2021 St. Louis Walk & Roll to Cure FSHD

2021 St. Louis Walk & Roll to Cure FSHD supporting FSHD Society
FSHD Society

About 2021 St. Louis Walk & Roll to Cure FSHD

SATURDAY, SEPTEMBER 18, 2021

Boulevard Park
2550 Lake Saint Louis Boulevard

Check in 9:00am  |  Walk Starts at 10:00am



The St. Louis Chapter of the FSHD Society will be participating in the International Walk & Roll to Cure FSHD - the only event focused solely on funding progress for FSH Muscular Dystrophy.

Every step matters. That is why we must continue to look to the future. 

Register for free 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!

On event day, you can join us for our "Everyone is a VIP" breakfast where we will celebrate together all we are doing to put an end to FSHD.

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

Date

Starts at:  September 18, 2021 9:00 AM
Ends at:  September 18, 2021 12:00 PM

Location

Boulevard Park
2550 Lake Saint Louis Boulevard
Lake Saint Louis,MO 63367 USA

Contact

Marsha Sverdrup
StLouisChapter@fshdsociety.org

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!