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...

So, last night was a Friday- had the fattest migraine, couldn’t see, walk or talk. Today is a Saturday- just choked myself silly trying to drink water 🤦🏻‍♀️ Smashed all my toes separately during the week stubbing my feet on door frames. Choosing to find this funny and giggle 🙃 Anyone else find...

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

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...

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...

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!!! ...