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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
In honor of Jessica Wallace Sergeant who fought LFS so courageously and for those out there still fighting it!
I'm supporting my friend Jenny Mills and as always remembering my best friend and Jenny's brother Eddie.
My daughter is a mutant and my grandchildren are mini-mutants. lost my first husband and my son to LFS .
LFS stinks!
Trishia Shelly-Stephens is our daughter and Tre Shellly is our grandson. Both are mutants that we hug as often as possible!
To support our family members who have this mutation