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?

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...

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 ...

Feeling confident

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