Dementia care offers support and services to an individual affected by the disease itself, which is dementia. It addresses the right and needs of the person with dementia and their families. Improving quality of life and changing attitudes towards dementia is the main goal of dementia care. Dementia care also provides quality of care, maintain dignity and promote health, security and comfort in consideration with the standard of care and ethical guidelines (Adams & Manthorpe, 2003). Understanding dementia care is necessary for those health care providers who are planning to handle dementia patients. Care worker should know their duties and responsibilities and have the required knowledge and skills to establish quality care. To find …show more content…
It also shows the need for more effective treatment method to stabilize the disease process and provide quality care for dementia sufferers. To achieve effective and excellence care on dementia, biological, psychological and social approach to dementia has to consider because it provides an understanding to people with dementia and help improved health practice, treatment and support for better dementia care (Bowers & Downs, 2008). Biological approach tackles the disease process of dementia, the cause of brain injury and the changes in behavior pattern of dementia sufferers. On the other hand, psychological approach to dementia involved the sufferer’s reaction to the injury, how they accept it and deal the situation. It also covers the effect of the disease process on their communication and action in relation to others. Particularly, people with dementia, mostly feel embarrassed and depressed by their brain injury. They are often angry, agitated and frightened because of the disease but maybe it also means seeking help to avoid embarrassment and disgrace. Dementia care in social domain explains the right of the person with dementia to enjoy and experience significant social interaction. Friendly environment and venues with sociable care provider that makes them comfortable and feels worthy is the focus. In addition, social identities of the people with dementia should be valued and social
2.1: Describe how current legislation, government policy and agreed ways of working support inclusive practice for dementia care and support
• 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.
In dementia care is a key aspect of best practice. It is a way of caring for a person with dementia as an individual with unique qualities. It means looking at the world from the person’s point of view ‘standing in their place’ as it were and appreciating how they may be feeling.
Living with dementia can be overwhelming, stressful and emotional. There is a lot to take in, appointments and assessments to attend, sorting out what support you are entitled to, care preparation, wishes and preferences.
As the disease progress, people might slowly lose their quality of life (QOL) in term of good health, mentality, communications and abilities that are considered crucial to their life. Patients might struggle to adapt with the new changes and disabilities happened to them and feel depress as they cannot live their normal life. There are three stages of Alzheimer which are mild, moderate and late stages. The mild stage of Alzheimer will starts affecting patient’s cognitive functions in which it might impair short term memories especially the one that are recently learn such as dates, recent events and people names. In terms of behavior, patients might experience depression and personality changes that could affect social relationships and everyday routines. Due to memory loss, family member relationship especially husband-wife relationship are also affected because patients might not remember their loved ones and they also lose sexual interest with their partner. It is hard for Alzheimer patients to live in the society and they are usually isolated because the society tends to assume these patients as crazy or
All organisations and authorities have a duty of care towards an Individual with dementia, GPs, Social
This report will assess the limitations in the current approach to patients with dementia following an observation undertaken within the hospital observing the care and awareness of patients with dementia.
Current legislation and government policy were put in place to ensure that care providers provide the best possible care for dementia patients. Government equally provide funding to improve care environments to help to manage the condition of people with dementia as they are less likely to get confused or become distressed within an environment designed with their needs in mind.
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
This essay will aim to introduce the term dementia including the types, causes, prevalence, young onset and models of care. This essay will continue to address what skill could be implemented to provide person centred care with understanding of health promotion and recovery concepts.
Dementia is typically a disease of "old age," and dementia was considered a normal part of aging for many years. In the advanced stages of dementia, patients typically lose the ability to communicate, and either the desire or the ability to take in nourishment. This stage is typically called the Terminal Stage or End-Stage Dementia. The absence of response to external stimuli does not mean that these individuals are not suffering. These patients still possess the ability to feel pain, fear, and to some extent can be comforted. Hospice and Palliative care programs exist to provide care for those approaching the end of life, and to give them the ability to pass in a peaceful way, with as the support of their loved ones and caregivers. Dignity and the absence of pain and stressors are an important part of this specialized care.
The development of a dementia environment approach will highly impact the improvement of life of people living with dementia involving their family and carers, evidently reducing the stigma linked with the condition. The need to physically and socially design an approach for the progressing ageing population, and better comprehension of the issues affecting the dementia suffering elderly. Life Community Village is a specially designed and self-contained village for dementia-affected people imitating a normal daily life. It visions a change of approach in dementia care in the future and cope with the growing number of issues of dementia in the ageing population. Its mission on the other hand, is focused on delivering a holistic and person-centric approach by leading and optimizing a normal life for dementia-suffering elderly. Also providing a dementia-friendly community and creating a society that the dementia-suffering person can engage in. In the current increasing population of older Australians, there is over a million that has received a form of aged care support and services every year. This is provided through the collaboration of funding and administration of the local, state and federal government. Meanwhile, according to Australian statistics, there are more than 353,800 who are living with dementia. In less than five years, it is projected to rise to 400,000; and due to the fact that there is currently no cure for the condition, and with the
Week 5 Nurs 8200 The article is titled “Dementia carer education and patient behavior disturbance. International journal of geriatric psychiatry” by Coen et al. (1999). The topic is on the topic of dementia carer with the purpose to evaluate the impact of dementia Carer Education Program on carer quality of life, wellbeing, and burden. The study was a Single group before and after the intervention study. The clear description of the study design makes it convenient to understand. A sample population of 32 dementia carers was taken. Thirty-two carers were enrolled for the successive three runs each about 8 months apart. They were interviewed prior to starting the study. Of the thirty-two carer, four were lost to longitudinal follow-up and the remaining 28 were interviewed again 6±7 months after the program. The intervention applied was clearly mentioned as eight weekly two hours support and education sessions by a Psychogeriatric clinical team. The interview was done by an experienced psychologist. The result of the study was, therefore, valid. The researcher did a Pre-programme and 6 months post-programme to obtain the data. The data source Measures included quality of life, burden, well-being, managing problem behavior, appraisal of social support, knowledge of dementia, and perception of the program. The Patients were characterized in terms of cognition, behavior disturbance, and functional status. With the two pilot runs of the program, out of the thirty-two enrolled in
Dementia is an umbrella term used to explain the gradual decline in multiple areas of functions, which includes thinking, perception, communication, memory, languages, reasoning, and the ability to function (Harrison-Dening 2013). Worldwide, 47.5 million people have dementia and there are 7.7 million new cases every year. Alzheimer's disease is the most common cause of dementia and may contribute to 60–70% of cases. (Alzheimer's society 2014). The complexity of dementia presents a number of behavioural challenges to those who live with dementia and their care providers. Aggressive behaviour seems to be one of the most prevalent challenging behaviours in the different stages of dementia (Weitzel et al 2011). As acute care
Alzheimer's disease is a progressive, degenerative disorder that attacks the brain's nerve cells, or neurons, resulting in loss of memory, thinking and language skills, and behavioral changes”(AFA 1). Millions of adults of the age 65 and older have been diagnosed with this serve diseases . Based on their condition they should be placed in a nursing home , because they're going to get the treatment they need . It also prevents the patients from hurting themselves and other members of the family. Nursing homes can benefit the patients in many ways and help, them accept their condition. Patients are able to interact with people with their same condition or have a different illness. They also provide counseling for the family members of the alzheimer's patients where they give them the support they need , and they’re able to learn more about the illness of their loved ones .