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Join TEAM DEBRA for the Crown Point Relay Runs on October 25, 2026, at beautiful Crown Point Park in San Diego, California!
Combine running and walking with a lively festival atmosphere, and you have the Crown Point Relay, 8K, and 5K. Set along the shimmering waters of Mission Bay, this flat and fast course welcomes runners and walkers of all abilities for a morning centered around community, teamwork, and fun.
Choose from the following events:
After your race, or between relay legs, enjoy the “Block Party by the Beach,” featuring live music, DJs, cold refreshments, and local food trucks. Whether you are chasing a personal best, enjoying a relaxed waterfront run, or completing a relay with friends, family members, or coworkers, you will experience beautiful bay views, cool coastal air, and an energetic finish-line celebration.
By joining TEAM DEBRA, you will help improve the lives of individuals and families affected by epidermolysis bullosa (EB). The fundraising minimums are:
TEAM DEBRA will cover the race registration fee for each participant.
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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Get in touch! or
© Copyright 2026, debra of America, All Rights Reserved | The Dystrophic Epidermolysis Bullosa Research Association of America, d/b/a debra of America is a registered 501(c)(3) tax exempt organization. | All Trademarks and Brands are Property of Their Respective Owners. debra of America does not endorse any drugs, tests, or treatments that we may report. This website is for informational purposes, always check with your physician before adopting any medical treatment. | EIN: 11-2519726
Crown Point Relay Runs
Sunday, October 25, 2026
,
Get in touch! or
© Copyright 2026, debra of America, All Rights Reserved | The Dystrophic Epidermolysis Bullosa Research Association of America, d/b/a debra of America is a registered 501(c)(3) tax exempt organization. | All Trademarks and Brands are Property of Their Respective Owners. debra of America does not endorse any drugs, tests, or treatments that we may report. This website is for informational purposes, always check with your physician before adopting any medical treatment. | EIN: 11-2519726
Crown Point Relay Runs
Sunday, October 25, 2026
,
Get in touch! or
© Copyright 2021, debra of America, All Rights Reserved | The Dystrophic Epidermolysis Bullosa Research Association of America, d/b/a debra of America is a registered 501(c)(3) tax exempt organization. | All Trademarks and Brands are Property of Their Respective Owners. debra of America does not endorse any drugs, tests, or treatments that we may report. This website is for informational purposes, always check with your physician before adopting any medical treatment. | EIN: 11-2519726
Crown Point Relay Runs
Sunday, October 25, 2026
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