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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 a mutant and my whole family has been effected by LFS!
Jen Mills and all of the Mutant Family. Stay strong!
I'm supporting my two mutant grandkids who have had cancer twice each. I'm excited about the research being done which is not just another chemo drug.
Friends of Ramer Nation!
Supporting my sister Laurie in her continued struggle. She is the most positive and supporting person I know. This is the least I can do for all she does for everyone around her. God bless us one and all.
I am supporting this campaign because my aunt and cousin are the most awesome "mutants" that I know who are affected by this. They have both went through so much and yet continue to stay positive and strong. Let's get the word out and make Lfs known!
Family.
I'm a living mutant!!