Meet Our Patients
Meet some of the amazing kids who have been treated in our UW Health Pediatric Neuromuscular Program and read their stories.
Samantha Ceplina has had her heart set on a career in health care ever since childhood. A strikingly beautiful, good-humored and determined young woman, Samantha could have easily viewed her life as the proverbial half-empty glass. Diagnosed at age 6 with spinal muscular atrophy (SMA), Samantha has not been able to walk for the past six years. Of course, she has no time for what others might view as obstacles. "SMA is something I have," she says, "but I have never let it define me. It has never changed what I have wanted to do." Read Samantha's story
Parker was born with a rare, incurable neuromuscular disease called SMA, or spinal muscular atrophy. Children with SMA typically become very fatigued, and things most of us take for granted - such as walking, eating and even breathing - can be an incredible challenge. But Parker, a social butterly with an infectious smile, manages to always see the positive in every situation. Read Parker's story