Hey, so just wondering how people cope with their pain. I have day too day pain in my legs, which some days is worse than others. I have pain relief for this but wondered if anyone had any other advice. I have relapsing remitting MS. Thanks ❤

Hi John ….you ok ? Tessa x

Hi everyone. Hope you’re all well. This is my first post and I hope it is shared in strict confidence. I am going to skip the details of diagnosis and move onto the biggest challenge I have faced since being diagnosed with MS. I would be so grateful of your opinions. I was diagnosed with M…

Hi everyone Just joined and new to these groups. I have relapsing remitting since 1997. Moved back to the east coast and noticed a change from living on the west coast. I have alot more symptoms and pains than i did. Not liking this change but will deal with it.

Do you think that interferon is effective DMT?

I am really interested in all the comments on Amantadine, mainly because I’ve got a box sitting in front of me but my GP prescribed it to be taken between 4-6pm and everything I’ve read says not after 2pm to prevent insomnia. My neurologist wrote to my GP to tell them to prescribe it, but I fee…

I just want to hear people’s stories, if there are any, about any experience with this virus and the possibility of it contributing to the cause of ms. I had Glandular fever at 16, and ten years later, DX with MS. Has anyone else experienced this or similar?

Hello everytime I go up or downstairs I go side way to hold the fense and never leave it untill I reach I sometime wonder should I go up running ir down of course down impossible and put my life on the top of my wing lol Im so imbalanced not sure if its 100% because of MS balance depends on severa…

https://www.mstrust.org.uk/a-z/evening-primrose-oil-epo

New to the group and hoping to learn from everyone else as well as my own experience.. ✌🏻❣