LFS and Living My Best was intended as a resource for explaining Li Fraumeni syndrome to children aged 8-13.
LFSA has other resources about living with Li Fraumeni syndrome that are located on their website. Some are linked below:
Their Genetic Counseling Advisory Group (GCAG) has resources to help newly diagnosed individuals, medical professionals, and the general public learn about LFS and navigate through a diagnosis/screening/treatment plan:
https://www.lfsassociation.org/genetic-couseling-advisory-group/
Their most recent awareness brochure is available for download in seven languages:
https://www.lfsassociation.org/lfs-awareness-brochure/
Kindly donated by the LFS Association
