So this is an offload really but thought I’d share and if anyone has similar experiences insured or not. Before I was diagnosed I was in the process of applying for life insurance and critical illness cover. It felt the right time as I have a mortgage and at the time a son on route to the world. ...

Still new so bare with me. I’ve been light headed and dizzy for a few days now and my left side has been sore with flashes non stop of nerve pain. Work today is rough

So, I have never taken any medication for relapsing MS. After nearly 20 years after being diagnosed, I have been prescribed amantadine. Am not decided and after reading about the possible side effects I am a bit reluctant. Does anyone take it and do the benefits outweigh any possible side effects?

I just got my MRI results. No new lesions!!! Sorry had to share. 🧡

Hi everyone, Is anyone else’s balance (or general symptoms) worsening this spring? I spend most of my time in temperature controlled environments (thank goodness) but my body is exhausted and going through the motions. The weather has been all over the place so I’ve been thinking it’s that, but if t...

Loading doses complete. Now I feel like I have the flu 🤧.. have a great day!

In the UK. Not ready for this heatwave coming next week. I’m already getting frustrated with todays heat, 24c.

How is everyone coping (in the uk) with this heatwave at the min? What's the best tips and tricks to stay cool

Has anyone tried cooling vests? Any idea where to get them from? Do they work?