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Make a donation and help fund research for a cure. Guaranteed entry with fundraising minimums depending on race. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.
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Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb). By joining team debra, you’ll be raising vital funds to support the eb community while taking part in one of the most memorable races in america For more information or if you have any questions, feel free to contact us at
Debra of america is part of debra international, a worldwide network of national groups working on behalf of all people living with epidermolysis bullosa (eb).
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