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Mental health policy and practice across Europe: an overview

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chapter<br />

fourteen<br />

The user <strong><strong>an</strong>d</strong> survivor<br />

movement in <strong>Europe</strong><br />

Di<strong>an</strong>a Rose <strong><strong>an</strong>d</strong> Jo Lucas<br />

Introduction<br />

This chapter explores the role of user involvement in mental <strong>health</strong> <strong>policy</strong> <strong><strong>an</strong>d</strong><br />

<strong>practice</strong> both at a <strong>Europe</strong><strong>an</strong> level <strong><strong>an</strong>d</strong> <strong>across</strong> selected countries. The issues we<br />

seek to elucidate are: the history of the user movement; its activities (i.e. what<br />

groups do); <strong><strong>an</strong>d</strong> whether or not these groups are user-controlled. We then briefly<br />

comment on the role users c<strong>an</strong> play in research <strong><strong>an</strong>d</strong> what influence they have, if<br />

<strong>an</strong>y, on <strong>policy</strong>.<br />

User involvement in mental <strong>health</strong> is one of the most exciting <strong><strong>an</strong>d</strong> innovative<br />

developments in the field of psychiatry. It empowers individual service users<br />

<strong><strong>an</strong>d</strong> enables them to org<strong>an</strong>ize collectively. Historically, users of mental <strong>health</strong><br />

services did not have such a voice but this has been ch<strong>an</strong>ging with involvement<br />

growing in a number of countries in recent years (Wallcraft et al. 2003; Rush<br />

2004; Campbell 2005; Chamberlin 2005).<br />

Clearly, moving towards greater user involvement is not without tensions<br />

with other stakeholders. When a disempowered group finds its voice <strong><strong>an</strong>d</strong> formulates<br />

a position from which to develop ch<strong>an</strong>ge, there will always be obstacles.<br />

While never underestimating the newly-found power of users, this chapter will<br />

also describe some of the hurdles that are still to be overcome.<br />

In addition to the strong ethical <strong><strong>an</strong>d</strong> democratic imperatives for user involvement<br />

in the pl<strong>an</strong>ning <strong><strong>an</strong>d</strong> delivery of activities, there is also <strong>an</strong> increasing, albeit<br />

still limited, body of evidence supporting the vital contribution that service<br />

users c<strong>an</strong> make to mental <strong>health</strong> research. Indeed, service users may be better<br />

placed th<strong>an</strong> professionals to assess how services address their needs (Thornicroft<br />

<strong><strong>an</strong>d</strong> T<strong>an</strong>sella 2005). It also has been shown, for example, that users report less<br />

satisfaction with services when interviewed by other service users (Simpson <strong><strong>an</strong>d</strong><br />

House 2002). User involvement in research c<strong>an</strong> also have benefits for the individuals<br />

involved, including the acquisition of new skills <strong><strong>an</strong>d</strong> knowledge, a sense

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