Body, Corporeal Space, and Legitimating Chronic Illness: Women Diagnosed with M.E.

The trendiness in using the body as a unit of analysis does not keep us from trying to understand how the body is part of the mundane stuff that makes up everyday life, particularly the chronically ill body. In our research with women diagnosed with chronic illness, we found that women experience their bodies, both sensorially and in their capacity for labor and leisure, through social scripts, seeming economic imperatives, and their own blood, sweat, and tears. The synchronous existence of the discursively ill and materially ill body seemed to be highlighted in these women's accounts of their experiences of myalgic encephalomyelitis (M.E., popularly referred to as Chronic Fatigue Syndrome or CFS). This spurred us to rethink the body in terms not just of embodied social practices but also of embodied experiences. In this paper we draw on women's experiences of M.E. as a way to assist in building a radical body politics. We first review and critique various attempts to come to terms with the simultaneity of the discursive and material body. We then present our empirical study comprised of in‐depth interviews with women diagnosed with M.E. and living in Victoria and Vancouver, British Columbia, Canada. We then elaborate the notion of corporeal space as a way to access embodied experience. We close with comments about how body and space create a nexus through which we can access bodily existence within space.