The Muscles for Mckenna Gala is a fundraising event, in honor of Mckenna Ellixson, with one goal: to fund a cure for spinal muscular atrophy (SMA). Mckenna is a beautiful 6-year-old girl diagnosed with SMA. The Muscles for Mckenna Gala will be held on Friday, March 18, 2016 at the Drexelbrook Ballroom in Drexel Hill, Pennsylvania. The evening will entail a night of dinner and cocktails, silent auction, raffle items, live music entertainment provided by The Heartbeats, and the opportunity to meet with some local Philadelphia icons. We invite you to join us for a memorable evening of food, dancing and most importantly, HOPE. What is Spinal Muscular Atrophy? SMA (spinal muscular atrophy) is a disease that robs people of strength by affecting the motor nerve cells in the spinal cord, taking away the ability to walk, eat, or breathe. It is the number one genetic cause of death for infants. There is no cure and no treatment – but we are asking you to help us change that. Cure SMA Cure SMA is dedicated to the treatment and cure of spinal muscular atrophy (SMA)—a disease that takes away a person’s ability to walk, eat, or breathe. It is the number one genetic cause of death for infants. Since 1984, we’ve directed and invested in comprehensive research that has shaped the scientific community’s understanding of SMA. We are currently on the verge of breakthroughs in treatment that will strengthen our children’s bodies, extend life, and lead to a cure. We have deep expertise in every aspect of SMA—from the day-to-day realities to the nuances of care options—and until we have a cure, we’ll do everything we can to support children and families affected by the disease. With your help, we will find a cure. Sincerely, Muscles for Mckenna Gala Committee