Tiny Washington state hospice accepts no federal funds, relies on community volunteers and donations to serve the dying.
Hospice care often prompts fear and misunderstanding, but the services provided can lead to less pain and trauma at the end of life.
As more patients receive hospice care at home, some of the powerful, addictive drugs they’re prescribed are ending up in the wrong hands.
This is the first federal website designed to help families choose a hospice, but experts aren’t impressed.
Traditionally there for mothers giving birth, a doula’s role has evolved to comforting seniors facing death.
A San Diego program helps chronically ill people avoid the hospital by teaching them how to better manage their diseases and telling them what to expect in their final years. Other health providers and insurers around the country are trying similar approaches.
Hospice groups are teaming up with specially trained paramedics to deal with common problems that worried patients or families incorrectly think need hospital care.
Ending pain and suffering has helped several states pass “right-to-die” laws, but dying patients are more concerned about controlling how they die and dying with dignity.
A Kaiser Family Foundation analysis sheds new light on a widely-held belief about the costs of end-of-life care.
KHN consumer columnist Michelle Andrews answers questions about Medicare beneficiaries’ costs associated with doctors who have concierge medicine practices, insulin pumps and respite care.
Hospice use has been growing fast in the United States as more people choose to avoid futile, often painful medical treatments in favor of palliative care and dying at home surrounded by loved ones. But some African-Americans have long resisted the concept, and their suspicions remain deep-seated.