The ms fight is one you just can’t win.

Hey I have been on several different ms medication and everyone of them just makes me worse or makes feel worse and makes me not being able to do alot in my life does anyone else experience this I'm on vurmity currently and it's making me feel worse more memory loss really bad hot flushes and itchy ...

Make today count! keep fighting you beautiful people and have a great week!

So many folks when seeing/talking to me ask “How are you doing?” They have witnessed my deterioration and know my health situation. I never know what to say and lately have been saying “I have good days and bad days.” What do you say?

Just wondered if anyone could share their experience of taking Cladribine? I’ve had RRMS for about 15 years with thankfully minor symptoms of numbness and fatigue with 4 relapses during this time , the last being this time last year. I’ve now been offered Cladribine which will the first drug I wil...

I think I did too much yesterday. My back is killing me and my fatigue levels are extremely high. Woops. 😁😁

As the title states my brother [29] was recently diagnosed with MS how can I best support him without overwhelming him? I want to give him space but also want to make sure he knows I am here in whatever capacity he needs