Ann Macfarlane OBE

Ann Macfarlane OBE

Monday 19 January 2015

‘Austerity’ strikes at the heart of Social Care: What contributes to this ‘austerity’ from a service user perspective?

Introduction
Contributing factors to this austerity include negative language, the lack of collective service user voices, placing people who require services in ‘silos,’ meetings by professionals each with their own agendas, power tensions, medical model training, restricted funding and ‘silo’ funding streams and institutional oppression to name but some.  An exploration of these issues reveals a very large ‘elephant’ that virtually defies edification, deconstruction and rebirth. 

Negative language such as ‘burden,’ vulnerable’ and ‘challenging behaviour’ used to describe people who need support enables professional people and groups to keep service users at a distance.  This in turn leads to professional inertia and a lack of support for service users.  This avoids tackling fundamental and basic issues such as spending time and talking with people who are isolated and lonely and doing tasks that are of concern to them.

The lack of service user voices or, as professional people often state, the lack of the ‘right’ service users voices means that they cannot do anything until these individuals and groups are identified and consulted.  Many consultations take place with service users and needs are known but there is seldom a report back to those who participated.   Services that do change or are extended often take months by which time further consultation takes place.  Service users who do participate often become disenchanted as their views are dismissed while the search continues for that elusive service user who will change the face of social care services.  Those service users with the tenacity and expertise to continue are often expected to contribute without acknowledgement of their skills and expertise, the need for expenses, the cost of attendance, lack of briefing or information in appropriate formats to enable them to have equality in a group setting.  The outcome of these experiences enables professional people to continue to think they ‘know best.’

Placing service users in silos, mainly according to impairment or situation, often denies potential service uses and those already receiving support, a person centred, holistic assessment or review.  This can compromise choice and control and the gateway to independent living.  Direct payments continue to be denied for certain groups of people, such as those in the mental health system.  On challenging this lack of information for the potential service user it transpires that social workers find the process and payments system difficult and tend to blame the service user’s inability to manage as the issue. 

Meetings that engage professional people from a number of disciplines is a costly exercise and seldom results in positive outcomes for service users.  Meetings take up vast amounts of time, with time taken to produce agendas, minutes and reports that seldom produce results conducive to improved lives for people who require support.  Meetings are often just a repeat of what has already been discussed with no tangible outcomes.  At a recent seminar that focused on social care at a time of ‘austerity’ the question at the end of the discussion was ‘so what do you think today has achieved?’  The response was a shocked ‘Now that’s an interesting question,’ followed by silence.  

Power tensions within health and social care structures show the difficulties that arise from the ‘silo’ approach in determining what outcomes will be achieved from a service user perspective.  Senior managers involved in managing budgets feel responsible for ensuring it is spent on achieving outcomes that will benefit their service user clientele.  Many needs may not be directly applicable to their budget and so the holder either has to become creative or waste it in trying to find alternative solutions.  Long delays ensue in providing any support as service user’s lives do not fit these silo arrangements.

Medical model training does not generally suit the social care sector and framework and what is offered does not always equip staff with the appropriate social model skills.  Far more service users trained to deliver a social model perspective and programme are required to present on professional courses and at seminars and conferences.  Service users are the experts in this field and yet their expertise and valuable contribution is often overlooked.  

The ‘elephant’ overarching these issues is funding together with an approach and attitude towards service users that is mainly negative, where they are viewed as a burden and incapable.  This leads to a reluctance to communicate, share power and budgets and creates a ‘them and us’ situation with mistrust by service users who realise and understand that nothing will change.

Institutionalised oppression continues to exist and makes it virtually impossible for service users to understand the systems and structures within which professional people work and the barriers that exist to keep service users out.  Professional people themselves often state they do not understand the systems and structures within their culture and so where does that leave the lives of service users.  Trying to break through them causes anxiety, distress, frustration and anger by service users, and often by professional people too.

From a service user perspective to watch and listen to professional people struggle to eat this gigantic ‘elephant’ one bite at a time is asking for an impossible outcome.  It devalues the lives of those who require support and wastes vast amounts of money and time and creates an unhealthy appetite as people spend time chewing.  The cost of the numbers attending meetings in any one week is phenomenal and is seldom evaluated in terms of what has been achieved and what the true costs are in any given period.  Professional people often declare that the lunch break brings welcome respite from this difficult ‘animal.’ Deconstructing this elephant is unpalatable and unlikely ever to occur and is made harder by the inequality of funding that exists with a health budget of £150 billion pounds against a social care budget of £8 billion pounds.   A whole systems approach to health and social care in this time of ‘austerity’ may be the ‘ideal’ but who dares take up the challenge? 






About Ann MacfarlaneOBE

Ann became a trustee at the Social Care Institute for Excellence in 2007. Ann, a wheelchair user, is a leading Disability Rights and Equalities Consultant, focusing on health and social care as it affects disabled adults, irrespective of age. She specialises in Independent Living, Direct Payments and Personal Budgets, and has been involved in the UK disabled peoples' movement for many years. Ann is an 'expert by experience' for the Care Quality Commission, and works with the Department of Health, the NHS and other national Organisations. She is recognised in her community and is a member of the Local Authority's Safeguarding Board, chair of their Users Adults at Risk Group and the local Patient-Wide Forum. She is Patron of Kingston Centre for Independent Living. Ann has lectured worldwide on health and social care. Ann received her MBE in 1992, and an OBE in the Queen’s Birthday Honours in 2009. She was also awarded a Paul Harris Fellowship. Ann has particular responsibilities in her local United Reformed Church and enjoys photography, travel, art and gardens.