It’s time to look back with you and celebrate all that we achieved together for the Li-Fraumeni syndrome community in 2023: Let’s Make 2024 Strong!
As we prepare to ring in 2023, we here at Living LFS want to take a moment to look back with you and celebrate all
5 years ago, I learned my Breast Cancer metastasized. I was terrified, angry, but not surprised. A close group of friends I met through the
In April 2018, Living LFS awarded 14 travel scholarships to members of our support group to help them attend the LFSA 2018 REACH International LFS
Women with Li-Fraumeni Syndrome have close to 100% chance of developing cancer in their lifetime. About half of all these cancers develop before age
Genetics are very complicated. There are so many factors that influence how we become who we are on the cellular level and beyond. A good
Few things are more frustrating than looking for answers and getting the response- we don’t know. Sometimes, a person agonizes over the decision to be
by Andi Last – Sean Hannity and Hercules have made Travis Tritt the first person to ever say the words “Li-Fraumeni Syndrome” in a major
November 9, 2017 was the first Genetic Counseling Awareness Day! Andi Last met up with Wendy Kohlmann, MS, CGC, a licensed genetic counselor at The University of
D’Ana and her sister Courtney helped found Living LFS. They soon became our mutant sisters as we worked to bring those living LFS together.
