2021 California Walk & Roll to Cure FSHD

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

About 2021 California Walk & Roll to Cure FSHD

The 2021 California Virtual Walk & Roll to Cure FSHD

Saturday, SEPTEMBER 18, 2021

The Bay Area, San Diego, Los Angeles, and Sacramento chapters
are coming together from across the state for one, amazing day
of walking & rolling to Cure FSHD!

Register 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!

This year you can Walk & Roll your way! We are planning a virtual walk and will join in on the Livestream Celebration with FSHD Radio, but we also have a few "pop up" celebrations across the state!

  • San Diego participants are invited to re:Connect and celebrate the Walk & Roll on September 14. Learn more and RSVP!
  • Bay Area participants are invited to a Walk & Roll day celebration luncheon in Santa Cruz - details emailed to all registrants in the area.
  • Los Angeles participants are invited to celebrate with us at the LA FSHD 360 at UCLA on September 25.
  • And everyone is invited to join the livestream on the 18th on Facebook@FSHDSociety.org!

HUGE THANK YOU  to the two amazing and generous anonymous donors who funded our matching grant challenge! All matching funds have been claimed, but you can still make a huge difference with your fundraising!

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


Starts at:  September 18, 2021 10:00 AM
Ends at:  September 18, 2021 2:00 PM


Your Yard or Neighborhood
Your Favorite Park or Trail


Amy Bekier or Sue & Kent Drescher

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!