Debra Australia is a non-profit organization dedicated to supporting individuals and families affected by Epidermolysis Bullosa (EB), a rare genetic skin condition that causes fragile skin and blisters. The organization provides vital resources, information, and advocacy to improve the quality of life for those living with EB. In addition to support services, Debra Australia raises awareness about the condition and funds research aimed at finding effective treatments and potential cures. They also offer financial assistance for medical needs and promote community engagement through events and fundraising activities.