Roberto Rodriquez Jr. was the first-ever fetal surgery patient at CHOP, undergoing a prenatal procedure to remove a lung lesion in 1995.

Casey and Bryan Kirsch were determined to give their son Jackson every chance to live a healthy life when they learned that he had a giant omphalocele.

After months of debilitating pain, Laurel found relief, support and healing from the Center for Amplified Musculoskeletal Pain Syndrome at The Children's Hospital of Philadelphia. 

Prenatally diagnosed with myelomeningocele (MMC), the most severe form of spina bifida, Sean Mulligan underwent fetal surgery at CHOP to repair the birth defect.

After learning their baby had CDH, the Pappas family traveled from Tennessee to seek care at CHOP's Center for Fetal Diagnosis and Treatment in Philadelphia.

Audrey Rose Oberio was prenatally diagnosed with myelomeningocele (MMC), the most severe form of spina bifida. She became CHOP's 1,000th fetal surgery patient.

Peyton Laricks underwent successful surgery at Children's Hospital of Philadelphia to repair a prenatally diagnosed congenital diaphragmatic hernia (CDH).

When Felix, who is from Caracas, Venezuela, was diagnosed with Gardner syndrome, a condition that often leads to colorectal cancer, his parents found him the best care at CHOP.  

After a poor spina bifida prognosis, Mia Lisa underwent fetal surgery for spina bifida at CHOP, where surgeons repaired the opening her spine before birth.

Luke Kelly came to CHOP for lifesaving care after being prenatally diagnosed with a type of lung lesion called bronchopulmonary sequestration (BPS).

Caoimhghin was diagnosed before birth with spina bifida, and was the very first baby delivered in the Garbose Family Special Delivery Unit at CHOP.

Born with a congenital condition that causes an irregular angle of growth to his lower legs and uneven lengths, Matthew Emerick found help from CHOP orthopedist Richard S. Davidson, MD.

A back brace kept Gina's idiopathic scoliosis in check for years until a growth spurt at age 15. That's when her family sought surgical help from spine experts at CHOP.

After an ACL injury sidelined football standout Justin Morrison from New Jersey, surgery and follow-up care at The Children’s Hospital of Philadelphia put him back on the gridiron.

Born with severe chest and spine deformities, Keegan's future looked dim until his parents found Robert M. Campbell, MD, and the innovative VEPTR device he created. 

Megan Ward is the mother of two childhood cancer survivors, Mollie and Grace. Ward's experiences with her two daughters has led her to become an advocate for childhood cancer research. 

Just two days after complaining that her leg hurt, 2 1/2-year-old Hailey Tamagno was with her family at CHOP getting a shocking diagnosis: acute lymphoblastic leukemia.

When a CT scan showed a tumor in Jake’s brain, he was sent to CHOP immediately for surgery. Doctors diagnosed the mass as Ewing sarcoma, a type of cancerous tumor.

Joey was diagnosed with acute lymphoblastic leukemia (ALL) when he was 6 years old. A year later, he and his family participated in the Parkway Run to raise funds for cancer research at CHOP.

Born with Down syndrome and a congenital heart defect, Alex Volz was diagnosed with acute lymphoblastic leukemia at 27 months old.