I got out of bed this morning at free-fall speed. Unfortunately, my legs hadn’t received the same instructions. I hit the floor like a bowling ball dropped into a lake, then walked to the bathroom like a newborn giraffe discovering gravity. I immediately knew I’d fucked up. Apparently, I’ve now g...

I had bad reaction to broumvi and its been awful since. I had it on 3rd of sept. Ive been gp, ive been a&e, contacted ms team multiple times. And here i am crying at home cause i cant take feeling this ill. I dont know what i need to do to get some help. Its so hard to cope with. I get take paraceta...

Is anyone in recovery who also has ms? I really need to talk to someone who gets it. Iykyk

I lived across three states Missouri Arkansas and Illinois when I was younger and I hate Having to be sick to the extent I can’t even get out of bed. They should be out there like me when I was younger not deliberately buying their properties as close as possible to mine is simply because they are w...

I’ve been having this weird issue with my sense of smell. Anytime I’m around a strong smell, like coffee or cooking, it seems to trigger this cigarette/smoky smell in my nose that I get stuck with for the rest of the day. Most of the time it doesn’t go away until the next day, and sometimes it can ...

Sitting at home all day gets old and exhausting and now I’m bored out of my mind. If it weren’t for MS I could be riding my ATV but my right hand is totally ruined from Rheumatoid Arthritis and I am right handed so I really miss riding bikes and four wheelers

I don't know who needs to hear this but the National MS Society in the US is absolute garbage! If I could share pics, I'd show the proof !! Over two years ago I was banned from the NMSS Facebook group over RELIGION*! When I talked to the group administrator, he spoke to me very disrespectfully, ref...

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

How does everyone deal with loneliness/unsupportive or emotionally absent partners? I’ve lost all my friends because of my diagnosis, I have no time to make new ones because every single day I have some kind of doctors appointment usually multiple. And I have no energy, when I need help with things ...