Explore new frontiers in Alzheimer's support systems! When Congress authorized the Alzheimer's Disease Demonstration Grants to States program in 1990, no one knew how effective the program would prove to be. A New Look at Community-Based Respite Programs provides you with results of the first major evaluation of ADDGS programs. Across the country, groups were able to develop specialized programs that reached traditionally underserved clients. A byproduct of many of the ADDGS programs was that they helped strengthen ties between communities and agencies, improving social services for both caregivers and people with Alzheimer's. A New Look at Community-Based Respite Programs examines: the profile of the average respite care user different challenges faced by urban and rural clientele how culture and ethnicity influence health care decisions ways to involve communities in respite care how understanding patterns of use makes for better program design and implementation A New Look at Community-Based Respite Programs provides you with detailed analyses of a variety of successful support service plans, including mobile day care, Latino-specific outreach, traveling dementia evaluation teams, and programs designed for people who live alone. You'll also read about the importance of complementing family caregivers instead of substituting for them. Throughout, helpful tables make the results of ADDGS programs clear. It is estimated that Alzheimer's will affect up to 14 million Americans by the year 2050. A New Look at Community-Based Respite Programs contains vital knowledge that you can act on now to help lay the foundations for a better future.
Explore new frontiers in Alzheimer's support systems! When Congress authorized the Alzheimer's Disease Demonstration Grants to States program in 1990, no one knew how effective the program would prove to be. A New Look at Community-Based Respite Programs provides you with results of the first major evaluation of ADDGS programs. Across the country, groups were able to develop specialized programs that reached traditionally underserved clients. A byproduct of many of the ADDGS programs was that they helped strengthen ties between communities and agencies, improving social services for both caregivers and people with Alzheimer's. A New Look at Community-Based Respite Programs examines: the profile of the average respite care user different challenges faced by urban and rural clientele how culture and ethnicity influence health care decisions ways to involve communities in respite care how understanding patterns of use makes for better program design and implementation A New Look at Community-Based Respite Programs provides you with detailed analyses of a variety of successful support service plans, including mobile day care, Latino-specific outreach, traveling dementia evaluation teams, and programs designed for people who live alone. You'll also read about the importance of complementing family caregivers instead of substituting for them. Throughout, helpful tables make the results of ADDGS programs clear. It is estimated that Alzheimer's will affect up to 14 million Americans by the year 2050. A New Look at Community-Based Respite Programs contains vital knowledge that you can act on now to help lay the foundations for a better future.
Most scholars do not consider the long-term nature of caregiving, but rather focus on a specific developmental period (e.g., old age) or a specific disability (e.g., cancer). Yet the most important lessons about caregiving may occur at any age, regardless of disabilities or other limitations. Caregiving is a lifelong process. It begins in a mother’s womb, continues throughout the lifespan, and ends after death. Caregiving Across the Lifespan emphasizes caregiving as a process that occurs throughout one’s life. It discusses infant care, the developmental needs of children and adolescents, the many caregiving issues in adulthood and mid-life, and finally end-of-life care and bereavement. Key coverage includes: Examining caregiving issues across a developmental perspective. Caregiving from infancy through early childhood through end of life. Mid-life and multigenerational bonds and responsibilities. Caregiver identity in older adults. Family caregiving at the end of life. This must-have volume offers a wealth of insights and ideas for researchers, practitioners, and graduate students across the caregiving fields, including psychology, social work, public health, geriatrics and gerontology, and medicine as well as public and education policy makers.
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