“…They may take up several roles ranging from administrative and fundraising to providing companionship and support (Emanuel et al, 1999;Handy & Srinivasan, 2004;Wilson et al, 2005), and can positively influence the quality of care for both terminally ill people and those close to them by reducing stress and offering practical and emotional support and providing a link to the community (Block et al, 2010;Burbeck et al, 2014;Luijkx & Schols, 2009;McKee, Kelley, Gulrguis-Younger, MacLean, & Nadin, 2010;Morris et al, 2012). Faced with increasing resource constraints in professional healthcare, some governments are turning to informal care to make up a greater proportion of care provision (e.g., through volunteerism) (Arno, Levine, & Memmott, 1999;Astrain, 2018;Fast, Keating, Derksen, & Otfinowski, 2004;Help the Hospices, 2006;Janssen, Jongen, & Schröder-Bäck, 2016;Knickman & Snell, 2002;Triantafillou et al, 2010). Volunteers can provide palliative, direct patient care in both dedicated palliative care and in generalist palliative care (i.e., palliative care provided by regular professional caregivers such as the hospital specialist, general practitioner, home-care nurses, nursing home staff) providing psychosocial, signalling (e.g., being an intermediary, communicating needs to professional caregivers, etc.)…”