Peutz-Jeghers Syndrome (PJS) Resources
Support and Education Groups
PJS and JPS is a free online support group for patients, family, friends, researchers and physicians, to discuss Peutz-Jeghers syndrome and Juvenile Polyposis Syndrome.
It addresses the growing concern surrounding the misuse of genetic information in health insurance and employment decisions.
The Colon Cancer Alliance is a nonprofit patient advocacy organization dedicated to increasing colon cancer screening rates and survivorship.
GeneReviews are expert-authored, peer-reviewed disease descriptions focused on the diagnosis, management and genetic counseling for people with inherited conditions.
The National Organization for Rare Disorders (NORD) provides advocacy, education and other services to improve the lives of all people affected by rare diseases.
GINA is a federal law designed to protect people in the United States from genetic discrimination in health insurance and employment.