Yolanda Case Study Essay

The memoir went exactly how I thought it would be. Bette Ann Markowitz’s situation of taking care of a parent who has Alzheimer is very common; having an aging parent who can no longer fend for themselves. Markowitz is not an only child so she had to constantly consult her sibling on “what is the best option” (Moskowitz41),

‘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.

She gives her account to how the help of clergy, friends, and family. Seeking help from clergy members it helped her differentiate visions from hallucinations. In her words she describes hallucinations as lacking sense. Visions are a message from God. Friends play a crucial role in someone with mental illnesses, because they can observe the patients to see if any changes happen that are too swift or too angry or too violent. Also keep constant contact with the individual, the constant presence of someone either through email or phone call really helps. Family can also play the same role of a loving

The term ‘dementia’ is used to describe a syndrome associated with an ongoing decline of the brain and its abilities. This includes problems with memory loss, thinking speed, mental agility, language, understanding, and judgment. People with dementia can become apathetic or uninterested in their usual activities, and have problems controlling their emotion. They also fine social situation challenging, lose interest in socialising and aspect of their personality may change. The majority of people who are diagnosed with dementia have either Alzheimer’s disease or vascular dementia, or a combination of the two. (Source 1) As the disease progresses, the person experiencing dementia becomes more vulnerable and their needs often complex; which requires appropriate care and management (Kitwood, 1997).this leads me to the next distinctive feature of patients with dementia.

Illnesses like Alzheimer's disease make it difficult for those who want to provide supportive care at the end of life to know what is needed. Because people with advanced dementia can no longer communicate, they cannot share their concerns. Is Uncle Bert refusing food because he is not hungry or because he's confused? Why does Grandma Ruth seem agitated, is she in pain and needs medication to relieve it, but can't tell you. As these conditions progress, they also obstruct efforts to provide emotional or spiritual comfort. How can you let Grandpa know how much his life has meant to you? How do you make peace with your mother if she no longer knows who you are? Someone who

After Sister Maria's death, the neuropathological evaluation found that her brain contained abundant neurofibrillary tangles and senile plaques: the characteristic lesions of Alzheimer's disease. When focusing on the life of Sister Dolores, Dr. Snowdon observed that higher education may lead to higher functioning in later life. She was a professor of elementary education at Mt. Mary College and then a degree in geography. One clear difference between Sisters Maria and Dolores is in education. The pilot study also found a correlation between higher education and healthy function in later life. Sister Maria's poor health began from the start of her first “bluebirds”, an assignment after taking their vows. Sister Maria's first assignment was to teach a second-grade class at St. Joseph’s School in Appleton, Wisconsin. The vow of obedience meant that she accepted it without question, but the isolation and stress of her first year in America had taken its toll. On her first day of teaching Sister Maria suffered a nervous breakdown, and this marked an episode of severe depression which could be attributed to her outcome. The lives of these Nun’s have provided insight to aging and Alzheimer's disease and exemplifies to researchers what is possible in old age, and further research on how the diseases may be

Mrs. Yowell is a 90-year-old woman who is a resident of a long-term care facility. She was alert and mentally quite capable until about a year ago when she began to manifest signs and symptoms of dementia. A review of her medical records failed to document a thorough analysis of her dementia, but a diagnosis of “probable Alzheimer disease” was recorded.

By the numbers, Alzheimer’s disease looks even worse than it may be. The cost of Alzheimer’s overwhelms the caregiver and everyone involved with the patient. The price businesses pay for Alzheimer’s it detrimental to their industry, show by “A 2002 study showed that United States businesses lost $36.5 billion that year because employees missed work or quit and had to be replaced so that they could care for someone with Alzheimer’s disease” (Adams 24). The caregivers play vital roles in the lives of the sufferer, but the business take an even heavier loss. Heath care is necessary for someone with Alzheimer’s disease, however it can get expensive “The costs of

Patients with dementia are highly subject to psychosocial interventions. Thus, frank will tend to rely on his two children (Thomas and Jenny) and staff at the residential home for support and protection. Psychosocial model of care involves psychological therapy, which can be delivered on a one-to-one/group basis to meet important psychological needs as well as have impact on physiological level (Bartle and Frankland, 2008). These psychological therapies include Cognitive stimulation therapy (C.S.T), Reminiscence and Animal

     It is inevitable that eventually each of us will grow old and begin to face more and more health problems as our age rises. Elderly people are challenged by many illnesses and diseases that unfortunately, are incurable. One disease that becomes more common as people age is Alzheimer’s disease. Alzheimer’s a common cause and a form of dementia and can severely damage a patient’s cognitive functions and can ultimately cause death. Living with Alzheimer’s disease can be saddening for both the sufferer and the family. Family and friends will find it very hard to cope when a loved one begins slipping away and losing memory of who they are.

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.

People lose height, skin becomes loose, hair becomes gray, people become covered in wrinkles and they start to become weak. Even though all of this may be true, older people still have purpose in life. Patients often feel stripped from their life from dementia. “Richard Leider, one of America's preeminent executive life coaches and renowned expert on purpose and meaning in life, has postulated that purpose is fundamental to an individual's health, happiness, and longevity”(Nakonetschny). With conducting activities into nursing homes, that sense of happiness and meaning will become reestablished more and more every day. Dementia patients have family that cares for them and wishes the best for them, they do not wish to see their relatives rot away in a nursing

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

of attending injured patients even if there was no power supply. Fortunately, DOH has been actively sending three generators to the district hospital, in addition to the two others that already arrived to prevent such difficulties to occur again in the future (Gitagano & Pineda, 2015).