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Mental health policy and practice across Europe: an overview

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The user <strong><strong>an</strong>d</strong> survivor movement 337<br />

of empowerment <strong><strong>an</strong>d</strong> being valued, <strong><strong>an</strong>d</strong> a better underst<strong><strong>an</strong>d</strong>ing <strong><strong>an</strong>d</strong> relationship<br />

with other researchers (Allam et al. 2004).<br />

User involvement c<strong>an</strong> take place at the <strong>Europe</strong><strong>an</strong> level as well as in individual<br />

countries. The m<strong><strong>an</strong>d</strong>ate that the <strong>Europe</strong><strong>an</strong> Union (EU) has to intervene to promote<br />

social inclusion, eliminate discrimination, protect hum<strong>an</strong> rights <strong><strong>an</strong>d</strong><br />

promote good <strong>health</strong> <strong><strong>an</strong>d</strong> well-being (see Chapter 13) provides opportunities for<br />

active user involvement at a p<strong>an</strong>-<strong>Europe</strong><strong>an</strong> level. Unfortunately, user involvement<br />

at this level today exists mostly in the virtual realm due to a lack of<br />

funding, <strong><strong>an</strong>d</strong> more generally, user involvement <strong>across</strong> <strong>Europe</strong> is very unevenly<br />

developed. This is partly due to differing social, economic <strong><strong>an</strong>d</strong> political conditions<br />

in the various regions, <strong><strong>an</strong>d</strong> differs from the disability movement which<br />

seems to be more well accepted <strong><strong>an</strong>d</strong> active at <strong>an</strong> EU level (e.g. the <strong>Europe</strong><strong>an</strong><br />

Disability Forum).<br />

Another factor influencing the level <strong><strong>an</strong>d</strong> nature of user involvement is the<br />

way in which mental <strong>health</strong> services are provided. On the one h<strong><strong>an</strong>d</strong>, the tr<strong>an</strong>sition<br />

to community care appears to facilitate the rise of user groups. On the<br />

other, harsh involuntary treatment legislation <strong><strong>an</strong>d</strong> <strong>practice</strong> appears to give rise<br />

to sympathetic professionals, including lawyers, forming non-user initiated<br />

groups to ch<strong>an</strong>ge these <strong>practice</strong>s. One exception to this pattern is the Netherl<strong><strong>an</strong>d</strong>s<br />

where there is a strong (albeit divided) user movement, even though mental<br />

<strong>health</strong> provision remains largely hospital-based.<br />

These structural differences in the way groups are formed present challenges<br />

when seeking to map user groups <strong>across</strong> <strong>Europe</strong>. Those familiar with the situation<br />

in the United Kingdom will know that a ‘user group’ is usually defined as a<br />

group whose members are users only <strong><strong>an</strong>d</strong>/or where the major decisions are<br />

taken by service users. This is not necessarily the case in all <strong>Europe</strong><strong>an</strong> countries.<br />

Groups may involve families (indeed they may be primarily groups of family<br />

members), sympathetic professionals <strong><strong>an</strong>d</strong> interested members of the general<br />

public. In the email survey for this chapter (see below) we included a question<br />

on whether or not groups were user-controlled, where this was defined as users<br />

controlling decision-making in <strong>an</strong> org<strong>an</strong>ization. Few groups outside the United<br />

Kingdom <strong>an</strong>swered this question, which may indicate that this concept is not<br />

known to them.<br />

Another challenge is that in most western <strong>Europe</strong><strong>an</strong> countries (but not all),<br />

groups are org<strong>an</strong>ized at both the national, regional <strong><strong>an</strong>d</strong> local levels. Such structures<br />

are well developed, for inst<strong>an</strong>ce in Sweden, Denmark, Fr<strong>an</strong>ce <strong><strong>an</strong>d</strong> Austria<br />

among others, where local <strong><strong>an</strong>d</strong> regional groups are often affiliated to national<br />

org<strong>an</strong>izations. The links in other countries are less clear. In m<strong>an</strong>y countries<br />

there also may be diagnosis-specific groups which again may be linked to<br />

national umbrella org<strong>an</strong>izations. In Fr<strong>an</strong>ce, for example, some diagnosis-specific<br />

groups are linked to the national French network of user org<strong>an</strong>izations – FNAP<br />

PSY (Fédération Nationale des Associations de Patients et [ex] Patients ‘PSY’).<br />

In the countries of eastern <strong><strong>an</strong>d</strong> central <strong>Europe</strong> there are no user groups with a<br />

national brief currently, although there are developments in both Lithu<strong>an</strong>ia<br />

<strong><strong>an</strong>d</strong> Georgia.<br />

A final challenge in mapping the <strong>Europe</strong><strong>an</strong> scene is the sustainability <strong><strong>an</strong>d</strong><br />

turnover of user groups. It is well known that user groups emerge <strong><strong>an</strong>d</strong> close<br />

down with some rapidity (Wallcraft et al. 2003). Even quite large org<strong>an</strong>izations,

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