Blog
Events
Contact
Menu
Blog
Events
Contact
Search
Close
Facebook
Instagram
Twitter
Linkedin
Youtube
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
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
DONATE
Events
Mutant Meetups
Since the beginning, Living LFS has been all about connecting “mutants” – those of us with Li-Fraumeni Syndrome – both in person and online. Enjoy these photos from our many Mutant Meetups over the years.
All 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
