I’d just like to say that I’m in the process of changing my neurologist as he is no help at all and isn’t able to put into action what he actually says when we meet so this app is my best source of information and advice. I just want to thank the creators of the app and everyone of you out there. Yo...

Might be my family situation!! Or my Ms 🤔 Feels like I can’t smile anymore ☹️unless I want tobe 😁in my own time. Just feeling miserable feel very annoying and lonely at times Hope I’m not the only one? Ms might doing this to us? 🤔

Hi everyone, hope everyone is doing well enough. It's been a while since my last post here 😅. Does anyone is having issues with Support on Hand for Kesimpta? They had a major update as the customer support told me ...and ever since then I cannot synchronise my phone with the app. I've been trying ...

Hello! I was diagnosed with RRMS in 2021 (right leg weakness, numbness in both legs and lhermittes sign). Currently on glatopa and I'm dairy free. ( Also 4 months postpartum with my second daughter) I've been very fortunate and have had extremely minimal symptoms since my initial diagnosis. However...

So I've been using a trekking pole for about 6 months. I probably should've been using one a lot longer, at least a year. I'm curious if anyone has been reliant on a walking aid for at least 6 months and was able to recover enough to not need one? If so what helped the most?

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’m getting my first delivery of kesimpta today and I AM NERVOUS AF!! Worrying about side effects, infection risk, and just being ill overall.. I’ve been on a natural supplement and lifestyle/diet change. Same 3 lesions on my brain for almost 2 years. Just wrecking my brain with injecting myself a...