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Frank Broyles, head football coach at the University of Arkansas from 1958-2005, applied his knowledge and skill as a coach to take on a personal experience in which he was ill-prepared for when his wife, Barbara was diagnosis with Alzheimer’s Disease (AD). Coach Broyles establish a long history in football by being a player and a coach. He is known as the University of Arkansas most winningest coach and became a legacy for the razorbacks by leading the team into consecutive wins (Fosil, 2005). With over 50 years of coaching experience, Coach Broyles faced his most challenging opponent yet.
The author wrote this book with a clear undeniable purpose in mind. Although a head football coach at a major university, it is his own personal experience, off the field that has qualified him to lead, instruct, guide and direct current and future caregivers who struggle to understand AD and the difficult journey though out each stage of the disease that lie ahead.
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Similar books on the subject of AD pale in comparison to Coach Broyles Playbook for Alzheimer’s Caregivers in several ways.
First, the author’s expertise is by personal experience which carries with it deeper meaning. Secondly, the author’s profession called for very tough decision making, where leadership is mandatory and team participation is required. Many readers may be unfamiliar with AD, yet know the dynamics of football or unfamiliar with football, but well verse in AD. Consequently, both psychological and emotional labor is needed for both. Finally, after reading the book from the early stage of AD to the final stage readers are equipped with skill and education on the subject of
AD. The use of this author’s profession clearly helped him create guidelines and recommendations in his book, Coach Broyles Playbook for Alzheimer’s Caregivers. This style of writing, which he identifies with on the field and now off the field, has resulted in an unprecedented and strategic way of understanding AD. In his easy to follow book, written with care givers in mind coach Broyles addresses the early stage of AD by explaining the changing behaviors of your love one, which may warrant a visit to the doctor. He points out the importance of accompanying your love one to the doctor, but make sure he or she does the talking and give answers to questions physicians may have. This is a valid point. In fact Coach Broyles continues to make points throughout his book for AD caregivers. He continues to give the charge of making sure you understand what the doctor explains by requesting to use layman’s terms and do not leave until you are certain your concerns are address. Another interesting fact for caregivers that Coach Broyles points out is how important it is to choose the correct doctor. One who has specialized training in this area and one that will not dismiss you and your love one’s concern to old age (14). For example, potential risk that involves memory loss versus occasional forgetfulness may signal to the physician specific test are needed. In addition, memory decline are common attributes among aging populations, while others may be a sign of something more serious. Signs of memory loss are additional main points Coach Broyles reveals when caring for AD patients or love ones. As an author, Coach Broyles incorporates his thinking as a head coach and director with his devotion as a husband and Father by using parallels of what makes a winning team. The author acknowledges a plan needs to be made and a team formed with everyone understanding their specific roles. Here, Coach Broyles makes another proclamation and that is to take care of you. This is when the “team” comes in. While experience and leadership skills are high valued qualities, no one can do this alone. The coach expresses this sentiment throughout his book and supports these ideas by giving results of the aftermath. Using practical ideas, the author recommends what helps and what is not helpful. In fact the entire book uses matters of practicality. Coach Broyles instruct such practical ways of interacting with your loves ones just a much as you did when she was strong and active. Allow her to be useful, show her how and keep answering her questions are all practical things caregivers should do. These practices must be implemented and can be consider “the playbook”. Each chapter indicates a need to follow his recommendations because the changes in the brain of loves one suffering with AD are followed by abrupt sometimes gradual abnormal behavior. He explains portions of the brain are damage in people with AD and they may not think, speak, or see the same and certainly those changes can cause family members overwhelming sadness and frustration, but this is not the time to give up. Coach Broyles supports his recommendations by suggesting the brain has changed in people with AD and their activities begin to decline. For example, love ones may not speak as much because many AD patients have a hard time with expression and communication. It may be hard to find the correct words and memory lost is also a hallmark of AD patients. Another area of the brain that affects AD patients is their ability to analyze the objects they are seeing. This is a critical fact for caregivers to be aware of and put into practice easy to see and understand objects in the environment around patients and love ones diagnosis with AD. The author covers every aspect, every concept, and legal details to prepare and train caregivers of AD suffer. This book is very useful and should be judge in the category of nursing. Our aging population is expected to increase as the youngest baby boomers turn 65 several years from now (AARP, 2015). Hospitals, nursing homes, private residence, assisted living apartments all should be train and guided by this book. According to the author these entities are known as “special teams”. The contents would bring many caregivers and love ones together as each try to understand and cope with their love one who may not recognize them. The book is unique in many ways because it addresses relevant realities as our society changes and our older loves ones may need more care and attention. Ironically, the last stages of AD are not all that different for older people with health related illnesses who may not suffer from AD at all. Coach Broyles reveals the last stages as the end of life. This section of the book deal with the harsh realities of letting go as your love one’s life start to slip away and death occurs. Coach Broyles points are well taken and this book will be useful among family members as well as caregivers, who may also be the caregiver of a love one suffering with AD. It is also very easy to see the analogy of a football coach and caregiver of AD suffers.
One word describes this woman successful, in her coaching and her will to fight weather it was trying to win a championship or trying to be the first woman to win over a disease like dementia. Pats childhood was rough and tough. She was and still is one of the best coaches to have coached at the college level. She is taking one day at a time to fight her disease.
Pat Summitt has been diagnosed with Dementia, early-onset Alzheimer’s type. Even though she no longer makes the play calls or runs the practices, she can still be found on the court yelling at players until her face turns blue. Summitt is very much still a large part of the Tennessee Lady Vols basketball team, and considers herself the “big gun”; her official title is Head Coach Emeritus. Her constant rock is her son, Ross “Tyler” Summitt, her pride, joy and greatest accomplishment; although Summitt did not want her son to follow in her footsteps, he is currently the head coach at Louisiana Tech and has succeeded expectations. Many of Summitt’s former players were inspired by her, and many have become outstanding coaches at every level of the game. From many famous college coaches like Sylvia Hatchell, Geno Auriemma, and Kim Mulkey, the game of women’s basketball is headed towards a bright
Pah-Lavan, Z. (2006). Alzheimer's disease: the road to oblivion. Journal of Community Nursing, 20(5), 4. Retrieved from EBSCOhost.
I worked with Dementia and Alzheimer patients as a Certified Nursing Assistant for almost three years. Working with the elderly has been one of my greatest achievements. I assisted my residents with bathing, grooming and making them feel comfortable. I was able to create a favorable environment for my residents while working with them. I had the opportunity to see patients go from early stage to their last stage of dementia. This gave me an opportunity to want to do more for people who are in need of my care. From my experience, I learnt that nursing is not just a job; it’s a responsibility and a calling, and it requires that you derive joy in what you are doing even in the toughest moment of caring for your
Foer vowed to show us how the game of soccer can impact different regions and cultures. He indicated us how these relationships (between different nations and beliefs), while there, are hard to apprehend on the global scale. But trough soccer, these relationships reveal themselves in a hesitant fashion.
The author covers the most prevalent groups and events relating to football. Some of them are pep rallies, marching band, cheerleaders / pep squads, spectators / ex-players, and the brains / farm kids / nobodies. The pep rally is a school-wide event,
football (soccer) is ‘weak and feminine. It is evident that these boys believed in sporting
(Davidson, F. G.) Due to the nature of dementia being a neuropsychological disorder, those affected by the disease tend to look like they will not require much care, which, in reality, they often require more care than the caregiver originally expected, leading to stress and burnout. Another effect caused by this can be the caregiver blaming themselves by feeling like they are failing to give proper care, which, in reality, can often be very far from the truth. If the caregiver does not receive help from anyone else, the task of watching over the victim becomes a daunting twenty for hour task. Sometimes, the caregiver won’t be allowed quality sleep. Over 66 percent of home caregivers suffer from some form of psychological or physical illness. The most common illness that is resulted from giving care to Alzheimer’s disease is depression. The caregiver needs to monitor their emotional well-being as well as the well-being as the person that they are giving care to. Usually, giving care to those with dementia is actually more stressful than giving care to those with cancer. When the caregiver is a family member and not a professional, the emotional toll is often even greater. It is important for caregivers to remember that they need to take care of themselves first and
The second view advocates the merits of research: AD research cannot be done without AD patients in all the stages of their disease. This is an indubitable fact, because how else can one track the development of the disease (especially the characteristic biological changes)? By invoking the argument of scientific progress and the possibility of finding a cure, the participation of Alzheimer’s disease patients in research is no longer a matter of possibility but of absolute necessity.
Alzheimer’s disease, named after Dr. Alois Alzheimer, is a disease that is on the rise in America and the rest of the world. People should learn as much as they want about this disease, because as you age, your chances of becoming an Alzheimer’s Disease, or AD, patient increases. It is estimated that approximately 3 percent of Americans between the ages of 65 and 74 have the illness, and more than half of all people over age 85 have the ailment.
In the film, “The Alzheimer’s Project: The Memory loss tapes” there was an 87-year-old woman with Alzheimer disease named Bessie Knapmiller. It seems as Alzheimer runs in her family because her older sister has the same disease. Bessie sister is 93 years old and she has lost her entire memory. Bessie sister does not even remember their family members. However, Bessie stage of Alzheimer is not as bad as her sister, she still drives and still remembers people. At times, Bessie does forget others. Bessie went to take a memory test in May and few months later, when she returned she did not remember her doctor or him giving her the exam. When Bessie took her first memory test she could not remember the previous president before George Bush. She
In the world of sport, soccer and football with respect to demographic has had numerous controversies. Although both sport are known famously around the globe, for many years fans from both sides are known for asking, is American football same as soccer? What’s the time limit on both sports? What’s the game objective? Do they use the same ball? However they both have similarities and differences which I will be talking about in this essay.
Alzheimer’s disease was found more than a century ago but still there is little known and understood about the disease. AD attacks the medial temporal lobes which interferes with memory and the ability to reason and pay attention. (Wierenga and Bondi, 2011). People with AD also have increased atrophy of brain tissue and the brain is clogged with neurofibrillary tangles and senile plaques which are both believed to produce Alzheimer’s symptoms by disrupting the impulses between neurons (Sue et al. 2013). A look into what it feels like to have AD may give a better representation of how the person feels and how their loved ones feel.
Alzheimer’s disease (AD) is a progressive, terminal, degenerative brain disease. It is the fourth leading cause of death in adults and currently affects over four million people in the United States. This number is expected to increase over the next several years as the baby boomers age, until it reaches fourteen million by the year 2025.
“Difficult, depressing, and tragic” are a few of the descriptions generally associated with illness. Those who suffer from dementia, especially, undergo a realm of these characterizations. With this adversity in mind, most people generate a basic understanding based on education rather than personal experience. It is this preconception that can prevent us from gaining a true insight of one’s reality.