“…Numerous researchers have examined the experiences of young caregivers (e.g., Aldridge & Becker, 1999;Antoun & Frank, 2003;Arnaud, 1959;Banks et al, 2001;De Judicibus & McCabe, 2004;Frank, 2002;Lackey & Gates, 2001;Olsen, 1996;Packenham & Bursnall, 2006;Power, 1977;Thomas et al, 2003;Warren, 2007), but few have specifically examined the intersection of their experiences as caregivers of mothers with MS and play. Given the importance of play, the purpose of this study was to describe how daughters who are caregivers to their mothers with multiple sclerosis experienced play.…”