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.

When antibiotics failed to resolve her C. diff, Avery became one of the first pediatric patients to benefit from FMT, a promising new kind of transplant.

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

For months, 8-year-old Evelyn’s symptoms were a mystery. When she discovered she had Crohn’s, she joined the search for a cure for the chronic disease.

After being diagnosed with non-Hodgkin lymphoma as a child, Matthew Ramirez set his sights on becoming a doctor and helping other kids with cancer.

When her pneumonia led to severe complications, Angelica Hale was given a second chance thanks to lifesaving procedures and a kidney transplant from her mother.

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.

After an X-ray revealed a growth in his hip, Jackson was diagnosed with pigmented villonodular synovitis (PVNS). His Children’s care team knew what to do.

After 19 surgeries, Teddy arrived at Children’s for help battling Hirschsprung disease. His care team helped him attend school without the worry of an I.V.

Having cystic fibrosis isn’t easy. But thanks to an innovative regimen of care and a committed team, Caleb is forging forward.