Abstract
Over a fourth of adults residing in the United States have a disability. Nevertheless, medical and mental health professionals have limited formal training in disability justice and disability-responsive care. Furthermore, the medical model of disability feeds the societal belief that deems people with disabilities as less than others while sustaining environmental structures rooted in ableist ideology, thus, limiting the quality of care provided to people with disabilities. This interpretative phenomenological analysis aimed to address an existing gap in the literature by examining an interabled couple's experience after one of the partners acquired a disability. We hope the results of this study to: (a) increase understanding of the lived experiences of an interabled couple after a partner acquired a disability; (b) highlight the importance of accounting for both partners’ experiences; and (c) increase awareness of disability-responsive strategies for serving interabled couples counseling.
Get full access to this article
View all access options for this article.
