MS, The 'Gift' That Keeps on Giving ...
Hi guys. First post, so here goes - I've gone from R/R to PPMS. It's a bit frightening but it's nice to talk to people who understand. I've been put on the W/L for Rituximab infusions although from what I'm reading the results aren't great for PPMS - anyone here have any experience? I'm determined to be as positive as I can and to find ways to adapt - hope you're all ok. Keep fighting πππ»
You donβt go from RR to PP, itβs RR to SP (Secondary Progressive) and as I understand it Rituximab is successful in its treatment
Well that's what I was told last apt. My Neurologist is lovely and I def have noticed a detioration in walking ability - anyway, what does it matter, I have this blasted condition and I'm going to have to get on with it (maybe it's always been Ppms) it is what it is ... Adapt n conquer πππ»