Emily was given a third chance at life when an experimental treatment for acute lymphoblastic leukemia at CHOP wiped out her cancer cells.

With help from CHOP’s Pediatric Headache Program, Haley found ways to manage her debilitating migraines made worse by a concussion, and get back to living her life.

Harrison, 14, suffered from digestive problems his entire life. Treatment from the Lustgarten Center for GI Motility has his digestive system working normally.

An advanced surgical technique helped Hamda, who is from the United Arab Emirates, regain a substantial amount of function in her right arm.

Sisters Julia and Claire both have cystic fibrosis (CF) and are treated by CHOP’s Cystic Fibrosis Center. The disease has created a strong bond between them.

Olivia has been treated for pulmonary hypertension since she was a baby. Now 9, she’s a happy, caring child who loves books and music.  

Genetic tests revealed that James had two rare, unrelated syndromes. His treatment plan was adjusted to address his unique needs, and he is now thriving.

Austin spent most of his life fighting leukemia and the disease seemed to be winning — until a pioneering treatment at CHOP changed everything.

Genetic testing at Children’s Hospital of Philadelphia found a mutation in Connor’s STAT3 gene, which led to a tailored treatment plan.

Genetics experts at Children’s Hospital of Philadelphia have helped Cortney and Ryan identify their daughter’s rare genetic mutation, leading to improved care.

Sara, 17, has her pulmonary hypertension and arrhythmia under control with help from the Pulmonary Hypertension Program.

Diagnosed with Ewing sarcoma at 14, Carly has endured months of intensive treatment, but her positivity has persisted through it all.

Twins, Shane and Nicholas, used to resist eating new foods. Now 3, they’re eating a variety of foods thanks to the Pediatric Feeding and Swallowing Center.

Emma, 9, has the energy to swim, dance and participate in the activities she loves thanks to the Pulmonary Hypertension Program at Children's Hospital of Philadelphia.

Twins Hattie and Nora were diagnosed with selective intrauterine growth restriction (sIUGR) before they were born, and monitored at Children’s Hospital of Philadelphia.

Noah, 4, used to have serious problems with chewing and swallowing solid food. Now he’s eating a balanced diet and is on track to be feeding himself.

Laney has been living with both Turner syndrome and Crohn’s disease since she was a toddler. Thanks to Children’s Hospital, she is a thriving 11-year-old.

The Martha Escoll Lubeck Feeding and Swallowing Center at Children’s Hospital of Philadelphia has helped Gracie overcome her fear of eating solid foods.

Emma has her complex heart problems, including pulmonary hypertension, under control thanks to the Cardiac Center at Children’s Hospital of Philadelphia.  

After years of searching, Chloe’s family found support at Children’s Hospital of Philadelphia, where doctors identified the cause of her rare form of leukodystrophy.