CHOP’s palliative care team supports a family through the tragic passing of their beloved daughter.

When Given’s parents learned their unborn baby had a sacrococcygeal teratoma (SCT), a tumor on the tailbone, they sought help and hope at CHOP.

After an international adoption, family turns to CHOP for support, surgery and therapy for son with brachial plexus injury.

Vomiting and swollen legs led to a shocking diagnosis: Jayden’s heart was failing. A heart transplant at CHOP has transformed his life.

Eliana inherited a rare condition affecting bone development from her mother. Both mother and daughter receive treatment at CHOP from a doctor with special expertise in the condition.

When Carolyn was 28 weeks pregnant with her third child and her doctor in New York discovered that her baby carried the gene for autosomal dominant polycystic kidney disease (ADPKD), she became dedicated to changing the historical lack of pediatric research on the rare disease.

For nearly 50 years, Bill needed frequent treatment for hemophilia — often every few days. A gene therapy changed everything.

Eliza’s family brought her to CHOP for its expertise in hyperinsulinism. She became the 600th patient to have pancreas surgery and went home cured.

Amir was born with multiple spinal problems. Surgeries at CHOP have helped straighten his spine, improving his self-confidence.

Just a few days after he was born, Kylen suffered four seizures and was diagnosed with epilepsy.

In 2000, Christian had fetal surgery for spina bifida at CHOP. Today, he’s an EMT. Follow his journey.

When their foster daughter faced insurmountable odds, a Delaware couple turned to CHOP for help with complications from spinal muscular atrophy.

Debilitating pain without a known injury can strike some of the most driven and high-achieving youth. A CHOP program offers support, treatment and relief.

After learning their unborn daughter’s life was at risk from a tumor growing on her tailbone, Lyra’s parents found hope in the SCT experts at CHOP.

Call it a mother’s intuition. Though Killian appeared to be growing and developing normally during prenatal appointments, Jennifer couldn’t stop worrying something was wrong.

When a 20-week-old fetus was diagnosed with a large goiter, CHOP experts offered a novel solution – regular infusions of thyroid hormone into the umbilical cord.

Fetal surgery for severe CDH gave AJ’s lungs a chance to grow before birth, improving his chances of a better outcome. Today, the 6-year-old is thriving.

Asher came to CHOP for a fetal surgery procedure called FETO to treat his severe CDH before he was born, giving him the best chance to survive and thrive.

While Julia’s diagnosis of a brain tumor was a shock to her family, the location and type of tumor meant surgery at CHOP was the only treatment she needed.

After Molly qualified for a kidney transplant, a new organ from a living donor was identified thanks to CHOP’s involvement with the National Kidney Registry.