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Back to Copaxone after 10 years without it--any advice welcome

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    Back to Copaxone after 10 years without it--any advice welcome

    I was on Copaxone for 3 years but stopped it in 2010. I'm about to start it again, this time in the generic (glatiramer acetate) form, with only 3 shots a week.

    There was a routine I had involving warm or cold gelpacks, or maybe it was both, to ease the injection reaction. I can't remember what that routine was.

    I'd appreciate any advice. Looks as if the 3-times-a-week injection has fewer problems than the weekly shot, and I'm glad of that.
    MEMBER OF MS WORLD SINCE 4/03.

    SPMS diagnosed 1980. Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Glatiramer acetate 40 mg (= Copaxone) 2021- 3/16/24

    #2
    I hope Copaxone serves you well.
    This link might answer your question about hot/cold packs:

    https://www.copaxone.com/injection-a.../how-to-inject

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      #3
      Thank you! Although I'm taking the generic form known just as glatiramer acetate (from Mylan) and not the brand-name Copaxone, I'm sure that the instructions on gel packs would be the same.
      MEMBER OF MS WORLD SINCE 4/03.

      SPMS diagnosed 1980. Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Glatiramer acetate 40 mg (= Copaxone) 2021- 3/16/24

      Comment


        #4
        I stopped taking glatiramer acetate 40mg 3 times a week on March 16, 2024, after checking with the neurologist about it. One of the side effects (bowel urgency) was becoming intolerable.
        MEMBER OF MS WORLD SINCE 4/03.

        SPMS diagnosed 1980. Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Glatiramer acetate 40 mg (= Copaxone) 2021- 3/16/24

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