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
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