FOR IMMEDIATE RELEASE: February 27, 2022 download as PDF Andi LastVice President, Living LFS, Inc.andi@livinglfs.org March is Li-Fraumeni Syndrome Awareness Month, and for the third
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
by Aimee I used to have a lot of issues with the term “previvor” because it frightened me. It was an acknowledgement that I was
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
by Ilonka Dee Dylan broke his arm two months ago. About a year and a half ago, we gave Dylan a skateboard after he nagged
If you regularly make large, generous donations to Living LFS or other 501(c)(3) non-profit organizations, make sure you’re getting the biggest tax break possible for
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
