LFS Association

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10+
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About this app

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.
LFSA Education, Research & Advocacy
Updated on
Aug 24, 2026
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Data safety

Safety starts with understanding how developers collect and share your data. Data privacy and security practices may vary based on your use, region, and age. The developer provided this information and may update it over time.
  • No data shared with third parties
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  • No data collected
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  • Data is encrypted in transit
  • You can request that data be deleted
Content rating
Everyone
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App support

About the developer
LI FRAUMENI ASSOCIATION INC
app@lfsassociation.org
196 Fletcher Cir Chicopee, MA 01020-3837 United States
+1 508-397-7397