Join LFSA on May 12 at 11 AM ET to Explore Essential Resources for LFS Families and Providers Presented by LFSA Genetic Counselor Advisory Group Co-Chair Megan Frone and LFSA President Jenn Perry, this session offers a clear, user-friendly tour of essential resources for families and healthcare providers navigating LFS. Register Today!
Monday, September 14, 2026 Makefield Highlands Country Club Yardley, PA Tee up for a day that drives real impact. The Hunt Fore a Cure Golf Classic raises vital funds for families living with Li-Fraumeni syndrome (LFS), a condition that causes a predisposition to cancer affecting both children and adults. The Li-Fraumeni Syndrome Association (LFSA) provides
8th International LFS Association Symposium Hosted by MD Anderson Cancer Center in partnership with the LiFE Consortium Our 8th International Li-Fraumeni Syndrome Association Symposium will be a hybrid event—both in-person and virtual—bringing together scientists, doctors, geneticists, and LFS families to make meaningful connections across borders. More Details Coming Soon!
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Phone: 1-833-4MYLFSA (1-833-469-5372)
Email: info@lfsassociation.org
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