Info Cards for International LFS Awareness! We’re excited to make new resources available to spread awareness of Li-Fraumeni syndrome (LFS) on May 3, International LFS
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
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
“Losing my voice does not mean I won’t be heard.” – Jennifer Mallory Today, October 5, 2021, is one year since Living LFS founder Jennifer
$36,320 in hardship grants awarded in 2021! Living with a genetic disease like Li-Fraumeni Syndrome (LFS) has devastating physical and emotional costs and losses. To
