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
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
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
Many of us met Andrea at an LFS conference in Boston a few years ago. She and her mother Kim are well known within our
Kelilah Vardah gives us her thoughts on the Living LFS question: “Do some of you think you can beat cancer with pure will (and medicine
It is difficult to imagine anything good coming from being diagnosed with Li-Fraumeni Syndrome. Yet as our members remind us, the good is in what
Lainie Jones has had five primary cancers, as well as Li-Fraumeni syndrome. But she’s stayed optimistic and refuses to let cancer control her life. Source:
World Rare Disease Day is February 29, 2016. Living LFS is teaming up with Global Genes to raise awareness about Li-Fraumeni Syndrome and Rare Diseases.
Brian Ries- No Matter the Odds, Keep Fighting. About a month ago, I reached out to the support group to see if anyone was willing
