Along with 60% of us MSers I’ve been having awful fatigue in the heatwaves we’ve had here in England. This is new to me, I was diagnosed almost 2 years ago and I’ve never suffered with fatigue pre diagnosis. My biggest issue when fatigue creeps in is sensory overload? I’ve zero tolerance to any ba...

I was on Kesimpta for about 9 months. It wasn’t working so my doctor switched me to Mavenclad a month ago. I am not sure if the things I’m experiencing are related to the medication or just my MS. I had some issues when I stopped the Kesimpta. My body was confused not having it. But now I feel the...

Lately whenever I try to do a “simple” task like cleaning the bathroom, or washing dishes I find myself getting frustrated because I can’t do it the way I used to be able to do it. I understand that my body is different now but what I’m trying to do is not get so in my head about it. what are som...

I've recently been changed from having Secondary Progressive MS to Relapsing Remitting. I've been offered 2 treatments (Ocrelizumab and Ofatumumab) Does anybody take either one? And what is your opinion of them?

Oh, good. Another man who can't handle that I've got MS.... Brilliant. 😎💪💃🙄

Do anyone of you find it hard being in large or small groups of friends? As I hardly chat to them 🙄😤😢. I do small talk or when I want to do a little chat 🤞😅. Most of them chat away and my mum does but I can’t do that!!!!! It’s our Ms isn’t? Hate finding things hard for me so frustrating!!! ...

Going on holiday soon and I haven’t been on one since I got diagnosed (2018). I’m going with family (not my partner who knows more about my day to day as I live with them). I want to know how to let family members know that I want to get a Rollator over using a wheelchair. I can still walk “fine” ma...

I know there’s been a few posts in the past regarding tiredness. But has anyone taken risk free or side effect free medication or supplements to tackle tiredness/fatigue? And how long it took for them to be more energetic.