Anti-oppressive practices with chronic pain sufferers

Chronic pain and (dis)Ability leaves one struggling for normalcy, trying to make sense out of the fundamental operations of one's body, the meaning of suffering, and the social construction of wellness (Jackson, 2002; MacDonald, 2000; Oliver, 1996; Thomas, 1999; Wendell, 1996). Social work and other helping professions need to find ways to learn from sufferers, to listen to their stories, deriving insight from their knowledge, in order to more effectively attend to their health care needs. Findings from a doctoral dissertation using a narrative "testimonial" methodology, framed within a postmodern anti-oppressive ideology, will be presented. This research listened to the stories of women in, or retired from, the helping professions, who are Sufferers of chronic pain, specifically attending to their experiences of living with chronic pain, dealing with the medical system, and the relationship of their pain and (dis)Ability with their helping roles. Six sufferers participated-two physicians, two nurses, and two social workers-providing a cross-disciplinary lens to both their personal and work experiences. The guiding research question was, "How can the stories of women in the helping professions, who are sufferers of chronic pain and (dis)Ability, inform an anti-oppressive approach to social work practice in working with sufferers?" A close read is provided into the sufferers' professional storying, including their insights, reflections, and critiques of health services. An anti-oppressive model of social work is highlighted, extrapolated from participants' storied practices and collaborative visions for best practices in working with chronic pain sufferers.