I finally quit doing all those sites, because I was simply not willing to hurt that much. I inject only in my abdomen, and only 4x per week, because Shared Solutions does not recommend using sites more than once per week. My MS Specialist is OK with that. (I actually made the change on my own, and told her about it several months later.) She says, "We do what we can." In spite of my decreased injection fx, Copaxone seems to be working. I had a UTI in December, which usually triggers a flare. This time, it didn't! ~ 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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02-01-2009, 01:27 AM
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Senior Member
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But I can only do shots in my belly. It hurts pretty well everywhere else. I have started doing them without the auto injector. They've come out with a smaller needle and it works pretty well for me. I really can't believe I got brave enough to try it w/out the injector...one day I just did it!
 My husband couldn't believe it...nor could I. But anyway, it leaves less problems at the site than when I use the injector.
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~ Friend2U . . HANG IN THERE! If I had to sum up FRIENDSHIP in one word, it would be COMFORT. ~Adabella Radici MS/dx2006 BETASERON (Quit May 2011) COPAXONE (Began June 2011) |
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