“…Calvey and Mee (2011) report that haemodialysis highlights a need for patients to define a new sense of self because of the illness. This is due in part to the chronic nature of the illness and the frustration (Polaschek, 2003a), loss of freedom (Hagren, Pettersen, Severinsson, Lützen, & Clyne, 2005), boredom (Moran, Scott, & Darbyshire, 2009) and dependence (Strandberg, Åström, & Norberg, 2002) that the illness creates. Polaschek (2003b) suggests that the strength of qualitative studies is that they offer a better understanding of the experience of people living on haemodialysis, and provide an opportunity for health professionals to gain insight into the experiences of the patient and therefore be able to provide more adequate support and understanding of the issues that haemodialysis patients face.…”