I have spent my entire adult life
working in urban, low-income communities. With a 96% poverty level, my school
where I was principal in Detroit had more homeless students than any school in
Michigan. If you are working to deliver palliative care to inner-city patients
and caregivers in these communities, you must become knowledgeable about the
social and economic barriers that can hinder their access to quality palliative care.
A healthcare focus group consisting of community stakeholders including healthcare professionals,
persons living with chronic illnesses, and caregivers in five inner-city
communities reported these five themes:
1)
Lack of family
support
2)
Communication
barriers with healthcare professionals
3)
Stresses of being
a person of color or another minority
4)
Caregiver burdens
5)
Lack of spiritual
support
Community outreach is
mandatory for reaching this population. Also needed are cultural sensitivity,
available resources, and services to improve access to care. Low-income
populations with chronic illnesses in urban communities are entitled to quality
of life just like everyone else. This isn’t only a healthcare issue. It’s a
moral one.
Frances Shani Parker,
Author
Becoming Dead Right: A Hospice Volunteer
in Urban Nursing Homes is available in paperback and e-book
editions in America and other countries at online and offline booksellers.
Hospice and Nursing Homes Blog
Hospice and Nursing Homes Blog