OK, friends. I’ve got some really great news. As you know, MDA’s commitment to improving the lives of young adults living with muscle-debilitating diseases is near to my heart. It’s why I chose to accept the role as the first adult MDA National Goodwill Ambassador. It’s been almost a year since we began implementing MDA’s . . .
When Zac Henderson could no longer play baseball, he joined the school jazz band. When he could no longer hold his instrument, he migrated to the local 4-H. Then it was on to managing his high school’s basketball team. Now Zac has his own film production company thanks to working on the basketball team’s highlight . . .
Since the tender ago of five, Hugo Trevino, who has Spinal Muscular Atrophy (SMA), has been involved with MDA. From participating in MDA Summer Camp as a child to rallying behind causes like Fill the Boot and Muscle Walk, Hugo has always been dedicated to helping others live longer and grow stronger. Now, as a . . .
13-year-old Melissa Shang is an activist, an advocate and an author. She’s spoken at the United Nations, given a TedX talk and just published her first book. She is a girl on a mission. And it all started with an American Girl doll named Isabelle. For Melissa, Isabelle was the last straw. Every year, American . . .
Noah Hometown: Cortland, NY Age: 17 Diagnosis: I was diagnosed with Duchenne Muscular Dystrophy (DMD) Favorite School Subjects/Activities: My favorite school subject is history. Favorite People: My favorite people are my parents and my sister Katie. I also love spending time with my grandpa and my cat, Smokey, who is 16 years old. Interests: I like to read and I also . . .
Navigating through college isn’t easy for anyone, but it can be especially tricky for people with disabilities. Here are some quick tips to help those of you heading off to college this fall — as well as anyone considering attending university one day. 1. Pick a school you want to attend, not one you are . . .
Latondra Chappell is like most teenagers. She drives, goes to prom and is attending college. However, at the age of 11, Latondra was diagnosed with congenital muscular dystrophy, which caused her muscles to break down and lose strength, putting her in a wheelchair. At her local MDA Care Center, Latondra’s doctor pushed her to live . . .
In an auditorium in Bearden, Arkansas, Doug Haynes was sitting in his wheelchair by the stage, dressed in his graduation robes. The high school senior had waited for this moment for four years. His physical therapist stood in front of him, pushing away the chair’s footrests and grasping the gait belt around Doug’s waist. Sensing . . .