What you guys do for this

Laila El Ashrafi is an individual residing in the Leicester area, known locally for openly navigating and advocating for those dealing with Multiple Sclerosis (MS). f Facebook • Multiple... +2 She is a prominent, active member in UK-based MS support and awareness networks, where she regularly shares...

Holidays don’t agree with me, every time I get a UTI, insomnia , oral thrush, dehydration and they think I’m going mad. Somedays I feel life with MS is going to make me mad. First time hospitalised for 8 days and they was trying to say mania, next holiday the same but I now know the signs so I calle...

I’m a lil upset as I just wrote a funny, meaningful post but there was an error :( I personally think it was the language I used. Anywho take 2 So I’m 37 female whose V has died. My OT says it’s my battery level and fatigue that’s causing me to feel this way. I want my sexy time back, life is grey...

How do I live without any income? I'm waiting to see if my disability goes through

Looking for people’s experiences with Kesimpta - I think my neuro wants me to go on this but I’m not keen following anaphylaxis with other self injectables. Hoping hearing good stories will help win me round

I got newly diagnosed (4 months ago) with rrms and had optic neuritis idk how to adapt and accept this new version of me it’s so hard on me. I’m pretty young and I get surprised glances from doctors and nurses who are shocked to see someone my age with ms. I’ve been dealing with unbearable headaches...

So I had a rant, yes I feel slightly better. Left without medication again so still not slept and it’s currently 4.35am 🤷🏽‍♀️Ms team I’ve been to you numerous times crying out for help. You’ve never helped. I tried to take my own life as I’m really struggling, crisis team reached out to you as the...

Has it really been 6 months? Ok, more like 7 month now. Hoping for another quick session with no issues.