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I have posted on here before about my son diagnosed with RRMS in 2014. He had lots of relapsing but no remitting. A couple of years ago it progressed to SPMS. Over the last year he got rapidly worse, couldn’t walk outside, furniture surfed around his house, regularly needed help to feed himself, fel...

Enjoy the day and make something you enjoy.

Hi everyone, Hope you're well. My name's Kelly and I work for Shift.ms on the Buddy Network. Are you newly diagnosed? Or just not sure where to turn? We can connect you with another MSer for free. The Buddy Network connects you with an experienced MSer, someone a bit further down their journey. G...

I tend to suddenly freeze with tremendous pain included! I always think it's just me but I'm sure someone comes close or closer to me 😔

Hi i just would like to know what everyone does in there free time i am a games and music host on TIKTOK what do you do and do you have tik tok?

My sofa is my gym on Tuesdays. Some Days, the walk from bed to the couch is the “workout.” And that’s okay. But keeping your ankles and spine moving is what keeps you independent in the long run. My bundle gives you 3 movements for the days you can’t move much at all. No gym, no gear, just you and a...

You can get a free cooling vest and I also got this neck wrap or headband. Just google MSAA and search cooling vest and fill out the application! I’m super pumped! People have said they get to go outside again! They give you backup ice packs as well! So when one melts you can just put new ones in!