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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
For my Mini Mutants and in honor of the Connolly's. I am very proud to a part of this LFS community!
I am so proud to be a part of this organization and am blown away by how much support we have received-Thank You! We will now be able to organize regional meetings at other cancer centers, providing support and awareness.
To love and support RamerNation and other families living with LFS.
If you know Linda Zercoe, you know why I'm supporting this campaign.