World Cancer Day 2018- What Mutants Wish you Knew About LFS.
Years ago, we asked our support group members, What is one thing you wish everyone knew about LFS? As always, the answers were heartfelt, emotional,
Years ago, we asked our support group members, What is one thing you wish everyone knew about LFS? As always, the answers were heartfelt, emotional,
So a big event is coming up that you really want to attend, maybe it’s in another state or another country, and your bank account
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
My name is Kathy Higgins. I have lost 4 family members to LFS. KERRY Kerry was first diagnosed with cancer at the age
Claire Roberts shares their family’s story of not only one, but two children facing cancer and learning some of the challenges families with Li-Fraumeni Syndrome
Odds are that Li-Fraumeni Syndrome is THE most devastating hereditary cancer syndrome that you have never heard of, unless of course you know one of
My name is Andi. That’s my husband Jay in the video with me. I’m the mutant, and he’s my warrior. In March 2015, at the
The 2016 Summer Olympics are underway in Brazil. We watch as the world comes together in Rio to celebrate and honor feats of strength, endurance