Do Good. Feel Good. Donate Today.
Li-Fraumeni syndrome (LFS) is both devastating in its impact and isolating in its rarity. Living LFS is a 501(c)(3) non-profit with the mission to encourage, empower, and educate those living with LFS.
Your donations allow us to connect LFS patients to care, resources, and each other, making LFS hardship grants and events such as the Jennifer Mallory Family Camp possible.
Living LFS is a 100% volunteer organization, which means 100% of your contributions support people with LFS. See Living LFS’ impact and ratings at Charity Navigator and Guidestar.
Thank you for putting your hard-earned money towards a community in so much need of your support. We pledge that every cent dedicated will be used to help patients live a better life with LFS.
Living LFS Federal Employer Identification Number (EIN): 47-1326501
Physical checks may be sent to:
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