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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
To support my cousin Jen and in loving memory of her families members.
I know a mom and her son who both have LFS and she is the most amazing person who's strength everyone could learn by!!
Never got to know the cousins that were lost, but the ones that are here remind me almost daily of why crappy stuff happens to us: because we are surrounded by love and can take anything. TEAM MILLS
The LFS is in my family!! And I have watched my cousin go through many different cancers, and I am so proud of her everyday!!!
We love our mutants!
Anything to help our friend Jen battle LFS!
We support this campaign in memory of, and in honor of the Mills Family Members.
For our awesome neighbors.
This gene has taken a heavy toll on my family. Many have not survived. I am fortunate enough not to be a carrier. This donation is for the ones fighting their battles everyday and night, year after arduous year. You are all in my prayers continually.