Translate »
LFS Association is on Facebook!
Get connected and stay up to date with the latest LFS news and events...Learn more!
Li-Fraumeni Syndrome Conference
Missed the conference? Don’t worry—watch the webcasts here!
Metformin Study for LFS Patients
Enrollment is limited. Learn more today!
What is LFS?

LFS Association

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.


Medical Resources

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 information.