You personally know what comes with dating someone with the same disease you have .

I was just diagnosed 4 days ago. My neurologist has me on IV steroids for 5 days to start and then will start a medication and has tasked me with searching my options. I don't know what I'm reading 😁 Can anyone point me in the right direction - oral, infusion, injectable?

If been on injections since 2022 anyone else having kesimpta injections do use think its helping use ?

Hi just wondering if anyone suffers with sleeping i take things to help me go asleep but seem to wake up multiple times through the carnt remember the last time i had a decent sleep starting to affect me drained lol

Hey 👋 Welcome to the Shift.ms community! Drop a comment below and let us know where you're from 👇 Whether you've got MS questions, you're seeking advice, or you just want to chat to other MSers, we've got you covered 💚 Take a minute to hear Sarah's MS story and learn how she gets the most out ...

I have, but it doesn’t seem to help

Hi Everyone! 👋 My name's Heidi! I'm new to the app, but not to MS. I was diagnosed in 2013 with RRMS, have been on a few DMDs, made numerous connections and kinda faded into the shadows when COVID hit. I'm now back ready to make new friends and push forward on this continued "journey" that is the u...