For nearly 100 years, the American Cancer Society (ACS) has worked relentlessly to save lives and create a world with less cancer and more birthdays. Together with millions of our supporters worldwide, we’re helping people stay well, helping people get well, finding cures, and fighting back against cancer.
Cancer Hope Network is a non-profit organization that provides free and confidential one-on-one support to cancer patients and their families. As our core offering, we match cancer patients or family members with trained volunteers who have themselves undergone and recovered from a similar cancer experience.
The Foundation for Women’s Cancer was founded by the Society of Gynecologic Oncology (SGO) in 1991. The Foundation for Women’s Cancer is a 501 (c) (3) not for profit organization dedicated to funding research and training, and ensuring education and public awareness of gynecologic cancer prevention, early detection and optimal treatment.
LFS Association provides a wide range of information, advocacy, and support services for individuals and families with Li Fraumeni Syndrome. We support a consortium of researchers, medical providers and caregivers to further research and promote optimal care for the LFS community.
The primary mission of Lynch Syndrome International (LSI) is to serve our global communities by focusing on providing support for individuals afflicted with Lynch syndrome, creating public awareness of the syndrome, educating members of the general public and health care professionals and providing support for Lynch syndrome research endeavors.
The National Cancer Institute coordinates the National Cancer Program, which conducts and supports research, training, health information dissemination, and other programs with respect to the cause, diagnosis, prevention, and treatment of cancer, rehabilitation from cancer, and the continuing care of cancer patients and the families of cancer patients.
Our mission, as an alliance of leading cancer centers devoted to patient care, research, and education, is to improve the quality, effectiveness, and efficiency of cancer care so that patients can live better lives.
We are a support group who aim to provide support and information to anyone whose lives are or have been affected by Familial Adenomatous Polyposis and Gardner’s Syndrome (FAP) plus Peutz Jegher’s Syndrome, Juvenile Polyposis and MYH (Mut Y Homolog) whether patient, family, friend or those with an interest in the Gene.
In 1985, compelled by the memory of her late father, Edward P. Richardson, who had died of cancer one year earlier, Carolyn Aldigé embarked on a mission. She founded the Prevent Cancer Foundation, a 501(c)3 nonprofit, with the hope of sparing others from the pain and suffering caused by cancer. Aldigé believed firmly that an emphasis on prevention, not just treatment, could help decrease cancer deaths and incidence rates. Since then, through its research, education and outreach efforts, the Foundation has worked hard to spread the prevention message to the public, spurring ground-breaking research and new ways to reach captive audiences.
PTEN World is for people with Cowden Syndrome/BRRS and their families and medical providers. Members may support each other on their profiles and in the discussion forum. If you are interested in learning more about our support group, then we hope you’ll sign up!