Alzheimer's Disease Case Study Essay

“Alzheimer`s disease is called a family disease” (ALZlive), because it impacts every family member who is slowly watching a loved one decline. Alzheimer’s disease has an impact on caretakers because caregivers can lead to a variety of emotions, from guilt to anger. When dealing with a client who has Alzheimer; caretakers have a huge responsibility, which can cause stress or depression. If the caretaking is a family member it might lead to finical problems, which can lead to the hard and controversial decision of putting someone in a nursing home, that is better equipped. Guilt is the main emotion that a caretaker can express “I have never spoken to my mother`s doctor, it occurs to me that other children of

When it comes to Alzheimer’s, I know firsthand how it affects individuals and their families. My great grandfather had Alzheimer’s for many years before his passing late last year, at age 92. Alzheimer’s is a disease that many individuals suffer with each year, but yet with all the advancements in modern medicine we still have no cure for it. There are different ways to conquer this disease, understanding the causes, knowing effects, and researching possible treatments.

This report provides detailed information regarding the Alzheimer’s disease, and how it affects the individual as a person. It examines the facts and statistics of Alzheimer’s disease, as well as cover the survival rate. It covers the cognitive impacts that Alzheimer’s has on the individual, and also the emotional profiles of each of its victims. Gives a general concept of how Alzheimer’s disease has evolved over the past years, and it also shares the advances that it has made. It addresses the role of the public health and aging services, and how it affects the person. It goes into detail on how the brain is affected by this disease, and the impact it can cause for the individual. Overall, it stresses the importance of being aware of the Alzheimer’s diseases because it allows for there to be support, encouragement, and hope for the victims. Just having someone there can make all the difference to someone suffering.

Certain qualities are consistently observed in the Alzheimer’s victim. These dysfunction’s, though, are not exclusive to Alzheimer’s disease. Consequently, declaring Alzheimer’s by these parameters is a matter of degree rather than an absolute. Characteristic dysfunction’s have been noted in Alzheimer’s victims, but the degree and severity of these varies from patient to patient. Thus, evaluation of the patient’s mental status must be made based on the sum, rather than a single characteristic. Memory is one of the first noticed deficiencies, beginning typically with the recent and short term memory, and progressing from there as the disease grows more severe. In addition, deterioration in language skills, attention span, praxis (performance of an action), and visuospatial skills are commonly seen. Also observed are changes in the actions and personality of the Alzheimer’s victim. These include changes in mood, motor activities, activities of daily living, socialization skills, psychotic disturbances, vegetative symptomology, and rise in anxiety levels. Again, the

In conclusion, I informed Jenny that there is a lot of information on the Alzheimer’s disease on the internet, libraries, hospitals and other places one can go to seek treatment. I told her that she and her grandmother are not alone. If she wants some really good information and help, she should turn to The Alzheimer's Association, which is the most trusted resource for reliable information, education, referral and support to

Dementia is an extremely common disease among the elderly, with 4 million Americans currently suffering from the Alzheimer’s type alone. Figures show that 3% of people between the ages of 65-74 suffer from the disease, rapidly increasing to 19% for the 75-84 age bracket, and as high as 47% for the over 85s. Therefore, it is easy to see why Dementia is such a large part of many people’s lives, whether they are suffering from the condition themselves, or have an elderly relative who requires full time care just to undertake simple day to day tasks. The disease can be extremely traumatic for the patient and their families, as the person, who may have been extremely lively and bright throughout their

It is a complex disease people often times do not know how to care for. Although a decline in memory and bouts of more forgetfulness are more common as one ages, spotting the difference between normal age-related symptoms and Alzheimer’s is important for families so that they can get their loved one the best care available. Even with proper care though, caregivers can misunderstand the symptoms of those afflicted, leading to an improper treatment of the patient. There are an estimated between 2.4 and 3.1. million AD caregivers in the United States, a majority of which are family members, who may not know proper care techniques or may be of older age themselves, as they could be caring for a spouse (Schulz and O’Brien1, 185-94). In fact, in a study of caregivers of those to patients with a memory ailment including Alzheimer’s or Dementia found that spouses have consistently been found to be more depressed than other relatives caring for a family member with a cognitive impairment (Schulz and O’Brien2, 771-91). To help in awareness, there are many new classes being offered in schools that can better prepare caregivers. The U.S. Department of Health and Human Service’s (DHHS) National Plan to Address Alzheimer’s Disease dedicated a major goal to “Enhance Care Quality and Efficiency,” with major strategies including building a workforce with the skills to provide high quality care, explore

There may be some sense of grief and disappointment but emotional support is garnered to strengthen the members from the family by the caregiver. The patient needs to be kept in a general well being condition regardless of the pace this illness is taking. The best of care services are extended to the patient at all stages of this illness regardless of its pace of deterioration. The dementia care rendered includes a normal life schedule as much as possible for the patient and the rest of the

In PSYC1002R, we have learned that dementia is simply a blanket term that best explains the gradual decline in multiple areas of function that define human existence. These areas include memory, language, communication, skilled movement, perception, recognition, decision-making, to name a few. In 2011, there were 747,000 Canadians suffering with dementia with 15% of them being 65 years old and older. (Tsuji, 2017) It is estimated that by 2031, that figure will rise to an alarming number of 1.4 million people. (Tsuji, 2017) Dementia is difficult for both the individual diagnosed with the disease and the patient’s family members or caregivers. It is difficult to watch a beloved one become more and more distant and estranged. In this short essay,

Psychosocial treatments can be affective for both the family as well as for the person who is diagnosed with Alzheimer’s. Part of this includes normalization of degradation of the illness, as well as providing the family with the proper tools to communicate with their loved one. For example, it can be important to learn to communicate questions that include the answer in them to ease the stress of the person who is trying to recall a word or person they may have seen. For instance, instead of asking “Who came to see

Alzheimer's disease (AD) is a serious form of dementia that involves the destruction of brain cells, and ultimately leads to death (1). What makes AD such a frightening disease, for both the patient and their family members, is the loss of "self" associated with the dementia. Those afflicted with AD can't understand the changes going on within themselves. Family members are upset by the loss of the "person" they once knew. It is common for daughters (for example) to say that a mother in the later stages of AD is not their "mom" because the personality displayed by the patient is so different from the personality they associate with "mom".

Alzheimer’s is a worldwide disease that many people over the age of 65 years old are diagnosed. Alzheimer’s disease is a current situation in my household the past three years. It is one of the many health issues that do not yet have a known cause or cure. In this investigative report I researched how Alzheimer’s patients affect their family caregivers. All my information was cited from the West Warwick High School research tool as well as google to find articles related to my claim. Many families around the world are going through the same struggles as my own and are seeking advice from others on how to carry on with this daily hassle. My family as well as other families are not alone. There are different ways to cope with our issues depending

aling with Alzheimer’s is hard on the individual going through the disease but also on the ones who have to watch them go through the disease. So how can I comfort them? There are care facilities and assisted living places for people to go if they cannot carry out life's skills and processes. These places are meant for people who cannot live at home anymore. There are a couple of options; retirement housing, assisted living, nursing home, and Alzheimer’s special care units (SCUs) also called memory care units.

In the pamphlet Basics of Alzheimer’s Disease, the Alzheimer’s Association adds late onset, traditionally known simply as Alzheimer’s, targets primarily people 65 and older. The disease follows a series of steps from mild decline with little noticed changes to very severe cognitive decline where the final stage of the disease is in progress (Basic 19-21). Throughout the stages, independence becomes lost and family members will become care takers and in the later stages nursing homes or hospice may be needed. One book encourages the care giver to communicate through body language, tone, and written instructions to help alleviate as much stress as possible for those living with Alzheimer’s (Living 47). The book further adds when caring for a person with Alzheimer’s remember to maintain patience and to show respect .

After Alzheimer's is diagnosed in a parent, or other elderly family member, the caregiver has the task of deciding what the best form of care for the patient is. In order to do this they have to fully understand what the disease is, and