Blog
Financial Support Available for Families Affected by High Cancer Risk During Li-Fraumeni Syndrome Awareness Month
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
2022 Year in Review
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
Perspective on Previving Cancer
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
How a Family Cancer Story Became The Hope of Elephants
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
Panic Attacks
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
8 Sophisticated Ways to Donate to Charity and Reduce Your Taxes
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
The Universe Had Other Plans: Lauren's Story
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
The Realities of LFS and Cancer: Elizabeth's Story
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
Identifying Li-Fraumeni Syndrome: Taylor's Story
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
Stay Strong and Live Life: Hailey's Story
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
2022 Living LFS Mandala
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
$12,000 in hardship grants to be awarded on Li-Fraumeni Syndrome Awareness Day, March 20
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
