Looking for
something specific?

Hello this is my first post, although I have been following the forum for several months. I was diagnosed in January and my MS nurse recommended the site. I want to say thank you to you all for all the support you give to each other and new people like me and loads of information that I have picked ...

I was supposed to have my first Ocrevus infusion today but it has been deferred in light of the coronavirus outbreak and I will be treated with Brabio for the time being instead. I had emailed some concerns to my hospital (The National Hospital for Neurology and Neurosurgery in London) as I was worr...

Love that ms nurse says oh I respond to emails faster... Last time I got no response at all. This time well I'm 4days in not holding much luck. Guess I'll phone tomorrow and see. Legs been giving out multiple times a day for almost three weeks now. Plenty of bruises have been collected and pulled m...

Remylination https://msguide.blog/2020/07/30/clinical-trial-appointment-week-52-of-the-remyelination-drug-elezanumab-for-multiple-sclerosis/

Since I've been told by the infamous Dr G (Dr Giavanoni) that it would be too expensive to clinically trial turmeric, I've created this Facebook group to share people's experiences with and document any benefits or side effects that they have after trying half a teaspoon of the stuff after eating

Hi all, - If you take ocrelizumab (Ocrevus) , as I do, and want to participate in a vaccine trial then have a read of this post on the Barts MS blog and get in touch with them via the blog. - https://multiple-sclerosis-research.org/2020/06/mscovid19-covax-or-coronavirus-ocrelizumab-vaccination-study...

I signed a contract for conducting clinical trials of the drug. My relatives did not approve of my decision and each time they scared me with scary stories and the fact that I would be an experimental mouse🤷. In Ukraine, MS treatment is very expensive, and I think that for me this is a chance to ge...

I've been waiting for PPMS therapy for a long, long time so... maybe 3 or 4 more yrs or so?: https://multiplesclerosisnewstoday.com/news-posts/2020/05/29/cell-therapy-ata188-safe-with-sustained-lessening-in-disability-trial-reports/?utm_source=Multiple+Sclerosis&utm_campaign=c80384abac-RSS_NON-U...