I’ve been diagnosed with MS for 3 years now and on days when my pain is constant what really helps me is the Voltaren gel.

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

Hi I hesitated before writing about this issue For private reasons But since a year now or so I can’t climb the stairs to second floor in my house I can go up and down stairs anywhere else but not my house Stair is built by marble I’m not sure does it scare me am I anxious or is it an ms thing Last...

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...

I got diagnosed with MS a couple of months ago and my neurologist was quick to recommend DMT infusions of Rituximab. I’m wondering what questions I should be asking my dr. about this?

My sofa is my gym on Tuesdays. Some Days, the walk from bed to the couch is the “workout.” And that’s okay. But keeping your ankles and spine moving is what keeps you independent in the long run. My bundle gives you 3 movements for the days you can’t move much at all. No gym, no gear, just you and a...

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

After nearly Two weeks of numbness in right side face & lip roof mouth numb .no steroids given because they thought they would wait&See also i didn't tolerate the steroids last year.!! Its soo frustrating just wish I could feel my face again. Diagnosed year ago want on a DMT soo badly tried...

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...

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