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The 2nd Annual "Living with LFS" Webinar Conference...coming to you!
January 28, 2015 at 5pm (EST). 4 Guest Speakers. Register for FREE!
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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