“…Studies either focus on a more diverse population of HMV users or focus on one aspect of care (Ingadóttir & Jonsdottir, 2006;Schaepe & Ewers, 2017). Several studies identify the quality of relationship with carer-givers as important (Dreyer et al, 2010a(Dreyer et al, , 2010bSchaepe & Ewers, 2017) and Ballangrud et al (2009) found feeling in control of one's care was important. Nurses and family members are the most prominent characters in descriptions of care for HMV, but there can also be a need for specialist care requirements like speech therapy (Laakso, Markström, Idvall, Havstam, & Hartelius, 2011).…”