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Hi all, first time on this site or any forum for that matter. Hope to make freinds and talk to others about ms, the roller coaster ride to diagnosis, and what happens next. Its taken me five years to get diagnosed and treated and ive been knocked back more times than I can remember. hope I can now...

...of how all the different MS drugs work. - https://youtu.be/Dr_2F-quv7Y

What do we know about MS and menopause? How do symptoms change, Is there an increased risks of getting a relapse? How do the disability level change? Thanks ladies and sorry gents.

Please let me start off by saying I'm not whining or being ungrateful...my current neurologist has been very efficient in organising scans and treatment over the years. But...I am wondering if I can change my neurologist. When I saw him about a year ago he encouraged me to get back with my ex husban...

You may have seen that Mike, Gemma and Zoe have been working through some ideas about building mental resilience with Neuropsychologist Jo Johnson… here’s the playlist in case you’ve missed the videos: https://www.youtube.com/playlist?list=PLm0sRroMtds267oPVxXSAR6bJEZ_Vr__f There are new episodes...

I was diagnosed with RRMS mid May 2020 at the age of 28. All rather shocking because the only symptom I've experienced is optic neuritis. It has been said that I need to start on Tecfidera next week. I'm feeling pretty anxious about this. More so because all my neurologist seems to say is 'No-one ha...

Hi all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...

Hi everyone, I have rrms. I have been getting this excruciating shooting pain in the side of my head, it usually only last a few seconds. The pain is so bad, you just have to sit and wait till it passes. The pain isn't on my face. I have had it for years but it would only be a couple of times a ...

Never meet a group of people that are not updated on new discoveries and cures.I posted a message here to help but it was removed because admin claimed i broke house rules..How am i suppose to help other patients in the community when i can not direct them where to get a cure???If you are still with...

Hi all Does anyone have additional illnesses like fibromyalgia? I have a lovely combination of illnesses and other conditions. I have had fibro and cfs since 2008/9. Has anyone managed to find the happy medium between rrms and fibro?