Author: Living LFS

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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The New

For those of you who are new, welcome, we are so happy you’ve joined us! For those who have been with us, we’re so glad

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