Connor’s Unexpected Battle

Connor’s accident happened in the blink of an eye. When his parents took him to the hospital closest to their home they were immediately sent to UPMC Children’s.

Harrison’s Journey to the Lab

Harrison, patient with Stage IV Hodgkin lymphoma

At age 14, Harrison was diagnosed with Stage IV Hodgkin lymphoma. He endured five rounds of chemotherapy and 14 radiation treatments as a high school freshman.

Braxton’s Time to Thrive

Braxton was born with 7q11.23 duplication syndrome, a genetic disorder that can cause a variety of neurological issues, developmental delays, and other conditions.

“BelleDozer” Triumphs over Thalassemia

Belle was adopted from China when she was 19 months old. When her parents first met her, they knew she was special. They also knew Belle had potentially devastating blood disorder called thalassemia, which would require a lot of medical care.

Living Proof of Donor Impact: Meet Taytum

At 9 days old, Taytum’s life hung in the balance due to a rare heart condition. Learn about her family’s unwavering determination and the extraordinary care provided by UPMC Children’s Heart Institute.

Meet Rosie

Shortly after Rosie was born, physicians diagnosed her with Maple Syrup Urine Disease (MSUD), a rare, life-threatening genetic disorder in which the body is unable to process certain proteins.

Taylor’s Road Home

In late September, following several failed attempts to wake Taylor from her now 10-week-long coma, neurosurgeon Taylor Abel, MD, suggested an experimental type of deep brain stimulation. The procedure involved implanting an electrode in Taylor’s brain to modify electrical signals.