Yes it's lovely outside BUT not for a person who's already dragging his self and feeling extra fatigued 🥵

The way I believe is this the pharmaceutical industry are the richest people in the world so I try not to take as much medicine as they suggest or just things that they suggest. I just get an infusion every 6 months and I noticed that I don't get the same feeling that I have in the past from getting...

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

Anyone have relatives with MS? Do you find it comforting? Or daunting? Do you find yourself or others comparing you?

I am not sure whether to have the flu vaccine or not. I am in Australia. Winter is coming the last time I had the flu vaccine. My MS symptoms flared up and was very difficult for me. I am in a wheelchair and secondary MS so not sure. I take medication Mayzent (ms) which has lowered my white blood ...

My vision is normally fine- I wear reading glasses that's it - but for the past while, if I walk too long or do too much my vision goes blurry. It's becoming the first sign I need to rest but it's a huge inconvenience - like I need to see!? I've had optic neuritis so I know it's not that as it's vas...

The humidity is making me feel dreadful. Can anyone suggest a quick fix?

Is anyone on this and how are you getting on with it? as I’m away to start.

Guys it’s helping me!! Normally if I’m moving about or doing some kind of physical work my legs and back would give in straight away as in within 40+ mins but I was doing something a few days ago and I was up on my feet for about 2-3 hours and didn’t struggle one bit so if anyone had problems with w...

This is so new to me. I was diagnosed in April 2026 after having optic neuritis. It was very scary and I thought the headache prior was just due to stressors of life. I am scheduled to start Ocrevus in the summer. I’m trying to keep a positive attitude, I exercise five days a week and walked 1-3 mil...