After a brain hemorrhage caused hydrocephalus, newborn Carston was facing a dire prognosis. Thanks to his care team at Children’s, he beat the odds.

After experiencing stomach pain, 13-year-old Chris discovered that he had a chronic illness called Crohn’s disease. Since then, he’s learned to manage the condition.

With dreams of becoming a marine biologist or a mermaid, Dakota won’t let a brain tumor get in the way.

Growing up, Paula Schirmer had never heard of pediatric scoliosis. As an adult, she discovered it affected all three of her daughters.

Dontavious, who is one of 2,000 patients treated for sickle cell disease at Children’s each year, is committed to bringing awareness to the condition at just 13.

Diagnosed with acute lymphoblastic leukemia, Hudson took her cancer diagnosis and treatment in stride, inspiring her parents to follow her lead.

A novel surgery called rotationplasty allowed Jude to maintain his mobility despite losing part of his leg due to osteosarcoma.

When newborn Locklyn was diagnosed with Down syndrome, a heart defect and an underdeveloped nasal septum, her parents turned to Children's for comprehensive care across multiple specialties.

After Lena was diagnosed with rhabdomyosarcoma, a rare childhood cancer, her family took her to Children’s. Today, they are beyond thankful they made the four-hour trek.

Born with dilated cardiomyopathy, Rynli needed a heart transplant in order to live. Children’s performed its 400th pediatric heart transplant to save her.