Advocacy in Health Care by Kevin Teasdale

By Kevin Teasdale

Advocacy in future health Care offers a research-based framework for advocacy that may be used as a advisor to daily medical perform. It discusses tips on how to communicate out on behalf of sufferers and consumers in addition to tips to empower them to talk out for themselves. the most subject matters are illustrated with case-study examples from normal hospitals and group settings, in addition to from the fields of studying disabilities and psychological health and wellbeing. This ebook will attract scholars, certified pros and self sustaining advocates operating with sufferers and consumers in the health-care process, together with nurses, medical professionals, social staff and people in professions allied to medication.

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Sample text

The pattern of risk in Graham Pink's case follows that described by Hunt & Shailer (1995). He at first believed that the problem was one of communication and once the management had seen conditions for themselves they would surely act. He soon discovered resistance to the substance of his complaints and was then placed in a disturbing ethical dilemma over loyalty to his patients and his profession against loyalty to his employers. By going public to a national newspaper, he placed his own job at risk.

If the specialists themselves believe this, then there is no reason to explain things to patients, other than to calm their nerves through bland reassurances. Pressures of time and workload have increased enormously within the health service, so the second part of the GP's statement adds to the pressure to conform by suggesting that asking for lengthy explanations will take up an unreasonable amount of the valuable time of the specialists, which could instead to be given to others in even greater need.

In the UK it is more frequently termed independent advocacy. Gates (1994) describes an early example arising from a conference on cerebral palsy in 1966 when a number of ageing parents expressed worries about the continuing welfare of their children after their deaths. It was suggested that a citizen advocacy service should be established to represent the children in their future dealings with health care organisations and other services. A condition of becoming citizen advocates was that individuals should be unpaid and unconnected with the care services provided for the children.

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