Its mission is to help patients, families, and doctors in countries where there is no DEBRA structure to support them and to assist new groups to form and develop.

Learn about Epidermolysis Bullosa (EB), a rare genetic disorder, its symptoms, treatments, and personal stories from the EB community at debra of America.

For more information or if you have any questions, feel free to contact us at: Email: [email protected] Phone: 833-debraUS (833-332-7287) Our team is here to support you with any questions or …

Your support is more than a donation —it's a lifeline. With your support, debra of America provides free programs and services that ease the unrelenting physical, emotional, and financial burdens of EB …

Oct 25, 2025 · Attend the 2024 debra of America Benefit on October 25, 2025 at Southern Exchange Ballrooms in Atlanta, GA. Featuring cocktails, hors d’oeuvres, auction, and dinner.

Learn about debra of America's team working to raise EB awareness, and provide EB support to patients and families affected by Epidermolysis Bullosa (EB).

Whether it’s finding answers to everyday challenges, accessing free wound care supplies, or connecting with others who understand— debra is here, every step of the way.

La pagina de internet de debra provee pacientes, cuidadores y profesionales de salud con la información mas reciente sobre EB, mientras ofrece un lugar donde la comunidad de EB puede …

Please complete our Participant Request Form below and we will respond shortly. For additional questions, email [email protected] or call 833-DEBRAUS (833-332-7287), ext. 104.

No one should face Dystrophic EB alone. debra of America offers free programs, personalized support, and trusted online resources to help individuals and families navigate life with EB.