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.
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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 TodayPPMS for 25 years (dx 1998)
~ Worrying will not take away tomorrow's troubles ~ But it will take away today's peace. ~
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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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