Holiday Giving: Transform Lives with a Legacy of Hope
As the year comes to a close, you can make a lasting difference for families living with Li-Fraumeni syndrome (LFS). The Li-Fraumeni Syndrome Association (LFSA) supports individuals and families affected by this rare genetic disorder through education, advocacy, research, and community connection.
Through our two-year Legacy of Hope campaign, we are raising $500,000 to advance research, expand access to genetic testing, and strengthen global advocacy for those impacted by LFS. Your year-end donation will directly support:
- The 2026 8th International LFSA Symposium, bringing together experts, researchers, and families to advance care and understanding of inherited cancer.
- Critical research initiatives, educational programs, and awareness campaigns that bring us closer to a future without LFS.
LFSA provides resources, educational forums, and support services for families living with LFS. We collaborate with physicians, genetic counselors, and medical centers to promote optimal care, raise awareness, and accelerate research.
This year, your generosity can create hope, connection, and meaningful change. By making a year-end gift, you join a community committed to transforming lives and building a better future for the LFS community.
Every donation matters. Make your gift today and be part of the Legacy of Hope.
The Li-Fraumeni Syndrome Association (LFSA) is a 501(c)(3) charitable organization. Donations are tax-deductible as outlined by IRS tax regulations. Our 501(c)3 federal tax exemption number is: 45-2284811.
Checks may be mailed to:
Li-Fraumeni Syndrome Association
P.O. Box 6458
Holliston, MA 01746
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