Neurofibromatosis Type 1 Patient Stories
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Neurofibromatosis Type 1: Conor’s story

Conor, 16, and his parents have been traveling to CHOP from South Carolina several times a year since he was an infant for NF1 treatment and clinical trials.
Hypothalamic/Optic Pathway Glioma NF1: Abby’s Story

When Abby was a toddler, she was diagnosed with a disorder that causes tumors and has been receiving treatments at CHOP. Abby is a Patient Ambassador for the 2016 Parkway Run & Walk. Read about her amazing efforts to help other kids undergoing chemotherapy.
Neurofibromatosis Type 1: The Camiolo and Schmidt Families’ Stories
Kelley Schmidt and Kristin Camiolo, who both have daughters followed by the Neurofibromatosis Program at The Children’s Hospital of Philadelphia, share their stories in hopes of helping other families who are facing an NF1 diagnosis.
Neurofibromatosis Type 1: Cullen’s Story

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.
Neurofibromatosis and Pediatric Stroke: Patrick's Story
Patrick suffered a stroke during surgery to remove a tumor on his cerebellum. Here, he shares the story of his recovery at CHOP.