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
We are racing for our dear friend, Noelle Johnson, and others like her with LFS. We are racing in the Boulder Sunset Sprint Triathlon to raise money and awareness for LFS. Please consider donating to this worthy cause.
webinars, and to find out about
LFS Awareness Brochure