Do Good. Feel Good. Donate Today.
March is LFS Awareness Month, and March 20 is LFS Awareness Day! This month, to highlight the importance of the TP53 gene, your donations of $5.30, $53, $530 – or any amount – can provide hardship grants to LFS families in need. Learn more.
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 made events such as our First Annual Living LFS Family Camp possible, and will fund the second Jennifer Mallory Living LFS Family Camp.
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