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One family took up the challenge of taking their mother, who had serious medical problems and the coronavirus, from the hospital to die at home. But because of the risk of infection, home hospice can be a daunting experience.
Fewer Americans are dying in a hospital, under the close supervision of doctors and nurses. That trend has been boosted by an expanded Medicare benefit that helps people live out their final days at home in hospice care. But as home hospice grows, so has the burden on families left to provide much of the care.
Kathy Brandt and her wife, Kim Acquaviva, national experts in hospice and palliative care, shared intimate details of Brandt’s experience with terminal cancer before her death Sunday.
For a generation of LGBTQ people who lived through unprecedented social change, getting older poses new challenges — lack of services, discrimination, neglect and even abuse.
Kathy Brandt and Kim Acquaviva are both leaders in the world of hospice and palliative care. When Brandt learned she was dying of ovarian cancer, the couple decided it could be a teachable moment.
In the bipartisan opioid bill headed to the president’s desk, hospice workers would be allowed to destroy patients’ unneeded opioids, reducing the risk that families misuse them.
A new government watchdog report outlines vulnerabilities in Medicare’s $17 billion hospice program, pointing to inadequate services, inappropriate billing and outright fraud.
Vietnam veterans’ wartime experiences — and their lasting psychological toll — can make it harder to treat their physical and emotional pain as they approach death.
Fewer than half of health care workers at a nonprofit Florida hospice had completed advance directives for end-of-life care.
During Northern California’s recent wildfires, dozens of hospice patients who had hoped to spend their last days in the comfort of their homes had to be relocated to evacuation shelters, assisted living facilities and relatives’ homes instead.
U.S. hospice agencies promise to be available around-the-clock to help patients dying in their homes. But a Kaiser Health News investigation shows that in an alarming number of cases, that promise is broken.
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.