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Join host Sabrina Rendon-Espinosa for the 2025 “DO IT FOR ELI” 5K Walk/Run Fundraiser — a day dedicated to raising awareness and critical funds for debra of America.
This isn’t just a fundraising event — it’s a powerful day of hope, unity, and the fight for a cure for Epidermolysis Bullosa (EB). As a community, we come together to show Eli that he is never alone in this fight.
Saturday, November 1st | 9:30 a.m.
The Greenline Small Pavilion #3
2532 Sidney Brooks, San Antonio, Texas
Registration: FREE
$5 Raffle Tickets — Chance to win a Dallas Cowboys Basket
“DO IT FOR ELI” T-Shirts — $20 Adults | $12 Kids
Let’s walk, run, and rally together for Eli, and for all those affected by EB.
Epidermolysis Bullosa (EB) is a group of rare disorders caused by a mutation in one of 18 genes. People with EB share the lifelong challenge of extremely fragile skin that blisters and tears from minor friction or trauma. The list of medical complications EB causes may be long and often requires multiple interventions from a range of medical specialists. There is no cure for EB but there are treatments that help alleviate some of the debilitating symptoms of certain types of EB. debra of America’s work led to the groundbreaking U.S. As of 2025, three therapies have been approved by the U.S. Food & Drug Administration, marking a historic shift in the landscape of care and a powerful step forward for individuals and families affected by this devastating disease. To learn more please visit here.
Our mission is to improve the lives of those impacted by Epidermolysis Bullosa (EB) — “The Worst Disease You’ve Never Heard Of.” We integrate direct-to-patient programs and services, education, advocacy, close partnership with treatment developers, and research funding to foster meaningful change for those living with EB. Each year, debra of America spends an average of $1.5 million on direct-to-patient programs and services to provide immediate relief to thousands of families across the country.
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