I have my face-to-face assessment tomorrow. This is my second attempt to get pip! I am so stressed...head is all over the place.

I am finding that as my mobility is not so good due to lead legs and fatigue my weight is creeping up, as my fitness is sliding down. Prior to MS I would usually put on 1/2 a stone in the winter and then lose it all in the spring. Unfortunately I now find it difficult to shed those gained pounds. I...

Kirstiewalls1 has changed her username! I am now Mintyrocksmaka. I thought it wise not to have my real name on here after all the replies to my post yesterday about men messaging and wanting to chat on other platforms. The Terry Pratchett fans among you will know the name from his fabulous Discworl...

I've recently had men ask to chat and I've accepted but then they pressure me into moving to WhatsApp, Signal or similar. These men don't have MS so not sure why they want to chat. One even deleted his profile when I made it clear I wasn't Interested in any relationships especially intimate ones. H...

Hi all. My lovely 15yr old was dx with RRMS 2yrs ago. She has gone from being an active, sociable “normal” teenager to spending most of her life trapped in bed. She missed 90% of school last year and is now in her final year with similar prospects. She is in debilitating pain all the time, and s...

Is it just me or do u feel funny telling new doctors that you have multiple sclerosis? I get the weirdest looks from primary doctors or dentist when I tell them that that's the reason I have a cane or that's why I'm not walking straight and take a bit longer to get to places.

Every month I get the reminder that I have this disease . It's on the day I self inject. I'll get other little reminders through out the month ... the fatigue, depression, and anxiety. But on the day of my dose , it's an extra hard reminder

This is one for the male MS sufferers, I've had MS for a long time now and am struggling with erection issues. Does any other male suffer from this? I am on a very high dose of Viagra but for the last year it rarely works and now it's starting to affect my long term relationship

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