Learn how Walk MS brings us together to rally for those affected by MS and take a step toward a world free of this disease.
How to Participate
Stay Tuned - More 2022 Walk MS sites coming soon! Sign up here to be the first to know when your event launches.
Can’t find a Walk MS event location that’s convenient for you? No problem! Register as a virtual participant for a Society-hosted event or sign up for Walk MS: Your Way to create your own day-of event experience – anywhere, anytime.
Antonia, diagnosed in 2017
I was a 27-year-old, very active equestrian when an emergency room visit changed my life – an MRI revealed I had multiple sclerosis. MS has taught me that you don’t know what someone is going through.
Pathways to Cures
The National MS Society paved the way for all MS treatment options that exist today and has funded over $1.1 billion in research since 1946.
Eric, diagnosed in 2003
The Walk is the culmination of months of effort by my family and friends to raise money to find a cure. And I think it really educates people on what this disease is, and what it does to people's lives.
Funds raised through Walk MS support programs and services – like Ask an MS Navigator – so that we can build a network to help people affected by MS live less isolated, more informed and happier lives.
Jennifer, diagnosed in 1999
I initially started doing the Walk because I was looking for community. My family and friends have been a huge support for me – I felt the need to kind of expand that support and be part of a community who had been affected in the way that I have been.
Pathways to Cures
“The National MS Society relentlessly pursues every pathway to every cure until we have stopped MS in its tracks, restored what has been lost and ultimately – have ended this disease forever.”