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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.

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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

After the loss of his family to LFS, Michael James celebrates the life he had with daughter, Dolly. Mr. James continues his fight and support by raising awareness of LFS and the LFS Association.

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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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