Family support

Last updated

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.

Contents

History

The late 1970s and early 1980s are considered pivotal times for the development of respite and family support services, particularly through the demands and initiatives of parents of children with disabilities. [1] [2] [3] [4] These initiatives occurred throughout the US concurrent with the formation of activist parent groups in the 1970s, in the state of New Hampshire, [5] [6] for example. Foster care, which involved "substitute care" from birth families, preceded this organization of parents nationally, and together, with group homes, was considered the primary form of community residential services in the US. [7] [8] [9] [10] However, by the 1990s, family support had become an established service reported regularly in the field of intellectual and developmental disabilities, and part of the States' and local service systems in the US. [6] [11] [12] Family support services were considered one of the better ways of supporting families and their children, including "building on natural supports" and encouraging the integration of children in the community. [13] [14] [15] [16]

Family models and services

By the early 1980s, states such as New York had established family support programs and agencies, New York State Office of Mental Retardation and Developmental Disabilities, and "model programs" [17] [18] were identified nationally which served children and their families in the community (e.g., MacComb-Oakland, Michigan, Dane, LaCrosse, and Columbia counties, Wisconsin). [14] New models of family support services were initiated, including professional models which involved both traditional respites for the families (i.e., the opportunity for a break from the stress of caring for children with "special needs") and individual recreation opportunities in generic agencies/sites for the son or daughter (versus traditional in-home babysitting child care). [19] Professional parents sought to have respite places available in group homes (e.g., a friend of the home), to develop small group respite settings, to hold parent-to-parent support groups and meetings, to establish councils, and to have cash subsidies to meet the extra expenses of raising a "disabled child" (e.g., Exceptional Family Resources, Syracuse, New York, 1985). By 1983, the State of New York had funded three major demonstration grants [20] and then Governor Mario Cuomo and his wife Matilda held the first Family Support Conference in Albany, New York. [21] New York State indeed by 1988 reported $16,536,000 in discrete family support initiatives [22] which did not include new agency family/cash subsidy demonstrations funded later in 1989–1990 in the state. [23] or agency cash subsidies included as part of family support demonstration programs (e.g., recreation/respite in generic agencies). [24] In the public policy arena, the respite was often explored in the context of child care for children with disabilities, [25] [26] and additional expenses of raising a child with a disability as especially critical in low income-families. [27] [28]

Promotion on behalf of families

In 1985, Syracuse University's Center on Human Policy was awarded a three-year Community Integration Project from the Federal Government (National Institute on Disability Research and Rehabilitation) to work with states and communities in the US. The project, based on a national search conducted by the Wisconsin Developmental Disabilities Council , identified state cash subsidy programs in 21 states in the US. [29] The project, together with a new national Center on Community Integration, prepared information on family support for distribution, including a news bulletin on family support based on the project's research studies, [30] an article on the case for family support for families, [31] bibliographic references, [32] [33] [34] [35] [36] innovative agencies and organizations, [3] and an introduction to family support issues, such as family-centered supports, individualized and flexible supports, empowering families, use of natural, community supports, and permanency planning. [37]

Family counseling

The purpose of family counseling

There are some great goals and things that can happen through family counseling or therapy, you can grow your family relationships, enhance communication in the family, talk through problems that create tension in the family, and more.  [38] There are many reasons why a family might start seeking help as well, you could be having trouble communicating and connecting with a child, a new adjustment to the family, or divorce.  [38] There are many reasons for families to go to counseling. Some of these reasons include coping with a family member that might be suffering from mental health issues, addiction, and the emotions that come with such changes. [39]

What happens during a session

For the first session, there is the consultation, in which the therapist, psychologist, or clinical social worker, will ask about why you are seeking help, get to know you, what you want out of these sessions, and let you ask any question they might have for them. [40]   For other sessions though, you will have discussions, develop skills and abilities to problem solve, and express feelings and thoughts in a productive manner. You will explore ways in which your family works, rules, and behaviors, that will help combat conflict. You will also strengthen one another, build trust, and confide in one another. [39] [38]

What to expect

When doing these family sessions, you need to make sure the appropriate people are in attendance, those that are directly involved in the issue that you are going to this counseling for.  [41] Family helps with coping strategies and working through problems and issues that occur during your life, which counseling can help enhance.  Sessions can be a bit time-consuming, 50 min to an hour, and the number of sessions may vary, depending on your issue, and how well the sessions go, so no two family sessions will be the same amount of time, activities, and conversations. [39] The sessions are oftentimes short-term, you won't be in therapy for long periods of time.  [39] The amount of time that will be dedicated to these family therapy sessions is decided by the psychologist, clinical social worker, or therapist that is working with you.  It doesn't immediately fix your issues, but when you stick with it, there has been a lot of positive feedback which has helped in learning great skills, and problem-solving. [39]

Basis in theories

Family support is based in part on theories related to families, particularly family systems theory, ecological and support theories, community support theories, life-span and life course theories, family psycho-social theories, family empowerment theory, the work-home resources model, and positivistic theories, such as the sociology of acceptance. [42] [43] [44] [45] [46] [21] [47] [48] [49] [50] [51] [52] In relation to services, basic policy concepts have included family-centeredness, capacity-based services, empowerment and participatory decision-making, and individualized (and appropriate) services, among others. [53] Between the 1970s and 1990s, family support was developed in the context of community integration, [54] building on the quarter-century work on the physical and social integration of families and their children. [55] [56] [57] It differs from other models of family support developed in the context of employment programs, housing programs, nutrition, transportation, health care, or city emergency programs. These included: the Family Support Services of West Hawaii (including community and economic development activities), Family Support Services|Family Support Services of Amarillo (including employee assistance and family therapy), Family Support Services of Southeastern Pennsylvania (e.g., child welfare and early intervention), City of Chicago Family and Support Services (e.g., domestic violence, senior services). (brief web review, 2011).

Growth in the US

By the 1990s, family support had gained great popularity in the field of intellectual disabilities, especially since 80-90% of children with disabilities continue to live with their families even today. [58] Yet, the Human Services Research Institute determined that only 1.5% of the state budget for developmental disabilities services was used to support these families as of 1990. [59] By 2006, family support spending was reported to be $2,305,149,428 in the US, [60] yet, in FY 2006, it remained at only 5% of total intellectual and developmental disabilities spending of $43.84 billion. [61] In the US, the costs of "family care" for intellectual and developmental disabilities have been studied, including direct financial costs met by families, indirect and opportunity costs, and indirect psychological costs. [62]

In related fields, though, family support is still often considered to be "unpaid", "voluntary support" by family members, family-to-family training programs, and self-help groups, often near forms of family interventions by professionals (e.g., behavioral training, [63] clinical assessments, [64] vocational training, family therapy, clinical community re-entry) in traumatic brain injury. [65] and in adult mental health. [66] In children's mental health, family support and advocacy organizations are viewed to be increasing at the systems and policy levels, with the late 1980s formation of the Federation of Families for Children's Mental Health [67] and the reformation of the National Alliance on Mental Illness, a strong parent organization from the late 1970s. Family support services today are viewed as important for families with individuals with diverse disabilities (e.g., motor-neuron disease, [68] AIDS, epilepsy cerebral palsy, autism)with a greater emphasis on choice in support services (e.g., counseling, [69] training and information, respite). [70]

As a parent-professional field

As family support would be considered a parent-professional field, the research studies documented diverse disabilities (e.g., epilepsy, sickle cell anemia, hearing/visual impairment, spina bifida, cancer, learning disability), household incomes, level of assistance by daily living activities, behavioral and medical needs, insurance coverage, daily routines, the impact of disability on the household, services for specialized needs, and so forth. [71] The field then was challenged in the 1990s to broaden approaches to families, including gendered caring, [72] [73] inner-city population groups, [74] rural areas of the country, [75] a "whatever it takes approach", [76] and over-professionalized approaches to people's homes. [77] This was followed by a national research study on these organizations supporting families in the community and those supporting adults with disabilities to live in their own homes., [78] two major national and international comprehensive reform efforts in community living. Baltimore, MD: Paul H. Brookes. [17] In addition, governmental policy today appears to continue to encourage adults with disabilities to live at home with parents or caregivers (2011); thus, family support funds are usually designated for families with children and adults living at home, including in families with aging parents. However, family supports are also integral to adoptive and foster families and may take the form of in-home aides or home assistance, provision of equipment, respite and home adaptations, and shared care options between birth and foster parents/families. [79]

As a caregiving model

In line with the parent-professional partnerships of the 1980s and 1990s, the Oregon Research Institute published a book on Support for caregiving families. [80] The book included the progressive professional stances on family stress and support,(For critique, see Racino & Heumann.) [81] [82] Value-based services based on the Center on Human Policy's statement in support for children and their families (1987), [83] the role of parents in quality services, [84] [85] [86] coping skills (often addressed by behavioral or skills training), [87] human development and informal support, [88] and family life cycles, including infants and early intervention, school-aged children (school programs), transition to adulthood (and supported employment), and eco-behavioral/clinical treatment of families (stronger in fields such as mental health), among others. [80] Family support and aging, a major concern in the 2000s due to the aging population in the US, was also the focus of service reform in the 1990s. For example, 700,000 people with developmental disabilities live with one or more parents over the age of 65. [89]

As a model of community services

As deinstitutionalization policies in the US moved toward the development of community services, [90] [91] community parents also became more interested in "out-of-home placements" (e.g., small group homes) of their children (e.g., children moving from the parental home and beginning adult lives). [92] This approach is valued internationally as one way for adults to attain adult status, especially in Western countries. [93] [94] In states like New York and Connecticut, this resulted in tension between "institutional" and "community parents" vying for limited public funds, and between providers of services for funding (e.g., state institutions and private, non-profit community sectors). However, as states began to close institutions, funding was often available primarily to relocate those individuals living in institutional care or those at risk of institutionalization (e.g., home and community-based Medicaid waiver, HCBS). [95] [54] For example, "15 states financed 90% or more of their family support services with Medicaid HCBS; 11 states financed their family support activities through state funding. [61] Since family support was recommended for children, options such as foster care (new models for adults and children)often included family support services, families on waiting lists were offered family support services, and a broader range of types of services was developed in different states (e.g., Wisconsin's menu of services). [96] [97] [98]

New and traditional population groups

In the 2000s, "new population groups" in family support, as part of family support theories in the US and worldwide, included:

Adolescent mothers and single parent families

Traditional groups known to be at risk of adolescent mothers were sometimes involved in social support and adolescent theories, as part of adolescent pregnancies and mothering research. [99] At-risk families with intellectual disabilities also may be single mothers and early recommendations were for additional support options such as boarding nearby to family, modifying apartment programs to allow children, and increasing family support services in private homes. Critical are personal and family values, empowerment of families and home visitors, parent-child activities, and cluster groups (e.g., neighborhood improvement, natural childbirth groups, toddler playgroups, team group support [100] ), among others (e.g., Cochran, et al., 1984). [101]

Multicultural and transnational families

In addition, the needs of multicultural families, based on changing US demographics, also resulted in greater attention to the major minority groups, including African-Americans, Asian Americans, native Indian Americans, and Hispanic/Latino Americans. [102] [103] [104] [105] [106] [107] Original approaches involved services to Native Americans on reservations (often poverty) or as "assimilation into white society" [108] in contrast to approaches involving housing integration of "diverse populations" (e.g., Asian Americans) in mixed-income housing in small cities. [109] Today (2012), the American Indians, for example, own and operate casino gambling in the US and obtain funds for their own social services. [110] In addition, new transnational families, who may be separated from their families by international migration, form part of the new face of families in the US [111] as does the gay, lesbian, bisexual, and transgender activist populations. [112]

Youth with disabilities

Youth with disabilities became an emerging "age group" [113] in the late 1980s and 1990s as family approaches (often parent-based) competed with approaches based more on the desires of youth with disabilities. For example, personal assistance approaches based on diverse lifestyles and hiring of aides by service users became a popular way of thinking about services. [114] [115] In addition, major federal initiatives in transition planning in the US resulted in a variety of approaches to moving from child-centered to adult services, based in part, upon theories of adolescent development. [116] [117] [118] Today, self-advocacy has grown worldwide and youth, in particular, have sought their own voices and futures. [119] [120]

Aging population

The changing demographics of aging in the US have been well documented in diverse fields [121] with its public-facing the need to revamp the nation's Social Security system. [122] The latter can no longer, as developed in the Depression Era, financially support the growing aging population which outstrips the younger generation paying into the system. For example, "between 2010 and 2030, the number of people aged 65 and older is projected to increase by 76%, while the number of workers supporting the system is projected to increase by 8%". [123] The elder population also is living longer, expected to have a marked increase in the people living over the age of 80, [124] involving an increase in "disabilities" such as dementia (e.g., Public Broadcasting, 2011), affecting social security disability benefits, [125] and also the discovery of older adults with lifelong disabilities in "community-dwelling" two-generation families. [126]

Youth, children and adults in mental health

Instead of family support in the field of mental health, parent organizations have formed state and national chapters independent of their children (e.g., National Alliance for the Mentally Ill). [127] In addition, community agencies often have developed parent education programs (which remains government-funded program in the US), and family therapists and counselors (often in private practice) tend to work with the whole family. Personal assistance and independent living approaches tend to begin with the desires and wishes of the youth or adult, and less often, the children; these approaches in mental health remain relatively uncommon though psychosocial approaches have some similarities. [128] While housing and support and employment support have been transferred across fields, greater reluctance exists in the field of mental health for "family support" (often starting with parental concerns) who often bill the parents as secondary service recipients.

In psychiatric rehabilitation, "families are a major resource impacting rehabilitation outcome" (families as allies) with 50-60% returning home from hospitals in the US (Anthony, et al., 2002, p. 185). Extended families are viewed as critical worldwide, and many approaches are categorized as "family management" (e.g., information, treatments, family management), family interventions, or "psychoeducational" (Ibid, 2002). [129] However, leading national research centers in the US examined state service systems and recommended prevention and family support for children in mental health and their families. [130] Such "ecologically-grounded models" which are expected to improve or "mediate child and parent outcomes" have often been the first targeted in difficult economic times; the "full-fledged family support movement" of community-based agencies was reported in 1992 as "struggling to operationalize a new set of services and a new way of doing business with families". [131]

Parents with intellectual disabilities

By the 2000s, internationally, the support of parents who themselves have intellectual disabilities moved to new prominence with extensive, multi-decade research [132] [133] [134] after initial programs and studies in the US as early as the late 1980s and 1990s. [135] [136] [137] [138] [139] [140] In addition, traditional parent training programs moved to community building [141] and parents/mothers with physical disabilities also prominently advocated for better lifestyles for themselves and their children, [142] [143] included as part of a new US National Resource Center for Parents with Disabilities. (April 1998). Through the Looking Glass administered the 5-year center on behalf of the "8 million American families in which one or both parents has a disability." [144]

Families with a member with a brain injury

In 2015, partially as a result of the Iraq and Afghanistan wars, veterans are returning home with head and brain injuries and then returning from hospital and rehabilitation to spouses and family. Common may be a referral to a support group for the spouse or caregiver who may experience "caregiver stress" and "burden of care", [145] the result of inadequate community services in homes and for families. In addition, brain or head injuries can be caused by vehicular accidents, sports injuries, falls or accidents, war and terrorism, and related medical conditions (e.g., brain tumor, stroke). Family support in these fields often refers to support groups or direct support from the family and neighbors to the individual with the brain injury or the rehabilitation or hospital program as the family support. [146]

US policy goals

In the National Goals and Research for People with Intellectual and Developmental Disabilities, [147] support of families and family life across the lifespan was considered one of the major goals of the extensive work group of leaders in that field (e.g., Ann Turnbull, Rud Turnbull, John Agosta, Elizabeth Erwin, Glenn Fujuira, George Singer, and Leslie Sodak, among others). [148] The overarching goal was: To support the caregiving efforts and enhance the quality of life of all families so that families will remain the core unit of American society. The five subgoals include:

Such efforts are critical as the US has often been criticized for having a lack of a coherent family policy for all its people (e.g., health care, housing, employment, leisure, community, and economic development). [149] [150]

International

Family support is indeed an international initiative with 1994 the International Year of the Family as proclaimed by the United Nations. Helle Mittler, from Great Britain, reported on the TASK Force of the International League of Societies for Persons with Mental Handicaps which highlighted Face to Face in the United Kingdom, Young Muslim Women's Association Comprehensive Programme in Jordan, Service Brokerage in Canada, Swasahaya Sumachaya, Mysore, and Karnataka Parents' Association in India, Market Place Support Group in Côte d'Ivoire, Africa, Brothers and Sisters Groups in Nicaragua and India, Fathers' group in the United Kingdom, and Parents and Professionals Learning Together in Bangladesh and Pakistan. [151]

In 2012, the international community is on individual and family life quality, [152] family support is a long-term service and supports (LTSS) in the US in communities [61] and a new chapter, "Family theories, family support and family studies" will be released in 2014.[ needs update ] [153]

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">Rehabilitation Act of 1973</span> United States law

The Rehabilitation Act of 1973 is a United States federal law, codified at 29 U.S.C. § 701 et seq. The principal sponsor of the bill was Rep. John Brademas (D-IN-3). The Rehabilitation Act of 1973 replaces preexisting laws to extend and revise the authorization of grants to States for vocational rehabilitation services, with special emphasis on services to those with the most severe disabilities, to expand special Federal responsibilities and research and training programs with respect to individuals with disabilities, to establish special responsibilities in the Secretary of Health, Education, and Welfare for coordination of all programs with respect to individuals with disabilities within the Department of Health, Education, and Welfare, and for other purposes. It created the Rehabilitation Services Administration.

<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.

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.

<span class="mw-page-title-main">Inclusion (education)</span> Where disabled students spend most of their time with non-disabled students

Inclusion in education refers to all students being able to access and gain equal opportunities to education and learning. It arose in the context of special education with an individualized education program or 504 plan, and is built on the notion that it is more effective for students with special needs to have the said mixed experience for them to be more successful in social interactions leading to further success in life. The philosophy behind the implementation of the inclusion model does not prioritize, but still provides for the utilization of special classrooms and special schools for the education of students with disabilities. Inclusive education models are brought into force by educational administrators with the intention of moving away from seclusion models of special education to the fullest extent practical, the idea being that it is to the social benefit of general education students and special education students alike, with the more able students serving as peer models and those less able serving as motivation for general education students to learn empathy.

"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." Normalization is a rigorous theory of human services that can be applied to disability services. 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.

In clinical diagnostic and functional development, special needs refers to individuals who require assistance for disabilities that may be medical, mental, or psychological. Guidelines for clinical diagnosis are given in both the Diagnostic and Statistical Manual of Mental Disorders and the International Classification of Diseases 9th edition. Special needs can range from people with autism, cerebral palsy, Down syndrome, dyslexia, dyscalculia, dyspraxia, dysgraphia, blindness, deafness, ADHD, and cystic fibrosis. They can also include cleft lips and missing limbs. The types of special needs vary in severity, and a student with a special need is classified as being a severe case when the student's IQ is between 20 and 35. These students typically need assistance in school, and have different services provided for them to succeed in a different setting.

<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.

A mental health professional is a health care practitioner or social and human services provider who offers services for the purpose of improving an individual's mental health or to treat mental disorders. This broad category was developed as a name for community personnel who worked in the new community mental health agencies begun in the 1970s to assist individuals moving from state hospitals, to prevent admissions, and to provide support in homes, jobs, education, and community. These individuals were the forefront brigade to develop the community programs, which today may be referred to by names such as supported housing, psychiatric rehabilitation, supported or transitional employment, sheltered workshops, supported education, daily living skills, affirmative industries, dual diagnosis treatment, individual and family psychoeducation, adult day care, foster care, family services and mental health counseling.

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.

Respite care is planned or emergency temporary care provided to caregivers of a child or adult.

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.

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.

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"

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. Cohen, S. & Warren, R. (1985). Respite care: Principles, programs and policies. Austin, TX: PRO-ED.
  2. Taylor, S., Knoll, J., Lehr, S., & Walker, P. (1989). Families for all children: Values-based services for children with disabilities and their families. In: G. Singer & L. Irvin (Eds.), "Support for caregiving families" (pp. 41-53). Baltimore, MD: Paul H. Brookes.
  3. 1 2 Taylor, S., Racino, Julie Ann, Knoll, J. & Lutfiyya, Z. (1987). "The nonrestrictive environment: On community integration for persons with the most severe disabilities." Syracuse, NY: Human Policy Press.
  4. Edinger, B., Schultz, B., & Morse, M. (1984). Final report: issues relevant to respite services for people with developmental disability. Part One: The research. In: Racino, Julie Ann (Ed.), "Final report of the Respite Project of Central New York". Syracuse, NY: Respite Project of Central New York, Transitional Living Services and the Syracuse Developmental Services Office.
  5. Shoultz, B. (1992b). "Like an angel they came to help us: The origins and workings of New Hampshire's family support network." Syracuse, NY: Research and Training Center on Community Integration, Center on Human Policy, Syracuse University.
  6. 1 2 Racino, Julie Ann (2002). "Community Integration and Statewide Systems Change". Journal of Health & Social Policy. 14 (3): 1–25. doi:10.1300/J045v14n03_01. PMID   12086010. S2CID   21862276.
  7. e.g., Hill, B., Lakin, K.C., Bruininks, R., Amado, A., Anderson, D. & Copher, J.(1989). Living in the community: A comparative study of foster homes and group homes for people with mental retardation. Minneapolis, MN: Center for Residential and Community Services, Institute on Community Integration, University of Minnesota.
  8. Provencal, G. (1980). The Macomb-Oakland Regional Center. In: T. Appoloni, J. Cappuccilli, & T. P. Cooke (Eds.), Towards excellence: Achievement in residential services for persons with disabilities. Baltimore, MD: University Park Press.
  9. Rucker, L. (1987). A difference you can see: One example of services to persons with severe mental retardation in the community. In: S. Taylor, D. Biklen, & J. Knoll (Eds.), "Community integration for people with severe disabilities". (pp. 109-128). NY, NY: Teachers College Press.
  10. Strully, J. & Strully, C.F. (1989). Family support to promote integration. In: S. Stainback, W. Stainback, & M. Forest, Educating All Students in the Mainstream of Regular Education. Baltimore, MD: Paul H. Brookes.
  11. Braddock, D., Hemp, R., Fujuira, G., Bachelder, L, & Mitchell, D. (1990). State of the states in developmental disabilities. Baltimore, MD: Paul H. Brookes.
  12. Knoll, J., Covert, S., Osuch, R., O'Connor, S., Agosta, J. & Blaney, B. (1992). "Family support services in the US: An end of decade status report". Cambridge, MA: Human Services Research Institute.
  13. Center on Human Policy. (1987-1989). A statement in support of families and their children. National Policy Institute on Families and their Children. Reprinted in: Racino, Julie Ann. (2000). "Personnel preparation in disability and community life: Toward universal approaches to support." (pp. 31-32). Springfield, IL: Charles C. Thomas Publishers.
  14. 1 2 Taylor, S., Bogdan, R., & Racino, Julie Ann (1991). "Life in the community: Case studies of organizations supporting people with disabilities." Baltimore, MD: Paul H. Brookes. ISBN   9781557660725 OCLC   23179646
  15. Bersani, H. (1991, January). "Case study of the family support services conducted by the United Cerebral Palsy Association of Philadelphia, PA". Salem, OR: Community Integration Associates (for the Pennsylvania Developmental Disabilities Council).
  16. Piersma, J. (2002). Family support services. In: R. Schalock, P.C., Baker, & M.D. Croser (Eds.), "Embarking on a new century: 'Intellectual disabilities' at the end of the 20th century". (pp. 143-152). Washington, DC: American Association on Intellectual and Developmental Disabilities.
  17. 1 2 Racino, Julie Ann (1991). "Organizations in community living: Supporting people with disabilities". The Journal of Mental Health Administration. 18: 51–59. doi:10.1007/BF02521134. S2CID   46194379.
  18. Osburn, Joe; Caruso, Guy; Wolfensberger, Wolf (2011). "The Concept of "Best Practice": A brief overview of its meanings, scope, uses, and shortcomings". International Journal of Disability, Development and Education. 58 (3): 213–222. doi:10.1080/1034912x.2011.598387. S2CID   143654105.
  19. e.g., Racino, Julie Ann (1985a). Respite program models — Use of generic services and family subsidy. In: Racino, Julie Ann. Respite services in New York State. (pp. 27-30). Syracuse, NY: Syracuse University, Maxwell School of International and Public Affairs.
  20. e.g., Racino, Julie Ann (1983). Respite grant awarded. Transitional Living Services News, I(4), 1.
  21. 1 2 Racino, Julie Ann (2000). Personnel preparation in disability and community life: Toward universal approaches to support. Springfield, IL: Charles C. Thomas Publishers.
  22. Braddock, D., Hemp, R., Fujuira, G., Bachelder, L, & Mitchell, D. (1990). New York State. "The state of the states in developmental disabilities". (p.336) Baltimore, MD: Paul H. Brookes
  23. Racino, Julie A. (1998). "Innovations in family support: What are we learning?". Journal of Child and Family Studies. 7 (4): 433–449. doi:10.1023/A:1022953926043. S2CID   141260429.
  24. Chapter 461, Laws of New York, 1984 and New York State Mental Hygiene Law, Secs. 13.03, 13.04 in Bates, M. V. (1985, July). State family support/cash subsidies programs. Madison, WI: Wisconsin Council on Developmental Disabilities.
  25. Lubeck, S. & Garrett, P. (1988, Spring), "Child care 2000: Policy options for the future. "Social Policy", 31-37.
  26. Walker, P. (1999, June). "Child care for children with disabilities: Addressing the unique challenges." Battle Creek, Michigan: The Arc of Calhoun County.
  27. Lukemeyer, A., Meyers, M. & Smeeding, T. (1997, July). Expensive children in poor families: Out-of-pocket expenditures for the care of disabled and chronically ill children and welfare reform. "Income Security Policy Paper No. 17." Syracuse, NY: Syracuse University, Maxwell School of International and Public Affairs.
  28. Bradley, V.J. & Agosta, J. (1985). Tax policy recommendation. "Family care for persons with developmental disability: A growing commitment". Boston, MA: Human Services Research Institute.
  29. Bates, M.V. (1985). Table of state family support/cash subsidy programs. Madison, Wisconsin: Wisconsin Developmental Disabilities Council.
  30. Shoultz, B. (1987, September). Families for all children. Syracuse, NY: Center on Human Policy, Syracuse University.
  31. Bradley, V.J. & Agosta, J.M. (1985). Keeping your child at home: The case for family support. Exceptional Parent, 10-22.
  32. e.g., Racino, Julie Ann (1988). Resources on supporting people with extensive health care needs in the community. Syracuse, NY: Center on Human Policy, Rehabilitation Research and Training Center on Community Integration, Syracuse University.
  33. Castellani, P., Downey, N.A., Tausig, M.B. & Bird, W.A. (1986). Mental Retardation, 24(2), 71-79.
  34. Bersani, H. (1987). "Site visit report: Calvert County, Maryland Arc family support services. Syracuse, NY: Center on Human Policy, Rehabilitation Research and Training Center on Community Integration, Syracuse University.
  35. Michigan Department of Mental Health. (1983). "Family support subsidy program". Lansing, MI: Author.
  36. United Cerebral Palsy Governmental Activities Office. (1987, Summer). "Family Support Bulletin". Washington, DC: Author.
  37. Walker, P. (1988, July). Resources on family support. Syracuse, NY: Rehabilitation Research and /Training Center on Community Integration, Center on Human Policy, Syracuse University.
  38. 1 2 3 RefreshMH (2021-01-12). "The Goals and Benefits of Family Therapy". Comprehensive MedPsych Systems. Retrieved 2022-11-28.
  39. 1 2 3 4 5 "Family therapy - Mayo Clinic". www.mayoclinic.org. Retrieved 2022-11-28.
  40. "What Can Family and Carers Do to Help a Person with OCD?" , Everything You Need to Know About OCD, Cambridge University Press, pp. 157–167, 2022-06-23, doi:10.1017/9781009004176.010, ISBN   9781009004176 , retrieved 2022-11-28
  41. "Family Therapy: What Are the Benefits?". Recovery First Treatment Center. Retrieved 2022-11-28.
  42. Bogdan, R. & Taylor, S. (1987). Toward a sociology of acceptance: The other side of the study of deviance. Social Policy, 18(2), 34-39.
  43. O'Connor, S. (1995). "We're all one family": The positive construction of people with disabilities by family members. In: S.J. Taylor, R. Bogdan, & Z.M. Lutfiyya, The variety of community experiences: Qualitative studies of family and community life. (pp. 67-77). Baltimore MD: Paul H. Brookes.
  44. Racino, Julie Ann (2005). Social support. In G. Albrecht, Encyclopedia on disability. (pp. 1470-1471). Thousand Oaks, SAGE.
  45. Bronfenbrenner, U. (1979). The ecology of human development: Experiments in nature and design. Cambridge, MA: Harvard University Press.
  46. Cochran, M. & Woolever, F. (1983). Beyond the deficit model: The empowerment of parents with information and informal supports. In: I. Sigel & L. Laosa (Eds.), "Changing families". (pp. 225-247). New York and London: Plenum Press.
  47. Maitz, E. (1994). Family systems theory as applied to head injury. In: J.M. Williams & T. Kay, Head injury: A family matter.(pp.65-79). Baltimore, MD: Paul H. Brookes.
  48. Macklin, E. (1973). "Adolescent development courses I and II: Life course theory". Ithaca, NY: Cornell University, School of Human Ecology.
  49. Andrews, Mary P.; Bubolz, Margaret M.; Paolucci, Beatrice (1981). "An Ecological Approach to Study of the Family". Marriage & Family Review. 3 (1–2): 29–49. doi:10.1300/j002v03n01_02.
  50. Olson, D. & Miller, B. (1984). "Family studies: Review yearbook". (Vol. 2). Beverly Hills, CA: Sage.
  51. Sprey, J. (1990). "Fashioning family theories: New approaches". Newbury Park, CA: Sage.
  52. Chan, Xi Wen; Kalliath, Parveen; Chan, Christopher; Kalliath, Thomas (2020). "How does family support facilitate job satisfaction? Investigating the chain mediating effects of work–family enrichment and job-related well-being". Stress and Health. 36 (1): 97–104. doi: 10.1002/smi.2918 . hdl: 10072/397497 . ISSN   1532-2998. PMID   31840406.
  53. Turnbull, H.R., Beegle, G., & Stowe, M. (2009). The core concepts of disability policy affecting families who have children with disabilities. (pp. 423-443). In: T.M. Skrtic, E. Horn, & G. Clark, Taking stock of special education policy and practice. Denver, CO: Love Publishing Co.
  54. 1 2 Racino, Julie Ann. (2011/2012). Outcomes of technical assistance in community integration in states in the US: A retrospective and prospective on the Rehabilitation Research and Training Centers. Rome, NY.
  55. Wolfensberger, W. (1972). "The principle of normalization in human services". Toronto: Canadian National Institute on Mental Retardation.
  56. Nirje, Bengt (1985). "The Basis and Logic of the Normalization Principle". Australia and New Zealand Journal of Developmental Disabilities. 11 (2): 65–68. doi:10.3109/13668258509008747.
  57. Thomas, S. & Wolfensberger, W. (1999). An overview of social role valorization. In: R.J. Flynn & R.A. LeMay (Eds.), "A quarter century of normalization and social role valorization: Evolution and impact". (pp. 125-159). Ottawa, Canada: University of Ottawa.
  58. e.g., Fujuira, G. & Braddock, D. 1999. Fiscal and demographic trends in mental retardation services: The emergence of the family. In: L. Rowitz (Ed.), Mental retardation in the year 2000. New York: Springer-Verlag. (Cited in: Stancliffe, R. & Lakin, K.C. (2005). Costs and outcomes of community services for people with intellectual disabilities. Baltimore, MD: Paul H. Brookes.)
  59. Knoll, J., Covert, S., O'Connor, S., Agosta, J., & Blaney, B. (1990). Family support services in the US: An end of decade status report. Cambridge, MA: Human Services Research Institute.
  60. Braddock, D., Hemp, R., & Rizzolo, M. (2008). The state of the states in developmental disabilities. Baltimore, MD: Paul H. Brookes.
  61. 1 2 3 Rizzolo, Mary C.; Hemp, Richard; Braddock, David; Schindler, Abigail (2009). "Family Support Services for Persons with Intellectual and Developmental Disabilities: Recent National Trends". Intellectual and Developmental Disabilities. 47 (2): 152–155. doi:10.1352/1934-9556-47.2.152. PMID   19368483.
  62. Lewis, D. & Johnson, D. (2005). Costs of family care for individuals with developmental disabilities. In: R.J. Stancliffe & K.C. Lakin, "Costs and outcomes of community services for people with intellectual disabilities". (pp.63-89). Baltimore, MD: Paul H. Brookes.
  63. Parsons, Marsha B.; Rollyson, Jeannia H.; Reid, Dennis H. (2013). "Teaching Practitioners to Conduct Behavioral Skills Training: A Pyramidal Approach for Training Multiple Human Service Staff". Behavior Analysis in Practice. 6 (2): 4–16. doi:10.1007/BF03391798. ISSN   1998-1929. PMC   5139667 . PMID   27999628.
  64. "Module 3: Clinical Assessment, Diagnosis, and Treatment – Fundamentals of Psychological Disorders". opentext.wsu.edu. Retrieved 2022-11-28.
  65. Williams, J. & Kay, T. (1991). "Head injury: A family matter". Baltimore, MD: Paul H. Brookes.
  66. LeGacy, S. (1978). "Training for parents of adults with mental illness: Series of sessions". Syracuse, NY: Transitional Living Services of Onondaga County, New York State, USA.
  67. Koroloff, N., Friesen, B., Reilley, L., & Rinkin, J. (1996). The role of family members in systems of care. In: B. Stroul (Ed.), "Children's mental health: Creating systems of care in a changing society". (pp. 409-426). Baltimore, MD: Paul H. Brookes.
  68. Australia, Healthdirect (2022-08-29). "Motor neurone disease (MND) – causes, symptoms and treatments". www.healthdirect.gov.au. Retrieved 2022-09-28.
  69. "Counseling Psychology". www.apa.org. Retrieved 2022-11-28.
  70. O'Brien, Mary R.; Whitehead, Bridget; Jack, Barbara A.; Mitchell, J. Douglas (2012). "The need for support services for family carers of people with motor neurone disease (MND): Views of current and former family caregivers a qualitative study". Disability and Rehabilitation. 34 (3): 247–256. doi:10.3109/09638288.2011.605511. PMID   22087569. S2CID   7369457.
  71. e.g., Knoll, J. (1992). Being a family: The experience of raising a child with a disability or chronic illness. In: V.J. Bradley, J. Knoll, & J.M. Agosta, Emerging issues in family support. (pp.9-56). Washington, DC: American Association on Mental Retardation.
  72. Traustadottir, R. (1991). The meaning of care in the lives of mothers of children with disabilities. (pp. 185-194). In: S. Taylor, R. Bogdan & Racino, Julie Ann. Life in the community: Case studies of organizations supporting people with disabilities. Baltimore, MD: Paul H. Brookes.
  73. Traustadottir, Rannveig (1991). "Mothers Who Care". Journal of Family Issues. 12 (2): 211–228. doi:10.1177/019251391012002005. S2CID   145408399.
  74. Walker, P. (1991). Anything's possible: Project Rescue. (pp. 171-183) In: S.Taylor, R. Bogdan & Racino, Julie Ann. Life in the community: Case studies of organizations supporting people with disabilities. Baltimore, MD: Paul H. Brookes.
  75. Shoultz, B. (1991). Regenerating a community: Residential, Inc., Ohio. (pp. 195-213). In: S. Taylor, R. Bogdan & Racino, Julie Ann. Life in the community: Case studies of organizations supporting people with disabilities. Baltimore, MD: Paul H. Brookes.
  76. Bersani, H. (1990) "Presentations on families and community integration". Syracuse, NY: Research and Training Center on Community Integration, Center on Human Policy, Syracuse University.
  77. Bogdan, R. (1991). This isn't a program, this is our home: Reflections on the over-professionalized approach to caregiving. (pp. 243-251). In: S. Taylor, R. Bogdan, & Racino, Julie Ann. Life in the community: Case studies of organizations supporting people with disabilities. Baltimore, MD: Paul H. Brookes.
  78. Taylor, S., Bogdan, R., & Racino, Julie Ann (1991). Life in the Community: Case Studies of Organizations Supporting People with Disabilities in the Community. Baltimore, MD; Paul H. Brookes.
  79. Walker, Pam. (1989, November). Family Supports in Montana: Region III: Special Training for Exceptional People (STEP). Syracuse University, Center on Human Policy, Rehabilitation Research and Training Center on Community Integration. Internet archive on 20 November 2014.
  80. 1 2 Singer, George H. S.; Irvin, Larry K (1989). Support for caregiving families : enabling positive adaptation to disability. Baltimore: Paul H. Brookes Pub. Co. ISBN   155766014X. OCLC   18682903 . Retrieved 29 June 2022.
  81. Racino, Julie Ann & Heumann, J. (1992). Independent living and community life: Building coalitions among leaders, people with disabilities and our allies. Generations, XI(1), 43-47.
  82. Racino, Julie Ann (1994). Creating change in states, agencies and communities. In: V.J. Bradley, J.W. Ashbaugh, & B. Blaney, Creating individual supports for people with developmental disabilities: A mandate for change at many levels. (p. 187). Baltimore, MD: Paul H. Brookes.
  83. Center on Human Policy. (1987). A statement in support of children and their families. "National policy institute in support of children and their families". In: S. Taylor, Racino, Julie Ann & P. Walker. (1992). Inclusive communities. In: S. Stainback & W. Stainback, "Controversial issues in special education." Boston: Allyn & Bacon.
  84. Lehr, S. & Lehr, B. (1990). Getting what you want: Expectations of families. In: V.J. Bradley & H.A. Bersani, "Quality assurance for individuals with developmental disabilities". (pp. 61-75). Baltimore, MD: Paul H. Brookes.
  85. Koroloff, N., Friesen, B., Reilley, L, & Rinkin, J. (1996). The role of family members in systems of care". In: B. Stroul, "Children's mental health: Creating systems of care in a changing society". (pp.409-426). Baltimore, MD: Paul H. Brookes.
  86. Warren, F. & Hopfengardner & Warren, S. (1989). The role of parents in creating and maintaining quality family support services. In: G.H.S. Singer & L.K. Irvin, "Support for caregiving families".(pp. 55-68). Baltimore, MD: Paul H. Brookes.
  87. Hawkins, N. E. & Singer, H.S. (1989). A skills training approach for assisting parents to cope with stress. In: G.H.Singer & L.K. Irvin, "Support for caregiving families". (pp. 71-83). Baltimore, MD: Paul H. Brookes.
  88. Dunst, C., Trivette, C.M., Gordon, N.J., & Pletcher, L. (1989). Building and mobilizing family support networks. In: G.H.S. Singer & L.K. Irvin, "Support for caregiving families". (pp. 121-141). Baltimore, MD: Paul H. Brookes
  89. The Arc and the American Association on Intellectual and Developmental Disabilities. (2008). "Family support". Washington, DC: Authors.
  90. Hayden, M. & DePaepe, P. (1994). Waiting for community services: The impact on persons with mental retardation and other developmental disabilities. In: M. Hayden & B. Abery (Eds.), "Challenges for a service system in transition." (pp. 173-206). Baltimore, MD: Paul H. Brookes.
  91. Taylor, S. & Searl, S. (1987). The disabled in America: History, policy and trends. In: P. Knobloch (Ed.), "Understanding exceptional children and youth." (pp. 449-581). Boston: Little, Brown.
  92. Moore, C. (1993). Letting go, moving on: A parent's thoughts. In: Racino, Julie Ann, P. Walker, S. O'Connor, & S. Taylor, "Housing, support and community". (pp. 189-204). Baltimore, MD: Paul H. Brookes.
  93. "Housing support community".
  94. Bjarnason, D. (2005). The dignity of risk: My son's home and adult life. In: K. Jonhson & R. Traustadottir, Deinstitutionalization and people with intellectual disabilities. (pp. 251-258). London: Jessica Kingsley Publishers.
  95. Research and Training Center on Community Integration. (1990). Consultations with states and communities on community integration. Syracuse, NY: Research and Training Center on Community Integration, Center on Human Policy, Syracuse University.
  96. Racino, Julie Ann (1999). A policy analysis of foster care: Children, adolescents and adults. In: Racino, Julie Ann. "Policy, program evaluation and research in disability: Community support for all." (pp. 289-314). London: Haworth Press.
  97. Wisconsin Department of Health and Family Services. (1999). "Family support services." Madison, WI: Author.
  98. Racino, Julie Ann (1999). The role of family case study research in family policy: Local agency delivery systems. In: Racino, Julie Ann. "Policy, program evaluation and research in disability: Community support for all." (pp. 235-262). London: Haworth Press.
  99. Secco, M.Loretta; Moffatt, Michael E.K. (1994). "A review of social support theories and instruments used in adolescent mothering research". Journal of Adolescent Health. 15 (7): 517–527. doi:10.1016/1054-139x(94)90134-o. PMID   7857949.
  100. "Support Groups: Types, Benefits, and What to Expect - HelpGuide.org". helpguide.org. Retrieved 2022-11-28.
  101. Cochran, M., Dean, C., Dill, M.F., & Woolever, F. (1984). Empowering Families: Home Visiting and Building Clusters. Ithaca, NY: Cornell University, Family Matters Project.
  102. McCallion, P. & Grant-Griffin, L. (2000). Redesigning services to meet the needs of multicultural families. (pp. 97-120). In: M. P. Janicki & E.F.Ansello, Community supports for aging adults with lifelong disabilities. Baltimore, MD: Paul H. Brookes.
  103. Harry, B. (1992). Cultural diversity, families and the special education system: Communication and empowerment. Baltimore, MD: Paul H. Brookes.
  104. Turnbull, H.R. & Turnbull, A. (1987). The Latin American families and public policy in the US: Informal support and transition into adulthood. Lawrence, KS: University of Kansas, Beach Center on Families.
  105. Karner, Tracy X.; Hall, Lisa Cox (2002). "Successful Strategies for Serving Diverse Populations". Home Health Care Services Quarterly. 21 (3–4): 107–131. doi:10.1300/j027v21n03_06. PMID   12665074. S2CID   20937800.
  106. Wang, Peishi; Michaels, Craig A. (2009). "Chinese Families of Children with Severe Disabilities: Family Needs and Available Support". Research and Practice for Persons with Severe Disabilities. 34 (2): 21–32. doi:10.2511/rpsd.34.2.21. S2CID   143289960.
  107. Chung, I. & Samperi, F. (2004). An east-west approach to serving Chinese immigrants in a mental health setting. In: D. Drachman & Paulino, A., Immigrants and Social Work. (pp. 139-159). Binghamton, NY: The Haworth Press.
  108. e.g., O'Connor, S. (1993). "I'm not Indian anymore": The challenge of providing culturally sensitive services to American Indians. (pp.313-332). In: Racino, Julie Ann, P. Walker, S. O'Connor, & S. Taylor, "Housing, support and community". Baltimore, MD: Paul H. Brookes.
  109. Racino, Julie Ann. (1993). Madison Mutual Housing Association and Cooperative: "People and housing building communities." (pp. 253-280). In: Racino, Julie Ann, P. Walker, S. O'Connor, & S. Taylor, "Housing, support and community". Baltimore, MD: Paul H. Brookes.
  110. Healey, J. (2010/2011). Appendix D: American Indians: Are they making meaningful progress at last? Race, ethnicity, gender and class. Los Angeles, CA: SAGE.
  111. Healey, L.M. (2004). Strengthening the link: Social work with immigrants and refugees and international social work. In: Drachman, D. & Paulino, A., Immigrants and social work: Thinking beyond the borders of the US. (pp.49-61). Binghamton, NY: Social Work Practice Press.
  112. Butler, S. (2004). Gay, lesbian, bisexual, and transgender (GLBT) elders: The challenges and resilience of this marginalized group. In: S.M. Cummings & C. Galambos, Diversity and aging in the social environment. (pp. 25-44). Binghamton, NY: Haworth Press.
  113. Macklin, E. (1975). Parent-teen panel. "Adolescents in Development, I and II". Ithaca, NY: Cornell University, College of Human Ecology.
  114. Litvak, S. & Racino, Julie Ann (1999). Youth and community life: Perspectives of adults with disabilities on personal assistance services. (pp. 207-224). In: Racino, Julie Ann. "Policy, program evaluation and research in disability: Community support for all." London: Haworth Press.
  115. Litvak, S. Zukas, H., & Heumann, J. (1987). "Attending to America: Personal assistance for independent living". Berkeley, CA: World Institute on Disability, Rehabilitation Research and Training Center on Public Policy and Independent Living.
  116. Blum, Robert WM.; Garell, Dale; Hodgman, Christopher H.; Jorissen, Timothy W.; Okinow, Nancy A.; Orr, Donald P.; Slap, Gail B. (1993). "Transition from child-centered to adult health-care systems for adolescents with chronic conditions". Journal of Adolescent Health. 14 (7): 570–576. doi:10.1016/1054-139x(93)90143-d. PMID   8312295.
  117. Rusch, R.R., Destefano, L., Chadsey-Rusch, J., Phelps, L.A., & Szymanski, E. (1992). "Transition from school to adult lives." Sycamore, IL: Sycamore Publishing Co.
  118. Powers, L.E. & Sikora, D.M. (1997). Promoting adolescent self-competence. In: S.M. Pueschel & M. Sustrova, "Adolescents with Down Syndrome: Toward a more fulfilling life." (pp. 71-89). Baltimore, MD: Paul H. Brookes.
  119. ADAPT. (2011). "Youth summit." Denver, CO and Austin, TX: Author.
  120. Dybwad, G. & Bersani, H. (1998). "New Voices: Self advocacy for people with disabilities". Cambridge, MA: Brookline Books.
  121. Meyers, J. (2001). Age: 2000 (Census 2000 Brief). Washington, DC: US Census Bureau, C2KBR/01/12. In: Kutza, E. (2005). The intersection of economics and family status in late life: Implications for the future. In: Caputo, R., Challenges of Aging on US families. (pp. 9-26). Binghamton, NY: The Haworth Press.
  122. Gregory, J., Bethell, T., Reno., V. & Veghte, B. (2010, November). Strengthening the social security system in the long run. Social Security Brief, 35.
  123. Nuschler, D. (2010, September). Social security reform: Current issue and legislation. Washington, DC: Congressional Research Services.
  124. US Bureau of the Census. (1998, December) International database [on-line]. Available https://www.census.gov/cgi/ipc/idbsum. In: Ansello, E.F. & Janicki, M. (2000). The aging of nations: Impact on the community, the family, and the individual. (pp. 3-18). In: M. P. Janicki & E.F. Ansello, Community supports for aging adults with lifelong disabilities. Baltimore, MD: Paul H. Brookes.
  125. Consortium of Citizens with Disabilities. (2012, March). Disability program reform principles. Consortium of Citizens with Disabilities Social Security Task Force. Washington, DC: Author.
  126. Ansello, E.F. & Janicki, M.P. (2000). The aging of nations. (pp. 3-18). In: M. P. Janicki & E.F. Ansello, Community supports for aging adults with lifelong disabilities. Baltimore, MD: Paul H. Brookes.
  127. Carling, P.J. (1995). "Return to the community: Building Support Services for People with Psychiatric Disabilities". NY, NY: The Guilford Press.
  128. Racino, Julie Ann (1999). Psychiatric survivors, the international self help movement, and personal assistance services. "Policy, program evaluation and research in disability: Community support for all." London: Haworth Press.
  129. Anthony, W., Cohen, M., Farkas, M. & Gagne, C. (2002). "Psychiatric Rehabilitation". Boston, MA: Center for Psychiatric Rehabilitation, Boston University.
  130. Friedman, R. M. (1994). Restructuring of systems to emphasize prevention and family support. Journal of Clinical Child Psychology, Volume 23 (Suppl.): 40-47.
  131. Weiss, H.B. & Greene, J. C. (1992, Feb & May). An empowerment partnership for family support and education programs and evaluations. Family Science Review, 5(1&2): 131-148.
  132. Llewllyn, G., Traustadottir, R., McConnell, D., Sigurjonsdottir, H.B. (2010). Parent with intellectual disabilities: Past, present and future. Malden, MA: Wiley-Blackwell.
  133. Booth, T., & Booth, W. (1996). Supported parenting for people with learning difficulties: Lessons from Wisconsin. "Representing Children", 9,2, 99-102.
  134. Booth, T. & Booth, W., (2000, February). Against the odds: Growing up with parents who have learning difficulties. "Mental Retardation", 38(1), 1-14.
  135. Peter, D. (1991). We began to listen: Training Towards Self Reliance, CA. In; S.Taylor, R. Bogdan & Racino, Julie Ann. "Life in the community: Case studies of organizations supporting people with disabilities". (pp. 129-138). Baltimore, MD: Paul H. Brookes.
  136. Heighway, S.M., Kidd-Webster, S. & Snodgrass, P. (1998, November/ December). Supporting parents with mental retardation. "Children Today", 17, 24-27.
  137. Whitman, B. & Accardo, P. (1989). "When a parent is mentally retarded". Baltimore, MD: Paul H. Brookes.
  138. Racino, Julie Ann (1990). "Research field notes on families". Syracuse, NY: Research and Training Center on Community Living (Syracuse University) and the Research and Training Center on Community Integration (University of Minnesota).
  139. Feldman, Maurice A. (1994). "Parenting education for parents with intellectual disabilities: A review of outcome studies". Research in Developmental Disabilities. 15 (4): 299–332. doi:10.1016/0891-4222(94)90009-4. PMID   7972968.
  140. Tymchuk, A. (1990). "Decision-making abilities of mothers with mental retardation". Research in Developmental Disabilities. 11 (1): 97–109. doi:10.1016/0891-4222(90)90007-u. PMID   2300689.
  141. Webster-Stratton, Carolyn (1997). "From Parent Training to Community Building". Families in Society: The Journal of Contemporary Social Services. 78 (2): 156–171. doi:10.1606/1044-3894.755. S2CID   144140098.
  142. Kirschbaum, M. (1988, June). Parents with physical disabilities and their babies. "Zero to Three", 8(5), 8-15.
  143. Kirschbaum, M. (1996). Mothers with physical disabilities. In: D. Krotoski, M.A. Nosek, & M. Turk, "Women with physical disabilities: Achieving and maintaining health and well being". Baltimore, MD: Paul H. Brookes.
  144. Through the Looking Glass. (1998, April). "Parenting with a Disability", 6(1), 1-8.
  145. Chwalisz, Kathleen (1992). "Perceived stress and caregiver burden after brain injury: A theoretical integration". Rehabilitation Psychology. 37 (3): 189–203. doi:10.1037/h0079103.
  146. Williams, J. & Kay, T. (1991). Head Injury: A Family Matter. Baltimore, MD: Paul H. Brookes.
  147. Lakin, K.C. & Turnbull, A. (2005). National goals and research for people with intellectual and developmental disabilities. Washington, DC: The Arc of the US and the American Association on Mental Retardation.
  148. Turnbull, A., Turnbull, R., Agosta, J., Erwin, E., Fujuira, G., Singer, G., & Sodak, L. et al. (2005). Support of families and family life across the lifespan. In: K.C. Lakin & A. Turnbull (Eds.), National goals and research for people with intellectual and developmental disabilities. (pp. 217-256). Washington, DC: The Arc and the American Association on Mental Retardation.
  149. Racino, Julie Ann (1999). The role of family case study research in family policy: Local agency delivery systems. In: Racino, Julie Ann "Policy, program evaluation and research in disability: community support for all". (pp.235-261). London: Haworth Press (now Francis & Taylor)
  150. Zigler, E. F., Kagan, S. L., & Klugman, E. (Eds.). (1983). Children, families and government: Perspectives on American social policy. New York: Cambridge University Press. Internet archive ISBN   9780521242196 OCLC   9080946
  151. Mittler, H. (1994). International initiatives in support of families with a member with learning disabilities. (pp. 15-31). In: P. Mittler & H. Mittler, Innovations in family support for people with learning disabilities. Lancashire, England: Lisieux Hall.
  152. Rillotta, F.; Kirby, N.; Shearer, J.; Nettelbeck, T. (2012). "Family quality of life of Australian families with a member with an intellectual/Developmental disability". Journal of Intellectual Disability Research. 56 (1): 71–86. doi:10.1111/j.1365-2788.2011.01462.x. PMID   21883595.
  153. Racino, Julie Ann (2015). Public administration and disability : community services administration in the US. Boca Raton: CRC Press. ISBN   978-1-4665-7982-8. OCLC   899156066.