We conducted a qualitative case study as part of a needs assessment for a d
ay hospice in a small Ontario city. Data were gathered from semi-structured
interviews with 28 stakeholders: nine health care administrators, 11 healt
h care providers, and eight lay people (terminally ill adults and informal
caregivers). Respondents described support, counselling, social activities,
and respite as key day hospice services. They also described several barri
ers to accessing services, including location, transportation, admission cr
iteria, referrals, and fees. For most respondents, the ideal staff mix incl
udes both volunteers and paid professionals in either a free-standing organ
ization or institutionally linked hospice. Although the vast majority of pa
rticipants were reluctant to impose admission criteria or other limitations
on hospice clientele, they expressed the need to ensure equitable access t
o this scarce resource. Opinions varied greatly across stakeholder groups,
highlighting the need to collect information from all relevant stakeholder
groups when planning hospices.