American Cancer Society
The American Cancer Society website offers helpful information about childhood cancer diagnosis, treatment, prognosis and resources.
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Showing 1 - 7 of 7 results
Neurofibromatosis Family Association (NFFA)
NFFA is a parent volunteer group that exists to support families and individuals at CHOP who are affected by neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) or schwannomatosis.
Thriving in School After Treatment
In this webinar CHOP experts discuss neuropsychological evaluation, the legal rights of students, and how to support your child as he returns to learning.
NF2 Crew
The NF2 Crew is an online support community for patients and family members (and other loved ones) with neurofibromatosis type 2.
Coronary Artery Anomalies — Data and Dilemmas
In this episode of Pediatric & Congenital Heart Talks, Julie Brothers, MD, addresses risk stratification in coronary artery anomalies and poses an algorithm for treatment approaches.
Virtual Driving Assessment: Preparing Teens to Drive Safely
Simulated driving assessments being piloted at select CHOP Primary Care locations gauge a teen’s ability to drive safely and avoid crashes.
National Organization for Rare Disorders (NORD)
The National Organization for Rare Disorders (NORD) provides advocacy, education and other services to improve the lives of all people affected by rare diseases.