What do you do, Sir? In my last blog I wrote about Magnesium, thus: Magnesium deficiency is increasingly recognised as a major health issue and can greatly increase the risk of sudden cardiac death.
This article has been cited by other articles in PMC. Abstract Family caregivers of people with dementia, often called the invisible second patients, are critical to the quality of life of the care recipients. The effects of being a family caregiver, though sometimes positive, are generally negative, with high rates of burden and psychological morbidity as well as social isolation, physical ill-health, and financial hardship.
Caregivers vulnerable to adverse effects can be identified, as can factors which ameliorate or exacerbate burden and strain. Psychosocial interventions have been demonstrated to reduce caregiver burden and depression and delay nursing home admission.
Who are informal caregivers? There are an estimated 30 million people with dementia worldwide currently, 1 and this figure is likely to double every 20 years.
Without caregivers, people with dementia would have a poorer quality of life and would need institutional care more quickly, and national economies would be swept away by the advancing demographic tidal wave.
However, this support comes at a cost of caregiver distress and poorer quality of life. The typical profile of a dementia caregiver is a middle-aged or older female child or spouse of the person with dementia.
One of the main differences between caregiving in the developed and developing world is the living arrangements, whereby persons with dementia in the developing world live in much larger households with extended families. Family caregivers may be motivated to provide care for several reasons: Gender, age, education, and ethnicity can also influence the way caregivers view their role.
Feeling more positively towards caregiving has been associated with lower educational level, greater social resources, satisfaction with social participation and better physical health status, being non-Caucasian, and being older.
Care providers provide hands-on care, dressing, assisting with finances and other daily activities, and care managers arrange for others to provide care, for example a nurse for personal care, an accountant to assist with finances.
Spouses tend to be care providers, and adult children and other relatives, care managers. Care providers tend to be more stressed than care managers.
Many studies have found that caregivers of those with dementia particularly care providers have higher levels of burden than other caregivers.
Over two thirds of caregivers sustained this commitment for more than 1 year and one third for 5 or more years.
They are at increased risk for burden, stress, depression, and a variety of other health complications.
Numerous studies report that caring for a person with dementia is more stressful than caring for a person with a physical disability.Your family and friends may hesitate to spend time with you and the person with Alzheimer's because they worry about not knowing what to do or say.
They also may not understand the behavior changes caused by the disease or might not be able to accept that the person has the disease. The latest news on healthcare advancements and research, as well as personal wellness tips.
Thoughtful and self-reflective, this collection of illuminating essays offers a rare glimpse into the often incomprehensible world of individuals living with Alzheimer's disease.
Information for those either just beginning their caregiving journey or veteran caregivers looking for more tools and resources online. Everything from home safety tips to financial advice are available. Connect with other caregivers from all walks of life to share personal experiences.
All about Lupron Depot (AKA - Leuprolide Acetate): this site explores the misuse, malpractice, withheld information, harmful off-label uses, investigations, litigations, and the many other issues involved with problematic so-called treatment using Lupron. The Effects of Alzheimer’s on Primary Caregivers and Their Families The article “ Family Caregivers of People with Dementia ” by Henry Brodaty, MD, offers professional insight into the effects of Alzheimer’s disease on the family unit.
Brodatyreviews some of the major areas where Alzheimer’s affects family members and states.