The Muscular Dystrophy Association (MDA) today announced that the 35th Annual Trans New Hampshire Bike Ride (TNHBR) held on June 25, starting and ending at the Portsmouth Senior Center in Portsmouth, New Hampshire, raised over $98,000 for the organization’s mission, with funds still cycling in. The event featured over 40 in-person riders as well as . . .
Thursday night, June 2, 2022, individuals from the Muscular Dystrophy Association (MDA), along with local volunteers, MDA families and MDA partners descended on Hotel ZaZa in Memorial City, Houston, Texas for what was truly a magical night. The evening consisted of a never-ending photo-op station, lots of conversation and reconnecting with friends, food AND the . . .
Eight years ago, if you were looking for Billy Zureikat you would find him on the basketball court. The 38-year-old, former ESPN producer and current logistics manager’s passion was on the court. That all changed when years of symptoms and eventually a diagnosis in 2021 of limb girdle muscular dystrophy (LGMD) began to impact his . . .
The relationships we at MDA form with our community is one of the most rewarding parts of our mission. One such relationship is our friendship with Jon Burcaw and his son Shane. As a long-time supporter of Schaeffer’s Harley-Davidson – a member of the Eastern Harley-Davidson Dealership Association (EHDDA) – Jon became a supporter of . . .
MDA’s Ambassadors are pivotal to our mission: empowering people living with muscular dystrophy, ALS, and related neuromuscular diseases to achieve their potential. We do that through care, research, and advocacy. Because the mission is big, we need big partners who can help evangelize what MDA is, what we do, and, most importantly, who we do it for. Enter, . . .
2021 was another challenging year for many, but once again, MDA’s grassroots advocates were relentless in ensuring lawmakers heard their voices. Throughout the year, our volunteers emailed, called, and met with important decision-makers urging them to act on vital public policy that will improve the lives of people living with neuromuscular disease and their families. . . .
Volunteers are a rich part of MDA’s 70-year history. Through volunteer committees, boards, community events, and Summer Camps where kids build confidence and independence, they are tightly woven into MDA’s fabric. This week is National Volunteer Week, and we couldn’t be prouder of or more grateful for the 33,000 volunteers across the country who make . . .
To kick off 2019 National Volunteer Month, the Muscular Dystrophy Association was honored to welcome Marriott International volunteers from all over the world into our Chicago offices on Friday, April 5, as part of Marriott’s Serve 360 event. Continuing its tradition of making its communities better places to live, work, and visit, Marriott International this . . .
Twin brother and sister Michael and Amy Schleicher’s story starts where a lot of kids’ stories do. They looked up to their big brother, Matt, and when he did something cool, Michael and Amy wanted to do it, too. In the case of the fateful summer that would point the twins in a long-term direction, . . .
January is a natural goal-setting time. The new year and its fresh calendar to fill out prompt a re-evaluation of how you want to spend your time and your resources. As you’re mapping out your 2019, MDA can fit into your fitness, financial and philanthropic goals — there’s an opportunity for every interest. Volunteer with . . .