I think I am 'borderline' SP/PP (diagnosed in my early 40's), and I am being prescribed at this very moment meds for mainly fatigue, bladder control and mobility.... As my EDSS has reduced with 0.5 over the last years, I am now 'eligible' for Siponimod.... (btw a recent repeat MRI did not show a lot of change over a significant number of years).
I don't really know what to expect, and I just wonder if any of you recognise themselves in the 'MS loop' I have been in so far?
Hello All, well I'm 64 with Clinically Isolated Syndrome MS,been on copaxone, and was allergic to it,now Avonex, Praying when I turn 65 I can be finished with this medication, I don't want to try anything else, I Pray ππ½ to God I'm finished with All this medication π€ππ€© Everyone have a wonderful night π΄
@A MyMSTeam Member I've been using glatmeir acetate (Copaxone) for over 25 years now. I also did a 5 year period with Betaserone (Avonex) plus Copaxone. I'm pretty much stable as I reach 62. Wish you all the best.
What can you expect when starting Siponimod (Mayzent) at 62 with borderline SP/PP MS?
Siponimod is approved to treat active secondary progressive MS, relapsing-remitting MS, and clinically isolated syndrome. It works by preventing white blood cells from leaving the lymph nodes and entering the central nervous system, which Show Full Answer
God Bless you Josephus.
My prayers go with you π
Best wishes blessings π joy
Stay young at heart π