2021 New England Walk & Roll to Cure FSHD supporting FSHD Society
FSHD Society

About 2021 New England Walk & Roll to Cure FSHD

The 2021 New England Walk & Roll to Cure FSHD Celebration Event

Saturday, SEPTEMBER 11, 2021

Join us for a Ballpark-themed lunch celebration on the Optum Rooftop in Boston!!

11:00am -2:00pm

REGISTER for the Walk & Roll HERE

Once you've registered for the Walk & Roll, we will send detailed information about the Walk Celebration on the Optum Rooftop!​ (You MUST REGISTER IN ADVANCE to gain access to the Rooftop!)

** The day will be filled with a luncheon catered by Tasty Burger, DJ'd by local radio personality Hank Morse, a silent auction, awards, and more! **

View and bid on Auction Items HERE.

** Tom Brady Autographed Football  ** 2 Tickets to a Patriots Game  ** 4 Tickets to the Revolution Game  **  4 Red Sox Tickets  **


Register today as a team or individual. 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!


Starts at:  September 11, 2021 10:00 AM
Ends at:  September 11, 2021 1:00 PM


Optum Building Rooftop
1325 Boylston Street
Boston,MA 02215 USA


Lexi Pappas

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!