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Needs of dementia patients
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In the book Jan’s Story by Barry Petersen, is a love story about how Alzheimer's disease stole his wife away. He gives an insight on her job as a an newscaster and how news was reported in places such as Moscow, Bosnia, Beijing, Africa, Baghdad, Tokyo and much more. At the age of 40 she started to slowly show signs and at the age of 55 it was confirmed that it was Alzheimer's. Once that was known, my heart sank, my first reaction was of course, these lovers have to fight this and she will win this battle. It was such a wild thought, to me that even when you say in your vows that it is death due us part but then have an expiration date. And before reading this and taking this class, I actually did not know much about the disease so this was …show more content…
This unforgettable fact was stated how “ten million people are unpaid caregivers for those five million with Alzheimer's.” However due to fundraising Alzheimer’s Association earned 94 billion and yet it seems this disease will spread to 16 million by 2050, so that’s 50 million people that will get this disease (Peterson,43). With that being said, the struggles for caregivers can be the anger, denial,depression, lack of emotion or conversation, social withdrawal, irritability, and more importantly, just overall, exhausting on both of you. Barry, did his best for such a long time with a caregiver until he had to put her in assisted living home. At first, this was hard for Barry and people but what Jan’s friends and family did not realize is the struggles Barry and Diane were facing, outsiders only see the Jan that they remember not what the disease has turned her
Informal supports, such as aid for housekeeping and running errands, are crucial to maintaining the lifestyle of individuals with Alzheimer’s in the community; however, the disease’s erosion of physical, cognitive, and communicative abilities often creates tremendous strain for family caregivers. Individuals and family caregivers dealing with Alzheimer’s often experience increasing social isolation as the disease’s progression undermines both mobility and the capacity for meaningful and appropriate engagement with the community (Banerjee et al., 2003). A number of studies have documented the physical and mental health costs borne by unsupported caregivers, and the link between caregiver stress and the institutionalization of their ill family members (Andren & Elmstahl, 2005; Banerjee et al., 2003). Taken together, the stress and isolation of dealing with Alzheimer’s disease undermine the health and quality of life of everyone involved, eventually precipitating institutionalization.
Illness and pain are by fare two of the worst things we could ever see happen to a loved one. Moreover, know that illness and pain is irreversible and sometimes fatal. Most illness in our older loved ones are caused by the fact that their body is aging. “Older adults experience more chronic illnesses than any other age group (Merck Research Laboratories, 1997).” (Brown 93). “The elderly, especially those over 80 years of age are the fastest growing population in the US, and the elderly report more pain than younger persons.” (Karen Bellenir 57). Michael Wolff discusses his mother’s illnesses and how it is effecting her everyday life. He goes a step further and paints a picture of how it makes him feel, in turn Wolff is able to capture the reader and draw them close to his opinion. “She strains for cognition and shockingly, sometimes bursts forward, reaching it – “Nice suit,” she said to me, out of the blue, a few months ago- before falling back. That is the thing that
Pam Belluck’s article entitled “Nuns Offer Clues to Alzheimer’s and Aging” focuses on the lives of the School Sisters of Notre Dame and a scientific experiment called the Nun Study. The Nun Study intends to find clues and answers about who gets Alzheimer’s disease and why. For fifteen years, these nuns have been tested on their ability to memorize, their strength, and even their genes have been analyzed. Dr. Snowdon’s research has theorized that a positive emotional state of mind earlier in life may lead to a longer, healthier life. But overall, a good portion of this article has little to do with scientific research, and much to do with the lives of nuns. The scientific research that the author does provide is not helpful in fully understanding this experiment. Belluck is not totally committed to this scientific study. Her main interest seems to be fixed on the lives of the nuns in this convent.
Charlotte Perkins Gilman's "The Yellow Wall-paper" is an excellent story on several levels. It works as a suspenseful thriller about the effects of mental illness. It also serves to make several points about feminism and the pervailing attitudes of her time.
The article “Cracking the Alzheimer’s code” by Linda Marsa discusses the history, discoveries and advancements for Alzheimer’s disease. The discovery of Alzheimer’s disease was revealed through a German physician named Alois Alzheimer. Alzheimer first discovered Alzheimer’s in the year 1901 while he was interviewing a mentally Ill patient named Auguste Dexter. The beginning of his discovery was due to the fact that Dexter was exhibiting uncontrollable behaviors that included jealously, screaming, confusion and paranoia. After Dexter had passed away, Alzheimer saw this as an opportunity to examine her brain under a microscope in thin pieces. To Alzheimer’s surprise, he discovered two abnormal substances on brain slices that were called amyloid
The researchers of this paper will be researching the effects of Alzheimer’s on society as well as the individual. Alzheimer’s disease is a disease that causes mental deterioration. The researchers will discuss the effects of Alzheimer’s disease on the individual, the effects of Alzheimer’s on the caregivers, and the effects of Alzheimer’s on society. Alzheimer’s disease is like many other diseases; early detection is best because deterioration of the brain cells can be delayed. Greutzner, H. Alzheimer’s disease has a tremendous effect on the lives of those who live with the disease.
Lisa Genova’s grandmother, who was 85 years old, had been showing signs of dementia for years; but she was a smart and independent woman who never complained, and she navigated around her symptoms. Her nine children and their spouses, as well as her grandchildren, passed off her mistakes to normal aging. Then they got the phone call when Lisa’s grandmot...
What is Alzheimer ? Is Alzheimer 's more difficult for the patient or for the patient’s siblings?
Dementia is the loss of a person’s mental skills from their daily routines. The symptoms of dementia could easily be over looked, they include forgetting things, daily routines are hard to complete, misplacing things, depression, aggravation and aggression, emotion are high, even feeling like someone is a threat to their life (Web MD,2012). Caring for someone with dementia can be difficult if with resources like healthcare, living facilities, nursing homes and medicine is involved, but sometimes healthcare and facilities do not provide the proper care. This disease is very common in the elderly community past the age of sixty-five. Finding out that a loved
The participation in leisure activities, such as dance, is related with a reduced risk of development of dementia, both Alzheimer's disease and vascular dementia (Verghese et al., 2003). Dementia is “a general term that describes a group of symptoms-such as loss of memory, judgment, language, complex motor skills, and other intellectual function-caused by the permanent damage or death of the brain's nerve cells, or neurons” (Alzheimer’s Foundation of America [AFA], 2015, para 1). Alzheimer’s disease is the most common cause of dementia in persons over the age of 65, representing about 60 percent of all dementias. Dementia is specifically characterized by “different pathologic, or structural, changes in the brain, such as an accumulation of
Slight Reminder of Credentials – In taking care of my mom, who was diagnosed with AD. I have learned first-hand that caring for a person with Alzheimer’s disease can be very stressful.
This theory views the family as a system containing interrelated and interacting parts. Whether something is affecting a family member positively or negatively, all family members are affected by these factors (Mitrani,Feaster, McCabe, Czaja, Szapocznik, 2004). In this case, the Howland family must cope with the vast changes in the cognitive function of their mother Alice. Throughout the film, we see how the impact of Alzheimer’s disease affects the family as a whole. Lydia who lives in California must move back home so that she can take care of her mother while her father is away at his new job. This is an example of how Alice’s Alzheimer’s diagnoses does not only affect her, but also affects Lydia’s life. Another example of how the disease affects the family system is when John and Alice are about to go for a run; Alice advises John that first she must use the bathroom before they part. Sadly Alice does not remember where the bathroom is in the house and she urinates in her
“Difficult, depressing, and tragic” are a few of the descriptions generally associated with illness. Those who suffer from dementia, especially, undergo a realm of these characterizations. With this adversity in mind, most people generate a basic understanding based on education rather than personal experience. It is this preconception that can prevent us from gaining a true insight of one’s reality.
A crucial scene that should not be unrecognized was when Alice told her husband that she wished she had Cancer. Alice explained that she wouldn’t feel so ashamed because people wear ribbons and go on walks to support the disease. This also underlines the stigma that follows Alzheimer’s because the imbalance between “physical” and “mental” illnesses is unbearable. For Alice, Alzheimer’s disease seems to be an invisible disease in her mind because people do not sympathize with it as opposed to other physical diseases such as Cancer, Heart disease, etc. It is very disheartening to recognize the negative connotations with mental illness as opposed to physical illness.
There is a 5 million estimate of the carers in the UK and figures are foreseen to upscale for the next 40 years to 9 million (O’ Dowd, 2007). With this high number of carers, for whom the carers can ask for support during times when difficulty arises in relation with taking care of people with dementia.