Alzheimer’s disease and the effects on family members
Diana Gonzalez
Community College of Aurora PSY 101-112 General Psychology I: SP17 3/8/2017
Introduction
There have been studies that examine the effects of family members who are diagnosed with Alzheimer’s disease being good or bad. Some studies looked at how care givers are effected. They can be known to depress prior to or after death of the person diagnosed with the disease (Stroebe, Zech, Stroebe, & Abakoumkin, 2005). Other studies showed how the family member with Alzheimer’s and the care giver interaction with the physician is known to result to the caregiver had more interaction than the patient does (Fortinsky, 2001). Another study showed how a family members
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(2007; 2009) did a diary study of persons with Alzheimer’s disease and their caregivers. This study included eighty-three ages 41-85 years. These 83 were people who volunteered to write a diary about being the family caregiver, and how their family member changes over time. These family caregivers provided the majority of home care of people with Alzheimer’s disease. In this study, it was discussed on how a family caregivers’ life orientation and changes in life orientation during the first year after the diagnosis of Alzheimer’s disease. The dairies were for the first six months after the family member being diagnosed with Alzheimer’s disease. The term “family caregiver” is used to refer to a person who primarily helps a person with Alzheimer’s disease with his/her daily life. A series of findings were made from the description being doubtful at first with a family member having Alzheimer’s to describing their new …show more content…
Either with their day to day activities, relationship, and with whom a physician goes to when it comes to a family who has someone who has Alzheimer’s. In the future, more studies about gender difference in caregiving behaviors should be done. With these studies, we could be able to see how the behaviors on how different gender influences the behaviors between the connections of spouses. Also, continued diary studies would be a great source to gather more and more information on how a caregiver’s life changes after a family members are diagnosed with Alzheimer’s
Being a caregiver to someone with Alzheimer’s is a title and life one must occupy and fully commit themselves to. In the beginning stages of Jan’s diagnosis, Barry vowed to himself that no matter what, he would be with Jan every step of the way, until the very end of her life. He was patient with her and only wanted to be with her every second of every day. In his mind, Jan was going to beat the odds. He would maintain his role as her sole caregiver and together they would struggle through the disease.
In Tiana Peele’s “Alzheimer’s: The Forgotten Issue” published by the University of Delaware Peele attempts to raise awareness of the forgotten issue of Alzheimer’s. Undoubtedly, Peele is drawn to this subject at matter because her grandfather was diagnosed with Alzheimer’s. This disease happens to be a form of Dementia and causes memory and intellectual abilities to deteriorate. Some of the early symptoms include short-term memory loss, and behavior changes. Furthermore, as one progresses into the later stages of this disease they become increasingly confused and become suspicious of loved ones.
Discussion 5- Advocacy According to recent data, the baby boom generation will have all retired by 2030, (AARP), which is only 15 years from now. The population in this generation will include 77 million more 65 and older individuals, not including the 54 million already in retirement and receiving Social Security and Medicare benefits. Please note that many seniors also receive some form of federal benefits such as military pensions, survivor’s benefits, annuities, investments income or an awarded settlement (Quad Agno, 14). Unfortunately, in our society driven many times by greed, this has placed our seniors in vulnerable positions, particularly when health and cognitive functions have declined; a slight disadvantage of becoming older (Quadagno,
Which brings me to how my research on dementia helped broaden my understanding on the short story "Babysitting Helen". It increased my knowledge the most in these three categories, the daily life affected, the symptoms of Alzheimer 's, and the struggles on the family. In the short story you can see the Alzheimer 's victim, Helen, was always being watched and always being taken care of. I now know why she was always on watch. As we can assume Barb is the caregiver for her mother and whenever she goes out she has to find someone to watch Helen.
Nurses in Complex Continuing Care Encountering Ethical Dilemmas of Autonomy and Wellbeing When Patient with Dementia Wants to go Home Bhakti Amin Student # A0622083 Professor S. Cairns NURS 2047 23 March 2018 Introduction Dementia continues to grow as a condition diagnosed among elderly females, researchers have hypothesized that this is due to longer female life expectancy (Podcasy & Epperson, 2016). Allowing a client with dementia to stay in their own can have several benefits such as joy, comfort, socially connected, maintain identity, and have meaning in life; however, in many cases, clients with dementia require complex continuous care (CCC) to support their health and wellness needs and the needs of their family (Lilly
This is more than just the financial resources that they have, but also their psychological and physical health and their spiritual outlook on life and the situation. One important factor is the caregiver's location and place of residence in relation to that of the person to be cared for. It must also be remembered that the carer has a life outside of this role and, therefore, important factors in caring include other day-to-day roles such as being an employee, a parent and a professional person. The carer is also affected by the opinions and demands of people outside the caregiving relationship. Caregivers are also facing a health care system that seems to be placing more responsibilities on caregivers while providing less and less
Communication Strategies Overview One of the many challenges posed by people suffering from dementia is communication. As this disease advances the brain begins to deteriorate by showing signs of lost memories, clear thought, and a lack of personal hygiene. In addition, mood swinges become evident stemming from the frustration of losing their ability to remember and communicate clearly with others. Other noticeable changes occur in the personality and behaviour patterns, such as a lower regard for personal hygiene.
Hillier and Barrow (2015), associate problems of caregiving with the responsibility itself, the caregivers personal health, role strains, strained family relationships, ect. With all of this strain on an informal caregiver it seems most beneficial to the caregiver and the elderly individual to consider admittance in to an assisted living facility. Once a basis has been established as to why an elderly person is admitted in to an assisted living facility, further insight shall be established to denote what is considered elder abuse. In this movie, Life and Death in Assisted Living Facilities, several
My mom is the primary caregiver for my elderly grandma, who has dementia. Personally, to be able to empathize more efficiently with my family it is important I gain understanding of caregiving elements. To connect to the ABC-X model, Caregivers, examines different coping mechanisms for adjustment and adaption given the unexpected development of Alzheimer’s disease. Ultimately, the pre-crisis is contributed to learning about the disease. From there, families had to pull together resources, including time, energy, financial, and social support.
Care givers: caring for a family member or friend with a physical or mental illness can be stressful, exhausting, both mentally and physically, and creates a physical and psychological strain for the care giver over a period of time. The psychological well-being such as depression and stress, are frequent consequences of caregiving. The age, socioeconomic status, and the availability of informal support that caregivers have access to greatly affect their own health and well being. Caring for a family member with a mental illness can differ from caring for someone suffering from a physical illness. In addition to the medical care and long term treatment of a family member, an open and liberal view of mental illness is almost an essential in being able to care for someone who is ill.
Working with older adults and their families - a review. The Association for Family Therapy,16,
The text describes eldercare as a "family process. " Explain this
This may be had at first if they are cognitively functioning, they may become depressed due to not thinking that their declining health. When this stage sets in a person knows that their life is coming to an end and they may not be ready, which can affect them negatively. Having a person like Joesy, that genuinely cares for their “Client/Patient” means a lot, hopefully they can come to terms with their declining health or at least they know that they are being loved for by a stranger. In conclusion, this article shows that even when family cannot care for their aging family, people in our communities will step in and take that role to care for our loved one.
Many children across the nation are taking their parent as get older and being to decline in vitality, many consider letting them move into their home. After all, it is easier to care for an elderly mother or father in a nearby room, rather than one who is across the street town or even in another state for the purpose of this week discussion this family in question will experience what is takes to take care of their elderly parent. As the older parents is preparing to the leave the acute care the coordination of care will approach and speak with the family to set up a plan of care for the elderly parent. This daughter who lives nearby will move her father who is 84 years old male that had changing in mental and physical health since he
Having lived in this situation, this video and topic struck home for me. My maternal grandmother lived with my family for the first fifteen years of my life and currently still lives with my mother. This situation has never seemed abnormal, particulate phenomenal or uncommon to me. In my culture (Japanese), it is expected that adult children will take care of their aging parent within their home; often times this is happening in conjunction with raising their own children. To place the care of one parents in the hands of a stranger (e.g. nursing home, assisted living, etc.) would be dishonorable and disrespectful.