We're a global charity of 60,000+ MSers, so you’re not in this alone. Find connection, access 1:1 support and get advice from the people who understand what having MS is really like.
Don’t wait until your next appointment to ask questions. Get proactive by searching topics that matter to you and watch, read or listen to our growing collection of MSer Stories.
Getting diagnosed, symptoms, treatments, lifestyle adaptations and everything in between. Learn how other MSers dealt with their diagnosis and are managing their MS everyday.
Got a pressing question? Ask the Shift.ms community in the live feed, have private conversations and feel secure knowing that support is just one tap away. Share your own experience to support other community members.
Multiple sclerosis is unpredictable, we get it. With MS community insights, short-form video and stories written by real MSers, there’s plenty of ways to learn about living well with MS.
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 more about the Buddy Network >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.
Read our impact report >