Five months pregnant with twins, Kim Hebron and her husband Vaughn learned their babies had a life-threatening condition called twin-twin transfusion syndrome (TTTS).

Meet Emily Ireland. Diagnosed with type 1 diabetes when she was 12 years old, Emily never lets her diabetes stop her from doing the things she enjoys.

Khloe was just 2 days old when doctors noticed she was having digestive problems. She was transferred to CHOP where doctors discovered she had Hirschsprung’s disease.

A mother tells the story of her daughter, Arianna, whose food anxiety and selectivity made mealtimes stressful and upsetting. The family turned to CHOP's Pediatric Feeding and Swallowing Center for help.

Thirteen-year-old Hannah Rowan has type 1 diabetes, hyperthyroidism, and was recently diagnosed with celiac disease. But all of these auto-immune conditions don't slow her down.

Hundreds of gravely ill newborns have benefits from EMCO, a machine that temporarily acts as the baby's heart and lungs, since 1990 when Katelyn became CHOP's first ECMO patient.

Katharina Lucas, Aaron's mother, describes how the Pediatric Feeding and Swallowing Center at CHOP helped teach her young son to eat after a diagnosis of failure to thrive.

Diagnosed with type 1 diabetes at age 8, Emily Gold has been working with her family and community to raise money to help find a cure for the condition.

Diagnosed prenatally with the abdominal wall defect gastroschisis, Vincenzo’s family traveled to CHOP for delivery and expert surgical repair. See how he's doing 10 years later.

Albe was rushed to the Emergency Department at Children's Hospital of Philadelphia for sudden cardiac arrest. The Critical Care Medicine team was ready to save his life.

Born with a heart defect called tetralogy of Fallot, Jack was just 9 days old when his family learned he also had chromosome 22q11.2 deletion, a rare chromosomal difference.

When Diana and Corey learned their unborn baby had tetralogy of Fallot, they came to CHOP's Fetal Heart Program to better understand the diagnosis, develop a birth plan and prepare for their baby’s open heart surgery. 

Rianna was diagnosed with diffuse hyperinsulinism when she was 10 days old. She was referred to the Congenital Hyperinsulinism Center at The Children's Hospital of Philadelphia for treatment.

Diagnosed with dilated cardiomyopathy as an infant, Julia was 13 when she had a heart attack at school. She received a life-saving heart transplant at The Children's Hospital of Philadelphia. 

Cardiologists at Children's Hospital of Philadelphia diagnosed Oliver with supraventricular tachycardia when he was 1, then found the right treatment to keep his heart beating normally.

Diagnosed with hyperinsulinism/hyperammonemia (HI/HA) syndrome, Natalie traveled to Philadelphia for specialized treatment at CHOP's Congenital Hyperinsulinism Center.

When Kendall was only 3 years old when he was diagnosed with a rare condition called Kawasaki disease, experienced a sudden heart attack, and received a life-saving heart transplant at CHOP.

Diagnosed with metastatic papillary thyroid cancer at age 12, Tanaya continues to receive expert care from the Pediatric Thyroid Center at The Children's Hospital of Philadelphia.

When Kristen and Tassos learned their unborn baby had hypoplastic left heart syndrome, they turned to CHOP's Cardiac Center for help and hope.

Born prematurely and with substantial hearing loss, Anna received a cochlear implant at CHOP — opening her world to language.