I was thinking about all the things I use to help manage MS and realised I’m basically being kept operational by Wi-Fi, batteries and my wife knowing all the passwords. I’ve got CCTV cameras around the house to help with memory and keep an eye on the kids. People think they’re for burglars. If a bur...

Just a question that's been on my mind 🤔 How do those of you with MS who live in hot countries manage your day to day life? Does the heat make your symptoms worse or have you found ways to adapt? Love to hear your experiences, routines and any tips that help you cope.

What careers are manageable and rewarding for people with MS?

My calves are chronically tight and painful. I have a stretching strap, Biofreeze, and just bought night orthotics. I also have a TENS unit and ice pack. They still hurt. I take meds and magnesium to help with spasms. Anyone have any recommendations for relief?

My neurologist said I need to take vitamin d tablets alongside my treatment, do you take vitamin d tablets and if so which ones 😊

I have been a little depressed lately. I was in and out of the hospital for a month now. I walk like I am drunk 😜and I really don’t want to be around anyone at the moment. It is July 4 and all I want to do is stay in my bed and rest. My back hurts from top of my spine to my left leg.

Has anyone had really bad dermatitis/ eczema after the first 2 cycles of Mavenclad? If so, what helped. Currently struggling with severe dermatitis/ eczema and nothing seems to be helping. Have gone to the dermatologist and all I was given steroid creams. Doesn’t seem to much help.

Just looking to talk to someone who can understand what I’m going through. My family and friends they don’t listen. They brush it off so I need to talk to someone just as friends someone who can understand what I’m going through and I can be there for someone who might need an ear to listen.

Mines, teaching my self to play the keyboard, Diamond painting, exercising, watching my favourite movies tv shows , listening to music, gaming.