Our identified population consists of family caregivers of people with dementia in Canada. As such, we need to implement our model in a way that it is accessible and usable for this population. The health promotion strategy that we intend to use is the development of a mobile application. The intention behind this app is to provide a free, accessible tool that caregivers of family members with dementia can use to mitigate the extremely high rates of depression, caregiver fatigue, and burnout, that are experienced by the family caregiver population (Snyder et al., 2015). The development of this mobile app would ideally involve the input of the stakeholders. The stakeholders would be engaged such that we, the app developers, would consult …show more content…
It would be irresponsible to presume that we are the experts, and therefore possess enough information to conclusively provide the best app possible. This is simply not true. Involving the people who love, work with, treat, and serve Canadians with dementia is the best plan of action to achieve a successful app that provides the information and support that caregivers need to lessen the burden of caring for a relative with dementia. Another reason for the focus groups and questionnaires involving stakeholders is to ensure that we are developing an app which will serve its purpose in informing and supporting family caregivers of people with dementia, without leading app users to believe that this app can be a substitute for medical input. We need to be responsible in the development of this app and be mindful that in no way should it be used as medical advice, nor should it lead a caregiver away from seeking appropriate care if they are experiencing severe psychological distress. Input from the Alzheimer’s society, physicians, and long-term care homes should ensure that the app is as helpful as it can be, without leading users away from more appropriate care when
Nearly 135 million people worldwide will be impacted by dementia by 2050 (Robinson, Tang, Taylor,. 2015). Dementia is not a disease, it is an overall term that describes a wide range of symptoms associated with the decline in memory and thinking skills. Dementia is a progressive illness that results in the loss of one’s sense of self (Burns, Byrne, Ballard, Holmes, 2002). The two most common forms of dementia are Alzheimer’s disease and Vascular dementia. Dementia is progressive and people with dementia experience complications with short-term memory, keeping track of personal items, paying bills, taking care of themselves and daily tasks (Haigh, Mytton, 2016). Due to the rising number of individuals developing dementia, it is causing major challenges in the healthcare systems and society (Angermeter, Luck, Then, Riedel-Heller, 2016). Utilizing psychotropic medications are often ineffective or harmful to the individual, therefore, many patients decide to utilize sensory therapy as a form of treatment instead (Livingston, Kelly olmes, et al., 2014). Caregivers of individuals with dementia can also experience health consequences related to caregiving at the end of life. Spousal caregivers are 40.5% higher odds of experiencing frailty as a result of caregiving (Carr, Dassel, 2017). Dementia does not only affect the individual, it affects those around them, society, and the healthcare system.
We know that a combination of lack of public and professional awareness, late diagnosis, negative media images, myths, stereotypes and negative experiences all contribute to a general fear of dementia. Individuals and carers can be supported to overcome their fears. There are many ways that individuals and careers can be supported is by gaining information and advice from going online, reading book’s/ leaflets, discussing the issue with other family members.
Instead of treating all people with dementia the same – it makes the care you give
• Every individual, including individuals with dementia, has their unique life history, lifestyle, culture and preferences, including their likes, dislikes, hobbies and interests, which makes an individualised approach in care necessary.
There are many different forms of dementia and each has its own cause. Some of the main type of dementia is Alzheimer’s disease, which is the most common form of dementia affecting 50%-70% of dementia patients (Alzheimer's australia, 2005). This is a degenerative illness which attacks the brain, this is achieved buy tangles which are in the middle of shrunken brain cells and plaques which eventually cause the brain cells to die meaning information can no longer be recalled or assimilated. There are also other types of dementia which include vascular dementia which is caused by circulation of the blood to the brain, Parkinson’s disease which is a disorder of the
Assignment 50: Unit 50: Enable rights and choices of individuals with dementia whilst minimising risks
Dementia does not only impact the people with symptoms and it also disturbs the people who must care for the person. It is estimated that 1.2 million people are involved in the care of people with dementia. It has a financial burden on the Australian economy $4.9 billion in 2009-10. (1)
Focusing on dementia, it is not constantly possible to involve the dementia sufferers in the decision making course of their care without encouragement and assistance by
Care staff will also be asked to perform self study research exercises in which they investigate aspects of dementia, for example person centred care. During this research exercise the students will be given internet time and at the end asked to feedback their findings to a small group, thereby also further developing their literacy skills. Use of the internet is not only an excellent way for learners to learn about dementia but also to develop their own personal ICT skills.
Buijssen 2005 suggests that depression is a main factor with dementia due to lots of feelings of helplessness and anxiety which can cause the service user to have challenging out bursts. To enable a person to remain in their home safely and independently other people will be involved. This depends on how advanced the dementia is, otherwise the service
The advisory committee is responsible to provide feedback on each of the programs components such as the brain bank, memory disorder clinics, respite care and model day care. The committee should oversee the training, research and coordination among all the components. The committee also enlists the services from a broad range of representatives that includes health care professionals, providers, individuals associated with the Alzheimer’s Association and other care givers to assist and seek direction in the fight against this disease.
The main motives include providing more knowledge and understanding of dementia and also its effect on behaviour as well as it progression rate. Provide carers with an impressive understanding of available local support services and how they can be accessed. It also aims at assisting in surpassing the shock relating to an initial diagnosis of dementia as well as ways to maximize life and well-being.
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
The older adult population in the United States has steadily increased thanks to technology and medical advances. While this definitely is an undeniable achievement, it also creates some challenges that society was not as prevalent to face before. Now that people are living longer it’s also means that often times family members are becoming caregivers to their loved ones during their so called golden years. Not only may it be difficult to care for a loved one, but it also becomes even more burdensome when their loved has a disability. In fact “dementia is one of the major causes of disability and dependency among older people worldwide.” (2016). Fortunately there are adult day centers that serve people with dementia and provide services that can benefit them. However many times caregivers are forgotten about and aren’t provided services that can also benefit them as well. While it does take a bit of pressure off of the caregivers while their loved ones are at the day center, it does not eliminate all the other effects. Many people may not be aware that there are detrimental effects that a caregiver may experience as a result of caring for someone with dementia.
Alzheimer’s disease affects 1 out of every 8 people in the United States. It is a long and debilitating disease that affects every aspect of a person’s life from the way they preform daily tasks, to the physical and mental abilities that are diminishing. Along with the lifestyle changes that Alzheimer’s disease presents, it also affects one’s psychological perspective as well their view on what they can offer their family and society. There are some ways to maintain a level of independence with a disease of this magnitude but there are also factors in lifestyle choices that can make it worse. Alzheimer cannot be cured, it cannot be slowed, but there are ways to keep the effected person at a certain level of comfort, independence and safety