Make a year-end donation to support families with Li-Fraumeni syndrome (LFS).
The Li-Fraumeni Syndrome Association (LFSA) supports families and individuals with LFS in ways that touch lives and inspire change. LFS is a rare genetic disorder that greatly increases one’s risk of developing cancer. Our efforts concentrate on raising awareness in the community, advancing medical and scientific research, and uniting patients and professionals who share our same goal.
We provide extensive resources, educational materials, forums, community events, and support services for those living with LFS and their loved ones. Our advocacy also extends to medical providers and thought leaders in furthering research and promoting optimal care for the LFS community. We are proud to work with respected physicians, genetic counselors and medical facilities to truly make a difference.
We are a community of Li-Fraumeni syndrome families and survivors. We are the building blocks of a future without LFS. Together we will bridge the gap between patients and medical professionals, changing lives and turning the tables for those impacted by LFS.
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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