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

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 😎✊👨‍🦽

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...

Hello hope everyones doing ok. anyone had an over the phone pip assessment i have one today and have no clue what to expect

It seems that these conversations are between young people who have children, jobs, and many other priorities than a retired 60-something has while managing MS. CAN WE OLDER FOLK CONNECT?

How do you cope?

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?

Good morning I'm up did my normal now I'm eating breakfast. I can't feel my hands or my legs or my feet. I've started a new MS infusion, I've only had one infusion so far my next one is next week so I hope the medicine will start to work because after my next infusion I would get my infusion every 6...

I’ve been on Ocrevus for three years ( 5 infusions) one coming up in December This time feels different weak legs , weak arms , numb feet & hands. Eyes unfocused , Constantly falling and tripping over own feet and exhaustion!!!!my mris came back and dr say leasons appear stable hmmmmm why do I feel ...

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...