2021 Columbus Walk & Roll to Cure FSHD

2021 Columbus Walk & Roll to Cure FSHD supporting FSHD Society
FSHD Society

About 2021 Columbus Walk & Roll to Cure FSHD

The 2021 Columbus Walk & Roll to Cure FSHD has gone HYBRID!

Join us online throughout the season, and back at the Coffman Park Pavilion in Dublin, OH on September 11, 2021!

​The Columbus Chapter of the FSHD Society will be participating virtually in the National Walk & Roll to Cure FSHD -  the only national event focused solely on funding progress for FSH Muscular Dystrophy. We will also celebrate our progress by coming together as a Chapter in September, as restrictions allow.

Our world has been highly impacted by the corona virus pandemic, yet our commitment to our families remains the same. Every step matters. That is why we must continue to look to the future. 

Register today, fundraise for the cause, and then join us if you're able in September. 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!

Event participants have a chance to WIN a 4-night RV rental from Road Adventures!! See our Prize Page to learn more! 


Starts at:  September 11, 2021 8:00 AM
Ends at:  September 11, 2021 10:30 AM


Coffman Park Pavilion
5200 Emerald Parkway
Dublin,OH 43017 USA


Susan Aumiller

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!