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 EB.

Non Profit

debra

debra's headquarters in New York, NY, United States

Brett Kopelan

Heather Fullmer

Jenna Kubeck

Mike Powers

Aigerim Saparova-Smith

Jason Kelly

Rob Rayl

Ryan Fullmer

J Alec Alexander

Angela Christiano

Thomas Trimarchi

Paul Honig

Kimberly D. Morel

Francis Palisson

Neil S. Prose

Juliette Prendiville

Amy Paller

Joseph McGuire

Andrew Tavani

Leslie Rader

James Wetrich

Arlene Pessar

William Cornman

Robert Ryan

Eugene A. Bauer

Alan Arbuckle

Gary Bellus

Susan Bayliss

Sharon Glick

Jonathan Alden Dyer

Richard A. F. Clark

Elaine V. Fuchs

Ervin Epstein

Nancy B. Esterly

Moise L. Levy

Gerald S. Lazarus

Dennis R. Roop

Lawrence Schachner

Daniel Siegel

Madeline Weiner

Mary K. Spraker

Timothy Wright

Elena Pope

Tor Shwayder

Anne W. Lucky

Laurence Miller

Anna L. Bruckner

John Lee

Jo-David Fine

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Thomas Trimarchi

Lambert Tamin

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