A Changing Mind
Have your parents started to forget things or struggle more in daily activities? It’s something we don’t imagine will happen to our parents. We can’t predict if it will happen; although, the older our parents get and if a family member has had the disease, it increases the risk. Alzheimer’s is a disease children don’t think could cause the death of their parents. It’s a disease that’s irreversible, with no treatment to stop the progression, and no cure. Children of aging parents are often unaware of the emotional and physical effects Alzheimer’s can have on their parents, family, and caregivers. The Alzheimer’s Foundation of America can provide support for all of those confronting Alzheimer’s, which is why it’s important to
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One of the advantages by placing a parent with Alzheimer’s in a care facility, aside from the fact they are very experienced, is the family can still be very involved in the care of their loved one. Mannion (2008) explained that many of the times family help assist in the care of their parent in the early stages of the disease and will continue to care for them while their parent is in a care facility, which averages approximately nine hours a week. Children tend to feel the need to provide care for their parent with Alzheimer’s, but can have negative side effects. One may feel cut off from social activities and may become depressed, anxious or develop anger from caring for a loved one with Alzheimer’s. Every loving, caring child needs to take a break from time to time when caring for their loved one, and respite care (temporary caregiver) is a wonderful way to achieve the needed time away (p.28). Caregiving, regardless of whether it’s the parent’s child or in a care facility, can be very difficult physically on an individual, especially in the late stages when they need a great deal of assistance in bathing, dressing, and moving from one place to another. Whoever the caregiver is, there are many services the Alzheimer’s Foundation of America can help with, such as finding support groups as well as social workers available for counseling to help caregivers caring for those with Alzheimer’s. Being a caregiver is a tremendous responsibility for an individual. Mannion stated “the wellbeing of a person with Alzheimer’s depends directly on the wellbeing of the person who is providing their care”
Alzheimer 's disease (AD) is a progressive degenerative disease of the brain from which there is no recovery. There are three brain abnormalities that are the hallmarks of the Alzheimer’s disease is initially caused by plaques buildup in the brain’s neurons as illustrated in figure 1. The support structure that allows the flow of the nutrients through the neurons gets damaged and ultimately there is loss of connection among the neurons and they die off (National Institute of Health, 2015). This causes the brain tissue to shrinks, which is called atrophies. All this ultimately lead the victim of this disease to face difficulties in governing emotions, recognize errors and patterns, coordinate movement, and remember. Ultimately, a person with AD loses all memory and mental functioning.
Alzheimer’s is a disease in the brain that affects a person’s memory, thinking, and behavior. It is the most common form of dementia and is common in adults older than 65. More than five million Americans are being affected by Alzheimer’s at this moment. Alzheimer’s comes in three stages; early, middle, and advanced. The disease is caused by the shrinking of the brain due to many risk factors and genetics.
Alzheimer’s Disease is a progressive disease that destroys memory and other important mental functions. Brain cells in Alzheimer’s disease dies and degenerate causing the loss of memory and mental functions. Alzheimer’s is the sixth leading cause of death in the U.S.A. Alzheimer’s Disease is named after Dr. Abis Alzheimer. In 1906, Dr. Alzheimer noticed changes in the brain tissue of a lady who had died of an unusual mental illness that was very unknown. The woman 's’ symptoms included memory loss, language problems, and unpredictable behavior that people with Alzheimer’s have almost often of times. Alzheimer’s disease is the most common form of dementia in this world and it’s thought to be the most progressive disease of all diseases. Also this disease gets progressively worse over time. The majority of people with Alzheimer’s are sixty-five years old or older, however, almost five percent of the people have early-onset Alzheimer’s. Early-Onset Alzheimer 's is known as Alzheimer 's at a younger age which appears at the ages of forties and fifties. In early stage Alzheimer’s, memory lost is very mild. With late Alzheimer’s, individuals lose the ability to carry on conversations and respond to their environment. People with Alzheimer’s often live an average of eight years after their symptoms become noticeable to others.
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 chapter 15 I found the part on Alzheimer’s disease very informative and interesting. Alzheimer’s and dementia are diseases that I find great interest in. My paternal grandfather was diagnosed with Parkinson’s disease when he was just over the age of 60. He proceeded to be diagnosed with Parkinson’s induced dementia, and then he later passed away from the disease. My maternal grandfather suffered from a severe stroke about 4 years ago, and is now suffering from stroke induced dementia. Seeing anyone who is suffering from Alzheimer’s and dementia of some sort is very sad. I work in an assisted living facility and we have a specialized facility of people who are diagnosed with Alzheimer’s or dementia. Working with these people on a daily basis
It is a complex disease people often times do not know how to care for. Although a decline in memory and bouts of more forgetfulness are more common as one ages, spotting the difference between normal age-related symptoms and Alzheimer’s is important for families so that they can get their loved one the best care available. Even with proper care though, caregivers can misunderstand the symptoms of those afflicted, leading to an improper treatment of the patient. There are an estimated between 2.4 and 3.1. million AD caregivers in the United States, a majority of which are family members, who may not know proper care techniques or may be of older age themselves, as they could be caring for a spouse (Schulz and O’Brien1, 185-94). In fact, in a study of caregivers of those to patients with a memory ailment including Alzheimer’s or Dementia found that spouses have consistently been found to be more depressed than other relatives caring for a family member with a cognitive impairment (Schulz and O’Brien2, 771-91). To help in awareness, there are many new classes being offered in schools that can better prepare caregivers. The U.S. Department of Health and Human Service’s (DHHS) National Plan to Address Alzheimer’s Disease dedicated a major goal to “Enhance Care Quality and Efficiency,” with major strategies including building a workforce with the skills to provide high quality care, explore
She welcomes anyone who comes into view yet stands near her husband. She develops small talk with her close knit family, the people she recognizes. Extended relatives and a few measly encounters do not form a new bond in her mind. She repeats stories, she repeats sentences and she repeats questions. She poses for a picture with her sister, lifts up the bottom crease of her sweater and pulls out a bright pink scarf to swing over her neck. She illustrates a world of imagination and fun through the playful pose. She represents a disease of heartbreak and loss. The woman shows early signs of Alzheimer’s. Alzheimer’s is a merciless disease in the family that killed her brother and is grabbing hold of the rest of her siblings.
Alzheimer’s disease is the most common type of dementia in the United States, with its commonness expected to increase dramatically in the coming decades. Although awareness of Alzheimer's disease has increased greatly among professional and amateur audiences, exact means do not exist to calculate how many Americans the disease affects. However, it is estimated that there are over 5.1 million people aged 65 or older with probable Alzheimer's disease. Alzheimer’s is also the sixth leading cause of death in America. Throughout, I will be addressing the issues that surround this disease: it is not an inevitable consequence of aging, the care and treatment, and end-of-life decisions. While explaining these issues, the goal is to achieve a better
Both age and genetics have been identified as risk factors, but many questions still remain. If a loved one were to face this horrible, deadly disease it can be quite the daunting task to be the primary care giver for someone going through Alzheimer’s. The Alzheimer’s Association of America reported in 2014, friends and family of people with Alzheimer's and other dementias provided an estimated 17.9 billion hours of unpaid care, a contribution to the nation valued at $217.7 billion. This is approximately 46 percent of the net value of Walmart sales in 2013 and nearly eight times the total revenue of McDonald's in 2013. Over half of primary caregivers of people with dementia take care of parents. But you are not alone in your efforts, there are a multitude of specialist and organizations that can help you with many different needs, hotlines in place to get information day or night about ways to make those affected by this disease more comfortable in their daily struggles.
“Alzheimer’s From A New Angle: A radical new approach to treating the fearful disease is showing promise” by Alice Park, an article found in the February 22/29, 2016 issue of TIME magazine, delves into encouraging new research being conducted to find a cure for Alzheimer’s disease, a progressive neurodegenerative condition that destroys the brain. Dr. Frank Longo, from the Department of Neurology and Neurological Sciences at Stanford University, School of Medicine, is leading the charge. This disease was discovered over 110 years ago by a German physician named, Alois Alzheimer. For so many years now, researchers have focused solely on treating/stopping Alzheimer’s once its devastation has already begun. In the last seven years, over
Alzheimer 's disease which chronically leads to Senile Dementia, is a horrific change in homeostasis for human beings. The most obvious change in homeostasis from Alzheimer 's is loss of memory. Memory loss can vary from short term to long term. Alzheimer 's disease has been occurring in humans for a long time. This is a disease that affects different body systems, and interrupts homeostasis to a significant point. As Alzheimer 's disease is further investigated, there are more discoveries with how it is caused, what it affects, and how to reduce the risk of developing it. Alzheimer 's disease is a frightening disease that is represented in humans. There are many concerns with this disease that are worth finding out for the future victims
In 1906 he noticed brain tissue in women changing and dying of an usual mental illness
Alzheimer’s disease slowly steals a person’s dignity and erases precious memories. The “Alzheimer’s Disease Guide”, found on WebMD explains that tasks become more difficult to do often leading to confusion and behavior changes. The article further explains the progression of the disease also brings hardship to family and friends (1). To best cope with Alzheimer’s we must better understand the disease.
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
Alzheimer is a degenerative disease that I lived closely with my great grandmother and it was difficult and sad how she kept deteriorating and see the woman that raised me had lost all of her abilities an independant woman, dominant that ran her home was depending on others to meet her basic needs, until the unwanted moment happened where she didn’t recognize me anymore it was awful and knowing that one of the most important persons in my world that I love and that she loved me so much was never going to know who I was anymore. “Family caregivers must be supported in dealing with their guilt at “failing” the person with AD” (Tablosky, 2014, p.631). This disease affects the patient but also the whole family and we have to do all the necessary