Aging Research Papers

In the U.S, one in four will be aged 60 years and older by 2050 (U.S. Census Bureau). This represents an overwhelming number of people who will either be in the caretaker role or be the ROC. Like today, most of the care will be provided by informal unpaid caregivers. The number of informal unpaid caregivers is expected to rise from 20 million in 2000 to 37 million in 2050 (Office of the Assistant Secretary for Planning and Evaluation [ASPE], 2003). Because of the burden of care giving, many caregivers will experience depression, poor health and quality of life (Etters, Goodall, & Harrison, 2008). Their well-being is an important public health concern.

Throughout this essay I will share the reasons I have found for there being difficulties and also rewards of being a carer for a family member. ‘A carer is someone of any age who provides unpaid support to care for family or friends who could not manage without this help. This could be caring for a relative, partner or friend who is ill, frail, disabled or has mental health or substance misuse problems.’ (Carers Trust) I will attempt to use my course materials to draw on the experiences of Ann Walker who cares for her elderly step father Angus who has developed Parkinsons’ disease. Firstly I will look at some of the following difficulties that I have identified and due to the limitations of this study I will then briefly discuss the

Our culture likes to ignore that everyone has sex for pleasure in some form or fashion. Created and preached has been a hard-fast narrative that sex only equals intercourse, and intercourse is only reserved for procreation or for the enjoyment of the young and beautiful, which very quickly begins to limit our understanding of the needs of those not using or falling into these realms, young or old. Consider that the young will age, the beauty will fade and procreation not forever possible. Things we cannot control will happen physically, causing our bodies to not be able to operate in ways that we once enjoyed, but that should not make us abstinent against our will. While some natural physical

According to Kim, Chang, Rose, & Kim (2011), care-giver burden has been defined as a multidimensional response to the negative appraisal and perceived stress resulting from the taking care of an ill individual (p. 846). More easily stated a care-giver is a person who assists another individual with one or more of their daily activities of living. A person who finds it necessary to care for a loved one suffering from dementia often finds the task daunting if not polarizing. The role of caregiver often times has a negative effect on the caregiver. These can include feelings of depression, isolation, fear and anger as well as the feelings of constant responsibility and social isolation (Kim et al., 2011).

Caregivers play a crucial role in the care of dementia patients. Providing care for dementia patients results in stress related health impacts to the caregiver. The caregivers go through a journey with the dementia patient and need a strong support system. The best approach to dementia care is for health care providers to provide information to and monitor the caregiver, in addition to the dementia patient, encourage the caregiver to take care of themselves, to seek support, and to work as a team to provide the best care for the dementia patient.

“The term ‘aging out’ refers to children within a state’s foster care system who are still in the system upon reaching the age of majority or when they have graduated from high school” (Craft, 2017, Aging Out). Many of these children “have not found permanency with an adoptive family … or they have not been able to return to their biological parents” (Craft, 2017, Aging Out). A child typically ages out at 18 years, “but some states have extended services beyond this age because so many young adults are just not ready to be thrust out into the world on their own at such a young age” (Craft, 2017, Aging Out). If a foster parent chooses to continue parenting the foster child once they have aged out of the system, they are able to as long as the foster youth is okay with this. If an individual continues fostering a child, they will no longer receive money from the state.

The well-being and safety of your aging loved one is important to you. Since you cannot be with them every day, you want to make sure they are receiving the best care possible. Although, you know that your senior loved one needs assistance at home they might not be as open to the decision. There are things that you can do to communicate your worries and concerns with your aging senior.

Millions of people are in the role of a part or full time caregiver in the U.S to family members who have a serious illness or disability. This a a very challenging and demanding role that needs to be recognized and appreciated.

In the U.S., there is an essential population of informal caregivers that devote a significant amount of time and resources to caring for older adults with impairments. However, due to the informal nature of these caregiver relationships, there is a lack of knowledge and understanding of this population. In “A National Profile of Family and Unpaid Caregivers Who Assist Older Adults with Health Care Activities (2016)”, Wolff and colleagues highlight the importance of understanding the responsibilities of caregivers and how this may affect their own health, as well as the need to identify the basic characteristics of informal caregivers. Therefore, the primary objective of this study by Wolff and colleagues (2016) was to characterize the common responsibilities of caregivers, their utilization of supportive services, as well as to identify the effects of caregiver-related responsibilities on their health. Ultimately, this information may inform future public health services and health care systems to provide much needed support and resources to these caregivers.

I found the most recent state plan on aging at http://www.dea.ri.gov/documents/RIDEA%20State%20Plan%20on%20Aging%20October%201%202015%20to%20September%2030%202019.pdf. The Older Americans Act requires states to submit this plan every four years and it provides updates on legislation and activities were done over the past time period to support older adults, as well as give updates on what will be worked on in the future. It is sent to the State of Rhode Island to ensure policies are up-to-date and will provide the best care for this population. This is necessary in order for taxpayers to see where their money is going and how the RI DEA is planning to care for the older adult population. Otherwise, without this document, the department

There are many articles regarding caregiver depression, stress and burnout. According to Black et al. (2010), the surveys performed in their study show caregivers of people with dementia have increased reports of fatigue, helplessness, stress and onset of depression symptoms. This study sheds light on the financial burden placed upon caregivers; they can spend as much as one thousand dollars a month for prescriptions

Maxine thought this question was quite basic. However, after much thought she stated that aging is simply "advancing in age." Upon further questioning she explained that her definition is a view of the "total process" of aging. She does not define aging in a biological, functional, psychological, sociologic or spiritual domain.

In the world of the senior community, caregivers must have the required skill set to provide residents with the medical treatment they need; however, the attitude of the caregiver must not be overlooked. As senior communities continue struggling due to the high employee turnover associated with this field of care, employers have started taking a unique approach to choosing new caregivers and keeping their current caregivers engaged, and happy.

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.

Many family members care for their senior loved ones who cannot maintain their independence and freedom without support. A recent study found that nearly a quarter of seniors over the age of 65 receive at least 20 hours a week of care. A quarter of those receiving care required over 50 hours a week. While caring for the needs of a loved one is a labor of love and brings with it many benefits, care is also taxing, exhausting, and can impact the health of the provider.