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.
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In this webinar CHOP experts discuss neuropsychological evaluation, the legal rights of students, and how to support your child as he returns to learning.
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.
The National Organization for Rare Disorders (NORD) provides advocacy, education and other services to improve the lives of all people affected by rare diseases.
The NF2 Crew is an online support community for patients and family members (and other loved ones) with neurofibromatosis type 2.
The American Cancer Society website offers helpful information about childhood cancer diagnosis, treatment, prognosis and resources.
Wondering whether you should take your child to an emergency room or urgent care? Learn about your options when you need help after the doctor’s office is closed.
A video presentation on Pediatric Airway Management
A video presentation by Mercedes Blackstone, MD, on Pediatric Drowning