Our patients' stories
Autosomal Recessive Polycystic Disease and Kidney Transplant: Marina’s Story
When Marina was 8, her family moved from Egypt to the U.S. to get the best care for her kidney condition. Today, Marina is in college.
Bilateral Renal Hypoplasia and Kidney Transplant: Rory’s Story
When Rory was a toddler, a kidney transplant at Children’s Hospital of Philadelphia (CHOP) saved his life. Today, he’s a happy and active 6-year-old.
Very Early Onset IBD: Landen’s Story
Diagnosed with very early onset inflammatory bowel disease (VEO-IBD) when he was only 18 months old, Landen is now responding well to treatment.
Alagille Syndrome and Liver Transplant: Alejandro’s Story
After a liver transplant at Children’s Hospital of Philadelphia with his father as the donor, Alejandro is an active and energetic 5-year-old.
Liver Transplant: Mia’s Story
Mia, 12, has the energy to enjoy her favorite activities like dancing after a liver transplant at Children’s Hospital of Philadelphia (CHOP).
Autism and Seizures: Massimo's Story
Massimo's participation in autism research at Children's Hospital of Philadelphia led to his early diagnosis of an unrelated seizure disorder.
Autism: Franco's Story
Diagnosed with autism at age 2, Franco has come a long way thanks to therapy at CHOP. Next up for his family? Tacking the Eagles Autism Challenge in May.
Beckwith-Wiedemann Syndrome and Cancer: Finn’s Story
Diagnosed with a rare genetic condition that predisposed him to developing cancer, Finn spent the first four months of his life at CHOP, where he survived heart surgery, abdominal surgery, liver cancer and chemotherapy.
Mitochondrial Disease: Matthew and Joshua’s Story
Matthew, 46, and Joshua, 42, are brothers who participate in studies that may lead to new treatments for their condition, mitochondrial disease.
Lymphatic Leaks: Naelani’s Story
Naelani was flown from Texas to Children’s Hospital of Philadelphia for an innovative procedure which worked to seal her lymphatic leaks.
With Hyperinsulinism, Experience Matters: Lily and Landon's Story
Siblings Lily and Landon were both treated for congenital hyperinsulinism at Children's Hospital of Philadelphia.
Hyperinsulinism Advocate Extraordinaire: Kaylee and Kathleen's Story
When her daughter's HI/HA was well managed, this mom turned her attention to advocating for her child's needs at school.
Hypoplastic Left Heart Syndrome: Francis’ Story
Francis was born with HLHS, a severe heart defect. After the first two of a staged series of three heart reconstruction procedures, he is doing well.
Ewing sarcoma: Sean’s story
Sean’s dream of becoming a kicker was put on hold, temporarily. Precision treatment for Ewing sarcoma put him back on the field, where he can one day make his dream a reality.
Reconstruction of the elbow: Clairianna’s story
Seven-year-old Clairianna had been living with a dislocated radius for nine months before doctors at CHOP made the discovery.
Thumb hypoplasia: Dean’s story
Dean was born without bone or muscle in his left thumb. Surgeons at CHOP created a thumb using Dean's index finger. He's been unstoppable ever since!
Surgery and Scar Tissue Removal for Compound Fracture: Kate’s Story
Two CHOP orthopaedic experts collaborate to help Kate regain full range of motion of her arm by removing scar tissue that had built up around a fracture.
Employee Story: Tailored Care for Every Child
Jessica Giannasca, Senior Director of IS Business Operations at CHOP, gained an intimate understanding of the patient family experience when her daughter Lily was treated at CHOP at 5 years old.
Ewing Sarcoma: Cameron's Story
A surgery to remove Cameron's right big toe and part of his foot to rid him of cancer did not stop him from enjoying his favorite sports.
Left Ventricular Noncompaction Cardiomyopathy: Lena’s Story
Lena suffered from a nearly fatal experience as a baby. She was saved by her ambulance team and by the Cardiac Center team at CHOP.