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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.

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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.

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LFS News

The cancer predisposition revolution
How was the inherited basis of cancer foreshadowed?
By David Malkin, Judy E. Garber, Louise C. Strong, Stephen H. Friend

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Community Events

TitanTough21 Foundation Launch Event
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.

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LFS Webinars

Check out our library to watch past LFS
webinars, and to find out about
upcoming webinars!

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LFS Awareness Brochure

Myriad Genetics is proud to partner with LFSA to launch the global LFS Education and Awareness Campaign!


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