Diagnosed at age 3 with a pediatric brain cancer called anaplastic ependymoma, Caroline continues to undergo treatment and is fighting for a full recovery.
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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 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.
Kaleb was diagnosed with cerebral palsy at 18 months. Thanks to a complex surgery and intensive therapy, he has built up his strength and is ready to run.
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 her sister was diagnosed with a genetic cancer, Sedona was monitored closely by the Cancer Predisposition Program at Children’s to help reduce her risk.
Adopted at 21 months of age, Tanvi had never seen a doctor. After being diagnosed with a rare spinal disorder, her family turned to Children’s for specialized pediatric surgical care.
One month into her first year of high school, Mary was diagnosed with two brain tumors. Her parents turned to the Aflac Cancer and Blood Disorders Center of Children’s for nationally-ranked care, and this unstoppable teen never missed a beat.
Diagnosed at birth with beta thalassemia, Nene endured two blood and marrow transplants before being cured at age 5.