I’ve finally got an assessment over the phone next week and don’t know what to expect. Could anyone shed any light? How long will it take and what will they be asking? Bit nervous about it.

What would you do with your life if you stopped having MS?

Hi everyone, my name is Taylah and this is my first post on here. I’m not officially diagnosed with MS, but I’m currently undergoing testing after being diagnosed with optic neuritis in my left eye. It all started with a persistent headache and blurry vision in my left eye, which led to hospital a...

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