Literature Review

All posts tagged with “Education | Community.”



There aren't enough dementia providers in Arizona. This unique campus offers training

11/18/24 at 03:00 AM

There aren't enough dementia providers in Arizona. This unique campus offers training KJZZ Phoenix, AZ; by Kathy Ritchie; 11/15/24 Arizona has the fastest growth rate of Alzheimer’s disease in the country. Yet there are not enough paid caregivers or even geriatricians — only 92 in the entire state — for this population. So how do you educate, even inspire, health care students to care about dementia? As the saying goes, if you build it, they will come. Judy Ward is chatting with three nursing students from Creighton University when a group of preschoolers toddle on by. ... The children attend a care center located at Hospice of the Valley’s Dementia Care and Education Campus in Arcadia. That’s also where Judy’s adult day club for people living with dementia is situated, along with a 12-bed assisted living community and a hospice unit. ...

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Death is a natural part of life, but our society struggles to support those who are grieving.

11/15/24 at 03:00 AM

Death is a natural part of life, but our society struggles to support those who are grieving. Iowa Public Radio (IPR); host Charity Nebbe; 11/14/24 After a profound loss, the instinct is often to try and ease the pain for those who are grieving, but grief counselor Lynette Jordan says the pain of grief needs to be felt. This hour, host Charity Nebbe speaks with Jordan as well as mother and son Brianna and Grayson Wills about how they developed an open dialogue of grief in the seven years since the death of Grayson's twin brother, Calder. She also speaks with CL Lepley, who through experiencing many difficult losses since age five has become an expert in supporting those who are grieving. Guests:

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It's not just pumpkin spice time--it's time for the family conversation!

11/15/24 at 03:00 AM

It's not just pumpkin spice time--it's time for the family conversation! Dunlap Bennet & Ludwig; by George Reilly; 11/13/24 “Quality family time” is a phrase often heard in the period from Thanksgiving to New Year’s, sometimes even with air quotes, to describe what many people believe to be a necessary, but not necessarily enjoyable, time of family togetherness. ... Whatever your perspective on this “quality family time,” chances are that for most of you, it was/will be a missed opportunity to discuss very important matters with your loved ones—namely what happens in the event of disability or death; who takes care of what; a parent’s (or grandparents, or your own) wishes on the end of life medical care and funeral/burial/cremation choices; your wishes on guardians for minor children; and other critical, but admittedly sensitive and gloomy topics. ...  Consider these statistics from surveys conducted by the Conversation Project: ... 92% of Americans say it’s important to discuss their wishes for end-of-life care, but only 32% have had such a conversation! [Click on the title's link to continue reading.]

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Busting myths about hospice care: Dr. Laura Godinez

11/05/24 at 03:00 AM

Busting myths about hospice care: Dr. Laura Godinez Cleveland.com, Cleveland, OH; by guest columnist Dr. Laura Godinez, MD, an associate medical director fo  Hospice of the Western Reserve; 11/3/24 In an era in which misconceptions about hospice care persist, it’s crucial to set the record straight. Let’s address some common myths.

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Governor proclaims Home Care, Hospice, Palliative Care Month 2024

11/05/24 at 02:30 AM

Governor proclaims Home Care, Hospice, Palliative Care Month 2024Governor.nc.gov - an official website of the State of North Carolina; by Governor Roy Cooper; 11/1/24A PROCLAMATIONWHEREAS, the State of North Carolina recognizes the importance and value of home care, home health, hospice, and palliative care in enhancing the well-being and quality of life for individuals and their families; andWHEREAS, home care, home health, hospice, and palliative care providers offer essential services and support to individuals of all ages, ensuring their ability to receive necessary care in the comfort and familiarity of their own homes; andWHEREAS, being able to receive care and support in the comfort of one's own home allows individuals to maintain a sense of dignity, independence, and quality of life; andWHEREAS, the dedicated professionals of the home care, home health, hospice, and palliative care industry work tirelessly to improve the lives of North Carolina residents, providing compassionate care, emotional support, and necessary medical assistance; and ...WHEREAS, North Carolina's home care, home health, hospice, and palliative care providers play a crucial role in promoting patient independence, reducing hospital readmissions, and minimizing the burden on our healthcare system; NOW, THEREFORE, I, ROY COOPER, Governor of the State of North Carolina, do hereby proclaim November, 2024, as “HOME CARE, HOSPICE, PALLIATIVE CARE MONTH” in North Carolina, and commend its observance to all citizens. [Click here to read the full proclamation.]

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Hawaii Care Choices kicks off talk show about health care

11/04/24 at 03:00 AM

Hawaii Care Choices kicks off talk show about health care Hawaii Tribune Herald; 11/1/24 Hawaii Care Choices has launched “Let’s Talk Healthcare Hawaii!” — a new TV talk show and podcast dedicated to palliative care education. [Access to the full story requires subscription.]

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Blue Ridge Care expands bereavement care with new Center for Hope & Healing

11/04/24 at 03:00 AM

Blue Ridge Care expands bereavement care with new Center for Hope & Healing Hospice News; by Jim Parker; 11/1/24 Blue Ridge Care has unveiled its new Center for Hope & Healing, a facility dedicated to offering comprehensive grief care. The Virginia-based nonprofit hospice, palliative care and PACE provider financed the center through philanthropic donations. The facility is located in the same building as Blue Ridge’s PACE program, according to CEO Jason Parsons. At the center, Blue Ridge bereavement care staff will offer specialized programs, workshops, support groups and individual counseling. “The center is a central organizing unit of our mission fulfillment in the areas of grief, family support and loss in a place people can come to that’s welcoming, inviting and centered around hope and healing,” Parsons told Hospice News. ... The center was built to create a relaxing atmosphere to help put visitors at ease, according to Parsons, with a sky blue color palette and several murals depicting natural scenes. In one display, a collection of rocks symbolizes the weight of grief. Visitors can write a message on the rocks to “leave that weight behind,” Parsons said. They can also paint their loved ones’ names on a mural of a branching tree in the lobby area. 

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The Alliance Celebrates National Care at Home Month

11/01/24 at 02:00 AM

National Care at Home Month 2024: Celebrating Care at Home in November National Alliance for Care at Home (formerly NAHC and NHPCO); 10/31/24 National Care at Home Month celebrates and supports paid and unpaid caregivers and builds on the existing work of National Family Caregivers Month. Customizable templates are available now. ... The National Alliance for Care at Home brings together two legacy organizations – the National Association for Home Care & Hospice and the National Hospice and Palliative Care Organization – representing, advocating for, educating, and connecting providers of care in the home for millions of disabled, elderly, and dying Americans who depend on that care. ... To represent this strength in unity, the Alliance is introducing National Care at Home Month, an annual observance recognized each November to inspire outreach to communities, media, and policymakers, recognize the valuable contributions of provider staff and volunteers, and continue building awareness of the home care continuum. To this end, we are paying special attention to different types of care at different points throughout November.

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Advance Directives: How to make sure your end-of-life decisions are followed

10/25/24 at 03:00 AM

Advance Directives: How to make sure your end-of-life decisions are followed Bottom Line Inc; by Mathew D. Pauley, JD; 10/24/24 Nearly 40% of older Americans have some form of advance directives, such as a living will to communicate wishes about life-saving treatment…or a medical power of attorney appointing a loved one as proxy if they’re incapacitated.  Problem: Your wishes may not always be followed in real-world situations. Examples: Emergency paramedics typically provide CPR to restart a patient’s heart even if that patient’s living will says otherwise. And complex medical circumstances at the end of life often arise that force your loved ones to make judgment calls about what you really want. Bottom Line Personal spoke to clinical ethicist Mathew Pauley about how to make sure hospitals, medical providers and family members follow your medical wishes.

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Aging Mastery: 10 weeks, 10 topics to empower seniors for healthy living

10/22/24 at 03:00 AM

Aging Mastery: 10 weeks, 10 topics to empower seniors for healthy living New Hampshire Union Leaders; by Kathleen D. Bailey; 10/20/24 Jen Brechtel, director of Community Health for the Granite VNA, said one of the biggest issues in the agency’s “Aging Mastery” program” is sleep. “It’s the topic people come in most for,” she said. “We partner with a sleep center to help them out. Another big one? Community engagement.” The Granite VNA and Hospice is interested in all factors affecting their senior clients. With a menu of data-driven programs, the agency is reaching out to help seniors master aging. The “Aging Mastery” program is a project of the National Council on Aging, according to Brechtel. ... The 10-week class, ongoing now in Sanbornton, has sessions devoted to the concepts that please (or plague) elders: navigating longer lives, exercise, sleep, healthy eating/hydration, financial fitness, advance planning, healthy relationships, medication management, community engagement and falls. Experts from the community take turns teaching the topics, with a VNA staffer as moderator.

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Death cafes: Demystifying the inevitable over tea and cookies

10/16/24 at 03:00 AM

Death cafes: Demystifying the inevitable over tea and cookies MD edge - Internal Medicine News; by Megan Brooks; 10/15/24 “Death cafes” — where people gather to discuss death and dying over tea and cookies — have gained momentum in recent years offering a unique way for people to come together and discuss a topic that is often shrouded in discomfort and avoidance. It’s estimated that there are now about 18,900 death cafes in 90 countries, with the United States hosting more than 9300 on a regular basis. This trend reflects a growing desire to break the taboo surrounding discussions of death and dying. But these casual get-togethers may not be for everyone, and their potential benefits and harms may depend on who attends and who facilitates the discussion. ... [Click on the title's link to continue reading these significant cautions.]

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Top questions people ask about hospice

10/14/24 at 03:00 AM

Top questions people ask about hospiceThe Star News, Medford, WI; 10/9/24

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Palliative and hospice care in the prehospital setting

10/11/24 at 03:00 AM

Palliative and hospice care in the prehospital setting

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Free access to Spanish digital nursing text--Oct 10 to 20--celebrating World Hospice and Palliative Care Day

10/11/24 at 03:00 AM

Free access to Spanish digital nursing text: Oct 10-20, honoring World Hospice and Palliative Care DayLife and Death Matters (Canada); Kath Murray; 10/10/24Life and Death Matters is giving free access to our digital nursing text Lo Esencial en Cuidedos Paliativos: Un Recurso Practico en Enfermeria (Spanish) and companion workbook to health care providers. October 12th to celebrate WHPCD.  Register and sign up below for free access to the digital text! [Updates, not on the webpage] Free access is being extended to healthcare clinicians and leaders throughout the United States, from October 10-20, 2024. Click here to register for free access.  Edits from Kath Murray, CEO/Founder of Life and Death Matters, updated information from this webpage:]

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Hospices leverage school-based partnerships to strengthen bereavement care

10/09/24 at 03:00 AM

Hospices leverage school-based partnerships to strengthen bereavement care Hospice News; by Holly Vossel; 10/7/24 Some hospices have increasingly recognized the value of collaborating with local educators when it comes to improving community grief support for bereaved children and their families. Establishing collaborative relationships with educational institutions can help hospices ensure that they’re developing age-appropriate grief services, according to Cole Warner, director of support services at North Carolina-based Hospice of Davidson County. The nonprofit provides hospice services across 10 counties in its service area and also offers bereavement and veteran programs. The ability to identify and communicate grief-related emotions ranges across different age groups, and bereavement care teams need to be well-versed on youths’ cognitive capacity, Warner said. This involves having educators weigh in the common challenges that kids experience along their grief journeys. ...

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Community Crisis and Grief: Public service video and resources for hospice organizations, communities, and persons whose "normal" hospice bereavement can be disenfranchised

10/01/24 at 03:00 AM

Community Crisis and Grief: Public service video for communities, healthcare orgs, and persons whose "normal" hospice bereavement can be amplified and/or disenfranchised Composing Life Out of Loss; by Joy Berger; originally 5/30/22 in response to Uvalde's shootings, updated 9/29/24 in response to Hurricane/Storm Helene September 29, 2024 – We send support to the many communities, families, and individuals affected by Hurricane/Tropical Storm Helene’s devastation and loss. This public service education video defines different kinds of community crises; different groups of persons impacted with basic roles and tasks before and during a community crisis; community grief; and potential effects of community crisis/grief for persons who are already experiencing the “normal” bereavement of a loved one. Editor's note: Disclosure, I am the author/producer of this video; Composing Life Out of Loss is a sponsor for this newsletter. To immediately share with this free, public service video, click here for the link. To embed this video on your website (and thus eliminate any Composing Life branding), click here and complete this contact form. Be sure to leave a phone number for faster turnaround. 

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Community partnership helps Veterans navigate their health care

09/30/24 at 03:00 AM

Community partnership helps Veterans navigate their health care U.S. Department of Veterans Affairs, Washington, DC; by Dr. Chien Chen; 9/27/24 VA’s National Center for Healthcare Advancement and Partnerships (HAP) helps create and manage partnerships between VA and community organizations. The goal is simple: bring together VA and those in the community who share the same goals and mission when it comes to providing Veterans with outstanding health care and support. They are called Veteran Community Partnerships, or VCPs. “Developing and nurturing strong partnerships with VA and community providers is crucial to supporting Veteran health care,” said Dr. Jamie Davis, HAP health system specialist. “VCPs are instrumental in ensuring these partnerships enhance the health and well-being of Veterans across the country.” The East Bay VCP at Martinez VA is part of Northern California VA. Martinez VAMC and Veteran Community Partnerships focus on getting Veterans access to all available health care services. 

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Improv for Caregivers receives a grant from the New Hampshire State Council on the Arts

09/25/24 at 03:00 AM

Improv for Caregivers receives a grant from the New Hampshire State Council on the Arts EINPressWire; by A. A. Cristi; 9/23/24 The New London Barn Playhouse received an arts in health grant from the New Hampshire State Council on the Arts to continue and expand their Improv for Caregivers program through a larger umbrella program titled “Improv for a Cause.” “Improv for a Cause” will encompass two communication programs that use a similar process to reach different communities. The first, Improv for Caregivers, in partnership with Lake Sunapee Region VNA & Hospice, is an ongoing communication workshop series for those who care for loved ones with dementia and Alzheimer's. ... Each improv workshop session combines insight from healthcare professionals with improvisational theatre techniques, with a goal of developing new communication skills, strategies to cope with stress, flexibility in relationships, and an understanding of loved ones' changing perspectives. With guidance from the VNA and caregivers in the community, the team of actors prepare short scenarios that portray situations caregivers commonly face, such as sundowning, taking away car keys, collaborating with care staff, and hallucinations. ...

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Top 5 regrets people have on their deathbeds: What they can teach us about living healthy, fulfilled lives, from an internal medicine doctor

09/25/24 at 02:00 AM

Top 5 regrets people have on their deathbeds: What they can teach us about living healthy, fulfilled lives, from an internal medicine doctor NBC-6 South Florida; by Alex Koller, CNBC; 9/23/24 To live a meaningful, fulfilling life, you have to accept that it'll eventually come to an end, says Shoshana Ungerleider. Over the years of caring for ill hospital patients, Ungerleider — a doctor who specializes in internal medicine — has observed regrets among people near the end of their lives, she tells CNBC Make It. Here are five regrets she says people often express:

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Guidelines for supporting the dying and their families

09/23/24 at 03:00 AM

Guidelines for supporting the dying and their families Psychiatric Times; by Ken Druck, PhD; 9/19/24 There are few subjects that most of us, including those who work in mental health, avoid more than death and dying. Meeting the needs of the dying and their families requires a deep and clear understanding of competent and compassionate care for health care professionals and caregivers. Since the death of my 21-year-old daughter several decades ago, I have had the honor and privilege of helping countless individuals, families, and communities that have suffered losses. I have also been given the opportunity to teach and train mental health professionals and developed several programs and guidelines for supporting the dying and their families. My top 7 guidelines to share with patients and their families are as follows:

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Mayo Clinic Minute: Palliative medicine for cancer patients

09/18/24 at 03:00 AM

Mayo Clinic Minute: Palliative medicine for cancer patients Mayo Clinic; by Sonya Goins; 9/16/24 Patients undergoing cancer treatments often use palliative medicine to cope with nausea, fatigue and other bothersome symptoms. Palliative medicine is a medical specialty whose main focus is supporting patients and families/caregivers who need help managing symptoms related to cancer or side effects related to the treatment of cancer, along with other life-limiting diseases. Dr. Touré Barksdale, a Mayo Clinic cancer rehabilitation and palliative medicine specialist, explains the benefits of palliative care.

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The patient care experience on full display

09/17/24 at 03:00 AM

The patient care experience on full display Modern Healthcare; by Mary Ellen Podmolik; 9/13/24 Art exhibits can promote a visceral reaction. The one that just opened along a hallway of windows on Thomas Jefferson University’s health sciences campus certainly does just that. The installation includes five hospital beds, life-sized mannequins inside large pill bottles, personal possessions and deeply personal quotes from five unnamed people who’ve gone through life-threatening trauma — a miscarriage, a pulmonary embolism, a wait for a kidney transplant, a case of undiagnosed paralysis and cancer. The Philadelphia artist behind the exhibit, Pepón Osorio, is the cancer patient. “Convalescence” is a complex and compelling exhibit of patient pain, reliance on drugs and inequitable care — part of the patient experience that can get lost in the daily tussle between providers and payers. “It is a critique of the healthcare system,” Megan Voeller, director of health humanities at the university, told me.

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The persistent stigma attached to dementia encourages denial

09/17/24 at 03:00 AM

The persistent stigma attached to dementia encourages denial InForum; by Carol Bradley Bursack; 9/14/24 Dear Carol: ... At age 70, I was diagnosed with mild cognitive impairment (MCI). Theoretically, that diagnosis means that I have a few more memory glitches than normal for my age. A percentage of people with MCI will develop Alzheimer’s disease, but not all. Yet, some family members treat me like I shouldn’t make decisions beyond what I want for dinner. ...Dear Al: The stigma attached to mental illness, cognitive decline, and even aging, illustrates widespread ignorance of facts. The more people like you speak up the better the future will be for others. ... For now, work on educating your family about MCI.  ... Here's a start: 

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Simon Boas’ ‘inspirational’ book A Beginner’s Guide to Dying is published posthumously

09/16/24 at 03:00 AM

Simon Boas’ ‘inspirational’ book A Beginner’s Guide to Dying is published posthumously Jersey Evening Post; by Rod McLoughlin; 9/13/24 Friends and family of the late Simon Boas gathered ... to celebrate the posthumous publication of his book, A Beginner’s Guide to Dying. The former Jersey Overseas Aid chief executive – who died from throat cancer on 15 July at the age of 47 – spent his last months developing into a book ideas first explored in articles for the Jersey Evening Post. Described by the Daily Mail as “an inspirational paean to the joy of life”, Mr Boas’ words reached a huge audience after they were reprinted in the national press and broadcast on the BBC’s Today programme. A proportion of the proceeds are being donated to the African Palliative Care Association and the International Children’s Palliative Care Network. Mr Boas’ inspiring writings in the face of his terminal diagnosis saw him awarded the Bailiff’s Silver Medal in May. Shortly before his death, he also received a personal letter from the King and Queen ahead of their visit to Jersey.

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Phoenix Home Care and Hospice shares Medicare Mondays on Silver Notes

09/16/24 at 03:00 AM

Phoenix Home Care and Hospice shares Medicare Mondays on Silver Notes NBC KSNF-16,  Joplin, MO; byWendi Douglas; 9/12/24 News segment for community education about Medicare for seniors, provided by a local hospice nurse.

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