Born prematurely and with substantial hearing loss, Anna received a cochlear implant at CHOP — opening her world to language.

Zoe was diagnosed before birth with small bowel atresia, a cause of fetal bowel obstruction, and underwent surgery at CHOP when she was just 1 day old.

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.

Peyton Laricks underwent successful surgery at Children's Hospital of Philadelphia to repair a prenatally diagnosed congenital diaphragmatic hernia (CDH).

Luke Kelly came to CHOP for lifesaving care after being prenatally diagnosed with a type of lung lesion called bronchopulmonary sequestration (BPS).

When Felix, who is from Caracas, Venezuela, was diagnosed with Gardner syndrome, a condition that often leads to colorectal cancer, his parents found him the best care at CHOP.  

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.

Born with severe chest and spine deformities, Keegan's future looked dim until his parents found Robert M. Campbell, MD, and the innovative VEPTR device he created. 

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.