Blog
Rethinking PINK in October- Why Andi Doesn't Do Pink and What YOU CAN DO To support Breast Cancer Awareness.
Andi Last is a breast cancer survivor. She has LFS and explains why she does not do PINK in October. She also gives us some
Raising Two Children with Cancer, The Roberts Family's story of living LFS
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
Positively Living LFS, It's NOT a Death Sentence.
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
Genetic Counseling in LFS.
What is Genetic Counseling? Genetic Counselors are a group of professionals with a Master’s level degree who work in clinics, hospitals, public health and private
Mutant Vs Monster: Andi Last's Tale of Li-Fraumeni Syndrome
My name is Andi Last. That’s my husband Jay Last in the video with me. I’m the mutant, and he’s my warrior. In March 2015,
Li-Fraumeni Syndrome- Cancer in Olympic Proportions. The Story of Brazil's p53 Mutation.
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
Regular Screening In LFS helps Survival
Video credit: CTV Toronto: Sick Kids Cancer genetics Program At age 3, now 14 year old Alaya was diagnosed with Leukemia. 10 years later, she
MO Songs for KERRY Fundraiser for Li-Fraumeni Syndrome
James Higgins lost his dad, his sister and 2 daughters to LFS cancers. Cancer came after him twice. This is his story and how he
Living with Tough LFS Decisions
There really are no easy decisions where cancer is concerned. It’s usually an exercise in choosing between a tumor and a hard place. Some people
COTI-2 - Big Excitement surrounding a SMALL Molecule.
One of the most exciting presentations at the REACH 16 International LFS Conference was information presented on COTI-2, a novel small molecule that helps repair
A Father's Day Tribute
Almost three years ago, the Peytavin family’s journey with cancer began. It is often said that when a family member gets cancer, the family gets
The REACH 2016 International Li-Fraumeni Syndrome Conference
On Wednesday, June 1st, 2016 the LFS family gathered at the Sheraton Capitol Square in Columbus, Ohio. This family includes people with TP53 mutations, those
