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
Click to View PDF...
Join or support Team Faces of LFS in The Color Run™ on June 11th, 2017!
webinars, and to find out about
LFS Awareness Brochure