Thank you for taking the next step in making a difference in the lives of our EB families.
Celebrate YOU by making a difference in the lives of the precious Butterfly Children. You can have friends and family donate and leave a message to your special page in lieu of gifts. It could be your birthday, wedding or any other special occasion.
A beautiful way to give back and celebrate you on your special day.
DEBRA Australia is a voluntary non-government funded support group that helps individuals and their families with Epidermolysis Bullosa, more commonly known as EB. An EB person has skin that is as fragile as butterflies’ wings so they are affectionately known as “Butterfly Children”. This rare genetically inherited skin disorder is incurable and requires painful 3 hour dressing changes every second day.
DEBRA Australia works to provide financial and emotional support to families with EB as well as advocating and providing vital funding to research for a cure.