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.

Sydney’s Story

Sydney was diagnosed with a rare genetic disorder called Urea Cycle Disorder / Ornithine Transcarbamylase deficiency (UCD/OTC) at just one year old.

Jimmy’s Life Defying the Odds

Jimmy, patient with an inoperable brain tumor

At four months old, Jimmy was diagnosed with an inoperable brain tumor and borderline hydrocephalus, and the prognosis looked grim.

A Rare and Life-Threatening Diagnosis

As a toddler, Cloud was your average, active little boy — climbing all over and getting into just about everything. Right before his 3rd birthday, that all changed.

The Road to Creating A New Standard in Behavioral Health

Many children with developmental and behavioral health needs experience a difficult journey toward wellness due to services that are fragmented or inaccessible. UPMC Children’s innovative Whole Child Wellness Clinic (WCWC) disrupts the current model of care with a new standard that better serves kids with behavioral health needs. 

Meet D’Kaiden

Doctors told Samantha to prepare for the worst — that her son D’Kaiden likely wouldn’t survive after birth.

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.

Rosie’s Future

PICU physicians diagnosed Rosie with acute meningoencephalitis. While meningitis is a condition that involves inflammation or infection of the protective layer of membranes that surround the brain (the meninges), encephalitis involves inflammation or infection of the brain tissue.