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Living LFS Have You Hugged a MUTANT Today?
Gildan 50/50 T-shirt
- Sizes YXS - XXXXXL
- View Sizing Guide
About this campaign
Li Fraumeni Syndrome is a hereditary cancer syndrome. Living LFS is a newly formed organization that aims to provide support and information to those with LFS. We want to help mutants get together, share their stories and help each other find the best resources to LIVE with LFS. We are organizing a Meeting in Portland, Oregon in October and funds will go directly towards providing a space for mutants to gather and find community. Our vision is to have meetings in many different locations and enough financial support to make meeting other mutants easier on this already physically and financially challenged population.
Supporters
I am happy to support my good friends living with LFS.
Mutants ROCK!
We love the Mallorys!
In support of my dear friend, Susan Frary and in support of all others who fight this challenge. I keep you all in my thoughts and prayers.
My beloved friend Laurie is one of the most inspirational people on the planet. She lives with LFS with great courage and love and I celebrate her with boundless gratitude!
Had to shop again to get the grandkids properly attired in the hope that it will never effect them or anyone else important in their lives.