A Cure for Cash: End Duchenne Muscular Dystrophy

Join Kate Skales and Shawn Gallagher for an evening of live music as they raise awareness about DUCHENNE'S MUSCULAR DYSTROPHY In early 2019 my cousin's Phil and Jena learned that their son Cash was living with Duchenne's Muscular Dystrophy. This is a rare disorder, affecting about 1 in 3,500 male births every year. There is currently no cure, but each day brings us a step closer to finding one. This disorder does not discriminate and can happen to anyone. Please join us for an evening of music and conversation to find a cure for Cash. During the event, we will hear from Cash's closest family members who will share their journey and insight into the fight against Duchenne's Muscular Dystrophy. In addition to purchasing a ticket, you can also donate at the silent auction with many wonderful items up for grabs. Your donations will be tallied up at the end of the night and donated directly to the Duchenne Research Fund in Cash's name. This event is all ages, BYOB, snacks and non-alcoholic beverages provided.