Palliative and End-of-Life Care for Sexual and Gender Minority Cancer Survivors: a Review of Current Research and Recommendations

2021 ◽  
Vol 23 (4) ◽  
Author(s):  
Kristin G. Cloyes ◽  
Carey Candrian
2022 ◽  
Vol 164 (1) ◽  
pp. 6
Author(s):  
Stephanie Rieder ◽  
Ellen Burgess ◽  
Shoshana Adler Jaffe ◽  
Ariel Hurwitz ◽  
Miria Kano

2018 ◽  
Vol 28 (2) ◽  
pp. 442-444
Author(s):  
Karolina Lisy ◽  
Andrew Ward ◽  
Penelope Schofield ◽  
Nicholas Hulbert‐Williams ◽  
Jim Bishop ◽  
...  

2021 ◽  
Author(s):  
Catriona R Mayland ◽  
Rosemary Hughes ◽  
Tamsin Mcglinchey ◽  
Warren Donnellan ◽  
Kate Bennett ◽  
...  

2020 ◽  
Author(s):  
Carey Candrian ◽  
Kristin G Cloyes

Abstract Lesbian, gay, bisexual, and transgender (LGBT) older adults are at particular risk for receiving inequitable end-of-life care. Their health care wishes may be ignored or disregarded, their families of choice are less likely to be included in their decision making, and they may experience increased isolation, bullying, mistreatment, or abuse, which ultimately contribute to receipt of poor-quality health care. This is particularly important during sensitive transitions along the care continuum to end-of-life settings; 43% of respondents of a 2018 survey of 865 hospice professionals reported having directly observed discriminatory behavior toward LGBT patients. Lack of visibility and accountability perpetuates vulnerabilities and the potential for discriminatory treatment. Unfortunately, while other areas of health care have prioritized and normalized collecting sexual orientation and gender identity (SOGI) data, hospices do not routinely assess patients’ SOGI in the context of end-of-life wishes and decisions. Drawing insight from a sample of 31 in-depth interviews with older LGBT adults, this paper focuses on one participant’s story—Esther’s. We chose her story to illustrate how care can be compromised at the end of life if an open discussion with patients about what and who matters most to them at the end of life, is avoided.


2019 ◽  
Vol 22 (8) ◽  
pp. 902-907 ◽  
Author(s):  
Teresa M. Cooney ◽  
Adam Shapiro ◽  
Channing E. Tate

2014 ◽  
Vol 23 (4) ◽  
pp. 173-186 ◽  
Author(s):  
Deborah Hinson ◽  
Aaron J. Goldsmith ◽  
Joseph Murray

This article addresses the unique roles of social work and speech-language pathologists (SLPs) in end-of-life and hospice care settings. The four levels of hospice care are explained. Suggested social work and SLP interventions for end-of-life nutrition and approaches to patient communication are offered. Case studies are used to illustrate the specialized roles that social work and SLP have in end-of-life care settings.


Sign in / Sign up

Export Citation Format

Share Document