@Marian_KielyΒ 

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Marian_Kiely

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 πŸ™‹πŸ€πŸŒ»
@watsoncraig

You don’t go from RR to PP, it’s RR to SP (Secondary Progressive) and as I understand it Rituximab is successful in its treatment

@Marian_Kiely

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 πŸ’ƒπŸ€πŸŒ»