Living LFS: Li-Fraumeni Syndrome https://validator.w3.org/feed/docs/rss2.html Andi Last Comparing MRI vs PET/CT Donate Living LFS Jennifer Mallory Family Camp 2026 Jennifer Mallory Family Camp Li-Fraumeni Syndrome Awareness Day and Month Volunteers Wanted for Living LFS Hanna whyte Linda Humpert Trishia Shelly-Stephens Jennifer Mills RD Mooney Greg Harper Carly Grant, MS, LCGC Catherine Wilsnack, MSW, LMSW Let's Turn $40K into $80K for Families Battling Cancer LFS Hardship Grants Jaclyn Schienda, ScM, CGC Kyu Kyu Cheng March is Li-Fraumeni Syndrome Awareness Month: Families With Devastating Cancer Condition to Receive Financial Relief One-On-One Support Tanya Lamons Robyn Hamilton Lisa Wickens D'Ana Reed Courtney Ma'at Ann Ramer Jen Mallory Tom Connolly Inge Vandormael Board of Directors Resources Living LFS Jennifer Mallory Family Camp 2024 Anna Carolina Macieira Feitosa Mota Kiera Families Facing Rare Cancer Syndrome to Gather for Empowering Camp Experience with Acclaimed Author Troy Mudgett Award-Winning Journalist and Author Lawrence Ingrassia to Join Family Camp for Those Impacted by Genetic Cancer Disorder Ami Gignac Charolette Elizabeth Smith Media Stories from the Li-Fraumeni Syndrome Community (Part 1) Families With High Cancer Risk Get Financial Relief During Li-Fraumeni Syndrome Awareness Month May 3 is International LFS Awareness Day - 5/3 for p53 Contact Us Port-a-Cath Pros and Cons: Should You Get a Port? 2023 Year in Review 2022 Year in Review 2023 LFS Adults-Only Nashville Getaway Memorials Home