LFS Association provides a wide range of information, advocacy, and support services for individuals and families with Li-Fraumeni Syndrome. We support a consortium of researchers, medical providers, and caregivers to further research and promote optimal care for the LFS community.
We are a community of Li-Fraumeni Syndrome families and survivors. We are the building blocks of a future without LFS. Together we will bridge the gap between patients and professionals who have the same goal.