“…This research has done much to illuminate the politics involved in expert efforts to identify and control particular (personal, environmental and/or cultural) factors understood to increase the prevalence of disease in targetable groups or communities (Herrick, 2007; Hyde, 2011; Kent and Farrell, 2014; Wentzell, 2011). It has also provided insight on how lay individuals interpret, rework and contribute to expert conceptualizations of bodily risks, especially as they relate to risks of becoming ill (Hallowell et al, 2015; Lock, 2005; Morden et al, 2012; Novas and Rose, 2005). Such studies have convincingly demonstrated that bodily risks are not experienced or governed uniformly: the perception and identification of risk factors indicating a higher chance of acquiring a disease, and the ability to develop ways of responding to, or minimizing, those risks, vary greatly according to the individual’s particular condition, her life history and her socioeconomic, not to mention cultural, background.…”