DebRA Australia
 Australia  |  Health/Medical

DebRA Australia provides ongoing support and information for individuals, families, and
professionals living and working with EB, ensuring all research and best practice treatments are
investigated leading to improved quality of life for all.

Epidermolysis Bullosa is rare skin disorder, both within Australia and globally. For many years, individuals and small state groups had been the primary source of services and support for families struggling with an EB skin disorder. A collaborative effort was made by the states in 2005 when we officially founded DebRA Australia, in order to create a larger network of support for these Australian families. DebRA Australia offers advocacy, financial support, emotional support and networking opportunities to families who are living with EB. DebRA Australia also uses donations to fund local and international research into a cure for EB. Our aim is to work for a life free of pain.
We want to investigate and implement ways to help sufferers in their daily lives, while educating the general public and health care professionals about EB.

Research & Resources

Create awareness

Advocacy

Emotional/financial support

Fundraising

Kid’s Camps

Manage Listing