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 will fund the second Jennifer Mallory Living LFS Family Camp, hardship grants for the LFS community, and more.
Your contributions allow us to connect patients to care, resources, and each other. 100% of all funds raised go directly back to our community. Everyone working at Living LFS does so on a strictly volunteer basis.
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