The consequences of the caregiver burden, particularly for those in need of Home Care in Puyallup WA, include negative consequences. Healthcare organizations play an important role in improving support structures for caregivers, especially in the Puyallup WA area. Caregiving is an increasingly common experience among middle-aged and older adults in Puyallup WA, affecting all demographics. The need for caregivers in Puyallup WA is expected to increase due to the continued increase in the population of older adults. Many middle-aged and older adults who are not currently caregivers hope to provide care in the future.
People are caregivers for various periods of time, but most people provide care for six months or more, and for many, this amounts to part-time work. These caregivers can bear a significant burden of disabilities and chronic illnesses when caring for others. The burden on family or informal caregivers is due to the multiple physical, psychological, social and financial stressors associated with the provision of care. The burden is particularly high in neurodegenerative diseases, given the progressive disability that occurs.
In a study conducted among caregivers of people with Parkinson's disease, 40% reported that their health had deteriorated due to the provision of care, and 65% reported that their social life had deteriorated. The same survey found that the burden borne by people who care for family members increased with the worsening of disability and symptoms of Parkinson's disease, especially mental health problems, such as depression, hallucinations or confusion, and with falls 74. Another survey found that people who care for their loved ones have a higher level of isolation from their loved ones compared to people who care for amyotrophic lateral sclerosis. This can be explained by the fact that patients with PD are generally older at the time of death, may have outlived many of their family members and peers, have often suffered a prolonged chronic course including dementia, and are more likely to die in nursing homes because no one can care for them in their own homes. 75 Family caregivers of ALS patients may also experience significant distress as the patient's functional state deteriorates and more help is needed, 76 In a In a survey of caregivers of people living with ALS, 64% considered that their own health had worsened and caregivers reported having higher stress levels than people living with ALS, 77. The caregiver burden is used to describe the cumulative emotional, physical, and financial cost experienced by family caregivers. Future research could take into account the duration and phase of the disease trajectory when investigating the burden trajectories of a patient's family caregivers at the end of life.
The same survey revealed that the burden borne by people who care for family members increases with the worsening of disability and symptoms of Parkinson's disease, especially mental health problems, such as depression, hallucinations or confusion, and with falls. The situation of very intensive care, the lack of time to relax, the sense of guilt for moving the person receiving care to a nursing home, or the feeling of guilt for not spending enough time with the person receiving the care are characteristics that have also been observed in caregivers with a higher burden. Caregivers, with an increasing burden, were unable to make the necessary adjustments, often leading to symptoms of exhaustion and sick leave. Financial and work strain The burden of caring tasks is complicated by the financial cost they pose to families. This is in line with the “wear and tear” perspective, which predicts that, over time, the burden on family caregivers will increase due to the cumulative effects of stressors that deplete their mental and physical reserves.
The burden that caregivers bear is defined as the set of global challenges that caregivers face with regard to their physical and emotional well-being, their family relationships, and their work and financial situation (Pearlin et al. In addition, changes in health and well-being sometimes affected the situation in several areas, for example, when caregivers faced an increasing burden and eventually retired from work due to illness. As the population ages and disability worsens, it is critical to understand the physical and mental health burden of caregivers, the variety of tasks caregivers can perform, and the social and economic impacts of chronic diseases or long-term disabilities. This study aimed to describe the trajectories of family caregivers who work and care for patients with a potentially fatal illness, and to identify work and care factors that are related to changes in burden over time.
This is a population of patients and families with high palliative care needs; however, evidence suggests that they rarely receive primary or specialized palliative care until the end of their lives. For some caregivers, the workplace and working conditions increased the burden over time, especially when they did not receive understanding and support, had a negative experience with a supervisor or colleague (table 2, first trimester), or were under pressure at work. Taking care of yourself is something you definitely have control over and can have a significant impact on your care burden. More information is needed about the nature of the burden caregivers bear and the existential and spiritual distress they experience.
this population.
