Is anyone else struggling to adjust (or did struggle) to their diagnosis? I was diagnosed with RRMS back in March of this year and I’m feeling low about it all, especially now I’m having to start to use a stick and my right leg is getting worse. I’m having to think of things like grab rails around...

Has anyone felt extremely lonely or isolated and lost a lot in different ways since being diagnosed? How do you navigate this please?

I originally joined this community to ask for advice as I was about to get my second ever MRI (first one gave me the diagnosis) 2 years later. Got scared, already have my results and fortunately there are no new lesions! So I guess I’m now sharing my happy news 😁. Would anyone want to connect? Here...

I've been on Kesimpta for 8 or so months and really struggled with feeling 'hungover' and fatigued on and off since the big crash of the loading doses. My nurse has agreed I need to change and has asked me to consider Briumvi, Ocrevus or Mavenclad while she chats to my neuro. If anyone has any exper...

Hi everyone last time I was on here things are going not very good and as of recently I’ve been registered as bed bound for the foreseeable future

I probably be wrong 😑 but just checking it might be me!!!!! I know Ms is different for all people ☺️. Probably sound stupid!!! But does Ms make you a horrible person? As I feel like I have a horrible Ms person in me!!!! 🙄 that’s why I’m like 🤐with my Ms dad!!!!!

Anyone Like To Make Friends

Hi guys! Please don’t judge but I’ve only found that drinking Monsters beats MS fatigue while at work. I know energy drinks are horrible for your heart so I was wondering what else I could drink or take to beat the fatigue on work days. Thank you for your insights and tips xxx