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Hi there, I'm testing the new swanky site on the hottest day ever in the UK. Fans are blowing to no avail. I think i fancy trying out the old hashtagging.. #toohot and @ting ... @maxllar

Hi I’m Christine This is my first post . Now I have PPMS . This has been a whirlwind of so many ups and downs . I was DX in 2003 with RRMS. Mine really started going down hill 5 years ago. I have been having so much pain in my shoulders and legs. My left foot and ankle swell really bad if I walk to...

Hi all, I am 22 and was diagnosed with rrms in July after an attack in May. I’ve just started a dmd. Still have some symptoms - fatigue, feeling faint and I overheat quickly. My managers know, but they just don’t get it. My job is so fast-paced and they still think I can do anything and everything...

I want to know where in this site do I get an answer if I have a question. I am new to this site and I am not sure how it works. I see there is some dialog between members but I don't see where I can get the answer to my question in my previous post.

Hey all, Hope everyone is doing we. I am hanging in there here. a bit run down today. Has been a busy few months and more recently in the last few weeks has gotten insane. Mostly all good things though so there is that at least. Firstly an up date on things with my son. Things are going so am...

Hi all. So, I know, a couple of weeks ago, I had an MDT DMT meeting, discussing my medication and recent relapses and new lesions. Still not received a letter from them, but I know that it can take a couple of weeks. However, a nurse from my MS team called me today, telling me that they'll be booki...

Hi I’m new to this iv had Ms along time iv never got over the lack of understand if you look ok you must be ok very frustrating just wanted to get it out there

Living with an autoimmune disease makes scientific pieces like this more understandable . https://multiplesclerosisnewstoday.com/news-posts/2020/07/24/dual-role-discovered-for-molecule-involved-in-autoimmune-eye-disease