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    Solumedrol and MS

    Also, I'm going to try starting a thread and adding tags to see if they are working. Sunshine raised a question about them.

    In another thread (started by Jen's Solitude/Dar) solumedrol was mentioned, and I said I didn't think it was used much any more. The National MS Society doesn't say that, though, and it looks as if it is still being used:



    Last edited by agate; 04-29-2021, 10:10 AM.
    SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

    #2
    Thanks for the link, agate. The information reminded me about the harmfulness of inflammation. I do recall that I always felt appreciative that solu-medrol took care of the inflammation, which made me feel better. In retrospect, if my neuro suggests it, I shouldn't fight him on it. I will keep an open mind when I talk to him on the 5th. I would still prefer to take prednisone pills, rather than the solu medrol infusion, but I will see what he suggests. Thanks again!

    Dar
    DAR
    R/R 1993
    Draw close to God and he will draw close to you. - James 4:8

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