2022 U.S. & International Virtual Walk & Roll to Cure FSHD

2022 U.S. & International Virtual Walk & Roll to Cure FSHD supporting FSHD Society
FSHD Society

About 2022 International Virtual Walk & Roll to Cure FSHD

​The Walk & Roll to Cure FSHD is the only international event focused solely on funding progress for FSHD. Led entirely by dedicated volunteers, supported by staff, events take place all over the US and Canada.​

JOIN US  to "walk or roll" today as a team or individual walker. Invite your family, friends, club members, neighbors, co-workers, classmates or congregation to join you. Everyone who registers will be given a free participant page and access to a state-of-the-art fundraising center. From there, you can share your story on social media and via email, and invite others to join you in getting us closer to a cure!

​Then, tune-in when our FSHD Radio podcast host, Tim Hollenback, holds a 4 hour, coast to coast, Walk & Roll celebration livestream on September 17th! Walkers and Rollers check in with us live from Florida, to Canada, to California - and all points in between. We celebrate teams and top fundraisers, share personal stories, and come together... one voice that is thousands strong, to say,  "FSHD does not get the final word; we will keep walking and rolling until a cure is found!"

We are working together to make a difference for those living with FSH Muscular Dystrophy!



Starts at:  September 17, 2022 7:00 AM
Ends at:  September 17, 2022 11:00 AM


Your Yard or Neighborhood
Your Favorite Park or Trail


FSHD Society

Why Participate?

FSHD affects nearly 1 million men, women and children worldwide, leaving them with the inability to walk, raise their arms, or simply smile. The FSHD Society is the largest network of patients, families, clinicians, researchers and friends - all advocating for FSHD. YOU are the driving force that enables the FSHD Society to support & empower families and to fund groundbreaking research to find treatments and a cure!

How Your Support Makes a Difference

Your support of the FSHD Society will be put to work right away, to push forward the most promising research, help empower patients and families to live stronger, healthier lives, and press the government and major institutions to give FSH muscular dystrophy (FSHD) the funding and attention it deserves. Your support ensures that no patient need ever face this disease alone, and pushes us towards our goal of delivering treatments to our families by the year 2025!

Thank You to our Generous Sponsors!