Is MS a long term condition like Parkinson's? I had thought that it was until I saw a few comments recently on here where people said that their Neurologist had said that their MS had gone. Is it to much to hope that it clears up after say 10/15 years? Or is it that MS treats everyone differently?

Honestly I did not think that I could be anemic I didn’t even know it was common with ms? What are some ways to handle it apart from vitamins of course

Feels like I haven’t got Ms anymore 😁😅 as I’ve been really well with it for a long time now 😁. I’ve been keeping very active and fit and looking after myself. doing well with my 4th Ocrevus treatment too 😁😅👍🧡.

“Try turning yourself off and on again, but don't be surprised if it doesn't fix anything.” Humor is my favorite survival tool at this point. What's your go-to coping mechanism when things get frustrating? 🤭

I haven’t got my Menopause yet 😅 with my Ms! I’m age 40. How many people have it on here? And who hasn’t?

Currently in Crete visiting friends and the summer season is pretty much ober but the 'cannibis' shop i go to has closed early so been trawling every since I got here to find summit to help with the pain😏. Come across a small shop that do vapes an edibles but looked like they sold out but explained...

I got permanent bracelets and I have to remove them every time. Sometimes they told me that if it’s gold it’s fine but I don’t even know what kind of gold. Any experience with that?