@I would love some feedback from people who have had RRMS and have progressed to SPMS. I was recently rediagnosed. I know MS is different for each individual but I’m wondering what I might expect the future to be like for me. on Shift.ms

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I would love some feedback from people who have had RRMS and have progressed to SPMS. I was recently rediagnosed. I know MS is different for each individual but I’m wondering what I might expect the future to be like for me.

First posted on the Shift.ms app

@LadyButterfly

Hello. I have SPMS now and use a wheelchair. Stiffness and spasticity is what I deal with. Botox can help. Baclofen as well. I am currently working with outpatient physical therapy. I’m dealing with weakness combined with stiffness. I know stretching is very important as well as strengthening exercises.

28 Jan 2026 17:03

@RC83

SP / PIRA for me has been slow gradual onset of new symptoms i haven't had during previous relapses and they get very very slightly worse year after year.

28 Jan 2026 17:16