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Dystrophic Epidermolysis Bullosa Research Association of America (debra of America)

Raise money for Dystrophic Epidermolysis Bullosa Research Association of America (debra of America)

The Dystrophic Epidermolysis Bullosa Research Association of America (debra of America) is the only U.S. nonprofit providing all-inclusive support to the EB Community, through funding research for a cure and by providing free programs and services for those with: Epidermolysis Bullosa (EB) — "The Worst Disease You've Never Heard Of."

EB is a rare genetic connective tissue disorder that affects 1 out of every 20,000 births in the United States (approximately 200 children a year are born with EB). There is no treatment or cure. There are many genetic and symptomatic variations of EB, but all share the prominent symptom of extremely fragile skin that blisters and tears from minor friction or trauma.

MISSION STATEMENT

The mission of debra of America is to improve the quality of life for all people living in the United States with EB, their families, and caregivers through free programs and services while funding research to find a cure and treatments for Epidermolysis Bullosa.

Teams

Click on a team below to make a donation.

Recent donors

Recent donors
Date Name Amount
May 01 Anonymous Undisclosed amount
Apr 30 Joyce Hall $54.43
Apr 30 Harlan Reichle $107.94
Apr 28 Anonymous Undisclosed amount
Apr 26 Joseph & Wendy Martin $107.94
Apr 24 Debra Valerio Undisclosed amount
Apr 23 Jamie Deighton Undisclosed amount
Apr 20 Jerry Carter Undisclosed amount
Apr 19 Sarah Obringer $27.68
Apr 19 Anthony Obringer $6.27