Congenital Hyperinsulinism Center Patient Stories

As a lifelong CHOP patient receiving care for a rare genetic disorder, congenital hyperinsulinism (HI), Katelyn now trusts the same care team for her son’s treatment.

Congenital hyperinsulinism runs in Kristen’s family. Discover how CHOP has helped Kristen and her daughter manage this rare condition across generations.

CHOP not only diagnosed Amelia’s extremely uncommon condition, it had the experts to treat her.

Caring for three siblings with hyperinsulinism — and keeping their blood sugar in the safe range — calls for creativity and guidance from CHOP.

Being part of a clinical trial as a patient of the HI Center research gave Nico the independence to be a normal kid and still safely manage his hyperinsulinism.  

Grandfather, mom and granddaughter have all been treated at CHOP for congenital hyperinsulinism (HI). This family’s history shows the evolution of HI care.

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.

After three months of searching for answers, Omar’s family found a diagnosis — and hope, at Children’s Hospital of Philadelphia.

When a rare disorder was diagnosed in two of their children, the Linares family found hope and expertise at CHOP.

Endocrinologists in New York didn’t have the knowledge of hyperinsulinism to help Dominique, 30, so she came to CHOP for treatment that controlled her HI.