Almost 15 years ago, Shift.ms was founded because of a lack in vital social and emotional support for MSers. Today, we're still trying to make the best community for you. Fill out our poll to let us know whether Shift.ms has helped you ⬇️ PS. Click the link to fill out our annual impact survey an...

So, I just discovered this word, ALLODYNIA. I believe "cold allodynia" is exactly what I'm feeling. It started very slowly and subtly around 10 years ago. Now, I can barely stand to go in the grocery store. Just the slightest exposure to cool air sends my whole surface area into painful icy cold bur...

We’ve just launched Shift.ms polls! Take part in the first poll below👇 *Bonus points if you can leave a comment and let me know: are you happy with how long it took?

I have my 2 hours routine MRI tomorrow! Any tips??

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 ...

According to the NHS app, I was 'seen at a neurology clinic' on 11th April, which is interesting, given that I had my MRI in the emergency dept (not neurology) on 3rd April (not 11th) and haven't been back since. After my first MRI, the letter arrived in the app on 23rd Jan, saying the doc had signe...

Hello fellow MSers, I have had a problem with ED for quite some time and I've been too afraid o admit it. It is SO frustrating and very degrading! So I am wondering if anyone could help me in what I could do? Thank you:-)

Finally, old enough to do anything I want, too tired to do any of it.

I’m literally 2 days from getting my infusion and I feel crappy feel like this last month I could feel the medicine wearing off then in the last two weeks I could feel symptoms coming back then this last week I was so tired, irritable, the works. I’m not going to lie while on infusion medicine I rea...

As World MS day approaches (30th May) we ask ourselves why have a World MS Day? The answer is simple it’s there to raise funds and awareness, for and of MS. Raising funds Raising funds is important as without funds, research can’t happen. Without research a cure will never be found and a cure is w...