As anyone on this group got MS after the covid vaccine,

I think the most surprising thing about having MS is when you are told after many MRIs. Is that you have no new lesions, but you are experiencing new difficulties or pain in other areas.

Hi guys I am new here, I was diagnosed with MS almost two years ago and life changed. I would love to meet people who understand what I am going through so I don't feel so alone.

What type of scan does the dr do to check for lesions on your spin?

Hi, I got told by Neurologist yesterday I have MS. I’m feeling a bit lost and confused and worried about how different my life will look now I have this condition. I’d be grateful to know if there are any things people wish they knew when they were first diagnosed that may help? I’ve just finish...

Hi, A question specifically for teachers in England. What things have work put in place to support you? Did you feel the need to get your union involved or were work supportive? Also what do you do when having a relapse? Work as normal on a full timetable or reduced hours?

Power yoga with weights this morning then later Pilates Followed by swim and jacuzzi 😁🧡

Hi, I’m a teacher in England. Diagnosed in September, awaiting to start treatment. I had optic neuritis last year and recently I’ve noticed a small patch of my eyesight blurring. I got in touch with the MS Team at the hospital, they said this is likely a relapse triggered by stress or other things, ...

I stop drinking by 4 pm go to sleep by 10, wakes up every 2 hours sometimes every hour to go. Anybody else experience this?