A series of surgical procedures at Children’s Hospital of Philadelphia corrected Brynn’s rare combination of heart defects.

With the help of the Niños Primeros en Salud Program led by CHOP's Global Health Center, Widni is now a healthy 5-year-old after years of treatment for malnutrition.

Chad, 11, is smiling again after multiple surgeries and ongoing treatment for CDH and pulmonary hypertension at Children’s Hospital of Philadelphia.

Ashley, 18, has her gastroparesis under control and the energy to enjoy her passions, thanks to the Suzi and Scott Lustgarten Center for GI Motility.

A new regimen of oral medications allows Stella, 10, to treat her pulmonary hypertension and live an active life.

Conjoined twins Abby and Erin were born connected at the head. After 10 months and multiple surgeries, the girls were separated.

Mitch suffered two relapses from acute lymphoblastic leukemia and was out of options until an experimental immunotherapy treatment at Children's Hospital of Philadelphia rid his body of cancer.

Lily, 8, has her complicated heart problems including pulmonary hypertension under control thanks to Children’s Hospital of Philadelphia.

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.