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Benefit for Li-Fraumeni Syndrome in Waverly

WETB’s Gayle Ong was one of several reporters covering the event and story of LFS and Mo Songs for Kerry, and was able to speak with LFS Association’s president, Jenn Perry about the significance of Kathleen and Jamie Higgins’ efforts!

Click here to see video and read the article on WETB’s website!

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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.

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LFS Association

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WETB’s Gayle Ong was one of several reporters covering the event and story of LFS and Mo Songs for Kerry.

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