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Living LFS Have You Hugged a MUTANT Today?
Gildan 50/50 T-shirt
- Sizes YXS - XXXXXL
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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
Our family has LFS. Good luck and God bless.
In support of the Connolly family...too many family members gone before anyone knew what took them. And because we are all mutants in our own way.
This goes out to our dear friend, Susan Frary! The strongest, toughest, and most amazing mutant I know! Love you!
My dear friend Coutney Ma'at and her sister are living with this syndrome. Wishing all of you the best and hoping to help fund research to help you all LIVE!
One word...RamerNation. Love them with all my heart and finding answers to help them live long, happy, healthy lives couldn't be more important.
Go Team Mallory!
My godsisters D'Ana and Courtney are living with LFS. Best of luck with your new nonprofit!
My childhood friend Courtney and her sister are both diagnosed with and living with this disease.