Login / Signup

A first voice perspective of people experiencing homelessness on preferences for the end-of-life and end-of-life care during the COVID-19 pandemic.

Cait VihvelinViraji RupasingheJean HughesJeff KarabanowLori E Weeks
Published in: BMC research notes (2022)
A key finding focused on the existential struggle experienced by the participants in that they did not care if they lived or died. The participants described dying alone as a bad or undignified way to die and instead valued an EOL experience that was without suffering, surrounded by those who love them, and in a familiar place, wherever that may be. This study serves to highlight the need for improvements to meet the health care and social justice needs of people experiencing homelessness by ensuring equitable, humanistic health and end-of-life care, particularly during the context of the COVID-19 pandemic.
Keyphrases
  • healthcare
  • mental illness
  • palliative care
  • mental health
  • public health
  • health information
  • quality improvement
  • affordable care act
  • chronic pain
  • decision making
  • climate change