I have had PPMS for many years now, having started with it in my 20s. I’m in my 40s now. I walk short distances with a rollator and am significantly affected by hand tremor and fatigue.
I would love to exchange with others who understand what I’m dealing with and share tips on coping.
Best wishes to all.
Hello there - better late than never! Must say you’ve done very well “out of the loop” all this time.
Just check in regularly and you’ll pick up lots of useful insight. We’re all different, so some will be relevant and others not. Progressive MS much less common than RRMS and there’s a PPMS section too which won’t therefore dwell on relapses and various DMT’s.
Graeme (also PPMS).