LFS Association

The LFS Association (LFSA) provides information, advocacy, and support services for individuals and families with Li-Fraumeni syndrome. LFSA also supports a consortium of researchers, medical providers, and caregivers to further research and promote optimal care for the LFS community. The LFSA event app supports this mission by providing attendees with access to educational sessions, event information, speakers, schedules, resources, and opportunities to connect with others in the LFS community. LFSA’s work is grounded in three key pillars: Research, Education, and Advocacy. Through this app, attendees can engage with educational content, stay informed, and make the most of their LFSA event experience.