Is Debra Murphree Still Alive? The Shocking Truth We Uncovered!

Attend the debra Care Conference to connect with and support the Epidermolysis Bullosa (EB) community and get the latest research and treatment updates.

Explore our Mentorship programs, EB Nurse Educator Program, New Family Advocate Program, debra Care Conference & additional support services.

Get to know the dedicated team behind debra of America, working tirelessly to support individuals and families affected by Epidermolysis Bullosa (EB).

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.

For more information or if you have any questions, feel free to contact us at: Email: staff@debra.org Phone: 833-debraUS (833-332-7287) Our team is here to support you with any questions or …

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

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).

debra of America is a non-profit organization providing free programs & EB support services to those living with Epidermolysis Bullosa. Make a donation and help fund research for a cure.

Founded in 1980, debra of America is dedicated to improving the quality of life of all people impacted by Epidermolysis Bullosa (EB) in the U.S. Learn more about our work.

1988 DEBRA MURPHREE THE PROSTITUTE RESPONSIBLE TELEVISION - Vintage Ph

debra of America is a non-profit organization providing free programs & EB support services to those living with Epidermolysis Bullosa. Make a donation and help fund research for a cure.

Founded in 1980, debra of America is dedicated to improving the quality of life of all people impacted by Epidermolysis Bullosa (EB) in the U.S. Learn more about our work.