News Archives - Page 9 of 9 - Li-Fraumeni Syndrome Association

Watch the Webinar!

Posted by LFS Association

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Watch the Living with LFS Webinar from May 21, 2013! Guest Speakers: Wendy Kohlman, Manager of Family Cancer Assessment Clinic, Huntsman Cancer Institute and Amanda Gammon, Genetic Counselor, Huntsman Cancer Institute Host: Bonita Kline, LFS Association Family Support Chair

Join Our Webinar – May 21, 2013

Posted by LFS Association

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Webinar: “Living with LFS” followed by Q&A Date: May 21, 2013 Time: 8:00-9:30pm (EST) Guest Speakers: Wendy Kohlman, Manager of Family Cancer Assessment Clinic, Huntsman Cancer Institute and Amanda Gammon, Genetic Counselor, Huntsman Cancer Institute Host: Bonita Kline, LFS Association Family Support Chair

Help Lead the Way

Posted by LFS Association

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The Pediatric Hereditary Cancer Predisposition Program at The Children’s Hospital of Philadelphia is currently conducting a research project to examine the challenges that parents face when deciding whether or not to have their children tested for LFS. Click here to read the article.

New Articles

Posted by Jennifer Perry

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Please read 2 new articles that we posted under our “research” section of our website: 1. 5 Questions on the development of p53 by Pierre Hainaut, PhD 12/11 2. Targeted Cancer Therapies – Awakening the “Guardian of the Genome” by June de Lartigue, PhD 12/11

LFS Launches New Website!

Posted by LFS Association

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Welcome! The LFS Association has launched a new website, a resource designed to provide a wide range of information, advocacy, and support services for individuals and families with Li Fraumeni Syndrome. We support a consortium of researchers, medical providers and caregivers to further research and promote optimal care for the LFS community. Be sure to