“…Family members of people who develop dementia are often the first to pick up on early symptoms or changes, but they may not understand the symptoms they are observing and, even with a diagnosis, experience difficulties in attributing changes to the person's dementia (Chenoweth & Spencer, 1986;Quinn, Clare, Pearce, & van Dijkhuizen, 2008). Studies exploring caregivers' understandings of dementia have found that caregivers may minimise the seriousness of symptoms by attributing them to ageing (Askham, 1995;Gray, Jimenez, Cucciare, Tong, & Gallagher-Thompson, 2009;Morgan & Laing, 1991), to the person never having had a good memory (Quinn et al, 2008) or to life events (Paton, Johnston, Katona, & Livingston, 2004).…”