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.

Lizanne Magarity Pando shares her daughter Jenna's story about living with Trisomy 21, also known as Down syndrome.

Born with ornithine transcarbamylase (OTC) deficiency, a rare metabolic disorder, Carter was 9 months old when he received a life-saving liver transplant at CHOP.  

A sensory processing disorder made eating a challenge for Toby. The Day Hospital Feeding Program at CHOP taught him how to like new foods.

Diagnosed with type 2 diabetes when he was 12, O'Dell Richardson has benefited from treatment and advice from the staff at CHOP's Diabetes Center for Children.

John and Sara have been coming to CHOP's Trisomy 21 Clinic, now the Trisomy 21 Program, all of their lives. The program provides care coordination for children and adults with trisomy 21.

William was born with tetralogy of Fallot, a heart condition that requires open heart surgery shortly after birth, and had surgery at CHOP.

Rowan was diagnosed before birth with a sacrococcygeal teratoma (SCT), a tumor located on her tailbone. She underwent surgery at CHOP the day after she was born.

In New Year’s Day in 2001, Chase Kroll was diagnosed with type 1 diabetes. Ten years later, he is headed to college. CHOP's Diabetes Center for Children helped him take control of his health.  

When Cristin needed to transition to adult healthcare, she had the support of the Trisomy 21 Program at CHOP to help guide her.

Parents say they see family-centered care in practice all the time at The Children's Hospital of Philadelphia. Here, they detail how CHOP is working to provide the best care for children and the most support for families.

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.