We are families, like you who have been devastated by the effects of Li-Fraumeni Syndrome, a hereditary cancer predisposition syndrome. Our hopes are to educate, raise awareness and find better screening programs and treatments for LFS.
We've compiled a list of doctors available to
answer your questions, LFS support and
treatment. They specialize in many different
areas, which have been listed with their
Given the speed of technological advancements in the prevention and treatment of cancer, it can be difficult for patients and advocates to stay up to speed on the latest information.
Dear Li-fraumeni Families, My name is James D. Everett and I’m the Chairman of the Board of the TitanTough21 Foundation and also a father of two children with Li-fraumeni Syndrome.
webinars, and to find out about
LFS Awareness Brochure