A girl struggles to decide whether to be tested for the genetic mutation linked to her father’s cancer. Would it be better not to know
I found out I was pregnant with my first baby three days after I was diagnosed with Li-Fraumeni Syndrome. My husband and I had been
I and my one year old baby both have LFS. Late last Fall my baby was diagnosed with Adrenocortical Carcinoma. Since then we have been
Hello. My name is Taylor. I am twenty years old and I was diagnosed with Li-Fraumeni Syndrome in December of 2021. When I was seven
My name is Hailey and in May of 2020, I found out I was pregnant with my now 1 year old. I also found out
Make a $530 donation to support Living LFS Hardship Grants and you can own this one-of-a-kind mandala, currently being hand-drawn by the illustrious Inge Vandormael
Living LFS will celebrate Li-Fraumeni Syndrome Awareness Month throughout March FOR IMMEDIATE RELEASE: February 6, 2022 Greg Harper President, Living LFS, Inc.greg@livinglfs.org Andi Last Vice
I had adrenal cancer as an infant in 1985, so the word ‘survivor’ has been part of my vocabulary my whole life. Even though I was too young to
The genetic mutation that causes Li-Fraumeni syndrome has the potential to unlock cancer FOR IMMEDIATE RELEASE: February 5, 2021 East Coast: Greg Harper President, Living
