Leila was diagnosed with Beckwith-Wiedemann syndrome and hyperinsulinism. She was referred to the Congenital Hyperinsulinism Center at The Children's Hospital of Philadelphia.
Charlotte's family came from California searching for answers about her persistently low blood sugar levels. They found answers and support at CHOP's Congenital Hyperinsulinism Center.
Frustration and fear led Max’s parents to bring him across the country to CHOP's Congenital Hyperinsulinism Center. After surgery to treat his diffuse hyperinsulinism, he's thriving.
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.
Lainie travelled from Michigan to the Congenital Hyperinsulinism Center at The Children's Hospital of Philadelphia for a cure for her focal hyperinsulinism.
Read Mackenzie's story about her and her family's experience with focal hyperinsulinism. Learn about her diagnosis and treatment at the Congenital Hyperinsulinism Center at The Children's Hospital of Philadelphia.
Born full-term after a healthy pregnancy, Nathaniel began developing low blood sugars — down to 20 mg/dL — a few hours after birth. His family turned to CHOP's Congenital Hyperinsulinism Center for help.
Katelyn was diagnosed with hyperinsulinism/hyperammonemia syndrome as an infant. Now a teenager, she has learned how to manage her condition and participates in clinical trials to help find answers that may benefit others.
Diagnosed with hyperinsulinism/hyperammonemia (HI/HA) syndrome, Natalie traveled to Philadelphia for specialized treatment at CHOP's Congenital Hyperinsulinism Center.