Normalization (people with disabilities)

Last updated

"The normalization principle means making available to all people with disabilities patterns of life and conditions of everyday living which are as close as possible to the regular circumstances and ways of life or society." [1] Normalization is a rigorous theory of human services that can be applied to disability services. [2] Normalization theory arose in the early 1970s, towards the end of the institutionalisation period in the US; it is one of the strongest and long lasting integration theories for people with severe disabilities.

Contents

Definition

Normalization involves the acceptance of some people with disabilities, with their disabilities, offering them the same conditions as are offered to other citizens. It involves an awareness of the normal rhythm of life – including the normal rhythm of a day, a week, a year, and the life-cycle itself (e.g., celebration of holidays; workday and weekends). It involves the normal conditions of life – housing, schooling, employment, exercise, recreation and freedom of choice previously denied to individuals with severe, profound, or significant disabilities. [3]

Wolfensberger's definition is based on a concept of cultural normativeness: "Utilization of a means which are as culturally normative as possible, in order to establish and/or maintain personal behaviors and characteristics that are as culturally normative as possible." Thus, for example, "medical procedures" such as shock treatment or restraints, are not just punitive, but also not "culturally normative" in society. His principle is based upon social and physical integration, which later became popularized, implemented and studied in services as community integration encompassing areas from work to recreation and living arrangement. [4]

Theoretical foundations

This theory includes "the dignity of risk", rather than an emphasis on "protection" [5] and is based upon the concept of integration in community life. The theory is one of the first to examine comprehensively both the individual and the service systems, similar to theories of human ecology which were competitive in the same period.

The theory undergirds the deinstitutionalization and community integration movements, and forms the legal basis for affirming rights to education, work, community living, medical care and citizenship. In addition, self-determination theory could not develop without this conceptual academic base to build upon and critique. [6]

The theory of social role valorization is closely related to the principle of normalization [7] having been developed with normalization as a foundation. [8] This theory retains most aspects of normalization concentrating on socially valued roles and means, in socially valued contexts to achieve integration and other core quality of life values.[ citation needed ]

History

The principle of normalization was developed in Scandinavia during the sixties and articulated by Bengt Nirje of the Swedish Association for Retarded Children with the US human service system a product of Wolf Wolfensberger formulation of normalization and evaluations of the early 1970s. [9] [10] According to the history taught in the 1970s, although the "exact origins are not clear", the names Bank-Mikkelson (who moved the principle to Danish law), Grunewald, and Nirje from Scandinavia (later Ministry of Community and Social Services in Toronto, Canada) are associated with early work on this principle. Wolfensberger is credited with authoring the first textbook as a "well-known scholar, leader, and scientist" and Rutherford H. (Rud) Turnbull III reports that integration principles are incorporated in US laws.

Academe

The principle was developed and taught at the university level and in field education during the seventies, especially by Wolf Wolfensberger of the United States, one of the first clinical psychologists in the field of mental retardation, through the support of Canada and the National Institute on Mental Retardation (NIMR) and Syracuse University in New York State. [11] PASS and PASSING marked the quantification of service evaluations based on normalization, and in 1991 a report was issued on the quality of institutional and community programs in the US and Canada based on a sample of 213 programs in the US, Canada and the United Kingdom. [12]

Significance in structuring service systems

Normalization has had a significant effect on the way services for people with disabilities have been structured throughout the UK, Europe, especially Scandinavia, North America, Israel, Australasia (e.g., New Zealand) and increasingly, other parts of the world. It has led to a new conceptualisation of disability as not simply being a medical issue (the medical model which saw the person as indistinguishable from the disorder, though Wolfensberger continued to use the term into the 2000s, [13] but as a social situation as described in social role valorization.

Government reports began from the 1970s to reflect this changing view of disability (Wolfensberger uses the term devalued people), e.g. the NSW Anti-Discrimination Board report of 1981 made recommendations on "the rights of people with intellectual handicaps to receive appropriate services, to assert their rights to independent living so far as this is possible, and to pursue the principle of normalization." The New York State Quality of Care Commission also recommended education based upon principles of normalization and social role valorization addressing "deep-seated negative beliefs of and about people with disabilities". [14] Wolfensberger's work was part of a major systems reform in the US and Europe of how individuals with disabilities would be served, resulting in the growth in community services in support of homes, families and community living. [15] [16]

Critical ideology of human services

Normalization is often described in articles and education texts that reflect deinstitutionalization, family care or community living as the ideology of human services. [17] [18] Its roots are European-American, and as discussed in education fields in the 1990s, reflect a traditional gender relationship-position (Racino, 2000), among similar diversity critiques of the period (i.e., multiculturalism). [19] Normalization has undergone extensive reviews and critiques, thus increasing its stature through the decades often equating it with school mainstreaming, life success and normalization, and deinstitutionalization. [20] [21] [22] [23]

In contemporary society

In the United States, large public institutions housing adults with developmental disabilities began to be phased out as a primary means of delivering services in the early 1970s and the statistics have been documented until the present day (2015) by David Braddock and his colleagues. [24] As early as the late 1960s, the normalization principle was described to change the pattern of residential services, as exposes occurred in the US and reform initiatives began in Europe. These proposed changes were described in the leading text by the President's Committee on Mental Retardation (PCMR) titled: "Changing Patterns in Residential Services for the Mentally Retarded" with leaders Burton Blatt, Wolf Wolfensberger, Bengt Nirje, Bank-Mikkelson, Jack Tizard, Seymour Sarason, Gunnar Dybwad, Karl Gruenwald, Robert Kugel, and lesser known colleagues Earl Butterfield, Robert E. Cooke, David Norris, H. Michael Klaber, and Lloyd Dunn. [25]

Deinstitutionalization and community development

The impetus for this mass deinstitutionalization was typically complaints of systematic abuse of the patients by staff and others responsible for the care and treatment of this traditionally vulnerable population with media and political exposes and hearings. [26] These complaints, accompanied by judicial oversight and legislative reform, resulted in major changes in the education of personnel and the development of principles for conversion models from institutions to communities, known later as the community paradigms. [27] [28] In many states the recent process of deinstitutionalization has taken 10–15 years due to a lack of community supports in place to assist individuals in achieving the greatest degree of independence and community integration as possible. Yet, many early recommendations from 1969 still hold such as financial aid to keep children at home, establishment of foster care services, leisure and recreation, and opportunities for adults to leave home and attain employment (Bank-Mikkelsen, p. 234-236, in Kugel & Wolfensberger, 1969). [29]

Community supports and community integration

A significant obstacle in developing community supports has been ignorance and resistance on the part of "typically developed" community members who have been taught by contemporary culture that "those people" are somehow fundamentally different and flawed and it is in everyone's best interest if they are removed from society (this developing out of 19th Century ideas about health, morality, and contagion). Part of the normalization process has been returning people to the community and supporting them in attaining as "normal" as life as possible, but another part has been broadening the category of "normal" (sometimes taught as "regular" in community integration, or below as "typical") to include all human beings. In part, the word "normal" continues to be used in contrast to "abnormal", a term also for differentness or out of the norm or accepted routine (e.g., middle class). [30] [31]

Contemporary services and workforces

In 2015, public views and attitudes continue to be critical both because personnel are sought from the broader society for fields such as mental health [32] and contemporary community services continue to include models such as the international "emblem of the group home" for individuals with significant disabilities moving to the community. [33] Today, the US direct support workforce, associated with the University of Minnesota, School of Education, Institute on Community Integration [34] can trace its roots to a normalization base which reflected their own education and training at the next generation levels.

People with disabilities are not to be viewed as sick, ill, abnormal, subhuman, or unformed, but as people who require significant supports in certain (but not all) areas of their life from daily routines in the home to participation in local community life. [35] With this comes an understanding that all people require supports at certain times or in certain areas of their life, but that most people acquire these supports informally or through socially acceptable avenues. The key issue of support typically comes down to productivity and self-sufficiency, two values that are central to society's definition of self-worth. If we as a society were able to broaden this concept of self-worth perhaps fewer people would be labeled as "disabled."

Contemporary Views on Disability

During the mid to late 20th century, people with disabilities were met with fear, stigma, and pity. Their opportunities for a full productive life were minimal at best and often emphasis was placed more on personal characterizes that could be enhanced so the attention was taken from their disability [36] Linkowski developed the Acceptance of Disability Scale (ADS) during this time to help measure a person's struggle to accept disability. [36] He developed the ADS to reflect the value change process associated with the acceptance of loss theory. [36] In contrast to later trends, the current trend shows great improvement in the quality of life for those with disabilities. [36] Sociopolitical definitions of disability, the independent living movement, improved media and social messages, observation and consideration of situational and environmental barriers, passage of the Americans with Disabilities Act of 1990 have all come together to help a person with disability define their acceptance of what living with a disability means. [36]

Bogdan and Taylor's (1993) [36] acceptance of sociology, which states that a person need not be defined by personal characterizes alone, has become influential in helping persons with disabilities to refuse to accept exclusion from mainstream society. [36] According to some disability scholars, disabilities are created by oppressive relations with society, this has been called the social creationist view of disability. [37] In this view, it is important to grasp the difference between physical impairment and disability. In the article The Mountain written by Eli Clare, Michael Oliver defines impairment as lacking part of or all of a limb, or having a defective limb, organism or mechanism of the body and the societal construct of disability; Oliver defines disability as the disadvantage or restriction of activity caused by a contemporary social organization which takes no or little account of people who have physical (and/or cognitive/developmental/mental) impairments and thus excludes them from the mainstream of society. [38] In society, language helps to construct reality, for instance, societies way of defining disability which implies that a disabled person lacks a certain ability, or possibility, that could contribute to her personal well-being and enable her to be a contributing member of society versus abilities and possibilities that are considered to be good and useful . [37] Society needs to destruct the language that is used and build a new one that does not place those with disabilities in the "other" category. [36]

Personal wounds, quality of life and social role valorization

However, the perspective of Wolfensberger, who served as associated faculty with the Rehabiltation Research and Training Center on Community Integration (despite concerns of federal funds), is that people he has known in institutions have "suffered deep wounds". This view, reflected in his early overheads of PASS ratings, is similar to other literature that has reflected the need for hope in situations where aspirations and expectations for quality of life had previously been very low (e.g., brain injury, independent living). Normalization advocates were among the first to develop models of residential services, and to support contemporary practices in recognizing families and supporting employment. [39] Wolfensberger himself found the new term social role valorization [40] to better convey his theories (and his German Professorial temperament, family life and beliefs) than the constant "misunderstandings" of the term normalization!

Related theories on integration in the subsequent decades have been termed community integration, self-determination or empowerment theory, support and empowerment paradigms, community building, functional-competency, family support, often not independent living (supportive living),and in 2015, the principle of inclusion which also has roots in service fields in the 1980s.

Misconceptions

Normalization is so common in the fields of disability, especially intellectual and developmental disabilities, that articles will critique normalization without ever referencing one of three international leaders: Wolfensberger, Nirje, and Bank Mikkelson or any of the women educators (e.g., Wolfensberger's Susan Thomas; Syracuse University colleagues Taylor, Biklen or Bogdan; established women academics (e.g., Sari Biklen); or emerging women academics, Traustadottir, Shoultz or Racino in national research and education centers (e.g., Hillyer, 1993). [41] In particular, this may be because Racino (with Taylor) leads an international field on community integration (See, Wikipedia), a neighboring related concept to the principle of normalization, and was pleased to have Dr. Wolf Wolfensberger among Center Associates. Thus it is important to discuss common misconceptions about the principle of normalization and its implications among the provider-academic sectors:

Wolfensberger himself, in 1980, suggested "Normalizing measures can be offered in some circumstances, and imposed in others." [42] This view is not accepted by most people in the field, including Nirje. Advocates emphasize that the environment, not the person, is what is normalized, or as known for decades a person-environment interaction.

Normalization is very complex theoretically, and Wolf Wolfensberger's educators explain his positions such as the conservatism corollary, deviancy unmaking, the developmental model (see below) and social competency, and relevance of social imagery, among others. [43]

Normalization has been blamed for the closure of services (such as institutions) leading to a lack of support for children and adults with disabilities. Indeed, normalization personnel are often affiliated with human rights groups. Normalization is not deinstitutionalization, though institutions have been found to not "pass" in service evaluations and to be the subject of exposes. Normalization was described early as alternative special education by leaders of the deinstitutionalization movement. [44]

However support services which facilitate normal life opportunities for people with disabilities – such as special education services, housing support, employment support and advocacy – are not incompatible with normalization, although some particular services (such as special schools) may actually detract from rather than enhance normal living bearing in mind the concept of normal 'rhythms' of life.[ citation needed ]

Some misconceptions and confusions about normalization are removed by understanding a context for this principle. There has been a general belief that 'special' people are best served if society keeps them apart, puts them together with 'their own kind, and keep them occupied. The principle of normalization is intended to refute this idea, rather than to deal with subtlety around the question of 'what is normal?' The principle of normalization is congruent in many of its features with "community integration" and has been described by educators as supporting early mainstreaming in community life. [45]

Arguments about choice and individuality, in connection with normalization, should also take into account whether society, perhaps through paid support staff, has encouraged them into certain behaviours. For example, in referring to normalization, a discussion about an adult's choice to carry a doll with them must be influenced by a recognition that they have previously been encouraged in childish behaviours, and that society currently expects them to behave childishly. Most people who find normalization to be a useful principle would hope to find a middle way - in this case, an adult's interest in dolls being valued, but with them being actively encouraged to express it in an age-appropriate way (e.g., viewing museums and doll collections), with awareness of gender in toy selection (e.g., see cars and motorsports), and discouraged from behaving childishly and thus accorded the rights and routines only of a "perpetual child". However, the principle of normalization is intended also to refer to the means by which a person is supported, so that (in this example) any encouragement or discouragement offered in a patronising or directive manner is itself seen to be inappropriate.[ citation needed ]

Normalization principles were designed to be measured and ranked on all aspects through the development of measures related to homes, facilities, programs, location (i.e. community development), service activities, and life routines, among others. These service evaluations have been used for training community services personnel, both in institutions and in the community. [46] [47] [48] [49]

Normalization as the basis for education of community personnel in Great Britain is reflected in a 1990s reader, highlighting Wolf Wolfensberger's moral concerns as a Christian, right activist, side-by-side ("How to Function with Personal Model Coherency in a Dysfunctional (Human Service) World") with the common form of normalization training for evaluations of programs. [50] Community educators and leaders in Great Britain and the US of different political persuasions include John O'Brien and Connie Lyle O'Brien, Paul Williams and Alan Tyne, Guy Caruso and Joe Osborn, Jim Mansell and Linda Ward, among many others. [51]

Related Research Articles

Supportive housing is a combination of housing and services intended as a cost-effective way to help people live more stable, productive lives, and is an active "community services and funding" stream across the United States. It was developed by different professional academics and US governmental departments that supported housing. Supportive housing is widely believed to work well for those who face the most complex challenges—individuals and families confronted with homelessness and who also have very low incomes and/or serious, persistent issues that may include substance use disorders, mental health, HIV/AIDS, chronic illness, diverse disabilities or other serious challenges to stable housing.

Developmental disability is a diverse group of chronic conditions, comprising mental or physical impairments that arise before adulthood. Developmental disabilities cause individuals living with them many difficulties in certain areas of life, especially in "language, mobility, learning, self-help, and independent living". Developmental disabilities can be detected early on and persist throughout an individual's lifespan. Developmental disability that affects all areas of a child's development is sometimes referred to as global developmental delay.

<span class="mw-page-title-main">Long-term care</span> Services for the elderly or those with chronic illness or disability

Long-term care (LTC) is a variety of services which help meet both the medical and non-medical needs of people with a chronic illness or disability who cannot care for themselves for long periods. Long-term care is focused on individualized and coordinated services that promote independence, maximize patients' quality of life, and meet patients' needs over a period of time.

Social role valorization (SRV) is a method for improving the lives of people who are of low status in society. 

Person-centred planning (PCP) is a set of approaches designed to assist an individual to plan their life and supports. It is most often used for life planning with people with learning and developmental disabilities, though recently it has been advocated as a method of planning personalised support with many other sections of society who find themselves disempowered by traditional methods of service delivery, including children, people with physical disabilities, people with mental health issues and older people. PCP is accepted as evidence based practice in many countries throughout the world.

Self-advocacy is the act of speaking up for oneself and one's interests. It is used as a name for civil rights movements and mutual aid networks for people with intellectual and developmental disabilities. The term arose in the broader civil rights movements of the 1960s and 1970s, and is part of the disability rights movement. Today there are self-advocacy organizations across the world.

<span class="mw-page-title-main">Deinstitutionalisation</span> Replacement of psychiatric hospitals

Deinstitutionalisation is the process of replacing long-stay psychiatric hospitals with less isolated community mental health services for those diagnosed with a mental disorder or developmental disability. In the late 20th century, it led to the closure of many psychiatric hospitals, as patients were increasingly cared for at home, in halfway houses and clinics, in regular hospitals, or not at all.

Supported living or supportive living refers to a range of services and community living arrangements (CLAs) designed with individuals with disabilities and their families to support disabled citizens to attain or retain their independence or interdependence in their local communities. Supported living is recorded in the history of the NASDDDS, celebrating its 50th Anniversary. Community Supported Living Arrangements (CSLA) was a landmark federal multi-state demonstration to illustrate the federal role in community living in the US. Supported living is considered a core service or program of community living programs funded through federal-state-local partnerships.

Wolf Peregrin Joachim Wolfensberger, Ph.D. (1934–2011) was a German-American academic who influenced disability policy and practice through his development of North American Normalization and social role valorization (SRV). SRV extended the work of his colleague Bengt Nirje in Europe on the normalization of people with disabilities. He later extended his approach in a radical anti-deathmaking direction: he spoke about the Nazi death camps and their targeting of disabled people, and contemporary practices which contribute to deathmaking.

A group home, congregate living facility, care home, adult family home, etc., is a structured and supervised residence model that provides assisted living and medical care for those with complex health needs. Traditionally, the model has been used for children or young people who cannot live with their families or afford their own homes, people with chronic disabilities who may be adults or seniors, or people with dementia and related aged illnesses. Typically, there are no more than six residents, and there is at least one trained caregiver there 24 hours a day. In some early "model programs", a house manager, night manager, weekend activity coordinator, and four part-time skill teachers were reported. Originally, the term group home referred to homes of 8 to 16 individuals, which was a state-mandated size during deinstitutionalization. Residential nursing facilities, also included in this article, may be as large as 100 individuals in 2015, which is no longer the case in fields such as intellectual and developmental disabilities. Depending on the severity of the condition requiring one to need to live in a group home, some clients are able to attend day programs and most clients are able to live normal lifestyles.

Psychiatric rehabilitation, also known as psych social rehabilitation, and sometimes simplified to psych rehab by providers, is the process of restoration of community functioning and well-being of an individual diagnosed in mental health or emotional disorder and who may be considered to have a psychiatric disability.

Citizen Advocacy organisations seek to cause benefit by reconnecting people who have become isolated from the ordinary community. Their practice was defined in two key documents: CAPE in 1980 and Learning From Citizen Advocacy Programs in 1987. The theoretical foundation of Citizen Advocacy is found in Citizen Advocacy and protective services for the impaired and handicapped. A central idea on which this practice is based is that the devaluation of a person or group by society has profoundly negative effects on their lives.

Supported employment refers to service provisions wherein people with disabilities, including intellectual disabilities, mental health, and traumatic brain injury, among others, are assisted with obtaining and maintaining employment. Supported employment is considered to be one form of employment in which wages are expected, together with benefits from an employer in a competitive workplace, though some versions refer to disability agency paid employment. Companies such as Skilcraft in the United States are an example of "supported employment" which is defined in law for state and federal reimbursements.

<span class="mw-page-title-main">Intellectual disability</span> Generalized neurodevelopmental disorder

Intellectual disability (ID), also known as general learning disability in the United Kingdom and formerly mental retardation, is a generalized neurodevelopmental disorder characterized by significantly impaired intellectual and adaptive functioning. It is defined by an IQ under 70, in addition to deficits in two or more adaptive behaviors that affect everyday, general living. Intellectual functions are defined under DSM-V as reasoning, problem‑solving, planning, abstract thinking, judgment, academic learning, and learning from instruction and experience, and practical understanding confirmed by both clinical assessment and standardized tests. Adaptive behavior is defined in terms of conceptual, social, and practical skills involving tasks performed by people in their everyday lives.

The Family Movement, also known in the past as the Parent Movement, is an arm of the disability rights movement, a larger social movement. The Family Movement advocates for the economic and social rights of family members with a disability. Key elements include: social inclusion; active participation; a life of meaning; safety; economic security; accessibility and self-determination. The family movement has been critical in closing institutions and other segregated facilities; promoting inclusive education; reforming adult guardianship to the current supported decisionmaking; increasing access to health care; developing real jobs; fighting stereotypes and reducing discrimination.

Community integration, while diversely defined, is a term encompassing the full participation of all people in community life. It has specifically referred to the integration of people with disabilities into US society from the local to the national level, and for decades was a defining agenda in countries such as Great Britain. Throughout recent decades, community integration programs have been increasingly effective in improving healthcare access for people with disabilities. They have been valued for providing a "voice for the voiceless"

Family support is the support of families with a member with a disability, which may include a child, an adult, or even the parent in the family. In the United States, family support includes "unpaid" or "informal" support by neighbors, families, and friends, "paid services" through specialist agencies providing an array of services termed "family support services", school or parent services for special needs such as respite care, specialized child care or peer companions, or cash subsidies, tax deductions or other financial subsidies. Family support has been extended to different population groups in the US and worldwide. Family support services are currently a "community services and funding" stream in New York and the US which has had variable "application" based on disability groups, administrating agencies, and even, regulatory and legislative intent.

Gunnar Dybwad (1909–2001) was an American professor and advocate for the rights of people with disabilities, particularly developmental disabilities. He is best known for his support for the social model of disability, reframing disability accommodations as a matter of civil rights, not medical treatment. The American Association on Intellectual and Developmental Disabilities gives out the Dybwad Humanitarian Award annually in his honor.

As of 2017, approximately 1.4 million Americans live in a nursing home, two-thirds of whom rely on Medicaid to pay for their care. Residential nursing facilities receive Medicaid federal funding and approvals through a state health department. These facilities may be overseen by various types of state agency.

The Connecticut Department of Developmental Services (DDS) is a state agency of Connecticut providing services to individuals with developmental disabilities and their families. Its headquarters are in Hartford. According to its official Twitter description, "CT DDS serves more than 20,000 individuals [with] intellectual disability and their families, including 4,000 infants and toddlers in the Birth to Three System."

References

  1. The basis and logic of the normalisatioprinciple, Bengt Nirje, Sixth International Congress of IASSMD, Toronto, 1982
  2. Wolfensberger, W. & Glenn, L. (1973). "Program Analysis of Service Systems (PASS): A Method for the Quantitative Evaluation of Human Services". Vol. 1. Handbook. Volume II. Field Manual. Downsview, Toronto, Canada: National Institute on Mental Retardation.
  3. Nirje, Bengt as cited in S. Cohen & C. Gothelf. (1988). A Preservice Trining Curriculum for Administrators for Community-Based Residential Programs Service People with Developmental Disabilities. NY, NY: City University of New York, Hunter College.
  4. Orientation Manual on Mental Retardation, Pt. 1. Downsview, Ontario: National Institute on Mental Retardation, Kinsmen NIMR Building, pp. 41-50.
  5. Misconceptions on the principle of normalisation, Bank-Mikkelsen, Address to IASSMD Conference, Washington, D.C., 1976.
  6. Allard, M., Howard, A., Vorderer, L. & Wells, A. (1999). "Ahead of His Time: Selected Speeches of Gunnar Dybwad." Washington, DC: American Association on Mental Retardation.
  7. Nirje, B. (1985). The basis and logic of the normalization principle. Australian and New Zealand Journal of Developmental Disabilities, 11(2): 65-68.
  8. Wolfensberger, W. (1983). Social role valorization: A proposed new term for the principle of normalization. Mental Retardation, 21, 234-9.
  9. The normalisation principle and its human management implications, in R. Kugel & W. Wolfensberger (Eds.) Changing Patterns in Residential Services for the Mentally Retarded, Washington, D.C: President's Committee on Mental Retardation, 1969.
  10. Wolfensberger, W. (1972). The Principle of Normalization in Human Services. Toronto, Canada: National Institute on Mental Retardation.
  11. Wolfensberger, W. (1972). The Principle of Normalization in Human Services Toronto, Canada: National Institute on Mental Retardation.
  12. Flynn, R. J., LaPointe, N., Wolfensberger, W. & Thomas, S. (1991, July 19). Quality of Institutional and Community Human Service Programs in Canada and the United States. ""Journal of Psychiatry and Neurosciences"", 16(3): 146-153.
  13. Wolfensberger, W. & Associates. (2001). "The 19th Century "Moral Treatment" Approach to Human Services, Especially to the Treatment of Mental Disorder, and Lessons for Services for Our Own Day". Syracuse, NY: Training Institute for Human Services Planning, Leadership and Change Agentry.
  14. Cashen, J. (1989, Nov-Dec). The need for value-enhancement training and informal support systems. Quality of Care, Issue 42: 1-3.
  15. Flynn, R.J. & Nitsch, K.E. (1980). Normalization, Social Integration and Community Services. (pp. 117-129). Baltimore, MD; Paul H. Brookes.
  16. Taylor, S. Bogdan, R. & Racino, J. (1991). Life in the Community: Case Studies of Organizations Supporting People with Disabilities. Baltimore, MD: Paul H. Brookes.
  17. Landesman, S. & Butterfield, E. (1987, August). Normalization and deinstitutionalization of mentally retarded individuals: Controversy and facts. "American Psychologist", 42: 809-816.
  18. Bruininks, R.H. & Lakin, K.C. (1985). Living and Learning in the Least Restrictive Environment". Baltimore, MD: Paul H. Brookes
  19. Racino, J. (2000). "Personnel Preparation in Disability: Toward Universal Approaches to Support". Binghamton, NY: Charles C. Thomas Publishers.
  20. Zipperlin, H. (1975). Normalization. In: J. Wortis (Ed.), "Mental Retardation and Developmental Disabilities, VII". NY, NY: Brumer Mazel Publishers.
  21. Chappell, A. (1992). Towards a sociological critique of normalisation principle. "Disability, Handicap and Society", 7(1): 35-51.
  22. Lippman, L. (1977). "Normalization" and related concepts: Words and ambiguities. Child Welfare, 56(5): 301-310.
  23. Phillips, M.J. (1992). "Try Harder": The experience of disability and dilemmas of normalization. aina; ap. Ferguson, D. Ferguson, & S. Taylor (Eds), Interpreting Disability: A Qualitative Reader. NY & London: Teachers College, Columbia University.
  24. Braddock, D., Hemp, R., Fujiura, G., Bachelder, L., & Mitchell, D. (1990). "The State of the States in Developmental Disabilities". Baltimore, MD: Paul H. Brookes.
  25. Kugel, R.H. & Wolfensberger, W. (1969). Changing Patterns in Residential Services for the Mentally Retarded." Washington, DC: President's Committee on Mental Retardation"
  26. Blatt, B. & Kaplan, F. (1974). "Christmas in Purgatory: A Photographic Essay on Mental Retardation". Syracuse, NY: Human Policy Press.
  27. Racino, J. (1999). Policy, Program Evaluation and Research in Disability: Community Support For All". London: Haworth Press.
  28. Blatt, B., Bogdan, R., Biklen, D. & Taylor, S. (1977). From institution to community - A conversion model - Educational programming for the severely/profoundly handicapped. In: E. Sontag, J. Smith, & N. Certo (Eds)., "Educational Programming for the Severely and Profoundly Handicapped" (pp. 40-52). Reston, VA: Council for Exceptional Children.
  29. Bank-Mikkelsen, N. (1969). Ch. 10: A metropolitan area in Denmark, Copenhagen. In: R.B. Kugel & W. Wolfensberger, Changing Patterns of Residential Services for the Mentally Retarded (now Intellectual and Developmental Disabilities, 2015). Washington, DC: President's Committee on Mental Retardation.
  30. Traustadottir, R. (1995). A mother's work is never done: Constructing a "normal" family life. In: S. Taylor, R. Bogdan & Z.M. Lutfiyya, The Variety of Community Experiences: Qualitative Studies of Family and Community Life. Baltimore, MD: Paul H. Brookes.
  31. Racino, J. & Rogan, P. (1990). RCE/SPE 636: Community Services and Systems Change: Syllabi. Syracuse, NY: Syracuse University, Division of Special Education and Rehabilitation, School of Education.
  32. Anthony, W., Cohen, M., Farkas, M. & Gagne, C. (2002). "Psychiatric Rehabilitation". Boston, MA: Boston University, Center for Psychiatric Rehabilitation.
  33. Johnson, K. & Traustadottir, R. (2005). "Deinstitutionalization and People with Intellectual Disabilities". London: Jessica Kingsley Publishers.
  34. Larson, S., Sedlezky, L., & Hewitt, A. & Blakeway, C. (2012/14). US direct support workforce. In: J. Racino, Public Administration and Disability: Community Services Administration in the US. NY, NY: CRC Press, Francis and Taylor.
  35. Walker, P. & Rogan, P. (2007). "Making the Day Matter: Promoting Typical Lifestyles for Adults with Disabilities". Baltimore, MD: Paul H. Brookes.
  36. 1 2 3 4 5 6 7 8 Groomes & Linkowski, D. A. G., & D. C. (2007). "Examining the structure of the revised acceptance disability scale". Journal of Rehabilitation. 73: 3–9. ProQuest   236273029.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  37. 1 2 Vehmas, Simo (2004). "Dimensions of Disability". Cambridge Quarterly of Healthcare Ethics. 13 (1): 34–40. doi:10.1017/S0963180104131071. PMID   15045913. S2CID   13467079.
  38. Eli Clare: The Mountain
  39. Wolfensberger, W., Thomas, S., & Caruso, G. (1996). Because of the universal "good things in life" which the implementation of social role valorization can be expected to make more accessible to devalued people. "International Social Role Valorization Journal", 2: 12-14.
  40. Wolfensberger, W. (1985). Social role valorization: A new insight, and a new term, for normalization. Australian Association for the Mentally Retarded Journal, 9(1): 4-11.
  41. Hillyer, B. (1993). Feminism and Disability. Norman, OK: University of Oklahoma.
  42. The definition of normalisation: update, problems, disagreements and misunderstandings, Wolfensberger, W. (1980) In R.J. Flynn & K.E. Nitsch (Eds). Normalization, social integration and human services. Baltimore: University Park Press
  43. Wolfensberger, W. & Tullman, S. (1982). A brief outline of the principle of normalization. "Rehabilitation Psychology", 27(3): 131-145.
  44. Wolfensberger, W. (1977). The principle of normalization. In: B. Blatt, D. Biklen, & R. Bogdan, "An Alternative Textbook in Special Education: People, Schools and Other Institutions". Denver, CO: Love Publishing Co.
  45. Yates, J. (1979). The Principle of Normalization, Guidelines for Tours, and Guidelines for Administrative Inquiries". Syracuse, NY: Training Institute on Human Services Planning and Change Agentry.
  46. Wolfensberger, W. & Glenn, L. (1975). ""PASS 3: A Method for Quantitative Evaluation of the Human Services Field. Toronto, Canada: National Institute on Mental Retardation"".
  47. Wolfensberger, W. & Thomas, S. (1983). ""PASSING: Program Analysis of Service Systems Implementation of Normalization Goals"". Toronto, Canada: National Institute on Mental Retardation.
  48. Flynn, R.J. & Heal, L.W. (1981). A short form of PASS 3: A study of its structure, interrater reliability, and validity for assessing normalization. ""Evaluation Review"", 5(3): 357-376.
  49. Demaine, G.C., Silverstein, A.B. & Mayeda, T. (1980, June). Validation of PASS 3: A first step in service evaluation through environmental assessments. Mental Retardation, 18: 131-134.
  50. Lindley, P. & Wainwright, T. (1992). Normalisation training: Conversion or commitment? In: H. Brown & H. Smith (Eds), "Normalisation: A Reader for the Nineties". London: Tavistock/Routledge.
  51. Williams, P. & Tyne, A. (1988). Exploring values as the base for service development. In: D. Towell (Ed.), "An Ordinary Life in Practice: Developing Comprehensive Community-Based Services for People with Learning Disabilities". (pp. 23–31). London: King Edward's Hospital Fund.

Further reading

Presentations

Syllabi: course readings

Assessment reports

Historical references