I never remit, hope that being older (46 at DX) means I'll be gone or close to it if it gets really bad (!), Have never (never say never with MS, who knows what may happen), had blindness, no numbness, only when trying to use it pain/discomfort in left knee, no tingling, other than STM loss, no real cognitive losses other than "Too "much of anything can feel overwhelming.
I do have PPMS, am in a chair (Wheelchair Kamikaze (Marc) has influenced me, tend to "zoom" whenever I can. DH gets no end nervous.) But what I'm saying is yes, it sucks, but it could be worse. Anyone with PP try LDN? VCCSI and stem cell interest me. Fingolimod does too (but is it I like the name?)