petek, 8. december 2017

Basic features and principles of deinstitutionalisation process




 [This we wrote for the Macedonian report. Hope it is useful!]

Stages in transformation of an institution
 

10 crucial steps of transformation process


In order to perform deinstitutionalisation in a most effective and smooth way possible the European guidelines suggest the following 10 steps (CEG):

  • Making the case for developing community-based alternatives to institutions
  • Assessment of the situation
  • Developing a strategy and an action plan
  • Establishing the legal framework for community-based services
  • Developing a range of services in the community
  • Allocating financial, material and human resources
  • Developing individual plans
  • Supporting individuals and communities during transition
  • Defining, monitoring and evaluating the quality of services
  • Developing the workforce

On a micro level of an institution or a region, six main tasks need to be achieved. Firstly, already inside the institution, the relationships between users and staff have to democratise and the status of residents improved. That means implementing new ways of democratic decision making on wards, opening the institution for the community and taking users to the community. The transformation or substitution of an institution needs to be planed therefore a vision of deinstitutionalisation needs to be created. The process of creating a vision also needs to be a dialogical process and everyone living and working in the institution should go true a process of its appropriation.
 
Resettlements of users are the next and important step when the place of work for the staff changes as well. Usually the first resettlement are to intermediate structures and foster care for children but latter on independent living should be developed as well. While resettling residents of institutions a whole range of other services (housing, employment, personal assistance, education, etc.) for ex- residents but also for other people that need long term care in the community.  

During the whole process quality, on-site practical training needs to be provided to staff and users. Deinstitutionalisation is a process connected to the whole society therefore it has to be connected to and integrated in the community since the first day.

Principles of deinstitutionalisation


Guiding principles of deinstitutionalisation process are, inter alia:

A.    Inclusion into the community
B.    Fostering enabling approaches in working with people
C.    Independent community living
D.    Ordinary environments and Social Role Revaluation
E.     Participatory action and dialogue with all the stakeholder, empowerment of users and relatives.
F.      Investment in staff and secured employment
G.    Users participation, choice and control
H.    Personalisation of care
I.       No restraint and coercion
J.       No skimming

Inclusion and community are the two most important concepts guiding DI activities. We need to stick to their real and original meaning – that the deinstitutionalisation process must provide means for the people, hitherto excluded, re-join their communities, be accepted, regain the status of full citizenship and step into new, and valued social roles. The goal of not just planning the shift to the care in the community, but envisaging the real community care, i.e. the care by the community thus strengthening the community itself, the processes of solidarity and ideal of conviviality – living together, must be pursued.

To achieve this, it is absolutely necessary to move from the personal deficiency based ways of looking at people with disabilities to enabling approaches. The starting point of any action that would strive for inclusion must be the strength perspective; i.e. valuing the existence of people now residing in the institutions, seeing them as able and making it possible, even in the adverse circumstances, to exercise their faculties, above all the basic one of free will. At this point standardised institutional or community responses need to be replaced by personalised care defined and tailored to each person individually.

Independent community living is thus not a solitary experience, even less the independence must be measured by the personal and social capital or normalised able body or able mind. Conversely, enabling approach must mobilise the environment, the community and the carers to enable people with disabilities to exercise their will, to empower them to make choices, friends and meaningful action.

However, this must not be seen as something special, even less as something separating or segregating people with disabilities (and especially future ex-residents) from the rest of us. Ordinary living must be a benchmark of success of deinstitutionalisation, a criterion upon which the society will measure the outcomes of the process. It must provide people who will resettle from the institutions with possibilities to enter into really valued social roles, exit not only the institution, but also their stigmatised, devalued (invalid) roles.

Goals, outlined above, cannot be achieved without the action that creates dialogue between all the stakeholders, without creating common understanding and common goal. What may seem utopian can be achieved if we truly make the participation of the people most concerned possible. Thus, ways of empowerment of the residents and their near ones must be part and parcel of the process of deinstitutionalisation.

Deinstitutionalisation is an investment in people, not walls. However, it is not only an investment in residents of institutions or people with disabilities; it is an investment in the people working for them. Therefore, the staff of institutions and future community services need to get quality training, but most importantly, they need to be rewarded fairly and to have secured employment. Nobody must lose their employment; they just need to learn to work in different situations and with different methods.

Users’ participation is needed at all stages of deinstitutionalisation. They do not need to have choice and control over their own care, but they need to be the main actors of the planning, implementing and monitoring the reform on the national level.

Community living and service cannot reproduce any of the institutional culture therefore all measures of restrain, coercion and formal or informal punishment have to be abolished immediately. Deinstitutionalisation should provide means of positive discrimination especially for people with the most complex needs. Therefore, there should be no skimming; users with most complex needs should be leaving institution first.

Therefore, a quality deinstitutionalisation agenda must embrace the principles of real inclusion, enabling, independent community living, ordinary environments and Social Role Revaluation, participatory action and dialogue, empowerment, investment in staff and secured employment, users participation, choice and control, personalisation, no restraint and coercion and no skimming. It has to have a steering body on the national level and many organisational and methodical changes in the practice. The organisational changes need to involve all stakeholders and most importantly users and enable democratic joint decision-making. Retraining is needed not only for the staff working in institutions but also for other professionals that will be working with people returning from institutions. The knowledge and technology of deinstitutionalisation needs to be created in the transforming institutions and communities not in offices detached from the people.

Claimer: This blog is intended as a part of Situation Analysis and Assessment/ Evaluation Report of Implementation of National Strategy on Deinstitutionalisation 2008-2018 which will be soon presented to the public within the EU framework project Technical assistance support for the deinstitutionalization process in social sector. For this blog Andreja Rafaelič is considered to be co-author.

Sources:
European Expert Group on the Transition from Institutional to Community-based Care (2012) Common European Guidelines on the Transition from Institutional to Community-based Care (Guidance on implementing and supporting a sustained transition from institutional care to family-based and community-based alternatives for children, persons with disabilities, persons with mental health problems and older persons in Europe), Brussels. [On line] Available at: deinstitutionalisationguide.eu/wp-content/uploads/2012/12/2012-12-07-Guidelines-11-123-2012-FINAL-WEB-VERSION.pdf

Flaker, V., Krstovski, V. (2017) Inception Report - Technical assistance support for the deinstitutionalisation process in social sector (EuropeAid/132633/C/SER/MULTI) European Union project; Skopje: A.E.S.A. Consortium & Alternative Consulting.

četrtek, 7. december 2017

Roadmap for Deinstitutionalisation – Common European Guidelines




“Though governments increasingly recognise the inevitability of deinstitutionalisation, there is less clarity with regard to the mechanisms that replace institutionalisation and what would constitute a human rights-based response.” [1]  This led to the development of The Common European Guidelines on the Transition from Institutional to Community-based Care[2] at commonly referred to as the “Common European Guidelines” brought together European and international best practices to “provide practical advice about how to make a sustained transition from institutional care to family-based and community-based alternatives.”

Common European guidelines are the only European document that is explicitly devoted only to deinstitutionalisation. The guidelines are a form of recommendations for member states and pre-accession states on how to implement the transition to community services. At the same time, they are a practical toolkit for stakeholders and practitioners on how to plan the process and how to implement it on an everyday level.

As the guidelines state deinstitutionalisation should base on a deep respect for human rights of people with disabilities, minimisation of risk and effectiveness for all stakeholders and actors of the process. Together with the institutional closure quality community services should be established. A good vision, community involvement, decision makers’ involvement and good leadership are key features of deinstitutionalisation. 

The document sets guidelines on how to create a good strategy and action plan based on dialogue and practical data, which legislation should be changed to enable community care, how to develop a range of community services, how to develop the workforce and steer the founding from institutions towards community, how to develop person centred care, how to plan institutional transformation and how to steer, monitor and evaluate the process.

Together with the Toolkit on the Use of European Union Funds for the Transition from Institutional to Community Based Care, they enable states to carry out deinstitutionalisation effectively and consistently without unnecessary investments in institutions.

Since the UNCRPD, a paradigm shift is occurring away from a medical model of care, towards a social rights model where individuals are supported to become active citizens making a contribution to their own communities. This has been accompanied by a wider understanding of the adaptations which society must make in order to ensure that the rights of people with disabilities are vindicated.[3]

A re-shaping of how services are provided is needed and the development of new services not currently available to meet new and changing needs and/or the integration in the services of a person centred, inclusive, participative and individualised approach, adopting the new social rights model of disability. One of the areas requiring improvements and/or changes is the way provision of long term and/or intense care is provided to persons with disabilities.

Common European Guidelines see it as an imperative that in managing the transition process people with significant disabilities and complex needs are not left behind. As this only generates additional needs. Promoting a person-centred approach will inevitably require innovative solutions, providing greater choice and control throughout life.

Regarding community based services; the guidelines refer to the spectrum of services that enable individuals to live in the community and, in the case of children, to grow up in a family environment as opposed to an institution. This encompasses the use of mainstream services, such as housing, healthcare, education, employment, culture and leisure, which should be accessible to everyone –regardless of the nature of their impairment or the required level of support. It also refers to specialised services, such as personal assistance for persons with disabilities, respite care and others. In addition, the term ‘community based services’ includes family-based and family-like care for children, including substitute family care and preventative measures for early intervention and family support.

Claimer: This blog is intended as a part of Situation Analysis and Assessment/ Evaluation Report of Implementation of National Strategy on Deinstitutionalisation 2008-2018 which will be soon presented to the public within the EU framework project Technical assistance support for the deinstitutionalization process in social sector. For this blog Andreja Rafaelič is considered to be co-author.



[1] COE Human Rights Commissioner, 2012.
[2] www.deinstittutionalisationguide.eu  The Common European Guidelines on the Transition from Institutional to Community-based Care, published in November 2012
[3] EASPD MAKING COMMUNITY-BASED SERVICES A REALITY - Roadmap on deinstitutionalisation

sreda, 6. december 2017

Special care to protect children against institutionalisation (UNCRC)




The UN Convention on the Rights of the Child (UNCRC) emphasises the need for special protection and care for children who are vulnerable and at risk. Both the declaration and convention of children rights recognize the rights to all children regardless of their disability or health condition. The roles of the family in caring for children and the state in providing support are highlighted.

Children living in institutions has been contrary to the Declaration of children’s rights already since 1959 since it states that ‘children have the right to live in healthy environment’. Already in 1951 Bowlby has proven that even a few days of institutional life for children is damaging for the development of their brain and has negative effects on a child’s well-being and behaviour. Therefore, institutions cannot be defined as healthy environment for children.

The UNCRC in the opening articles (article 2) declares children with disabilities as having equal rights as others and they should not be discriminated against.

Article 7 sets the right to know and be cared for by their parents which usually is not the case for children growing up in institutions. It is really hard for a child to get to know their parents when they live separately and see each other a few times a year or every few years as it usually happens to children living in institutions.

Children have the right to live with his or her parents (article 9) unless this is deemed incompatible with his or her best interests. Even when separated from them they have the right to maintain contact with both parents. Institutions do not explicitly forbid or prevent contacts with parents, but they also do not act upon enabling children to exercise their right to keep in contact with their parents.

The article 18 states that parents have joint primary responsibility for raising the child and the State shall support them in this. This is in particular the case for parents of children with disabilities where the main support that parents get is institutional care. In order to enable the parents to take responsibilities to raise their children with disabilities at home adequate support service should be provided. 

Children should be protected from all forms of physical or mental violence, injury or abuse, neglect or negligent treatment, maltreatment or exploitation, including sexual abuse (article 19).  Especially in institutions physical abuse and neglect can be observed as a routine. Children tied to cot beds, left alone in one room without any care and left to bang their heads until bleeding is typical for institutional abuse and neglect. 

Article 20 recognizes the right of children without family life for support and care especially in foster care and adoption and in special cases care in suitable institutions. Large institutions cannot be interpreted as suitable institutions as they breach many other rights from the convention. Suitable institutions are group homes (where max. 4 children live together) that provide children with a life as similar as possible to family life.

Article 23 is particularly aimed at children with disabilities. They have the right to live in dignity, self-respect and environments that enable their participation and inclusion in society. This right can be exercised only if suitable services in community are established and institutionalisation prevented.

The right to education (28. And 29. Article) is totally denied to children with disabilities in institutions. Instead of having a family life and being included in mainstream school system, they are placed in the social care system with very few education possibilities.

Article 37 most explicitly forbids the depriving children of their liberty unless in extreme cases and even that should be performed for an as short time as possible. This should be interpreted very narrowly; which means that it should be understood that the shortest possible time should be counted in hours and not in days or years. The same article states that every child deprived of their liberty should not be institutionalised together with adults but should have special services for themselves.

Family reintegration is the return of a child on a permanent basis to the family of origin who has been provisionally separated by an alternative family care placement or more usually a stay in residential care.  Where it is safe family reintegration constitutes the most desirable permanent solution for a child who has been in care. It should be sought as a priority, even if the family of origin does not seem “ideal” or their customs and ways of life are different from those of the majority of the population.

United Nations (1990) UN Convention on the Rights of the Child. Available at: http://www.unhcr.org/uk/4d9474b49.pdf

Claimer: This blog is intended as a part of Situation Analysis and Assessment/ Evaluation Report of Implementation of National Strategy on Deinstitutionalisation 2008-2018 which will be soon presented to the public within the EU framework project Technical assistance support for the deinstitutionalization process in social sector. For this blog Andreja Rafaelič is considered to be co-author. Acknowledgment to Andrew Dunn (UNICEF expert) for useful contribution.