“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

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...

Today I took my Wife and 3 of my kids to Kenny Wood and I ate like a king all the bad things I use to eat I went in and i feel no guilt I feel worse when I don't live my life I refuse too let my illness keep me in a cage so I'll just pray and live 🙏🏿✌🏾

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

Had anyone used this biofeedback device to help with their foot drop?

Does anyone else have a burning numb arm and wrist, and know of anything to help?