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…

Hi MSers! Hope all of you are fighting fit and keeping all symptoms at bay! I have a small problem to share with you all and hope to receive some positive feedback. My wife is an MSer for the past 5 years. She is on Tecfidera which has helped to keep her RRMS under control. Everything was hunky do…

hi all i have just started on the stage 3 biotin trial at newcastle , just wondered if any other forum members were on trial , and if they had noticed any benefits or side effects yet ? yours hank