2022 Arizona Walk & Roll to Cure FSHD

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

About 2022 Arizona Walk & Roll to Cure FSHD

2022 Arizona Walk & Roll to Cure FSHD

Saturday, September 17

Choose your walk site - either Tucson or Scottsdale:

Primary Walk & Roll Location hosted by the Arizona Chapter:  Gene C. Reid Park - Ramada #01, 100 S Country Club Rd, Tucson

-OR-

Join the Red Scooter Riders at their Neighborhood Pop-up Location: 20750 N 87th St Unit 1111, Scottsdale


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

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!

Date

Starts at:  September 17, 2022 10:00 AM
Ends at:  September 17, 2022 1:00 PM

Location

Gene C. Reid Park, Ramada #01, Tucson or 20750 N 87th St. Unit 1111, Scottsdale, AZ
,AZ USA

Contact

Ally Roets
ArizonaChapter@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!