Diagnosed with dilated cardiomyopathy as an infant, Julia was 13 when she had a heart attack at school. She received a life-saving heart transplant at The Children's Hospital of Philadelphia.
Lachlan travelled from Australia to the Congenital Hyperinsulinism Center at Children's Hospital for treatment of his congenital hyperinsulinism.
Quinn was diagnosed with a type of coronary artery anomaly called anomalous left coronary artery from the pulmonary artery (ALCAPA) and treated by the Cardiac team at CHOP, giving him a better chance at survival.
Abby was diagnosed with double inlet left ventricle, a severe heart defect, and underwent several surgeries at CHOP's Cardiac Center.
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.
Born prematurely and with substantial hearing loss, Anna received a cochlear implant at CHOP — opening her world to language.
A back brace kept Gina's idiopathic scoliosis in check for years until a growth spurt at age 15. That's when her family sought surgical help from spine experts at CHOP.
At 15, Carly Stephens was diagnosed with acute myelogenous leukemia. She received several rounds of chemotherapy at CHOP and today, she's a happy, healthy college student.
Malcolm was just 11 when he started to feel pain in his hip. A few months later, he was diagnosed with Ewing sarcoma, a rare bone tumor, and began treatment at CHOP.