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 with a severe congenital diaphragmatic hernia (CDH), Emerson’s family turned to CHOP, where an expert, multidisciplinary team made all the difference.

Colin has eosinophilic esophagitis, a rare inflammatory condition of the esophagus, and receives care at CHOP, which is one of the few pediatric hospitals with a specialized program for the condition.

Emily Kelly underwent successful fetal surgery at Children’s Hospital of Philadelphia to remove a cervical teratoma, a type of giant neck mass.

Diagnosed with bilateral hearing loss at 20 months old, Maggie's family sought help from CHOP's Center for Childhood Communications.

Mason was prenatally diagnosed with LUTO (keyhole bladder) and successfully treated with fetal surgery at Children's Hospital of Philadelphia.

Diagnosed with childhood apraxia of speech when he was 3 years old, Seth continues weekly speech therapy at CHOP Specialty Care Center in Bucks County, PA.

Bette Mickley didn't believe her daughter Amber had growing pains, for one simple reason: Amber wasn’t growing. Instead, the family learned Amber has Gaucher Disease, a rare genetic disorder.

After a diagnosis of GE reflux and failure to thrive, a mother tells how the Day Hospital at CHOP's Feeding and Swallowing Center helped her son Jack learn to eat.

When Phoenix was born profoundly deaf, his family turned to CHOP for help. At age 2 and 5 he received cochlear implants to help him hear. 

When Diana Huang learned her nephew, Steven, was sick with Gaucher disease in his native China, she helped him come to The Children's Hospital of Philadelphia for treatment.

Born prematurely with an enlarged area on his upper intestine, Jack was diagnosed with multiple jejunal atresia. Though it occurs only 1 in 3,000 live births, the expert team at The Children's Hospital of Philadelphia knew how to treat his rare condition.

The Feeding Program at The Children's Hospital of Philadelphia taught Luke to eat after a diagnosis of failure to thrive.

Lynne and Bill Garbose provided the lead gift to create the Garbose Family Special Delivery Unit (SDU) at CHOP, a specially created birthing suite for mothers carrying babies with known birth defects.

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.

Paige had severe tracheal stenosis, a life-threatening airway narrowing. Doctors recommended major surgery – a fix made riskier since she had just one lung.

Lily was diagnosed with hypoplastic left heart syndrome (HLHS) and underwent several surgeries at CHOP's Cardiac Center to treat the complex congenital heart defect.