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Patient Patients? - Achieving Patient Empowerment through Active Participation, Increased Knowledge and Organisation
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198 b
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There is much debate over what motivates individuals whosuffer from diabetes seeking greater empowerment over theirtreatment and life situation. The Swedish Health Law states thatpatients have the right to full information about their disease andto determine what treatment to receive. This book focuses upon theexperiences of members of two diabetes branch organisationsinvolved in prosecuting the empowerment of their members. Theextent to which patient organisations exert their rights isexplored via extensive surveys and interviews among the membershipof two particularly influential Swedish diabetic organisations. Inlight of all the arguments in favour of empowerment, it isconcluded here that the organisations? members were more interestedin receiving personal information and socialising with each otherthan gaining greater influence and empowerment. This finding maypartly be due to their confident belief in the Swedish health caresystem. Whatever the case, it is evident that patients and theirorganisations still have not yet fully explored the potential forgreater empowerment.
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