Li-Fraumeni Syndrome Association Canada

We are families, like you who have been devastated by the effects of Li-Fraumeni Syndrome (LFS), a hereditary cancer predisposition syndrome. Our hopes are to educate, raise awareness, and find better screening programs and treatments for LFS. By forming relationships with and supporting the variety of researchers and medical staff who can help achieve this, we wish to help provide a better understanding of a complex syndrome to those who need it. We welcome communication with all professionals, researchers, scientists, doctors, patients, and families in the hopes that the bridges formed by these communities will lead to an end of the devastating effects of Li-Fraumeni and other Li-Fraumeni-like syndromes.
For more information, please contact Founder & Co-Chair of LFSA-Canada Chiquita Hessels at: [email protected]