Skip to main content

Patient Stories

Our patients' stories

Patient story

Trisomy 21: Bryant’s Story

A year into the COVID-19 pandemic, Bryant’s family received a wake-up call from the staff at the Trisomy 21 Program. Instead of steadily improving since his last visit, Bryant’s behavior had become troublesome, he’d gained a significant amount of weight and his blood work was concerning.

Patient story

Desmoid Tumor: Vaida’s Story

Vaida’s tumor is in her cheek, a rare location for a desmoid tumor. After surgery at CHOP, this 2-year-old has retained an impressive amount of facial muscle function.

Patient story

Esofagitis eosinofílica: La historia de Princess

Hace años que Princess lucha contra una enfermedad inflamatoria del esófago poco frecuente. Gracias a CHOP, un nuevo medicamento y el apoyo de su familia, ahora está mejorando.

Patient story

Coming Full Circle: MarlaJan’s Story

From a tetralogy of Fallot patient to a Cardiac Center nurse, MarlaJan’s heart journey has made her an advocate for children with CHD.

Patient story

Chronic Lung Disease: Ethan’s Story

While doctors at CHOP helped Ethan’s premature lungs develop, other staff helped his family manage the stress of having a sick newborn.

Patient story

WAGR Syndrome: Miranda’s Story

CHOP researchers have published the most comprehensive description of WAGR syndrome, which affects less than 450 people worldwide, including Miranda.

Patient story

Eosinophilic Esophagitis: Princess’ story

Princess has struggled for years with a rare inflammatory condition of the esophagus. Thanks to CHOP, a new medication and family support, she’s now thriving.

Jump back to top