Does anyone else feel like people (friends) want to talk to you when it suits them like your a convenience to them ever since you got MS?

I have Multiple sclerosis and learning disability needs too 😢😤 Find that frustrating!!!! What other illness have you got with your Ms if any has?

Do you think stress makes your MS symptoms worse?

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 ...

About to have 1st infusion

It’s been a while since I’ve been here. I got my first MRI results since being on Kesimpta for 5 months. Good things, no new lesions and the inflammation seems smaller. But I didn’t leave feeling better. I feel foggy, forgetting words in the middle of sentences. Trying to figure out what will make i...