Our mission is to bring Li-Fraumeni families, Li-Fraumeni researchers, and Li-Fraumeni doctors together, all of whom are interested in the understanding of LFS, to identify the best LFS cancer treatments, LFS screening protocols, advocacy & awareness, and hopefully some day a cure for Li-Fraumeni Syndrome.
We here at Li-Fraumeni Syndrome Association are people like you; we wonder how one family could be plagued with so many cancers, multiple cancers and childhood cancers. We have seen generation after generation affected by cancer, but only recently have we learned why. Through LFSA, we hope to educate and raise awareness of this rare condition. Those with LFS have similar stories, but despite the rarity of this disease, the people who face it have a physical and a spiritual strength that is truly unique.
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