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I agree with Bird - let them know and then let us know what they say about the resistance pushing the med in - that is odd - haven't had that problem - have had a little of it oozing back out so leave needle in until count to thirty - that seemed to work for that problem -
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I'm not on Copaxone anymore (not related to any "equipment" problems), and didn't have the dull needle problem that I'm aware of (used the Autoinject).. But I DID have a gnarly batch where the glass would break when the Autoinject hit it, shoving the entire needle as far as possible into my bod.. Needless to say, that made me a little paranoid every time I had to inject, but it was just in the one box...
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I would have been more then a little paranoid - why did you stop the Copaxone ??
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It was something my neuro had me use, even though he says I'm PPMS, which theoretically does not respond to CRABS..So when my company changed insurance companies last year and I had to go without for a couple weeks, I realized it was kind of a waste, so I quit..Everything is pretty much the same ~ just a very slow, steady decline..As long as it stays slow, I guess I'm happy with that..
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Was on a very slow decline til last October then had a bad relapse out of no where and continue to. Have been on Copax since October but recently stopped due to 2 bad reactions from Copax.
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I've been on Copaxone for 5 months now and so far so good.I had only one IRPI reaction it was with my first shot. I hate doing my shots in my thighs it hurts alot,but I think almost everybody hates that injection area.
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It's really funny about those thighs...I couldn't stand them with Rebif (subcu), but I don't mind them with Copax....
Avonex (intramuscular) had to go straight down anyway, so I didn't mind them there either with Avonex.... J, did you have the "dreaded" reaction or allergic reaction? or what? |
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