2022 Intermountain Walk & Roll to Cure FSHD

2022 Intermountain Walk & Roll to Cure FSHD supporting FSHD Society
FSHD Society

About 2022 Utah/Idaho Walk & Roll to Cure FSHD

The 2022 Intermountain Walk & Roll to Cure FSHD!

Saturday, September 17, 2022

Canyon Rim Park, Millcreek UT

                                                         Check-in & Pancake Breakfast: 8:30am

                                                                       Walk Starts: 9:45am

Click here for more: Event Information


The Utah Chapter and the Idaho Chapter of the FSHD Society will be combining and participating in the Walk & Roll to Cure FSHD - the only international event focused solely on funding progress for FSH Muscular Dystrophy. 

We will start our day with a pancake breakfast, and there will be a bounce house and games for the kids as well!

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! 

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


Date

Starts at:  September 17, 2022 9:30 AM
Ends at:  September 17, 2022 12:00 PM

Location

Canyon Rim Park
3100 South Grace Street
Millcreek,UT 84109 USA

Contact

Kathryn Pyne
UtahWnR@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!