Welcome to EBAers, a group dedicated to raising awareness of and interest in Epidermolysis Bullosa Acquisita (EBA) and providing support and guidance for all those that are affected by this condition.

EBA is a very rare chronic autoimmune blistering disease of the skin and mucus membranes and its frequency of occurence is currently unknown. Whether you are directly affected by the condition, know someone who is or are simply interested in finding out more about it, our site provides a section with more information about EBA and its management that we hope will be of interest for you.

While we hope you find the information about EBA and its management useful and interesting, our strength as a group is our accumulated first-hand experience of dealing with the condition. The Personal Cases section of our site is all about the members of the group and their experiences with EBA.

The best way to get in touch with the group is through the Contact Us section of the website.

Thank you for visiting the website of the group and we hope you find your visit useful, informative and encouraging!

The EBAers Group