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Menu
About LFS
FAQ
History of LFS
LFS Cancers
Resources
Screening
Clinical Trials & Studies
Online Resources
Care
Podcast
Blog
Get Support
Become A Mentor
Memorials
Our Work
LFS Awareness
Events
History of Living LFS
Partnerships
Board of Directors
Press Releases
Financials
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Events
Living LFS Jennifer Mallory Family Camp 2022
10/28/21 WEBINAR: Talking to Kids About LFS
2021 Virtual Rare Disease Week on Capitol Hill
Li-Fraumeni Syndrome Awareness 2021
Mutant Meetups
2020 Rare Disease Week on Capitol Hill
2019 Living LFS Family Camp
2018 LFS REACH 18 International Symposium
2017 Rare Disease Week on Capitol Hill
