Question 1 Last week I undertook the Montreal Cognitive Assessment at home and the assessor was my husband. Leading up to the assessment I felt anxious, nervous and scared thinking about how my dyslexia, especially with numbers would impact the results. During the test I knew when asked about numbers that it took longer to answer the question and asked for them to be repeated. Since last week I thought how would have compounding issues like dyslexia with impaired cognitive ability affect the results. Can you imagine if you had cognitive impairment and were dyslexic as well? It is important as an assessor to know the complete personal social and medical history, to allow the test to run smoothly and allow extra time if the person suffers existing …show more content…
At the time of diagnosis, David and Irene may have protected themselves from negative stigma by saying to themselves that David’s current cognitive and physical capacity does not match their belief of what dementia is. So they remain in a state of instability, until carer roles and understanding of the disease process develops over time (Stirling, Campbell, Bentley, Butcher & Morrissey, 2016). The case manager can support them through the whole journey and ensure central and personalized care as they know David’s history (Hughes, Lloyd-Williams, & Sachs, 2012). They can provide early support and educational information and direct support as soon as possible after diagnosis is made (Downs & Bower, 2014). Early support allows David to be involved in his care planning whilst he still can. Early initiation of an advanced care plan is one way to reduce Irene’s carer stress, by making her aware of available support. Evidence has shown early support delivers longer periods of higher quality care at home (Crisp, Tabberer, Thomas, & Goddard, 2012) and delayed nursing home admissions (Downs & Bower,
I have been in care for a while and started out as a health care support worker so I have seen all different levels of progression with all different types of dementia. However the importance of early diagnosis is the same.
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.
The medical model of dementia dominated the traditional approach to dementia care until the 1990’s. The emergence of a social model of dementia after that time was partly to this dominance. It was also part of a wider social and civil rights movement at that time which people with disability were viewed and
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.
‘A retired teacher, Betty (65 years old), was diagnosed with Dementia. She lived at home with her husband Arthur (70 years old) who had been caring for her for several years. When she was diagnosed, No information was given to the couple. They had no relatives that they could rely on around them for support.
Early diagnosis of dementia can have a huge impact on the individual and their family and friends.
Instead of treating all people with dementia the same – it makes the care you give
Explain why individuals with dementia need to be supported to make advance care plans as early as possible
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.
When living at home with dementia the individual will have professional help come to them to help with daily tasks such as supervising medication intake, enabling optimum health and safety at home, providing a patient listening ear and friendly face, cooking, housekeeping and general errands, helping to facilitate routine, familiarly and comfort for their loved one at a difficult time. When someone moves from their home into a care home it can be very
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
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
In many cases patients with dementia wait a long period of time to go to the doctor after they start experiencing symptoms because they think it is a natural part of aging. The patients with dementia notice symptoms far before their care givers do but do not explain them to anyone. The fact that the patients wait so long to see a doctor about their symptoms and the lack of knowledge of the disease by the patient and care givers is a major hindrance to getting an accurate diagnosis and care. The care givers of the dementia patients play a major role in the diagnosis process as results showed they either promote or hinder the start of the diagnosis process. Early detection is essential to helping the patients live the best lives possible with dementia. Although treatment does not cure dementia it is usually much more effective in slowing in the progression when started in the early stages and an early diagnosis
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