I’m looking for advice on applying for SSDI. Long story, starting from 2006. They said I had MS by a spinal tap, after a third opinion… I was given the diagnosis of CIS. Years later, in 2022 I got the full diagnosis. Because of the years that has past, now I have PPMS, on a slow decline. I’m pushi...

Just got contacted by someone on here trying to basically use this app as a dating site. When I asked him if he had MS he said no then asked for my snap after that I blocked him.

I decided to write down some of my thoughts about living with MS. It turns out I had loads to say. It turned into a book. I published it today! I just wanted to gush. I’m sure you understand lol 😎✊👨‍🦽

People spend half their lives wishing they had a rewind button. If you could press play on a director's cut of your own past, would you actually change your worst mistakes, or are those the exact scars that made you who you are today? Let's hear it.

I always thought light weight trainers is best but was recently told a firm sole with them being ankle . What are peoples thoughts and findings?

I live in Maryland and recently they canceled my insurance I have been without my meds now for months. I need help

Has anyone swapped from Ocrevus to Kesimpta?

I been diagnosed with MS for 6 years and I thought I had passed my period of grief. But I was wrong. I attendee a party yesterday and I wore a dress and some low heels boots I love dancing and back in my good days I did it a lot so I thought why not try to at least. I did and I had fun. Then I start...

Honestly I did not think that I could be anemic I didn’t even know it was common with ms? What are some ways to handle it apart from vitamins of course