Hello all, I'm brand new to this group. I am hoping to just find support to help me navigate this lovely terrible disease.

Hey all, I have become more and more frustrated with loved ones in the family who seem to forget I have MS and how things have changed so much with it too. My memory has got worse and worse and I have to repeat myself as never sure if have already sparked up a topic or conversation but then get shot...

I was recently diagnosed. I haven’t started any kind of treatment yet. We’re having an appointment on the 12th to discuss that right now. I feel extreme fatigued body having a body aches and exhausted. I just don’t feel good. I don’t wanna get out of bed. I don’t wanna move. I don’t want people to ...

So how do you give yourself a break mentally? Some context, i no longer work due to my MS like alot of people on here but everyone around me is working and getting on with life, no they dont have MS but they have their own issues, everybody does, but I can't help but compare myself to everyone and ...

Happy Sunday!! I am struggling with the fatigue on a daily basis and its drying me insane!! I understand you need to rest, listen to your body which i am doing but it feels like my fatique is getting worse daily. How do people handle it? 😞

Does anyone have this experience. Because I am currently going through it and it is Plegridy side effects x100!