Literature Review
All posts tagged with “General News | Changing the Culture of Dying.”
End-of-life care needs cultural humility and social justice
12/22/25 at 02:00 AMEnd-of-life care needs cultural humility and social justice BMJ; by Jamilla Akhter Hussain, Rekha Vijayshankar, and Mary Hodgson; 12/18/25 Death, dying, and grief are not medical events—they are profoundly social, relational, and shaped by the histories people carry into their final days. ... [A] key question is: how can end-of-life care services become more trustworthy? Too often, institutions respond with so-called cultural competency initiatives. ... What is needed is cultural humility and social justice. Cultural humility involves ongoing self-reflection and acknowledgement of bias at individual, organisational, and system levels. Palliative care must prioritise cultural humility and social justice: trust grows not through outreach alone but through shared creation of knowledge, meaning, and care—and at the end of life ...
She has a young hospice patient who can’t financially afford the $2,400 to die
12/19/25 at 03:00 AMShe has a young hospice patient who can’t financially afford the $2,400 to die ChipChick; by Emily Chan; 12/17/25 Most people worry about how they’ll live, not how much it costs to die. But for TikToker Jordan ..., who is a hospice nurse, one heartbreaking conversation with a young patient exposed a reality that many people don’t want to think about. She has a young patient who is dying and needs to make plans for the end of her life. She was looking into cremations because those are usually cheaper than caskets. Still, they are expensive, and this patient told Jordan that she cannot financially afford to die.
Is moral adequacy possible in the face of structural disadvantage? The experiences of health and social care staff in supporting homeless people using substances at the end of life
12/19/25 at 02:00 AMIs moral adequacy possible in the face of structural disadvantage? The experiences of health and social care staff in supporting homeless people using substances at the end of life Palliative Care and Social Practice; by Gary Witham https, Gemma Anne Yarwood, Sarah Galvani, Lucy Webb, and Sam Wright; 11/26/25 Background: Homeless people using substances at the end-of-life face many challenges in accessing and receiving good care. These can relate to poor interdisciplinary working by health and social care practitioners, stigma and structural disadvantage. Results: The data analysis resulted in three key discourse positions relating to how practitioners position themselves in relation to the practice challenges of supporting homeless people using AODs and approaching end of life. These were as follows: (i) what constitutes a good death and where, (ii) the limitations of professional boundaries and (iii) maintaining moral adequacy in the face of traumatic death.
Perceptions of family caregiving change across demographic lines
12/16/25 at 03:00 AMPerceptions of family caregiving change across demographic lines Hospice News; by Holly Vossel; 12/12/25 Family caregiver burden may be falling heavier on the shoulders of certain demographic groups compared to others, a new survey has found. Perceptions of family caregiver roles and responsibilities vary vastly across different age groups, geographic regions and genders, a new survey from BURD Home Health has found. Survey responses were analyzed by demographics such as gender, income, age and geographic location. Among the main goals was to identify patterns and disparities in how caregiving duties are perceived and distributed, according to Justin Colline, director of marketing at BURD Home Health.Editor's Note: Key findings from the source survey include ..
My patient was gone. I had to help his family see it: The art of medicine means sitting with families’ grief and hope
12/16/25 at 02:00 AMMy patient was gone. I had to help his family see it: The art of medicine means sitting with families’ grief and hope Stat10 - First Opinion; by Raya Elfadel Kheirbek; 12/15/25 Bullets tore through Michael Thompson’s car at a stop sign, ending the life of a 35-year-old father in an instant. Just minutes earlier, he had dropped his 8-year-old daughter, Emma, at dance class, her pink tutu bouncing as she waved goodbye. Now, in the ICU, his young body lay tethered to machines — ... a ventilator’s hiss forcing his chest to rise. ... His family’s grief filled the room, raw and heavy, as I prepared to document our meeting. On the screen, a pop-up appeared: “Patient is deceased; do you want to continue?” Its cold bluntness paled against their pain. Michael looked alive. His chest rose and fell with the ventilator. ... Medicine isn’t just tests or machines. It is presence — sitting with families in their grief, faith, and love. Our tools should support that presence, not interrupt it with cold prompts. ... Most U.S. hospitals lack clear guidelines for these situations, leaving families and clinicians alike in limbo. They also worried about organ donation — a decision fewer than 1% of families consent to after brain death, often because the body still looks alive.Editor's Note: We thank the palliative care physicians, nurses, social workers, and chaplains who provide sensitive presence with families in the unbearable spaces between hope and loss, especially when life support decisions arise. In this season, may we pause to honor those who carry this sacred work—and remember the families who have had to accept harsh truths while machines still “breathe.”
A flight to the North Pole
12/15/25 at 03:00 AMA flight to the North Pole Fairfax County Times, Reston, VA; by Kristin Johnson; 12/12/25 Last Saturday morning [12/6], Gate D15 at Dulles Airport was filled with families wearing Christmas sweaters and pajamas. They were waiting for a 10 a.m. departure to the North Pole. The Fantasy Flight is a 30-minute plane ride that takes off annually on the first weekend in December. The event is for the families of children currently in hospice or long-term care. ... The mood at the gate is festive, but a little chaotic. The busyness helps to dull Tabitha Johnson’s grief. Her son died in hospice three weeks ago. She decided the family should still come.
Award-winning documentary chronicles hospice nurse’s final 39 days
12/12/25 at 03:00 AMAward-winning documentary chronicles hospice nurse’s final 39 days Hospice Foundation of America (HFA) and TGBeyond, Washington, DC; Press Release; 12/1/25Hospice Foundation of America (HFA) and TGBeyond today announced the release of A Butterfly Has Been Released, an award-winning short documentary, alongside a new professional continuing education program, From Caregiver to Patient: Hospice Nurse Allyson’s Final 39 Days. Pre-purchase is available now, with formal release in January 2026. The 36-minute film follows Allyson, a hospice nurse with more than 20 years of experience guiding patients and families through death and grief, as she navigates her own final 39 days after a life-limiting diagnosis. Through candid kitchen-table conversations, a 150-person living funeral, and a natural green burial, Allyson demonstrates what she spent decades teaching others: live with purpose, presence, and connection until the very last day.Editor's Note: Is the concept of a "living funeral" new to you? I've seen this moving film several times, with a group discussion among healthcare professionals led by its producers Jason Zamer and Barry Koch. Click here for its 2-minute trailer.
From compliance to cultural conscience
12/05/25 at 03:00 AMFrom compliance to cultural consciencePharmaLive.com; by Adela King, Inizio Evoke; 12/1/25 If patients can’t see themselves in your ads, they won’t see themselves in your brand. ... But don’t mistake this as a call to diversify casting alone. It’s a call to dig deeper and connect with cultural relevance, not just appearance.
Rediscovering purpose in the hardest moments of cancer care
11/26/25 at 03:00 AMRediscovering purpose in the hardest moments of cancer care Medscape; by Mark A. Lewis, MD; 11/7/25 ... I'm a GI oncologist, and about a quarter of my patients have metastatic pancreatic cancer. Treat that awful disease often enough and, believe me, you start to doubt your own abilities as a supposed healer. I mean, talk about overpromising and underdelivering. ... When you judge your worth by your outcomes, especially longevity, imposter syndrome sets in like dry rot, and feelings of ineffectiveness lead to therapeutic nihilism in the very caregiver that patients look to for hope. It turns out, though, the best antidote to self-pity is right in front of me every day: my patients. ...
Letters without limits: Jesse Tetterton
11/25/25 at 03:10 AMLetters without limits: Jesse Tetterton The Johns Hopkins News-Letter; by Omkar Katkade; 11/22/25 Letters Without Limits, founded by students at Johns Hopkins and Brown University, connects volunteers with palliative care and hospice patients to co-create “Legacy Letters.” These letters capture memories, values and lessons that patients wish to share, preserving stories that might otherwise be lost. By honoring these voices and preserving legacies, Letters Without Limits hopes to affirm the central role of humanism in medicine, reminding us that every patient is more than their illness and that their voices deserve to be heard.
Geisinger medical students accompany Scranton, Wilkes-Barre Allied hospice patients with No One Dies Alone program
11/25/25 at 03:00 AMGeisinger medical students accompany Scranton, Wilkes-Barre Allied hospice patients with No One Dies Alone program WWIA/PBS/NPR; by Lydia McFarlane; 11/23/25 Tommy Ahlin was very close with his grandfather. He looked up to the man he called “Pap-Pap” for his military service, wisdom and family values. He spent the last few months of his life in a nursing home under hospice care, where he died at age 97. “Unfortunately, on the day he passed, he did pass by himself and was alone for a couple of hours before anyone got to him," Ahlin said. ... Ahlin, a second-year student at Geisinger Commonwealth School of Medicine, or GCSOM, is now a representative for the No One Dies Alone program, which partners the medical school with Allied Services Hospice. Program volunteers vigil sit, which means to provide company to hospice patients whose loved ones can't be with them.
Community puts together Christmas parade for 6-year-old in hospice care
11/19/25 at 03:00 AMCommunity puts together Christmas parade for 6-year-old in hospice care NBC WSAV-3, Savannah, GA; by Ava Cartes; 11/16/25 A Savannah community came together Saturday evening at a rally behind a little girl and her family. A six-year-old girl from the Willow Point neighborhood in Savannah recently entered hospice care, and after learning the news, her community came out to celebrate Christmas—her favorite holiday. Neighbors organized a display of Christmas lights and even a parade to show their support for the family.
How one Lafayette man's offer to cook for families in need turned into a mission
11/18/25 at 03:00 AMHow one Lafayette man's offer to cook for families in need turned into a mission The Acadiana Advocate; by Adam Daigle; 11/17/25 Kent Zerangue planned to open a catering business when he retired in 2017, but one experience overshadowed any need to make money. ... He began cooking for families in need and launched Food With Love, “a heart centered ministry of Hospice of Acadiana.” ... He had 10 families in six months. ... Today, Food With Love serves about 135 families and prepares about 800 meals a week.
What is healthspan, and how can you extend yours?
11/13/25 at 03:00 AMWhat is healthspan, and how can you extend yours? MSN - Everyday Health; by Sarah Klein; 11/11/25 Many people want to live as long as possible. But what about living as well as possible? Thats the idea behind extending whats called your healthspan. Healthspan is the length of time you live in good health, able to stay active, independent, and mentally sharp while doing the things you enjoy, ...
Pidgie Chapman marks nearly four decades as a hospice volunteer
11/12/25 at 03:00 AMPidgie Chapman marks nearly four decades as a hospice volunteer The Pilot; by Maggie Boncurrter; 11/7/25 The ladies weren’t exactly Thelma and Louise of big screen fame, but they probably looked very similar driving through the Moore County community of Addor. FirstHealth Hospice volunteer Pidgie Chapman had a patient decades ago who loved to dress up and wear fancy hats. Chapman had quite the chapeau collection, so she presented her patient with a giant, floppy hat while donning a similar one. “In those days we could drive our patients around,” said Chapman, who has been a hospice volunteer since 1986. “We got in the car and visited all her friends – in our hats. She was absolutely delighted.” ... Chapman is one of the area’s most seasoned hospice volunteers, starting her career soon after the philosophy of care took hold in Moore County.
* "The Wounded Generation": Bearing the invisible scars of war
11/11/25 at 03:00 AM"The Wounded Generation": Bearing the invisible scars of war CBS News; by Lesley Stahl; 11/9/25 In 1984, President Reagan commemorated the 40th anniversary of the invasion of Normandy, and paid tribute to the World War II soldiers known as "The Greatest Generation." ... But in his new book, historian David Nasaw calls them "The Wounded Generation." "They are the Greatest Generation, but they returned from war, bringing wounds home with them that are invisible; they're psychic wounds," he said. "Now we know that a lot of those wounds were PTSD. But PTSD was not diagnosed for 40 years after the return of the World War II veterans. ... Nasaw said [of his own father,] "He came home smoking three or four packs of Luckys a day. He came home with a heart condition from the war. He dies at age 61. And I had never had the chance to find out what happened in Eritrea, what he went through. So, what do I do as a historian? I can't find out his story, so I jumped in to find out the story of his generation."Editor's Note: While most World War II veterans are now gone, many of today’s hospice patients—particularly those who served in combat—carry similar invisible scars. Their psychic wounds, once unnamed, often resurface in life’s final chapter. This story also echoes in their adult children, who now seek to understand the unspoken pain that shaped their families. For more insight and support—especially regarding post-9/11 veterans—see the Wounded Warriors Project.
Hospice of Orange & Sullivan’s sixth annual community breakfast features caregivers’ emotional stories of courage, compassion and dignity
11/11/25 at 03:00 AMHospice of Orange & Sullivan’s sixth annual community breakfast features caregivers’ emotional stories of courage, compassion and dignity FocusMedia, Middletown, NY; Press Release; 11/7/25 Hospice of Orange & Sullivan Counties, Inc.’s Sixth Annual Community Breakfast celebrated the profound difference Hospice makes through caregivers who shared touching stories of supporting patients during their final life journey. The ”Real Stories, Real Impact” panel discussion was moderated by Eric Gatsik, President and CEO of Hospice of Orange & Sullivan Counties and Heather Bell-Meyer, President and CEO of the Orange County Chamber of Commerce. About 115 attendees at the Barn at Villa Venezia connected, reflected and were inspired by stories of love, dignity and trust offered to patients at the end of their lives.
Non-profit that brought beauty, joy to hospice patients closes its doors
11/10/25 at 03:00 AMNon-profit that brought beauty, joy to hospice patients closes its doors Gold Country Media, Auburn, CA; by Midori Sperandeo; 11/4/25It has been said flowers are sunshine and medicine for the soul. For 12 years, that was the mantra of volunteers for The Petal Connection, who collected donated flowers from local businesses and created lovely bouquets – a little sunshine in a bottle – for people who needed them most. The special floral deliveries were made to hospice patients and senior citizens throughout the region, in Auburn, Folsom, Lincoln, Roseville and Rocklin. During the time The Petal Connection was in existence, volunteers delivered almost 130,000 bouquets, bringing brightness to people whose outlook could often be bleak.
Influencer Kaelin Bradshaw's tragic death at age 29 shared by her husband
11/06/25 at 03:00 AMInfluencer Kaelin Bradshaw's tragic death at age 29 shared by her husband Distractify; by Kelley Schepper; 11/3/25 Searches for Kaelin Bradshaw's cause of death surged after the TikTok creator’s tragic passing. Kaelin had documented her symptoms, diagnosis, and hospice move with unflinching honesty. She died on October 27, 2025, at the age of 29, peacefully and surrounded by family, according to her husband. ... Her last videos back that up with a clear timeline.
The Valerie Fund pledges $3.5 million to establish new pediatric pain and palliative care program at Hackensack Meridian Joseph M. Sanzari Children’s Hospital
11/06/25 at 03:00 AMThe Valerie Fund pledges $3.5 million to establish new pediatric pain and palliative care program at Hackensack Meridian Joseph M. Sanzari Children’s Hospital News Wise, Hackensack, NJ; by Hackensack Meridian Health; 11/3/25 Hackensack Meridian Joseph M. Sanzari Children’s Hospital today announced a transformative, 5-year, $3.5 million commitment from The Valerie Fund to significantly expand its Pediatric Pain and Palliative Care Program. The landmark donation will establish The Valerie Fund Pediatric Pain and Palliative Care Program at the Joseph M. Sanzari Children’s Hospital, located at Hackensack University Medical Center in Hackensack, NJ, ... This new partnership will allow the hospital to care for more people annually, growing from approximately 1,750 to 3,500 patient visits.
Alive Hospice founders mark 50 years by reflecting on how their first patient molded them
11/05/25 at 03:00 AMAlive Hospice founders mark 50 years by reflecting on how their first patient molded themThe Tennessean; by Brad Schmitt; 11/2/25 ... The third hospice program in the world launched in Nashville in 1974 with coffee and doughnuts. One of its cofounders, Vanderbilt psychiatrist David Barton, felt the hospitals could be institutionally apathetic toward terminally ill patients. "There was a bit of aversion to being constantly around people whose lives are ending," Barton said. So, after studying about dying and reading about hospice care facilities that had opened in London and Connecticut, he bought refreshments and invited eight people to his West Meade home. ... Barton pitched the idea to those eight, who included a few other doctors, a neighbor with cancer, his rabbi, and his wife, who by that point had become a clinical social worker. At meeting's end, he had pledges of support. Within a year, they had raised $57.
How to prepare for your death [podcast]
11/04/25 at 03:00 AMHow to prepare for your death [podcast] MedPage Today's KevinMD.com; podcast by KevinMD with Joseph Pepe; 10/31/25 Physician executive Joseph Pepe discusses his article, “A doctor’s guide to preparing for your death.” He shares practical and compassionate advice on planning for life’s inevitable end, from organizing essential documents and creating a “death folder” to protecting loved ones through wills, trusts, and life insurance. Joseph explains why facing mortality head-on allows people to live more freely and meaningfully.
HBO’s ‘The Pitt’ inspires viewers to consider organ donation, end-of-life planning
11/04/25 at 03:00 AMHBO’s ‘The Pitt’ inspires viewers to consider organ donation, end-of-life planning WBOG Country 101.3; by Ozzy; 10/28/25 A University of Southern California study reveals HBO’s Emmy-winning The Pitt motivates viewers toward organ donation and end-of-life preparations. Research examining two multi-episode storylines shows 26.9% of surveyed audiences sought organ donation information while 17.2% shared donation details with others. The organ donation narrative particularly resonated with Black viewers, a demographic overrepresented on transplant waiting lists yet underrepresented as donors. Editor's Note: The Pitt's storyline involving organ donation is from Season 1, Episode 6, titled' 12:00 P.M."
Health Talk: National Care at Home Month
11/04/25 at 03:00 AMHealth Talk: National Care at Home Month Rutland Herald, Rutland, VT; by Nicole Moran; 11/1/25 Throughout the month of November, VNA & Hospice of the Southwest Region (VNAHSR) will join organizations across the nation in recognizing and celebrating National Care at Home Month.Editor's Note: This article demonstrates great community outreach and education through local new outlets and national observances. For more visit our post, "November 2025 Healthcare Observances," and our ongoing Healthcare Observances webpage for additional dates.
Hospice of the Valley launches support group for people with mild cognitive impairment
11/04/25 at 03:00 AMHospice of the Valley launches support group for people with mild cognitive impairment Lovin' Life; by Lin Sue Flood; 11/2/25 Living with mild cognitive impairment (MCI) can be an isolating experience, but a new program from Hospice of the Valley offers a welcoming space for connection and support. GATHER is a peer-led group where individuals diagnosed with MCI can share their experiences, navigate emotions, and discover new coping strategies together. ... GATHER provides a safe environment for members to lead their own discussions. Unlike traditional support groups, members are empowered to guide conversations toward topics that are most relevant to them. This novel format models successful programs in Europe.
