Help Daisy and the Thousands Like Her
Daisy was born with Epidermolysis Bullosa (EB) —or what we call, “The Worst Disease You’ve Never Heard Of.”
About 200 babies are born with EB every year in the United States. Founded in 1980, debra of America is the only U.S. nonprofit organization that helps families like Daisy’s by funding research for a cure and by providing free critical programs and services to ease the physical, financial, and emotional burdens of the disease.
Just $25 allows us to send a package filled with expensive wound care supplies through our Wound Care Distribution Program, a program that has helps Daisy and her family tremendously.
Please join us in our mission by making a tax-deductible gift today. Your gift will allow us to continue to support families across the country. Every dollar counts!
Give with Confidence
debra of America has earned the highest possible rating of 4 stars from Charity Navigator, the nation's leading charity evaluator. A 4-star rating means that we adhere to sector best practices, execute our mission in a financially efficient way, and are committed to accountability and transparency.
Related Resources
EB in Depth
EB is a rare genetic connective tissue disorder that affects an estimated 1 out of every 20,000 births in the United States.
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Annual Reports & Financials
Take a look at our Annual Reports and Financial Statements to see how your donations are being put to work.
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More Video Stories
See Epidermolysis Bullosa (EB) up close and personal in the video stories of individuals impacted by EB.
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