The words ‘patient’ and ‘client’ are such words. To be a patient is to have things done to one; to have things prescribed for ; to be passively accepting of what one is told; to be condescended to; to be patronised; to be at the wrong end of an imbalance of power. To be a client has similar but slightly different labels.
The phrase ‘People who use services’ has none of these labels and accompanying expectations. Neither does the term ‘Service User’. Indeed it implies expectations of ‘expertise by experience’ and equal partnership in service planning and development and delivery.
So, in a practical example, a ‘patient’ seeing a medical consultant, for instance, can be (as commonly happens) talked down to, can have whatever they might say about their own condition phoo phood by the consultant and can have requests turned down by the consultant. The ‘service user’, on the other hand will go into the consultant meeting with full expectations of making an equal contribution to the assessment and problem solving and will take an assertive part in the process, not allowing any consultant arrogance or condescension.
Well, it is happening. The last few years has seen a positively growing development of concerted voices and I have listed three of the bodies who are becoming increasingly succesful at making the service use voice heard. The following links will take you to their external websites:
I've included the last link (no pun intended) because the statutory installation of LINks is patently the best opportunity for service user and carer involvement there has ever been. As I wrote recently on mesomoco:
Real service user and carer involvement and influence is now making a tangible difference and in the latter part of 2008, facilities have begun to mushroom around the concept of the user as an equal expert in her/his own right in heath and social care.Tokenism still exists: take for example the several websites set up by the "NHS Centre for Involvement" run entirely by civil servants, resistant to any suggestion of real service user and carer involvement and operating on vacuous government rhetoric.
On the other hand the National Association of LINks Members (NALM), a body set up by those previously involved in Patient and Public Involvement Forums, independent of political influence and sceptical of the way Government had run PPI via the QUANGO Commission for Patient and Public Involvement in Health (CPPIH), is doing great things. Interesting that many of the civil servants who inhabited CPPIH are now working at the NHS Centre for Involvement (NCI). NALM said in its recent newsletter it is in regular discussion with the CeO of NCI but they are unable to get any co-operation. In contrast, NALM has very positive discussions and partnership arrangements with the independent www.patientopinion.org.uk (very well worth looking up) and www.nationalvoices.org.uk - the new umbrella of organisations representing service user involvement - used to be the Long Term Conditions Alliance). The latter also has a membership list page (organisations only - no individual membership) which is very useful as a reference tool.
So, you lot. Get out and join your LINks - you can make a vast difference to service delivery, deficiences in service, inadequate practice and malpractice - IN THE NHS AND IN SOCIAL SERVICES.
The concerted national voice we have been battling for over forty years is here. USE IT!!!!!!!!!!!!