A $5 million gift from Irma and Norman Braman helped create the Suzi and Scott Lustgarten Center for GI Motility, a new center at CHOP to treat gastrointestinal motility disorders.
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.
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.
Born with nephrotic syndrome, Dede was sick her entire life. After years trying to manage the disease, Dede’s doctors recommended she receive a kidney transplant.
Matthew was diagnosed with several atrial septal defects during the first weeks of life and received expert care at CHOP's Cardiac Center, including open heart surgery.
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.
Lachlan travelled from Australia to the Congenital Hyperinsulinism Center at Children's Hospital for treatment of his congenital hyperinsulinism.