Abstract
The primary aim of this qualitative study was to describe the lived experiences of men and women in Hawaii who were diagnosed with obsessive-compulsive disorder, and in so doing to provide an avenue for exploring health disparities involving this illness. Ten in-depth interviews revealed distinguishable similarities and differences in experiences of obsessive-compulsive disorder and suggested ways of understanding these similarities and differences. This research emphasized that in order to address disparities between the diagnosis and treatment of obsessive-compulsive disorder, as compared to other neurobiological disorders, we must meet the critical need for education about this illness among clients, families, and clinicians.