Papers On Alzheimer's Disease

“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

Caregivers play a crucial role in the care of dementia patients. Providing care for dementia patients results in stress related health impacts to the caregiver. The caregivers go through a journey with the dementia patient and need a strong support system. The best approach to dementia care is for health care providers to provide information to and monitor the caregiver, in addition to the dementia patient, encourage the caregiver to take care of themselves, to seek support, and to work as a team to provide the best care for the dementia patient.

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

This stems from frustration, misunderstanding, and often times an actual inability for those afflicted to express themselves. Lives are forgotten, simple daily tasks become insurmountable feats, and those suffering can even have a distaste for the ones they love the most. The impact can be equally devastating for their family members and caregivers. A New York Times article even equated the emotional and physical toll of caregiving as similar to the effects of Post Traumatic Stress Disorder (Graham). Over time, this disease becomes exponentially more domineering and destructive. Until we can better understand the functionally of Alzheimer's, people associated with the disease can seek counseling, support groups, and information on more efficient ways to cope. There is even a great outlook for these services to increase as The U.S. DHHS also included a goal to “Expand Supports for People with Alzheimer's Disease and Their Families” in the National Plan to Address Alzheimer’s Disease. As part of this goal, nationwide strategies include providing the resources to help family caregivers continue to provide care while maintaining their own health and well-being; assisting families in planning for future care needs; and helping to maintain the dignity, safety, and rights of people with Alzheimer’s (National Plan to Address Alzheimer’s Disease). As a result, quality of emotional

Alzheimer’s disease is the most common form of progressive dementia currently affecting 5.3 million Americans. Of the 5.3 million, 5.1 million people are the elderly population with two-thirds of those affected being women. There is no treatment available to cure dementia but measures can be taken to sustain the quality of life. Dementia not only affects the patients directly, but also family members and caregivers as well. Family members deal with patient’s memory loss, changes in personality and also have to take care of the ill patients financially. According to WHO, the cost of dementia in 2010 worldwide was estimated to be $604 billion dollars. Apart from the economic pressure, family members also deal with the physical and emotional pressures that come with dementia.

Although, according to Williamson, “many caregivers adapt quite well to their role” (Williamson). Before my pap started losing his memory, I didn’t realize how hard it was to watch a loved one with this disease, let alone care for a patient with Alzheimer’s. According to an article that explains a few coping strategies for caregivers of people with Alzheimer’s disease, “caregivers of people with dementia experience high rates of clinically significant anxiety and depression” (Cooper). This article explains various emotion-focused strategies, problem-focused strategies, and dysfunction-focused strategies for those caring for a person with Alzheimer’s. An experiment was conducted on caregivers of patient who have Alzheimer’s that explains which of these strategies were

Alzheimer’s disease is a form of dementia, a disease that according to the Alzheimer's disease Education & Referral Center is defined as: “…a group of symptoms that are caused by changes in brain function”. According to the National Institute on Aging in a book entitled “Alzheimer’s Disease, Unraveling the mystery” the authors chronicled that Alzheimer’s disease affect people in different ways. The most common and noticeable symptoms are: 1). Memory loss that disrupts daily life 2). Challenges in planning or solving problems

However, in a study by Brodaty and Luscombe, there were associations between psychological problems and the severity of the dementia (Brodaty and Luscombe, 1998). Caregivers need different ways of coping during each stage of Alzheimer’s similar to the patient themselves. In the beginning stages (early/mild), the caregiver is dealing with the emotional stress of seeing their family member decline slowly. They are dealing with the transition in their life of gaining another person to care for. The patient has good and bad days during this time period which causes the caregiver to be confused as to the level of the disease (Callone, 2006).

Alzheimer’s disease, the most common form of dementia, is a progressive neurological disease afflicting 24.3 million people worldwide. 4.5 million people in the United States are diagnosed with this illness annually (Leifer, 2009). Victims of Alzheimer’s disease reach a stage when they are no longer self-sufficient. Those with severe symptoms or lacking family support systems are relegated to nursing homes. Although scientific studies indicate that Alzheimer’s disease leads to a loss of memory and independence, researchers have proven that caregivers are also affected both physically and emotionally. Research is currently being conducted in finding ways to treat Alzheimer’s and helping their caregivers in the process.

Alzheimer’s Disease affects millions of men and women each day. Those affected face many struggles and live a hard life as their memory slowly deteriorates. Some situations they face we would never wish upon someone else and at times can be very sad to see. Alzheimer’s Disease affects those surrounded by it just as much as it affects the person struggling with the illness. To be able to understand Alzheimer’s it is key to know the symptoms and complications, what it is like to live with the disease and the treatment.

Alzheimer is a silent disease that primarily attacks the brain having the effect of the gradual memory loss of the patient, what this means is that Alzheimer is the most common form of dementia, which is a loss of brain function that occurs with certain diseases in this case combined with Alzheimer’s patients suffers from memory loss and other intellectual abilities that interfere with daily life. Alzheimer patients cannot follow instructions, suffers confusion and disorientation in time and space, and may even become lost in familiar places for them. In addition, the person may have impaired judgment, confuse their loved ones and in many cases even unknown themselves, in other words, patients

Envision living the great life, surrounded by the ones you love the most, continuing to be cheerful and ecstatic. Now imagine to slowly be forgetful of silly daily life objectives. For example, like forgetting where you left your phone or your car keys.Then eventually you forgot about your loved one’s birthday or to make that appointment. All of a sudden, you can’t seem to remember how your loved ones looked, or who you even are. As time quickly runs by, you’re now forgetting how to talk, and how to take care of yourself. This crazy forgetful concept is a disease called Alzheimer’s, and today there are over 5 million americans living with this disease.

Alzheimer’s disease (AD) affects everyone involved: the victim and his/her’s loved ones. First of all, caregivers are often overlooked, and never realized for what sacrifices they give up to care for their loved one. Secondly, the financial burden of caring for someone with Alzheimer’s is a big job that can hurt the opportunities that needed more time to get a better degree. Thirdly, although the victim of Alzheimer’s disease is the ill one, usually, they aren’t the only one suffering from this terrible disease. People must know that the caregivers are fighting just as much as the victim of the disease.

Has someone in your family ever been diagnosed with Alzheimer's disease? Alzheimer's disease is a form of dementia. Alzheimer's is a disease that is hard to understand. There are different types or severities as well as symptoms and treatments for this disease.

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