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Social & Public Policy of Alzheimer's Disease in the United States (Hardcover, 1st ed. 2019)
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Social & Public Policy of Alzheimer's Disease in the United States (Hardcover, 1st ed. 2019)
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This book focuses on the public policy and political dimensions of
Alzheimer's Disease and other dementias (AD/D) in the United
States, with coverage of the global dimensions and relevant
examples from other countries. Starting off with a discussion on
the characteristics of AD/D and competing theories of their causes,
their human and financial costs, and the increasing burden they
place on all societies as populations age, the book examines in
detail the range of policy issues they raise. These include funding
policies, payment policy and regulatory functions, long-term
services and support (LTCS), public health and prevention policies.
The book analyses the big business surrounding AD/D and shows that
the strong public fear of developing dementia heightens the
likelihood of exploitation of vulnerable people looking for a
technological fix. It examines both informal and formal caregivers
and the heavy burden placed on families, primarily women, and
recent policy attempts to strengthen LTCS. It also examines the
latest evidence of potential risk-reduction and prevention
strategies and the difficult issues surrounding advance directives,
assisted suicide, and definitions of death that increasingly face
policy makers. It concludes by analyzing the policy implications on
possible technological scenarios.
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