The Eisenstein family struggled to help their young daughter maintain a healthy body mass index (BMI), until they sought the help of experts in CHOP’s Healthy Weight Program.

When it was time for Lilly Moore to have her third surgery for HLHS, her parents made the decision to travel 2,300 miles from home to the Cardiac Center at CHOP.

After being prenatally diagnosed with congenital diaphragmatic hernia (CDH), Parker, now 11, was treated with extracorporeal membrane oxygenation (ECMO) on her first day of life.

At just one day old, Emily underwent surgery to remove a sacrococcygeal teratoma (SCT), a large tumor that had grown to be a third of her size by the time she was born.

Camryn found all the help she needed in the CHOP Care Network to overcome a variety of health issues so she can now enjoy preschool like any other 3-year-old.

In the summer of 2012, Tim was diagnosed with type 1 diabetes. He knew he needed to get control of his diabetes so he could fully enjoy high school and all it offered: meeting new friends, learning new things — and even playing football.

Cullen Mitchell has neurofibromatosis, a genetic disorder. His parents, Kelly and Ken, credit the Neurofibromatosis Program at CHOP with helping them manage the complexities of caring for a child with this condition. 

After a stroke at age 17, Avery worked her way back to the basketball court — thanks to neurology, rehabilitation and sports medicine experts at Children’s Hospital of Philadelphia.

Felicia thought her long childhood battle with cancer was over until she was diagnosed with a new cancer — papillary thyroid cancer — in her sophomore year of college.

Michael Jr. was one of the Center for Fetal Diagnosis and Treatment’s first patients, where he had surgery to repair a congenital diaphragmatic hernia (CDH).

Olivia and Stella were diagnosed in utero with twin-twin transfusion syndrome (TTTS), a life-threatening condition in which blood circulates unequally between the twins.

Yousuf, who lives in Qatar, fell gravely ill. He was diagnosed with Guillain-Barré syndrome and transferred via air ambulance for treatment.

During a routine ultrasound, Tara and Travis Markel learned that their baby’s bladder was the size of his head, indicating a serious birth defect. Their research led them to the Center for Fetal Diagnosis and Treatment at The Children’s Hospital of Philadelphia.

After learning that their unborn baby had heterotaxy syndrome and CHD, Alison and Philip turned to The Children’s Hospital of Philadelphia for hope.

After suffering through multiple kidney infections and failed treatments, Taylor’s family turned to CHOP’s specialized Pediatric Kidney Stone Center for answers.

After a year of intensive treatment, 14-month-old Evan Stickle is finally home. His family credits his turnaround to CHOP’s Newborn and Infant Chronic Lung Disease Program.

Reid was diagnosed with hypertrophic cardiomyopathy shortly after he was born and had a defibrillator implanted at age 12.

Ben was born with hypoplastic left heart syndrome (HLHS) and underwent open heart surgery at CHOP's Cardiac Center.

Ben was born with hypoplastic left heart syndrome (HLHS) and underwent open heart surgery at CHOP's Cardiac Center. Watch his story.

LJ was diagnosed before birth with transposition of the great arteries (TGA) and treated by CHOP's Fetal Heart Program. Watch his story.