Author: Living LFS

2022 Living LFS Mandala by Inge Vandormael

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

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Treva Vetter at Rare Disease Week 2021

Rare Disease Week 2021

Treva Vetter is a Registered Nurse, survivor, and patient advocate who is living with Li-Fraumeni Syndrome. Treva represented Living LFS during the Virtual Rare Disease

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