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Journal of Palliative Medicine|April 11, 2003
Correlates of health status for family caregivers in bereavementKevin Brazil, Michel Bédard, Kathleen WillisonJournal of Palliative Medicine|October 17, 2006
Caregiving at the end of lifeRandy S Hebert, Richard SchulzJournal of Palliative Medicine|April 30, 2005
Reciprocal suffering: the need to improve family caregivers' quality of life through palliative careD W ShermanJournal of Palliative Medicine|March 28, 2008
What questions do family caregivers want to discuss with health care providers in order to prepare for the death of a loved one? An ethnographic study of caregivers of patients at end of lifeRandy Scott Hebert, Richard Schulz, Valire Copeland, et al.Journal of Palliative Medicine|November 5, 2008
Family discord and proxy decision makers' end-of-life treatment decisionsLaraine Winter, Susan Mockus ParksJournal of Palliative Medicine|June 11, 2009
Assessing families in palliative care: a pilot study of the checklist of family relational abilitiesVictoria M Wilkins, Timothy E Quill, Deborah A KingJournal of Palliative Medicine|March 4, 2009
Pediatric palliative care: describing hospice users and identifying factors that affect hospice expendituresCaprice A Knapp, Elizabeth A Shenkman, Mircea I Marcu, et al.Journal of Palliative Medicine|May 8, 2026
"We Talk About Everything": Experiences with Digital Health Communication in Palliative CareSarah Nouri, Courtney R Lyles, Carly Zapata, et al.Journal of Palliative Medicine|May 4, 2026
Top Ten Tips All Palliative Care Clinicians Should Know About Anorexia Nervosa and Eating Disorder CareGregg A Robbins-Welty, Julie Childers, Elaine Morgan, et al.Journal of Palliative Medicine|May 7, 2026
Left Behind: Addressing the Impact of Family Separation Due to Immigration Policies on the Suffering of Patients with Advanced CancerMonica Agosta, Gladys Janice Jimenez-Torres, Eduardo Bruera, et al.Pageof 414