Apologies for the sarcasm in the topic title, yesterday I read that public enemy number one AKA N.i.c.e had provisionally scuppered the go ahead for ocrevus to be funded as a NHS approved treatment. The only drug that showed any potential improvement to people living with ppms, yet only a couple o…

Hey, so I’m just about to go on a medical trial in Canada for new ms med, but first they are switch me to ocrevus infusion. Any one have information on this med for positive or negative effects?

Hi all, I’m curious to know if there’s anyone around here who has had an improvement in MS symptoms after going on Clemestine Fumarate (antihistamine) as was suggested in the remyelination trial. Thanks.

Hey everyone I really want to have the stem cell treatment, my neuro has said if I relapse again on tysabri then I’d be put forward, anyone know how I can get put forward for a trial without having to have another relapse? Thx in advance

Hi all Me agaim . 4am i woke up and my thoughts sre on …. stem cells I am upset, yes. Upset by doctors still focusing on newly diagnosed patients only , they say or excuse themselves saying they can not measure improvement in walking on us spms because we no longer walk . That is such rubbish…

I am sure most of ye have seen this tonight or watched the related Panorama program about same.. anyhow just sharing as the results are almost out on the HSCT international trial which includes the UK and they are very encouraging. http://www.bbc.co.uk/news/health-43435868 Note the trails were RRMS…