News

The DebRA Japan, a patient association for the rare and intractable skin disease Epidermolysis Bullosa (EB / Epidermolysis Bullosa), has created a disease awareness video to commemorate its 15th anniversary.

In this video, three groups of patient families appear and talk about their concerns, thoughts, and dreams for the future from their respective perspectives. In addition, as a current treatment for epidermolysis bullosa, our autologous cultured epidermis is also mentioned. It is a very rich video that deepens the understanding of the disease through the patient's unvarnished life.

Watch the video here: https://www.youtube.com/watch?v=rel8eIVxoF0
※The video shows the affected area and treatment of patients with epidermolysis bullosa.