2021 New England Walk & Roll to Cure FSHD supporting FSHD Society
FSHD Society

About 2021 New England Walk & Roll to Cure FSHD

The 2021 New England Walk & Roll to Cure FSHD

Saturday, SEPTEMBER 18, 2021


Though our date is set, we are still figuring out the best ways to connect our community this year. Stay tuned for more information about where and when we might be able to gather and celebrate our progress together. 
Ideas are welcome! Please contact us here with any suggestions. In the meantime: 

Register 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!

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



Date

Starts at:  September 1, 2021 7:00 AM
Ends at:  September 18, 2021 11:00 AM

Location

Your Yard or Neighborhood
Your Favorite Park or Trail
, USA

Contact

Lexi Pappas
alexipappas19@gmail.com

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!