Li-Fraumeni Syndrome Resources
The American Cancer Society website offers helpful information about childhood cancer diagnosis, treatment, prognosis and resources.
It addresses the growing concern surrounding the misuse of genetic information in health insurance and employment decisions.
GeneReviews are expert-authored, peer-reviewed disease descriptions focused on the diagnosis, management and genetic counseling for people with inherited conditions.
LFS Association provides a wide range of information, advocacy and support services for individuals and families with Li Fraumeni Syndrome.
NCI's website includes links to information about treatment, clinical trials, testing and research.
The National Organization for Rare Disorders (NORD) provides advocacy, education and other services to improve the lives of all people affected by rare diseases.
Stupid Cancer is an all-inclusive young adult cancer community that empowers those affected by young adult cancer.
GINA is a federal law designed to protect people in the United States from genetic discrimination in health insurance and employment.