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...

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

The steroids make me stronger how about you and I know I ask before how others cope?

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...

“Try turning yourself off and on again, but don't be surprised if it doesn't fix anything.” Humor is my favorite survival tool at this point. What's your go-to coping mechanism when things get frustrating? 🤭

Feels like I haven’t got Ms anymore 😁😅 as I’ve been really well with it for a long time now 😁. I’ve been keeping very active and fit and looking after myself. doing well with my 4th Ocrevus treatment too 😁😅👍🧡.

I have a telephone assessment coming up. I'm a bit nervous about it after reading some stories. Any tips? Also, it says in my letter that I can request at the start for it to be recorded and they will send a link at the end. Is it worth asking for this?

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