Looking for
something specific?

What VitD are you all taking ie what Strength?

Hi I’m Sarah 42 RRMS been on kesimpta just over a year I’m from the uk 🇬🇧 stockport (Manchester)

Don’t really know what to say or where to start really! I got diagnosed June this year I’m still coming to terms with it I think! I have managed to go back to work full time, but I am realising just how hard it is but I can’t find the words to explain why! I work in a school. And I’m feeling at the ...

Hi everyone my name's Amy and even though I have had MS since July 2000 this is my first time in a support group.

Hi everyone, just joined, am keen to meet others of a like mind in my area which is Derby. I’m very sociable & am wanting to expand my ‘ms world’ as I call it .. Who’s out there ? It would be great to be able to make new friends & meet up socially rather than just on line.. Louise 😃

Just wanted to know if anyone else gets anxiety with depression? I'm really feel like I'm going crazy my husband who works in the medical profession says it's nothing to do with my MS that's all in my head and snap out of it.

Hi

I was diagnosed in 2008, I'm so tired of being tired. I miss working. I'm 43 years. I had hopes and dreams. But that went away. Can anyone offer words of hope. There are days I feel like God has forgotten me. I have talked people out suicide, mentored others. But helping myself. Friends say I miss c...

I just wanted to say hello and introduce myself after recently joining the site. I have RRMS and am currently not on any medication not sure if this is the right path? I was mis diagnosed 10 years ago after s bout of optic neuritis then in 2011 suffered uveitis in both eyes and various tests confirm...

I'm new here so just wanted to say hello to everyone. Diagnosed January this year after having pins and needles in my legs early last year and my eyesight getting worse but that was thought to just be because of my overactive thyroid. From August last year my eyesight got very bad (now I know it w...