The Successful Caregiver's Guide
By Rick Lauber
()
About this ebook
So many children are caught unprepared when physical and mental health declines in aging parents. Life cannot readily prepare you to furnish excellent eldercare while balancing the demands on your time. This book provides practical tips, realistic guidance, encouragement and insight into the time ahead.
Among other things, it answers:
• How do you decide when your parent stays at home or moves to
assisted living?
• What should you expect when caring for your elderly parents?
• Who should you ask for help?
• How do you balance caregiving responsibilities with your personal life?
The Successful Caregiver’s Guide includes extensive explanations of your options and checklists for differing types of eldercare to help you choose the best care possible for your loved one.
Rick Lauber
Rick Lauber is the Edmonton-based author of Caregiver's Guide for Canadians published by Self-Counsel Press. In this book, Rick shares his own caregiving experiences and provides recommendations for other family members who are just stepping into this role. Rick has written extensively on caregiving issues for local newspapers and magazines plus serves as the Contributing Editor for both the Alberta and the Island Caregiver magazines.
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The Successful Caregiver's Guide - Rick Lauber
Introduction
Residents of the United States have weathered hurricanes (e.g., Galveston, Texas, 1900; and Hurricane Katrina, 2005), faced fires (e.g., Yarnell Hill Fire, Prescott, Arizona, 2013), and coped after world terrorism (911, New York City, 2001). After each catastrophe, Americans have proven themselves to be admirably resilient by surviving and rebuilding. However, there is a brewing problem throughout the country and it requires immediate attention: The country’s aging population. As of 2010, 40.3 million seniors (those 65 and older) were living in the United States — a notable jump of 15.1 percent of the country’s population between 2000 and 2010.[1]
With aging baby boomers (defined by the US Census Bureau as children born between 1946 and 1964 and directly following World War II), these numbers will most certainly increase. More and more adult children will see their own parents age and decline due to physical or mental health issues. As parents age, many sons and daughters will become caregivers who will help and support their aging parents in any number of ways. While aging, sickness, and eventual death are not pleasant topics to think or talk about, denial of these facts is not an answer. Mom or Dad may seem fine today, but she or he could easily fall and break a hip tomorrow. Realistically, one must expect and prepare for the future caregiving role.
With the population of the United States rapidly aging, more adult children are scrambling to find and provide help for their own parents. Unless those family members have been fortunate enough to work in the health-care, financial, legal, or social-work fields, they often lack the necessary skills, attitudes, and experience to adequately help.
When it comes to caregiving, there is a huge sense of responsibility, obligation, and even guilt for these adult children who may silently believe, Mom and Dad cared for me; now it’s my turn.
In turning the tables, adult children do what they can but must frequently learn on the job
while giving their parents the best quality of life possible. (My decision to write this book was prompted by this very situation.) Often, there is not much time allowed for a caregiver to research an issue, deliberate with other family members, and/or reach a decision as to what to do. Commonly, family members serving as caregivers suffer from a sense of imbalance, stress, and myriad emotions that include anger, depression, confusion, and grief. Considering the consequences, this is not always best for either the family caregivers or their parents.
Whether you are becoming a caregiver, anticipating eventually taking on the role, currently providing parental care, or know of someone else wearing the caregiver’s shoes, you are likely entering into foreign territory. There is no road map or tour guide to steer you in exactly the right direction. As a caregiver, you will be called on to make difficult lifestyle, health-care, and financial decisions affecting your own parents. You will struggle and question yourself as to whether you made the right and/or best choices. Learn to accept your own decisions, your own shortcomings (you cannot do it all for your parent), and the crucial importance of personal respite (i.e., taking a personal break).
Trust me, this is not easy. I’ve served as a caregiver not once, but twice — for both of my aging parents. My Mom had Parkinson’s disease and Leukemia while Dad developed Alzheimer’s disease. With Mom and Dad becoming sick simultaneously, my caregiving duties doubled and there was no rest between them. Through my experiences, I have developed a newfound respect for those working in care; specifically, for untrained family members (like me) who, often, have been thrust unknowingly and unprepared into a caregiving role. I have also gained more respect for myself and know my own strengths and weaknesses far better, as well as when it is necessary to take a break.
As you look ahead with uncertainty or trepidation to provide elder care, know that this is not a typical self-help book which simply aims to encourage or inspire you to learn something new or change your own life for the better. The issues I speak of in this book are very real, and the tools and strategies I suggest can be very effective. I will share stories with you as to what caregiving mechanisms were helpful for me, and I will also discuss what was not helpful.
For the sake of conciseness, I have chosen to remember my Dad for the most part throughout this book. While my Mom’s medical case certainly presented numerous challenges, my Dad outlived her and my caregiving responsibilities were extended. Not all of this may be exactly relevant to your own situation, but please glean what you can from it. It is my hope that when you have finished reading this book, you will have learned at least one new thing about what to expect or how to cope as a caregiver.
There are stories of confusion, worry, and neglect that surround the role of caregiving. These stories greatly sadden me, but I would like to emphasize that caregiving is not all doom and gloom or death and despair. While your parent’s situation (and perhaps your own) may seem bleak to you, there is great joy to be found here as you will see in the following pages.
1 65+ in the United States: 2010,
Loraine A. West, Samantha Cole, Daniel Goodkind, and Wan He; United States Census Bureau; accessed April 2015. https://www.google.ca/?gws_rd=ssl#q=2010%2C+40.3+million+seniors+%28those+older+than+65%29+were+living+in+the+United+States—a+notable+jump+of+15.1+percent+of+the+country%E2%80%99s+population+between+2000+and+2010
Chapter 1
Defining Caregiving
One person caring about another represents life’s greatest value.
— Jim Rohn
It’s interesting (and somewhat unsettling) that, while the word caregiving
is becoming much more used these days, the term remains largely misunderstood. There could be any number of reasons why including a lack of understanding about the job, a feeling of shame or discomfort (people may not readily admit they are doing this), or a sense of obligation (since Mom or Dad took care of me, it’s now my turn to care for them).
A friend of mine explained that she routinely visits a blind woman to open and read her mail. When I immediately defined my friend as a caregiver
she hesitated initially, but soon admitted that she was indeed providing care and support — what she was doing was an important task — albeit on a smaller scale than what others might do.
While many have chosen to ignore or completely dismiss the impact of caregiving on others, the facts point to this as an ever-growing problem and growth trend. Undeniably, the United States has a graying population. The children of World War II (those born between 1946 and 1964) are growing older. These are society’s baby boomers; I’m in this category myself.
According to the Family Caregiver Alliance, 65.7 million caregivers make up 29% of the US adult population providing care to someone who is ill, disabled, or aged.
[1] You don’t have to look too far to find other statistics echoing this magnitude. The Alzheimer’s Association reports that 43.5 million of adult family caregivers care for someone 50+ years of age and 14.9 million care for someone who has Alzheimer’s disease or other dementia.
[2] The United States Census reveals that the country had 40.3 million people 65 or older in 2010 — the highest number of seniors since the Census Bureau began keeping records more than a century ago. Not surprisingly, California is the state with the largest number of residents 65 and older with 4.2 million; followed by Florida with 3.3 million; New York and Texas are tied with 2.6 million; and Pennsylvania with 2 million.
These numbers are certainly not stagnant. They are, in fact, expected to skyrocket. By 2035, the country’s 65-plus population is expected to more than double. While this will be good news for those in senior-serving professions (as it results in more work and more opportunities), it will result in many more family members stepping forward to provide care for loved ones. Without proper preparation and education, these family members will be caught improvising and struggling (as I did).
A high population of seniors is not just an American issue; it is fast becoming a global concern. Caregiving does not have any borders. In Canada, almost 15 percent of the country’s population is now aged 65 years or older. According to the International Alliance of Carer Organizations, there were 6.5 million caregivers in the UK (2009), 1.3 million caregivers (aged 18+) in Sweden (2012), and 2,694,600 caregivers in Australia (2012).[3] Another report from the National Bureau of Statistics of China noted that the number of people, nationwide aged 60 years and older reached 167 million (or 12.5 percent of the total population) in 2009.[4]
Should these numbers not speak to you, know that aging is a natural course of life and a high population of seniors is almost guaranteed as baby boomers age. This is an oncoming speeding train that cannot be avoided. We can neither jump out of the way of nor blindly ignore this problem. With the rise of seniors expected, there will also be a correlating rise in the number of professional and private caregivers.
1. The Different Types of Caregivers
A caregiver can be simply defined as anyone who helps with the needs of others impacted by disease, disability, or aging. It’s important to realize that caregivers exist on many different levels. There are, of course, the medical doctors who practice full-time, the nurses who travel from hospital room to hospital room, and the volunteers who push around patients in wheelchairs. A caregiver may also work part time and may not even identify as someone caring for another. A neighbor could mow the lawn or shovel the snow for a housebound senior, a friend could drop in for a coffee and a chat, or an adult child could prepare and deliver a home-cooked meal. A minister can provide care on a spiritual level. A musician can visit a long-term care center and entertain residents with songs. No matter what level a person serves as a caregiver, he or she is doing noble work.
Caregivers are most often identified as adult children caring for aging parents; however, caregivers can be anyone. The list can include friends, spouses, partners, parents, and even grandparents. Care can be provided at many levels. In my friend’s case, she reads a blind woman’s mail; however, a caregiver can visit with a senior, provide transportation to medical appointments, serve as an advocate, manage finances, and help with hands-on care (e.g., clothing, toileting, or bathing). The list of caregiving jobs can seem endless and is rarely routine from one day to the next.
While caregivers may be handling tasks previously unknown to them, it’s important for them to keep in their own comfort zones. I never helped my parents with bathing or showering, I felt this was better left to professionals who had more experience in this and knew how to keep a senior safe on a wet bathroom floor. The last thing I wanted to have happen is Mom or Dad falling as a result of my own inexperience in this area. The same can be said for physically lifting or transferring a senior. Doing this requires a certain procedure and expertise, and I knew full well that I was not the best person for this job.
Even young children can help to provide care. While they may not completely understand a senior’s medical condition, young children can bring great joy and a breath of fresh air to a senior, so invite them along on visits. Note: When explaining the situation to children, it is important that they understand whatever ailment has been diagnosed is not anybody’s fault and not contagious.
We often think of parents providing care for their own children. This is one of those most obvious examples of caregiving. With the United States’ aging population, we are rethinking that norm and now understand and accept that adult children can easily become caregivers for their own parents.
Caregiving can inch up on you (e.g., a parent’s chronic health condition) or it may happen overnight (e.g., a parent falls and as a result, becomes disabled). You can never forecast the future. For example, my father was always a little forgetful, so Alzheimer’s disease was not a total surprise. My mother’s conditions, conversely, came without any warning.
Other unexpected caregivers are not even human. Many seniors’ homes are providing residents dogs or cats for pet therapy.
There is something very comforting and soothing about petting a dog or having a cat sitting on your lap. If you want to bring in the family dog or cat, please check with the care facility staff first. Depending on the size of the animal, it may startle or scare other residents. The best type of pet to bring will be one that is tame, quiet, and gentle around other people. Consider also that the sudden excited barking of a dog could upset other residents, and the cat could cause unpleasant and potentially dangerous allergic reactions for others. My parent’s first residence when they returned to Edmonton was home to two colorful budgies. Mom and Dad, along with other residents in the building, found comfort and enjoyment watching and listening to the birds.
Caregivers can also be differentiated by being described as formal or informal caregivers. The formal
group are often health-care professionals who work in a related field. Informal
caregivers are those family members who have little or no related experience and don’t know what to expect. Formal and informal caregivers also have been categorized as paid
and unpaid.
Family caregivers can, however, receive some kind of financial stipend paid from the parental bank account, should other family members agree.
No matter what type of health condition exists (e.g., cancer, multiple sclerosis, kidney disease), caregivers can face a steep, and often sudden, learning curve to become more knowledgeable. They will need to research the condition to become more knowledgeable with the symptoms, outcomes, and possible treatments.
Sometimes, family caregivers feel shame about having to care for aging parents. Feared humiliation or a lack of understanding from other individuals can lead to silence or reluctant whispers of admission. This is most unfortunate as caregivers should be proud of their role. By speaking out, caregivers may also find others willing and able to help them.
2. What Type of Caregiver Are You?
When it comes to caregiving categories, there are numerous types. There are many people who do not simply and neatly slide into one such category. Instead, they will show interest in a number of different areas and display different character traits. The trick is to know what you are best at and proceed accordingly.
It is perfectly natural to feel uncomfortable performing certain tasks for your loved