About Li Fraumeni Syndrome Association Canada
We are a community of Li‑Fraumeni syndrome families, researchers and care providers. We are the building blocks of a future without LFS.
LFS Association provides a wide range of information, advocacy, and vital resources for individuals and families with Li-Fraumeni syndrome. We are at the helm of a consortium of researchers and medical providers to advance research and promote optimal care for the LFS community.
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