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.

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

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.

Diagnosed with hip dysplasia at 6 weeks old, Quinn needed surgery. When her brother saw her spica cast, he made a heartwarming Christmas wish.

When the usually active Joseph was struck by sudden knee and hip pain, his doctor was baffled. Children’s helped solve the mystery and identify a rare condition.

An enthusiastic ballet dancer, Zoe couldn’t wait to dance en pointe. But Sever’s disease and heel pain got in the way. With the right care, she danced again.

In seven months, Ryder was diagnosed with medulloblastoma; had brain surgery, chemotherapy and stem cell transplants; and entered remission. Then his family gave back.

Diagnosed at age 3 with a pediatric brain cancer called anaplastic ependymoma, Caroline continues to undergo treatment and is fighting for a full recovery.