Katelyn was diagnosed with hyperinsulinism/hyperammonemia syndrome as an infant. Now a teenager, she has learned how to manage her condition and participates in clinical trials to help find answers that may benefit others.
Diagnosed with hyperinsulinism/hyperammonemia (HI/HA) syndrome, Natalie traveled to Philadelphia for specialized treatment at CHOP's Congenital Hyperinsulinism Center.
Caila was diagnosed with hypoplastic left heart syndrome (HLHS) and treated at CHOP by the Cardiac Center team, which is at the forefront of diagnosing and treating HLHS.
Lily was diagnosed with hypoplastic left heart syndrome (HLHS) and underwent several surgeries at CHOP's Cardiac Center to treat the complex congenital heart defect.
When Kristen and Tassos learned their unborn baby had hypoplastic left heart syndrome, they turned to CHOP's Cardiac Center for help and hope.
Two families with children diagnosed with HLHS find support and friendship through their shared experiences at CHOP's Cardiac Center.
Xavier was diagnosed with hypoplastic left heart syndrome before he was born. At CHOP's Cardiac Center, he's undergoing life-saving surgeries to treat this congenital heart defect.
After living with vocal cord paralysis for six years after a tumor was removed, Michael and his family found CHOP's Center for Pediatric Airway Disorders and laryngeal nerve reinnervation, a procedure that would give him his voice back.
When Kendall was only 3 years old when he was diagnosed with a rare condition called Kawasaki disease, experienced a sudden heart attack, and received a life-saving heart transplant at CHOP.