Abstract: The burden experienced by cancer informal caregivers is enormous. However, little is known about the burden experienced by informal caregivers of cancer patients in Nigeria. Thus the study determined the level of burden among cancer informal caregivers at the Department of Radiotherapy, University College Hospital, Ibadan, Nigeria. It also compared caregivers’ characteristics against the level of burden of care and investigated caregivers’ feelings of impairment to their health on account of giving care. A questionnaire consisted of socio-demographic/other variables and the Zarit Burden Interview was administered on 135 consecutive caregivers. Almost half (36.3%) of the caregivers had high level of burden. Relationship to …show more content…
Owing to the chronic nature of cancer, its debilitating features and the fact that there is some improvement in the treatment, the role of family of informal caregivers in the management is on the increase. For example in the United States health care system, caregivers support therapy like multimodality treatment protocols that are administered in outpatient and home settings (Schumacher, Stewart, Archbold et al., 2008). Caregivers provide support that cut across responding to the physical and psychological needs of the cancer sufferers (Honea, Brintnall, Given et al., 2008). Their roles in the management of cancer patients is totally …show more content…
Eighty six point six percent of caregivers who were above 60 years reported feeling of impaired health sometimes to nearly always while 16.7% of those 20-40 years reported feeling of impairment of health sometimes to nearly always. It is worthy of note that 80% of those who were 18-25 years never had feeling of impaired health on account of caregiving. Those who are above 60 years may be less energetic and may suffer from some illnesses that may come with age. These may add to the burden they experience while being a caregivers of a cancer patient. Older cancer caregivers have been reported to experience the highest level of burden (Given, Wyatt, Given et al.,
The time of life we call dying is an extremely difficult part of the life cycle, but a normal part," says palliative-care physician Ira Byock, author of Dying Well. "The nature of it isn't medical, it's experiential. " My grandfather had stage 4 lung cancer with metastatic to liver . Only palliative care advised by doctors. He was an strong personality .He loved all his grand kids too much.
On 6/29/15, Ms. Wendy Sanders and Mr. Charles Ray Hamilton visited the DHR office. Ms. Sanders is interested in becoming Mr. Hamilton 's rep. payee and caregiver. According to Ms. Sanders, she needs somewhere to live because she recently moved to the Carbon Hill area after getting out of an abusive relationship. She has been cleaning Mr. Hamilton 's home getting it ready for her son who is 13 years old. Worker explained to Ms. Sanders how his grandchildren have caused problems in the past for people who have tried to help Mr. Hamilton.
The services provided by Hospice are emotional support, medical services and spiritual resources for people who are in their last stage of a serious illness. Family members are not forgotten as services are provided to them for managing practical details and emotional challenges of caring for someone who is dying. The loved one that comes to Hospice is usually within the life expectancy of 6 months. BBH uses a team approach to provide professional services to provide individualized care to the client. The health care team includes attending physician, the registered nurse, hospice aides, social workers, the hospice chaplain, music therapist, trained volunteers and
They areinvolved in providing palliative care,into a system of medical care that emphasizes palliation and psychosocial support of patients diagnosed with a life-limiting illness, through professional nursing or other therapeutic services, such as physical therapy, home health aides, nurse assistants, medical social work, nutritionist services, or personal care
This study found that caregivers experience uncertainty in similar ways to patients who have life altering
In this assignment, I am going to be focusing on a teenager who has a terminally ill parent and how they would cope within the situation and what key issues you need to focus on in order to make the transition/change a success. The age group I am focusing on would be 16 – 18year old's. This is going to be a very difficult time in the teenager’s life so it is important that the correct support and planning is put in place to help make this experience easier. There are many key issues that you need to focus on when it comes to a young adult dealing with a close bereavement such as a parent, however there are going to be two key issues that I am going to be focusing on and that will be planning and the overall effect it has on the young person. I think this is important because " every year around 0.3% of all families with children under the age of 18years encounter parental cancer, and 3.1% of minors and 8.4% of young adults have a parent that has been diagnosed with cancer" (ncbi.gov, 2012)
This is more than just the financial resources that they have, but also their psychological and physical health and their spiritual outlook on life and the situation. One important factor is the caregiver's location and place of residence in relation to that of the person to be cared for. It must also be remembered that the carer has a life outside of this role and, therefore, important factors in caring include other day-to-day roles such as being an employee, a parent and a professional person. The carer is also affected by the opinions and demands of people outside the caregiving relationship. Caregivers are also facing a health care system that seems to be placing more responsibilities on caregivers while providing less and less
Hospice and palliative care can be easily intertwined; they are both concerned with promoting comfort and relieving patient pain. Hospice and palliative care, however, are different in some aspects. Patients who receive hospice care are nearing the end of their lives and there is no effort to cure their disease; the goal is to provide pain relief, a sense of belonging from family and friends if desired, support through the dying stages, and to assure that the person is able to die with dignity. Palliative care is also focused on reducing discomfort; however, the patient receiving care can be at any stage in their disease. Additionally, palliative care can also be administered during a time when a patient is receiving treatment to cure their illness.
Care givers: caring for a family member or friend with a physical or mental illness can be stressful, exhausting, both mentally and physically, and creates a physical and psychological strain for the care giver over a period of time. The psychological well-being such as depression and stress, are frequent consequences of caregiving. The age, socioeconomic status, and the availability of informal support that caregivers have access to greatly affect their own health and well being. Caring for a family member with a mental illness can differ from caring for someone suffering from a physical illness. In addition to the medical care and long term treatment of a family member, an open and liberal view of mental illness is almost an essential in being able to care for someone who is ill.
In all my experiences as a nurse, I’ve realized the importance of communication, providing holistic care to an individual and empowering them with the knowledge to manage their health. When an illness strikes a person, it affects not just his body, but also his mind and spirit. The art of communication is invaluable to patient interaction and establishing a therapeutic nurse-patient relationship, that facilitate coping mechanisms for patients, moreover it prepared myself as a nurse to meet their individual needs. Furthermore, there is at the moment an insurmountable demand for survivorship care as a result of the advancement in technology and medicine, which made living beyond life expectancy possible for increasingly more people. Living after cancer treatment is not free of complications as there are acute and chronic side effects of treatment that requires constant monitoring and attention, and this information spurred me to shift my focus from palliative to survivorship care.
SDLA 4: Activity 1 Palliative care continues to evolve in providing better end-of-life care and so does nursing care. Thus, nursing practice is enhanced to satisfy the demand of the palliative care. A nurse provides complex care and fulfils the needs of the patients. Nursing involves in caring work, which focus on patient experiencing agony in palliative and haematological cancer care. Nurses worked in a taxing environment, that can be highly stressful, and often they experience physical, psychological and spiritual exhaustion.
“Your grandma has cancer,” These four words were very difficult to swallow at a young age. Dealing with death so young can be very confusing and difficult to cope with. Not only is losing a family member tragic, but losing a family member who you cared so much about can really take a toll on your life. I know it took a toll on me when I lost my grandmother. It still does till this day.
According to a Child Protective Investigation, there are approximately half a million children in the U.S. foster care system, otherwise known as congregate care (group homes and institutions). Children are placed in congregate care when they are found to be in an unsafe environment. Usually children of abuse or maltreatment are placed first (Font, 2015). Out-of-home-care causes increased problems of attachment, behavioral, and psychological disorders in the developing child. Child safety is the primary goal of out-of-home-care; however, maltreatment investigations are still reported in those institutions.
Kaakinen et al. (2015) states that approaching family as a client is centered on each individual family members well-being that create the sum of a family. An example of this approach is well demonstrated by my family’s primary care provider (PCP). My mother, father, sister, and I all routinely see the same primary care provider. Near the end of 2014 my mother was diagnosed with breast cancer, and in early 2015 my father was diagnosed with colon cancer.
Caregivers Who are caregivers? Caregivers are either paid or unpaid individuals who work at hospitals, clinics, age-old homes, and patients ' residence to provide personal care. They perform all sorts of menial job like feeding, bathing, walking, dressing, exercising, laundry, grocery shopping, and transporting home to medial setting and vice versa besides caring. The basic aim of caregiver profession is to care for elderly and all-aged patients, and help them live a normal and healthy life.