Cherish’s rare and extremely serious heart condition went undiagnosed for years. CHOP experts gave Cherish and her family, at first, hope, and then a new heart.

Born with a severe congenital heart defect, 17-year-old Brendan is now an accomplished swimmer after treatment from Children’s Hospital of Philadelphia.

Brenna first came to CHOP with a lymphatics condition so severe she could hardly function. A collaboration between lymphatics, genetics and oncology changed her life.

Michael, 5, is meeting all his developmental milestones after surgeries for a severe heart defect. He was closely monitored by the Cardiac Kids Developmental Follow-up Program at CHOP.

Born with a severe heart defect, Hudson experienced a harrowing journey before he had a heart transplant at Children's Hospital of Philadelphia.

Doctors and genetic researchers at CHOP teamed up to find the gene mutation responsible for Daniel's painful lymphatic disorder, and successfully treat it.

Ryan had no idea anything was wrong with his heart. But a frightening diagnosis meant he had to take a break from sports to fight for his life.

Diagnosed with chylothorax at birth, Lucas needed expert lymphatic care at Children's Hospital of Philadelphia (CHOP) to survive. 

After Samad was diagnosed with a rare genetic heart disorder, his family underwent genetic testing and discovered they too had the disorder.

Born with a serious heart condition, Disha has grown up under the care of CHOP's Cardiac Center and now has a family of her own.