We’re a global charity that supports recently diagnosed people as they make sense of MS. We’re independent and our app is free.
Connect with other MSers, get 1:1 support and thrive with a community that gets what you’re going through.
Don’t wait until your next appointment to ask questions. Learn how other MSers deal with their diagnosis and are managing their MS.
Learn about multiple sclerosis and talk openly with other MSers about your experiences. Whether you want to know more about diagnosis, symptoms, treatments, lifestyle adaptations, or anything else MS, you’ve come to the right place.
I would recommend [the app] to anyone newly diagnosed with MS. All the information about your MS is right there.
It's a community without having to leave your house. Everything we need is there, with information for a plethora of questions. Plus, it's private and accessible right on your phone.
Sometimes other [MSers] describe symptoms so similar to me that I have been unable to describe to anyone else. Sometimes I am the person that can help someone else... or at least listen.
Multiple sclerosis is unpredictable, we get it. Ask the Shift.ms community anything in the live feed, have private conversations, see how other MSers are making decisions through community insights, or lose yourself in our video library.
The Buddy Network connects you with an experienced MSer. Get emotional support, tailored advice, and coaching to make proactive decisions right from the point of diagnosis (and make some really good friends along the way).
Learn about the Buddy Network >Our members are the heart of everything we do. From liking a post, to making video content, to fundraising for us, members keep Shift.ms a supportive and inclusive community.
We’re not a regular social network. We’re a small team, overseen by a board of trustees and we don’t have any investors or advertising partners. Our community is the driving-force behind Shift.ms.
Learn about our work >
MS begins with symptoms. Read up on common (and not so common) MS symptoms
So you’ve been (or might be) diagnosed with MS? What to do next and where to go for support
MS is highly treatable for many people. Know your options to manage symptoms and slow progression
MS is different for everyone. This is what you need to know for life after diagnosis
