Literature Review

The hospice moratorium: what CMS is really signaling about the future | part one Teleios Collaborative Network (TCN); podcast hosted by Chris Comeaux with Dr. Jennifer Kennedy; 9/2/26 In Part One of this timely conversation, host Chris Comeaux and co-host Cordt Kassner,  sit down with Dr. Jennifer Kennedy, Vice President for Quality, Standards and Compliance at CHAP, to unpack what the CMS hospice moratorium means, why it was implemented, and what hospice leaders should be watching next.  Jennifer explains how escalating concerns around fraud and abuse, rapid market expansion, transactional hospice models, accreditation oversight, and Medicare enrollment have created an unprecedented regulatory environment.  She also shares why she believes the moratorium could be extended as CMS continues strengthening enrollment screening and program-integrity efforts.

Stillwater Hospice brings palliative care to rural populations Hospice News; by Jim Parker; 9/2/26 Indiana-based Stillwater Hospice recently completed a rural palliative care pilot that the nonprofit plans to extend into a long-term program. The program’s roots were planted in October 2025. It emerged from a collaboration with Cameron Health, a community hospital in Angola, Indiana. ... Through the program, seriously ill patients who have been recently discharged from Cameron have access to a nurse practitioner for symptom management, patient and family education and goals-of-care conversations. Patients receive a phone call within three days of discharge and a visit within a week, ...

Levels of memory care and how they match changing dementia need The Good Men Project; by Alexander Reid; 8/31/26 Dementia care changes as memory impairment affects safety, communication, movement, and personal tasks. Early assistance might involve reminders, while advanced services can require continuous observation and extensive physical help. Families benefit from recognizing these changes before a crisis occurs. A careful review considers current abilities, medical conditions, personal preferences, and possible future needs. This process helps relatives compare residences confidently while preserving dignity, comfort, and familiar routines.

Bloom Healthcare expands Dallas-Fort Worth presence with acquisition of Christian Care House Calls Business Insider, Denver, CO; Press Release by GlobeNewswire; 8/31/26 Bloom Healthcare, a passionate team of medical providers specializing in in-home primary care for seniors with complex health needs, today announced its acquisition of Christian Care House Calls, a Dallas-Fort Worth-based home primary care practice. Effective August 31, Christian Care House Calls will operate under the Bloom Healthcare name, strengthening Bloom’s presence in the region and expanding its ability to provide high-quality primary care to patients in their homes and senior living communities. ... Through Bloom’s integrated Hospice, that coordinated approach can continue through end-of-life care, with individualized care plans that honor the wishes of patients and families and keep primary care closely involved throughout the care journey.

Priorities for advancing palliative care for Amyotrophic Lateral Sclerosis: a consensus report from a palliative care for ALS working group in the United States Muscle & Nerve; by Kara E. Bischoff, Yaowaree L. Leavell, Jessica M. Besbris, Christi Lero, Kelsey Noble, Astrid Grouls, Jerome Kurent, Benzi M. Kluger, Steven Z. Pantilat, Ambereen K. Mehta, on behalf of the International Neuropalliative Care Society's Palliative Care for ALS Working Group; 8/31/2026 The Palliative Care for ALS Working Group was formed within the International Neuropalliative Care Society, consisting of interprofessional ALS and palliative care clinicians, researchers, advocates, and patients and care partner representatives who are committed to improving palliative care for people living with ALS. The group engaged in a strategic planning process to determine what is needed to advance palliative care for people with ALS over the next 3–5 years. This report outlines the core recommendations from that strategic planning process. Recommendations are divided into five sections: (1) clinician education, (2) clinical service expansion, (3) research, (4) public awareness, and (5) policy change. Editor's Note: ALS is an especially devastating, demanding disease for patients, caregivers and families, for your clinical staff and volunteers. What disease-specific education and resources do you provide? How many ALS patients have your organization served in "x" years? Do you partner in any way with your regional ALS association? For non-clinical leaders, an important, easy distinction for you to remember the clinical, deeply personal differences between ALS versus ALZ: 

Beloved celebrities who opened up about their battles with dementia MSN; by Travis Reeed; 8/31/26 Dementia and Alzheimer’s disease have affected people from many walks of life, including some of the most recognizable figures in entertainment, politics, and culture. Their experiences helped bring greater attention to memory loss, cognitive decline, and the challenges faced by families and caregivers. From Hollywood legends to celebrated musicians and political leaders, these individuals continued to leave lasting legacies despite their health struggles. Their stories also helped encourage public conversations about conditions that were once poorly understood or rarely discussed openly. [Click on the slides to see personalized stories of Tony Bennett, Sally Kirkland, Ronald Reagan, Sean Connery, Margaret Thatcher, Rita Hayworth, and Jimmy Stewart.] 

Patient and caregiver perspectives on communication quality in tele-palliative care Journal of Palliative Medicine; by Julia I. Bandini, PhD, Elaine Li, BA, Dio Kavalieratos, PhD, FAAHPM, Natalie C. Ernecoff, PhD, Kimberly Curseen, MD, and Jordan Harrison, PhD; 8/27/26 Objective: To qualitatively explore patient and family caregiver experiences with telehealth and in-person visits for outpatient palliative care, including preferences related to mode of care and any perceived differences in communication quality by mode in a post-pandemic context. Results: Three themes emerged: (1) participants weighed convenience, symptom burden, and visit reason in choosing mode of care; (2) opinions differed on the authenticity of communication via telehealth; and (3) comfort and privacy shaped communication quality. Some patients and family caregivers perceived communication via telehealth as comparable to in-person care, while others felt in-person visits allowed for more authentic interactions. Many found that the convenience of telehealth outweighed any perceived differences in communication quality. In addition, some patients noted that without the option for telehealth, the benefits of an in-person palliative care visit may not have outweighed the travel burden.

Record-breaking Lube-a-Thon for Hospice GreatNews.Life; by Center for Hospice Care; 8/31/26 On July 31, Tom’s Car Care Center hosted the 21st Lube-a-Thon for Hospice. At this one-day event, customers get an oil change – full- or semi-synthetic oil, it doesn’t matter – and a car wash for a minimum donation of $50 to Center for Hospice Care. This year’s event broke the “modern-day” record for the number of cars serviced and the amount of money raised to support our promise that no one eligible for hospice care will ever be turned away, regardless of their ability to pay. The team at Tom’s changed the oil in 177 vehicles that day. The doors on the two bays opened just before 7am and there were cars in each of them until just before 6pm. In fact, cars started to line up at 6am – a full hour before the event began. Including donations and sponsorships, the event raised over $12,500, with all proceeds benefiting Center for Hospice Care.

AHA comments on CY 2027 Home Health proposed payment rule American Hospital Association; Press Release; 8/28/26 On behalf of our nearly 5,000 member hospitals, health systems and other healthcare organizations, including approximately 1,000 hospital-based home health (HH) agencies, our clinician partners — more than 270,000 affiliated physicians, 2 million nurses and other caregivers — and the 43,000 healthcare leaders who belong to our professional membership groups, ... The AHA has two significant concerns. First, CMS’ proposed payment update of 2.4% is inadequate. ... Second, the proposed rule includes substantial changes to Medicare provider enrollment authorities that would apply not only to HH agencies but also to all providers and suppliers enrolled in Medicare. 

The death I feared, and the peace I found Gillette News Record; by Michelle Mathal; 8/29/26 ... From the dreaded day my brother was diagnosed, to two years later when my parents tragically died in a car accident and I surfaced from the glacial water knowing I had to live to be his caregiver, to grieve alone. ... We enrolled in hospice earlier than most because Tomas was falling and losing movement in his left hand. ... No one told me that caring for a dying person would be so intimate. When I dressed him in the morning, I realized we had the same hands and feet, big enough that we should’ve been a foot taller. No one told me about the deep trust between caregiver and patient. It is a sacred pact not bound by blood, but an understanding that we would be seen at our most vulnerable and sensitive times, but not judge each other for these moments, but respect one another despite them.

[France] 'You cannot have a good assisted dying law without good palliative care’ GuardianTV; Press Release; 8/30/26 François Picard is pleased to welcome Anne Reynaud, Board Member of the Association for the Right to Die with Dignity. France’s long awaited assisted dying legislation marks a profound shift in the country’s approach to end of life care, but as Reynaud makes clear, the parliamentary vote is less the end of a debate than the beginning of a new ethical and legal era. Speaking from both personal experience and her professional role, Reynaud argues that the law represents meaningful progress while remaining more restrictive than the recommendations of France’s Citizens’ Convention. 

'They took care of me too': HIA Heather's House marks 1-year, nearing 400 patients InForum | Fargo Forum, Fargo, ND; by Kevin Wallevand; 8/28/26 Heather's House is celebrating its first year open, with nearly 400 patients receiving care through HIA so far this year. [HIA's Heather's House is North Dakota's first freestanding, inpatient hospice house. HIA had previously been known as Hospice of the Red River Valley before changing its name in June.] Editor's Note: Congratulations on this significant success. From an article we posted one year ago when they opened: "Ground was broken for the facility three years ago and administrative offices were moved into the building in February, but the dream began many years before that with hospice trailblazers Mary Lou Dahms, Sonia McManus and Edie Lohr." Be inspired by connecting-the-dots between their "dreams" and your own with today's "Today's Encouragement."