“…For most people in Western health care systems, the first point of contact for health related concerns is a primary care provider À most often a primary care physician. Yet, we know from the literature that primary care physicians often lack knowledge about dementia (Koch & Iliffe, 2010;Pimlott et al, 2009a;Renshaw, Scurfield, Cloke, & Orrell, 2001;Reuben, Roth, Kamberg, & Wenger, 2003), lack confidence in recognizing the symptoms (Harris, Chodosh, Vassar, Vickrey, & Shapiro, 2009;Iliffe & Manthorpe, 2002;Koch & Iliffe, 2010;Pimlott et al, 2009b), are unsure about how or if to conduct cognitive screening (Harris et al, 2009), face constraints in providing the time-intensive support required for patients and caregivers (Harris et al, 2009;Hinton et al, 2007;Koch & Iliffe, 2010;Pimlott et al, 2009b), lack knowledge of how to manage behavioural or psychological symptoms (Harris et al, 2009;Koch & Iliffe, 2010;Reuben et al, 2009), and often harbour beliefs that little can be done therapeutically in any case (Koch & Iliffe, 2010;Renshaw et al, 2001). The complexity and increasing prevalence of this chronic disease caused us to wonder about how the science of primary care reform was influencing the literature around primary care support for people living with dementia in the community.…”