American Cancer Society
The American Cancer Society website offers helpful information about childhood cancer diagnosis, treatment, prognosis and resources.
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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.
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.
Neurometabolic Optical Monitor: A Game-changer for CPR and Critical Care
Researchers at Children's Hospital of Philadelphia are working to create a non-invasive device to measure brain oxygenation during CPR and critical care, with the goal to reduce brain injury and death.
Braden QD Scale Education Module
The Braden QD education module is designed to educate staff on different components of the new Braden QD scale and provide case scenarios to practice using the tool.