Posts Tagged ‘Hospice’

Symptom Relief for Terminal Illness

Thursday, November 19th, 2009

Caring for a loved one.

Caring for a loved one.

If you are a caregiver, you may have had training in symptom relief for terminally ill patients. But, many family members now take care of their loved ones at home, and training may come through experience only. If you are one of those latter individuals, spend some time at the library, as many books about caregiving can be found on the book shelves. Also, calls to local hospice organizations or training programs offered by hospitals can help provide information as well.

Some basic information about symptom relief is listed below, and these solutions apply to any person at any age — even if they do not have a terminal illness. These problems may frighten a caregiver at first, but they are common problems, and solutions are available. Remember to rely on a trained hospice worker, a trusted nurse or a doctor for specific directions for your ‘patient’ before you take extreme measures.

Constipation: This is a common problem during the last stages of terminal illness, because the patient may not be physically active. Some solutions include increasing fiber in the diet with foods such as prune juice and bran cereal. Sufficient fluids also help to resolve the problem in many instances. Only give stool softeners or laxatives as a doctor may recommend. He or she may recommend them, as constipation can be a side effect of some medications. The warning sign for severe problems – one that warrants a call to the doctor – is constipation for more than three days or blood in the stool.

Eating and Drinking: Smaller and more frequent meals may resolve the eating problem. Some physical activity, if the patient can tolerate it, also helps stimulate appetite. Fluids are, sometimes, the most important issue. Dehydration can develop rapidly in people who do not drink enough fluids. Use a straw or offer ice chips to suck. Be aware that too many fluids also are dangerous and providing intravenous fluids to a person who is dying may result in respiratory distress. Follow a doctor’s instructions on how much food and fluid is ‘normal’ for your patient’s situation.

Breathing Problems: Breathing problems can occur during the final stage of any illness and may require oxygen. Another way to help open breathing passages is to elevate the head of the patient’s bed or to move the patient to a recliner. A doctor may prescribe small doses of liquid morphine or bronchodilator drugs. Follow orders for these prescriptions carefully. Opening a window on a mild day or running a fan in the patient’s room also can help improve air circulation.

Nausea and Vomiting: This problem may occur as a side effect of some medications or as a result of the disease. Do not force a nauseated person to eat. Use ice chips instead of drinking to help retain body fluids. Overt vomiting is an issue, however, as the patient may not be able to keep down medication. A doctor may order medication in suppository form if the patient continues to be nauseated.

Dry Mouth: A dry mouth can be caused by medication or by the disease or by a lack of fluids. Go by the doctor’s advice on the amount of fluids to provide, and if the patient continues to have dry mouth, contact the doctor. You may need to provide glycerin swabs or artificial saliva for the inside of the mouth and a lit coating of lip balm for dry or cracked lips.

Itching: Dry skin, a new reaction to a laundry product, medications or the disease may cause rashes, dry skin and discomfort. To stop the itching, you can apply a soothing  skin cream (alcohol-free, as alcohol-based products can further dry the skin) or calamine lotion to itchy areas. Cornstarch, baking soda or baby powder may work, too. Use a humidifier during the fall and winter when heat is used to help moisten the air. You may need to experiment if none of this solutions work. Change laundry detergent or avoid dryer sheets to see if those solutions help.

Thinking About Death May Change Your Life

Friday, November 6th, 2009
Facing the reality of death may bring serenity to your life.

Facing the reality of death may bring serenity to your life.

Have you faced the reality that, one day, you will die? If you haven’t faced this fact, don’t feel alone. Denial of death is a popular pastime in developed countries, as people don’t want to die any more than they want to pay taxes.

But, if you take the time to realize that you will die one day, your outlook on life may change and you may experience serenity. People who believe they will live forever (including many teens), often take more risks and make decisions that may take longer to resolve. The resulting chaos can be used as a means to avoid deep introspection, a skill that takes time to develop in many people.

One way to build that skill is to take life slowly and deal with situations as they arise. The person who tries to deal with situations or events that have not yet arisen and that may never arise can feel overwhelmed. This type of thinking also wears on a person’s health. Worrying about “what if” situations can become an addictive behavior, especially when an individual begins to think about his or her death.

Before you work yourself into a depression while thinking about life ending in death, think about a person who has been diagnosed with a terminal illness. Unfortunately, in many cases, a terminally ill person feels isolated and rightly so – the fact that many people do not want to face death in this society tends to spill over into real life as people avoid terminally ill loved ones.

But, dying is not a contagious disease. It is a fact of life. Still, many people treat death and dying with a hands-off attitude, mainly from fear. Many people equate death with pain, but physical pain can be endured or treated. Emotional pain often is the issue here. Fear of separation, fear of abandonment and fear of the unknown are real fears. These fears can be diminished by talking about them with a counselor or with your family and friends.

Alcoholics Anonymous deals with these fears in a twelve-step program [PDF] that addresses emotional issues and day-to-day activities that can prevent serenity. Since alcoholism is seen as a terminal illness among many recovering alcoholics, the individuals who seek treatment for their alcoholism (or drug abuse) can walk away with skills that can help many other people learn how to deal with life and death.*

Outside the twelve-step program, life plans also can be simplified further into four basic categories (not listed in any particular order):

  • Relationships with family members and friends
  • Job or career goals
  • Health issues
  • Spiritual questions

Taking each one of the four issues listed above, you can list obstacles that exist for you in any area within that category. Ask yourself questions such as:

  • Do any of my past relationships remain unresolved?
  • Do I have financial problems to address?
  • Do I exercise enough or can I eliminate foods that are not good for me?
  • What do I believe, and can I find support for my beliefs or do I need to change that perspective to find peace?

Although you deal with these four issues continuously throughout life, the answers to your questions may change as you age. The analogy would be like a movie you watched ten years ago or a book you read when you were younger. If you watched that movie or read that book again, you might see the content differently than you did ten years prior. AA calls this practice “taking inventory.” The average person might call it, “taking stock.” No matter what you call this personal interrogation, a constant desire to seek answers to life’s current dilemmas can help you to understand yourself and your loved ones better.

This willingness to take stock and to understand shifts in your perspective may show that you have grown emotionally, spiritually and in knowledge.

To realistically plan for your life to end one day is a practical exercise, and one that many hospices employ in their care-giving. But, if you think about the end of life now, rather than waiting for a time when you face death head-on, your willingness can present new opportunities rather than close doors. Facing the reality that life ends in death, always, may help you avoid chaos and worry and live a more peaceful life filled with satisfying relationships and goals.

*Note: Many addiction programs allow recovering addicts to replace “God” with “higher power” to help avoid resistance to recovery.

Some Terms to Define Advance Directives

Friday, September 25th, 2009
Learn more about advance directives

Learn more about advance directives

The following definitions are used by the American Hospital Association to define terms used in and about advance directives. These terms, which are part of a brochure provided to help patients, families and the hospitals that serve them, presents key resources to enhance educational efforts and to raise awareness around the important issue of advance directives.

Learn more about advance directives, get your questions answered and find more links that talk about this end-of-life planning at the American Hospital Association site, Put It In Writing.

  • Advance Directive: A document in which a person either states choices for medical treatment or designates who should make treatment choices if the person should lose decision-making capacity. The term can also include oral statements by the patient.
  • Artificial Nutrition and Hydration: A method of delivering a chemically-balanced mix of nutrients and fluids when a patient is unable to eat or drink. The patient may be fed through a tube inserted directly into the stomach, a tube put through the nose and throat into the stomach, or an intravenous tube.
  • Cardiopulmonary resuscitation (CPR): A medical procedure, often involving external chest compression, administration of drugs, and electric shock, used to restore the heartbeat at the time of a cardiac arrest.
  • Decision-Making Capacity: The ability to make choices that reflect an understanding and appreciation of the nature and consequences of one’s actions.
  • Declaration: One type of advance directive, commonly referred to as a living will.
  • DNR: Do Not Resuscitate; a medical order to refrain from cardiopulmonary resuscitation if a patient’s heart stops beating.
  • Durable Power of Attorney for Health Care (DPOA): An advance directive in which an individual names someone else (the “agent” or “proxy”) to make health care decisions in the event the individual becomes unable to make them. The DPOA can also include instructions about specific possible choices to be made.
  • Hospice: A program that provides care for the terminally ill in the form of pain relief, counseling, and custodial care, either at home or in a facility.
  • Legal Guardian: A person charged (usually by court appointment) with the power and duty of taking care of and managing the property and rights of another person who is considered incapable of administering his or her own affairs.
  • Life-Sustaining Treatment: A medical intervention administered to a patient that prolongs life and delays death.
  • Palliative Care: Medical interventions intended to alleviate suffering, discomfort, and dysfunction but not to cure (such as pain medication or treatment of an annoying infection).
  • Persistent Vegetative State: As defined by the American Academy of Neurology, “a form of eyes-open permanent unconsciousness in which the patient has periods of wakefulness and physiologic sleep/ wake cycles but at no time is aware of himself or his environment.”
  • Proxy: A person appointed to make decisions for someone else, as in a durable power of attorney for health care (also called a surrogate or agent).
  • Terminal Condition: In most states, a status that is incurable or irreversible and in which death will occur within a short time. There is no precise, universally accepted definition of “a short time,” but in general it is considered to be less than one year.
  • Ventilator: A machine that moves air into the lungs for a patient who is unable to breathe naturally.

25 Top Hospice, Death Care and Eldercare Blogs

Friday, August 21st, 2009
Portrait of old woman sitting by a window by Chalmers Butterfield.

Portrait of old woman sitting by a window by Chalmers Butterfield.

Are you seeking expert advice on how to work with an elderly parent? Do you want to find information about your own aging? Many experts, including lawyers, hospice nurses and nursing home advocates, have taken to the Web to offer their advice and knowledge through the following up-to-date blogs. Their information may be what you need to answer your questions about aging, deathcare and eldercare.

The following list of hospice and eldercare blogs are listed in alphabetical order to show readers that we do not favor one blog over another:

  1. AARP: Can’t live with out AARP if you are age 50 or older. This site provides advocacy, information, resources and even a game section. It’s more of a portal than a blog, but it’s a raging good resource.
  2. About.com Palliative Care: This site is designed for patients, families, and caregivers who are faced with life-threatening illness and are seeking information about palliative care or hospice.
  3. Caregiver List: This blog focuses on resources for caregivers for the elderly.
  4. Death Care Law Blog: William Stalter focuses his law practice on preneed and death care compliance, serving banks, funeral homes, crematories, and cemeteries.  He has written multiple published articles on the subject of preneed and is a member of The International Cemetery, Cremation Funeral Association.
  5. Dethmama Chronicles: This hospice nurse is off the charts – funny, intense, philosophical and nurturing, she provides an insider’s perspective into death care.
  6. Eldercare ABC Blog:If it requires a village to raise a child, then what does it take to care for an aging parent? This blog tries to answer that question with a myriad of resources.
  7. Eldercare Diary: This site is more of a portal than a blog, but it does contain a blog as well as a forum, articles and resource directory.
  8. ElderCare Expert Blog: “Dr. Cheryl” is an owner of a Geriatric Care Management business in Southern California, and she offers information on eldercare advocacy and information for caregivers and for eldercare professionals.
  9. GeriPal – A Geriatrics and Palliative Care Blog: This blog is a forum for discourse, recent news and research, and freethinking commentary. They welcome the perspectives of generalists, specialists, gerontologists, palliative care clinicians, and anyone else interested in care of the elderly or palliative care.
  10. Hospice Blog: This blog is dedicated to all of the hard working hospice professionals across the nation.
  11. Hospice and Caregiving Blog: Sponsored by the Hospice Foundation of America, this blog offers stories and articles about the end-of-life experience.
  12. Hospice and Nursing Homes Blog: Frances Parker is a consultant, hospice volunteer and former school principle, and her blog focuses on Parker’s experiences and knowledge about hospice care.
  13. Hospice Physician’s Blog: This fellowship-trained and board-certified hospice and palliative medicine physician shares insights into patient experiences from a hospice and palliative care point of view.
  14. How We Die: Ok, so this is not a blog – but, it’s a “can’t miss” site that may hold you spellbound. The founders explore how our most personal experiences have shaped what we believe about death and dying, and about the decisions we make for ourselves, for loved ones, or for patients at the end of life. The site welcomes stories from patients, their families, loved ones and friends, and doctors and healthcare professionals.
  15. Inside Eldercare: One man’s mission – to educate and inspire readers to make their elder care experience a positive. Ryan is the creator of the “by families, for families” approach to elder care which teaches families how to make elder care a positive experience.
  16. Lasting Tribute: This blog celebrates the lives of family, friends and people in the public eye who are no longer with us. It also allows members of the public to leave their own personal messages and upload photos.
  17. Medical Futility Blog: Thaddeus Pope tracks judicial, legislative, policy, and academic developments concerning medical futility and the limits on individual autonomy at the end of life.
  18. My Better Nursing Home: Dr. Eleanor Barbera frequently lectures on subjects related to psychology, aging, and nursing homes. Read her blog to gain insight into those topics.
  19. My Elder Advocate: Jack Halpern has held several key leadership roles during his 30 years in the nursing home industry, and he shares his current perspectives on eldercare with readers.
  20. Palliative Care Success: Tim Cousonis is a certified health care executive who has worked for the past 20 years to improve end-of-life care in the U.S.
  21. Pallimed: This blog is a hospice and palliative medicine blog that focuses on education about the hospice movement and industry.
  22. Risa’s pieces: This blogger is a palliative care provider who writes about his experiences with death and dying individuals.
  23. The Good Death: Jessica Knapp is a PhD student and freelance writer who wants to help people better handle all facets of death and dying. Her posts are filled with facts, questions and many links to other resources.
  24. The New Old Age: This New York Times’ blog focuses on Baby Boomers who face the challenge of parents who are living longer.
  25. The Nursing Home Administrator: Learn more about nursing home matters from Matthew Maupin, who writes about topics ranging from diseases to tech tools.

The Best Place for Hospice Training

Tuesday, August 4th, 2009
Volunteer at a Hospice.
Volunteer at a Hospice.

Do you care about people, especially those individuals who are terminally ill? This type of care requires a special affinity for understanding and some psychological training. While many social workers and psychologists may be called to caring for hospice patients, others may not have the college degree that seems necessary for this job. You may be surprised to learn that many hospice workers are volunteers who may not have a college degree, and the only requirement is registration for local classes or training at a local hospice program.

For instance, Santa Fe Springs hospice volunteers need to be at least 18 years old and have their own transportation. They should be able to donate at least two hours a week as they provide relief for family members, run errands, help with meals or transportation, read to the patient or write letters, play cards, games or listen to music, and provide companionship. “Some visits are very short, perhaps only 15 to 30 minutes, and others up to the maximum four hours (which is enough to go to the hairdresser, bank, post office and grocery store for the regular caregiver).”

If you want to take this service further with more intensive training, you might seek classes held by hospices or hospitals. In one case, the Marion General Hospital Hospice program in Ohio offers Hospice 101, a one-hour introduction to the rewards of being an active volunteer. Fingerprinting and background checks for interested individuals will begin that evening and classes begin in mid-September.

Concord Regional Visiting Nurse Association in New Hampshire is offering a nine-week Hospice Volunteer Training Session that starts on Wednesday, Sept. 9 from 6-8 p.m. This is an ideal time for those who work to make the classes to learn more about how to offer companionship and support to terminally ill patients and their families.

If you don’t have time now for a long class, shorter classes are available from many hospice centers. In some cases, fingerprinting is necessary to meet regulations and other facilities may have rules for volunteers, such as no heavy lifting. In most all cases, hospices are pleased to obtain new volunteers, especially individuals who care about what they do and can show compassion rather than fear and hope rather than despair for their patients.

If you plan to make nursing a career, some work as a hospice volunteer may help you decide if you’re cut out for a career as a nurse or nurse’s assistant. Although, in most cases, you must be over age 18 to serve as a volunteer, you may be working with individuals who are as young as five or as old as 95. This range of terminally ill patients may wear on you, as each case is different and each one can affect you in different ways. This is another reason why training is important, as classes or work sessions can provide you with the support and knowledge you need to volunteer effectively.

Open Courseware on Death and Dying

Thursday, June 18th, 2009

Do you want to learn more about aspects of death and dying, but don’t want to pay an arm and a leg for a college course? Take advantage of open courseware, then. These courses, offered by major universities, government entities and businesses, are courses offered online. While they offer little to no credit, they’re free and you can learn at your own pace.

The following short list of open courseware about death and dying provides some examples of what you can expect to find. The list is in alphabetical order, and we do not favor one course over another:

  • Death: This course examines a number of issues that arise once we begin to reflect on our mortality. Are we immortal, or does life really end at death? Discussions on suicide, attitudes toward death and other issues are offered by this Yale course.
  • Health Across the Life Span: Frameworks, Contexts, and Measurements: Johns Hopkins provides many excellent courses on health, and this one is an example. This course introduces and examines the basic principles that guide growth and development and the health of individuals across the lifespan, from the prenatal period through senescence.
  • Health Issues for Aging Populations: Another course from Johns Hopkins that introduces the study of aging, its implications for individuals, families, and society, and the background for health policy related to older persons.
  • Human Growth and Development: While addressing health care professionals, the layman can learn much about various developmental tracks that follow a person from birth to death.
  • Living with Death and Dying: The Open University provides a course that explores how knowledge and beliefs about death and encounters with death affect peoples’ lives.
  • Managing Long-Term Care Services for Aging Populations: This course reviews care and service systems from the unique perspective of an aging population, including the physiological and psychological changes common among seniors.
  • Medical Terminology: While not dealing with death and dying specifically, this course can help anyone (including nurses) understand more about the terms used by those in the healthcare profession.
  • Moral and Ethical Principles in End-of-Life Care: Another Open University course that addresses issues in hospice, or palliative care.
  • Moral Problems and the Good Life: MIT offers this course, which includes readings and lecture notes. Topics include: euthanasia, gay marriage, racism and racial profiling, free speech, hunger and global inequality.
  • Transitions into Residential Care: The Open University offers this course, which considers working with people in group care and residential settings.

Why You Might Need Long-Term Care Insurance

Sunday, June 14th, 2009

Most people associate long-term care with the elderly. But, long-term care also applies to the ongoing care of individuals who no longer can perform tasks independently – no matter the age. These activities of daily living, also called ADLs, include bathing, dressing and eating. The inability to conduct an ADL includes illness, injury or a cognitive disorder.

Assisted living or long-term care is offered by private homes, assisted-living facilities, adult daycare centers, hospices and nursing homes. While some folks already plan for alternatives to long-term care insurance, others may need to think about buying insurance. Even if you never need long-term care, you might want to be prepared for the possibility.

Here’s what Michael Chapman from Provident Capital Management, Inc. says about long-term care insurance:

…Long-term care is often very expensive. Although Medicaid does cover some of the costs of long-term care, it has strict financial eligibility requirements–you would have to exhaust a large portion of your life savings to become eligible for it. And since HMOs, Medicare, and Medigap don’t pay for most long-term care expenses, you’re going to need to find alternative ways to pay for long-term care. One option you have is to purchase an LTCI policy.

However, LTCI is not for everyone. Whether or not you should buy it depends on a number of factors, such as your age and financial circumstances. Consider purchasing an LTCI policy if some or all of the following apply:

  • You are between the ages of 40 and 84
  • You have significant assets that you would like to protect
  • You can afford to pay the premiums now and in the future
  • You are in good health and are insurable

You might want to read that article at Chapman’s site, as he also provides tips on how to shop for LTCI. For instance, before you buy LTCI, it’s important to shop around and compare several policies. Read the “Outline of Coverage” portion of each policy carefully, and make sure you understand all of the benefits, exclusions, and provisions. Once you find a policy you like, be sure to check insurance company ratings from services such as A. M. Best, Moody’s, and Standard & Poor’s to make sure that the company is financially stable.

Finally, when comparing LTCI policies, you may wish to seek assistance. Consult a financial professional, attorney, or accountant for more information.

National Nursing Home Survey Just Released

Thursday, June 11th, 2009

This new report presents an overview of the nursing homes and residents surveyed in the 2004 National Nursing Home Survey (NNHS), the seventh in a series of periodic surveys of nursing homes conducted since 1973 by the Centers for Disease Control and Prevention’s National Center for Health Statistics, Division of Health Care Statistics.

Nursing homes are a crucial component of the long-term care system. According to the 2004 NNHS, there were almost 1.5 million nursing home residents in 16,100 facilities. This number of current residents is similar to survey results from 1985 but still represents a decrease of more than 136,100 residents from 1999. The most recent projections indicate that the number of Americans needing long-term care will double between 2000 and 2050. Policymakers, health care providers, and consumers all need accurate and representative information on the characteristics of nursing homes and their residents to best plan for a continuum of long-term care and to determine the most appropriate location for care.

Other statistics from this report include:

  • Most of the nursing homes were proprietary (61.5 percent); 30.8 percent were operated as voluntary nonprofit facilities, and the remaining 7.7 percent were owned by government and other entities.
  • More nursing homes were certified by both Medicare and Medicaid (87.6 percent) than in 1999 (81.8 percent).
  • More than two-thirds (67.7 percent) of all nursing facilities were located in MSAs (Metropolitan Statistical Areas), and 66.6 percent were located in the Midwest and the South.
  • Nursing homes were either independently operated (45.8 percent) or were part of a chain with a common affiliation (54.2 percent).
  • Selected services provided to nursing home residents are delivered through formal contracts with outside providers. Pharmacy (84.1 percent) and medical director (83.5 percent) were the services most commonly provided under contract. Other services commonly provided by outside sources included hospice (78.1 percent), therapy services (68.7 percent), podiatry services (66 percent), dental and oral services (62.5 percent), and diagnostic services (58.9 percent).
  • Nursing homes used different and multiple arrangements to provide medical services, including using private physicians from the community (85.9 percent), contracting with physician group practices (30.1 percent), and employing physicians on staff (19.6 percent).
  • A total of 936,000 persons (registered nurses, licensed practical nurses, certified nursing assistants, nurse’s aides, and orderlies) provided nursing care to nursing home residents. Of these workers, the majority were employees of the nursing home and 18,600 were contract workers.
  • Certified nursing assistants (600,800) represented the majority of all nursing staff employed in nursing homes.
  • Of the 1.5 million nursing home residents, 88.3 percent were aged 65 years and older and 45.2 percent were aged 85 years and older.
  • Midwestern states had 68.2 nursing home residents per 10,000 civilian residents, whereas states in the West averaged 31.5 per 10,000 population. There were 60.8 residents per 10,000 population in the Northeast and 47.7 per 10,000 in the South. About 73.5 percent of Hispanic or Latino nursing home residents were located in the South and West.
  • Black residents were twice as likely as white residents to be under age 65 years (21.9 percent versus 10 percent) and were less likely to be aged 85 years and older (30.2 percent versus 47.7 percent). About 84.7 percent of black residents were from MSAs, compared with 74 percent of their white counterparts.
  • Of the nursing home population reported to be of Hispanic or Latino origin, 22.8 percent were under age 65 years, compared with 11.2 percent of not Hispanic or Latino residents. Conversely, 24.6 percent of Hispanic or Latino nursing home residents were aged 85 years and older, compared with 46.1 percent of residents who were not Hispanic or Latino. MSAs accounted for 86.6 percent of Hispanic or Latino nursing home residents, compared with 75 percent of not Hispanic or Latino residents.
  • Of all nursing home residents, 71.2 percent were female. About 59.5 percent of Hispanic or Latino nursing home residents were female, compared with 71.6 percent of their not Hispanic or Latino counterparts. Among black residents, 63.5 percent were female, compared with 72.6 percent of their white counterparts.

To learn more about how this study was conducted and more information about length of stay averages and more, download the PDF report.

How You Can Help Your Local Hospice

Sunday, June 7th, 2009

NHF (National Hospice Foundation) supports the National Hospice and Palliative Care Organization’s quality and research initiatives, hospice/palliative care provider education activities, consumer engagement and caregiver services and global hospice partnerships.

While many people do not know that Medicare can pay for hospice care, Medicare cannot spread the word about hospice or palliative care services like local outreach. And, Medicare Part A cannot pay for custodial care.

You can visit your local hospice and offer your services to help patients. If you do not like dealing directly with death care or patients, perhaps you can help organize a fundraiser to help raise awareness about local hospice facilities. Or, you can take a look at what some other people are doing to help make the transition from life to death easier for others. All the events listed below occurred in 2009:

  • Beautiful weather helped to draw a big crowd for the 8th annual Walk for Hospice in Albany, New York on Saturday, 6 June. According to the news story, the event raised about $115,000.
  • Hundreds of motorcyclists (including one 62-year-old Harley lady) will ride to rise money for the first Ride for Hospice of Hamilton, which will benefit the nonprofit agency’s indigent fund that ensures uninsured and underinsured terminally ill patients receive care. This ride took place today, 7 June.
  • The annual St. Catherine’s Hospice ball, held on Saturday night, 6 June, in the UK, attracted 400 guests and has raised about £20,000 for funds.
  • Hospice of Marshall County in Alabama received a $25,000 donation from Larry Fortenberry on behalf of the SpringBash ‘09 on Thursday. 4 June. This was the second year for the SpringBash and Fortenberry, the director, said he was already working on improving it for next year.
  • Cora Goyette learned Hospice of Orleans County, New York, needed special bed linens and gowns for Hospice patients. Hospice loans hospital beds and mattresses to patients, but regular-size linens do not properly fit a hospital bed. So, Cora started a Comfort Fund she calls, “Making a Difference, One Bed at a Time.” She contacted all the emergency services personnel in Orleans County – fire chiefs, veterans organizations and police agencies – and asked them if they would each donate $50 to the Comfort Fund. “As a result, we have been able to purchase gowns and linens for our patients,” Goyette said.
  • Thom Gill has become somewhat of a fixture at Hospice Home at High Point, North Carolina. Twice a week, the 57-year-old High Point man shows up with his Michael Kelly resonator guitar, takes his spot across from the nurses’ station and serenades the patients and staff with his laid-back acoustic music. This is a lovely story, and one that may stir your heart to help your local hospice!

Dying at Home: The Alternative to Hospitals

Wednesday, May 27th, 2009

Have you thought about dying at home? In the past, that’s all that our ancestors could do – provided they weren’t killed or died accidentally away from the home. In Canada, it seems that more people are choosing the option to die at home, despite free medical care at their hospitals.

According to a new study published in Social Science & Medicine, University of Alberta researcher Donna Wilson looked at mortality data of Canadians dating back to 1950. Up until 1994, 80 per cent of Canadians were choosing to pass on in a hospital bed. But since the mid-’90s there’s been a drastic change in the number of people going to hospital to die. The number is now down to 61 per cent.

“So after years of [the numbers] going up, we have completely reversed that and are now at the 1960 level, before there was free hospital care in Canada,” said Wilson, who adds the decrease in numbers of people dying in hospital has happened without direct health policy or government planning.

Her next study she wants to find out why this trend is happening. But she already has some ideas on the huge swing.

“My guess is that a lot of it has to do with the fact that death is no longer unexpected,” said Wilson. “A lot of people are dying at an advanced age and you begin to accept that fact that it’s going to happen and it [can be] a dignified event. If you take the person to the hospital . . . care is by strangers rather than family members.”

Wilson predicts the number of people dying each year will double, maybe even triple, in the next 10-20 years because of the aging baby-boomer population. And, despite the fact that the Canadian government hasn’t been involved in the stay-at-home deaths to date, Wilson would like to see more involvement and encouragement for the death-at-home option.

“We need to start putting more money in to home care and develop some hospices, have some courses for families and maybe build a few more nursing home beds,” said Wilson, who adds this not only helps the health-care system but also can provide a more dignified and potentially less painful death for the patient.

“All the drug therapies that keep people comfortable in hospital can be used at home,” said Wilson. “You’ve got much more choice. You’re not going to be force-fed; you’re not going to have an intravenous drip started on you that is painful.

“I think we have a very healthy population who can look after dying people.”

Considering the growing hospice care industry, this trend may already be active in the U.S. as well. Hospice care workers are well trained in helping the dying and their families with this life transition. Dying at home among family and friends may be a much more personal and meaningful option than dying in a hospital room amongst strangers.