Many of you know the reason we walk, Jaxon. Our oldest son was diagnosed with Duchenne Muscular Dystrophy when he was 3 years old. The diagnosis changed our lives and we look forward to a day when families no longer have to deal with the debilitating effects of this or other types of muscular dystrophies. The way for this to happen is for people to support organizations like MDA fund research, provide support for families, and hope for those affected by neuromuscular disease.
Our team has partnered with MDA to lead the fight to free individuals and the families who love them from the harmful effects of muscular dystrophy, ALS and related muscle-debilitating diseases that take away physical strength, independence and life.
Join our team or make a donation to support the 100,000 kids and adults who will be served by MDA this year.
See you at the MDA Muscle Walk!