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    Flare after infusion

    Has Anyone had a flare after an infusion? I feel like my hands and legs have been more numb after my August infusion. It always took me a while to recover from Tysabri and now I feel the same way after Ocrevus.

    #2
    I had mine last Tuesday. The steroids made me feel better for two or three days but the last two days I have been totally wiped out.
    No fun.
    It was one agains't 2.5million toughest one we ever fought.

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      #3
      Hey Kat and oceanpride!

      This article might help with some questions about Ocrevus.

      Hot off the press!

      MS symptoms can fluctuate while on Ocrevus, but 'wearing off' not likely | Disease's 'natural' variability likely cause of shifts between infusions | Multiple Sclerosis News Today
      PPMS for 26 years (dx 1998)
      ~ Worrying will not take away tomorrow's troubles ~ But it will take away today's peace. ~

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        #4
        Thanks for this interesting article KoKo
        I did not have the “crap gap” this time but the infusion itself seem to hit me a little harder.
        Maybe it’s just me getting a little older.
        With every infusion I think… or hope…
        that I will bounce back better than ever.
        Maybe this one will do the trick ?
        Or maybe my bouncing days are over.
        It was one agains't 2.5million toughest one we ever fought.

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          #5
          It could be from a true relapse, and just a coincidence with the timing of your infusion.
          Kimba

          “When you change the way you look at things, the things you look at change.” ― Max Planck

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