You can help us help the ENTIRE Li-Fraumeni syndrome community! Note, these are not in order of importance – every volunteer, in any capacity, has
As Li-Fraumeni Syndrome Awareness Month approaches in March, we are gearing up for our fifth year of awarding LFS Hardship Grants on March 20th: LFS
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
