Hiya, I am newly diagnosed with RRMS and I just have some questions about the medication options. I have opted for the self injectable ofatumamab (I think that’s how it’s spelled) as I know I will not deal well with being on a drip every 6 months due to fear with intravenous experiences I’ve had ...

Not sure if this is a MS symptom but I get watery eyes that blur my vision. Does this happen to anyone?

What age did you get diagnosed with MS. I was 30 and you?

Hi all 👋 Bit of a pathetic post, I'm sorry, but I need this. Would anyone be willing to be a friend? Since my symptoms really started getting bad around 18m ago, my mood has just been getting worse and worse and now I just don't know what to do. I have a husband, I have my daughter. They are wonder...

I find that I need to tell my wife and others what I am feeling when I say I have MS. I try to tell them that I feel like pins and needles on my legs and arms. I explain that it is like walking on balloons. I tell them that when I lower my chin to my chest I feel like elastic buzzing in my body. D...

Does anyone feel like your #Diagnosis is not real?? LOL I have been “Living” with MS for 3 going on 4 years but, even still sometimes I feel like this is not my Reality. 🙃🫤😅👸🏽

Has anyone tried going to an MS support group? If so, what were your thoughts on it?

Every new day is a quiet reminder that strength doesn’t always look loud or dramatic. Sometimes, it looks like getting out of bed when your body feels heavy. Sometimes, it’s choosing hope when yesterday was hard. And sometimes, it’s simply breathing through the moment and saying, “I’m still here.

Hi after seeing a new neurologist today who wondered why i was not on any treatment hes reccomending i start mavenclad. Im happy with decision but also kinda nervous as i dont take much medicines in life. I know everyone is different, i was wondering if anyone has any positives to share about taking...