Chapter 11: Disability and Social Work Practice

Chapter 11: Disability and Social Work Practice

Outline

  • Defining disability

  • Theorizing disability

  • Categorizing disability

  • Prevalence of disability in Canada

  • History of disability policy in Canada

  • Social work practice with individuals with a disability

Learning Objectives

  • To understand how theoretical frameworks inform disability-focused social work practice.

  • To understand how disability emerges through the interaction between bodily impairment and the environment.

  • To identify complex social, economic, and physical barriers to the inclusion of persons with disabilities from historical and contemporary perspectives.

  • To recognize how policies influence the delivery of health and social services to individuals with disabilities and their families.

  • To identify the links among theory, research, policy, and practice and to apply these links to addressing issues facing individuals with disabilities.

Defining Disability

  • No universal definitions of disability exist in Canada.

  • Definitions of disability have significant implications as they shape policies, programs, and services.

  • Different government agencies define disability in various ways:

    • Definitions used in surveys (to determine prevalence rates) differ from those used for benefit redistribution (e.g., income tax credits).

Theorizing Disability

The Medical Model of Disability
  • Also known as the biomedical model, disease model, clinical model, or individual model.

  • Views disability strictly as an individual deficit, as inherently biological.

  • Pathology or deviance from normality is diagnosed by “experts” who control access to services.

  • Shortcomings of the medical model:

    • Disability is seen as a static, uniform pathological characteristic.

    • It objectifies individuals with disabilities.

    • Does not consider social or environmental factors contributing to disability.

The Social Model of Disability
  • Emerged as a critique of the medical model.

  • Views people with disabilities as an oppressed group, distinguishing impairment from disability:

    • Impairment: results from physical limitations.

    • Disability: arises from social oppression and exclusion.

  • Asserts that disability is constructed by social factors (economy, culture, language).

  • Shortcomings of the social model:

    • Risks overlooking individual differences.

    • Assumes all individuals with disabilities experience oppression uniformly.

    • Suggests a barrier-free world is an unrealistic goal.

The WHO’s International Classification of Functioning, Disability and Health
  • Defines disability as an umbrella term encompassing impairments, activity limitations, and participation restrictions.

  • Definitions:

    • Impairment: Problem in body function or structure.

    • Activity Limitation: Difficulty executing tasks or actions.

    • Participation Restriction: Problems with involvement in life situations.

  • Stresses that disability is not just a health issue but a complex phenomenon reflecting interaction between individual health and societal features.

Table 11.1: Applying the WHO’s International Classification

Health Condition

Impairment

Activity Limitation

Participation Restriction

Leprosy

Loss of sensation in extremities

Difficulties in grasping objects

Stigma leads to unemployment

Panic disorder

Anxiety

Not capable of going out alone

Diminished social relationships due to people's reactions

Spinal injury

Paralysis

Not able to use public transportation

Lack of accommodations leads to diminished participation in community

Juvenile diabetes

Pancreatic dysfunction

None (controlled by medication)

Stereotypes about disease restrict educational participation

Vitiligo

Facial disfigurement

None

Stigma results in limited social relations

Individual with mental health problem

None

None

Denied employment due to employer prejudice

Categorizing Disability

The Categorical or Diagnostic Approach
  • Focuses on identifying the causes and effects of deviations from normal bodily function.

  • Utilizes assessments and tests to classify these deviations (e.g., scans, tests, assessments).

  • Benefits:

    • Standardizes care across contexts.

    • Facilitates medical specialization and clinical research.

    • Allows tracking of public health statistics.

    • Aids community building among individuals with a shared diagnosis.

  • Challenges:

    • Risks blurring the differences between individuals with similar diagnoses.

    • Clinical studies may neglect rare disorders due to small sample sizes.

The Non-Categorical or Functional Approach
  • Emphasizes level of functioning over diagnostic labels to assess participation and outcomes.

  • Considers the interaction of impairments, activity limitations, and environmental factors.

  • Benefits:

    • Acknowledges the role of the environment in impairments.

    • Reduces stigma surrounding specific diagnoses.

    • Provides individualized areas for intervention based on daily life.

  • Challenges:

    • May complicate classification for medical research.

    • Could be time-intensive in practice, requiring a nuanced understanding of the individual's context.

Table 11.2: Types of Disabilities

Type

Category

Hearing

Sensory

Seeing

Sensory

Mobility

Physical

Flexibility

Physical

Dexterity

Physical

Pain

Physical

Learning

Cognitive

Cognitive

Cognitive

Mental health-related

Developmental

Memory

Mental health-related

Other/Unknown

Unknown

Prevalence of Disability in Canada

  • Canadian Survey on Disability (CSD):

    • Measures disability considering severity and frequency of activity limitations.

  • Statistics from 2017:

    • 22.3% of Canadians aged 15+ reported disabilities (total: 6.2 million).

    • Disability prevalence by gender:

    • 24.3% of women and 20.2% of men aged 15+.

    • Among people aged 65+:

    • 37.8% reported disabilities.

  • Most individuals reported family and friends as their primary source of assistance.

Table 11.3: Prevalence of Disability by Age in Canada

Age Groups

Total Population

Population with Disabilities

Total Disability Rate

15-24

4,155,440

546,410

13.1%

25-44

8,940,410

1,368,270

15.3%

45-64

9,695,840

2,359,650

24.3%

65 and over

5,217,160

1,972,310

37.8%

65-74

3,241,250

1,036,580

32.0%

75 and over

1,975,920

935,730

47.4%

History of Disability Policy in Canada

Early Beliefs about Individuals with Disabilities
  • Historical views of disabilities are shaped by societal norms.

  • Example: Ancient Greeks perceived physical impairments as divine punishment.

  • Initial care for individuals with impairments provided by religious entities.

  • Common practices involved housing individuals in prisons, workhouses, or almshouses if they appeared different.

  • In early 1800s Canada, there was no state support for individuals categorized as “lunatics” or “insane.”

Asylum, Confinement, and Institutionalization
  • The Provincial Lunatic Asylum opened in Toronto City Jail in 1841.

    • Commitment could occur through two routes:

    1. Designation by two physicians;

    2. Statement from a justice of peace.

  • Institutions served as a catch-all for any undesired population.

  • The rise of the eugenics movement in the early 1900s aimed to improve genetic stock.

    • Resulted in sterilization laws passed in Alberta and British Columbia.

Deinstitutionalization
  • In the 1970s-80s, changes in care and support practices emerged.

  • Patients transitioned from large institutions to hospitals, and then community living arrangements.

  • This move led to significant reductions in funding for individuals with disabilities.

  • Non-governmental organizations helped mitigate the impact of funding cuts.

  • The deinstitutionalization movement recognized the segregation of individuals as oppressive, advocating for better care within communities.

The Independent Living Movement and the Dignity of Risk
  • The Independent Living (IL) movement began in North America in the 1970s.

    • It posits that individuals with disabilities have the right to live in communities despite societal barriers.

  • Key components of IL philosophy include:

    • Individuals best know their own needs.

    • The need for integrated and community-based services.

    • Enhanced self-representation and self-determination through deprofessionalization of services. - Individualized support services including peer support and direct funding.

  • Normalization principle (Bengt Nirje): Access to life patterns similar to typical community conditions.

  • Social role valorization (Wolf Wolfensberger): Provides opportunities for dignity, respect, and participation through access to valued social roles.

Progress and Development of Disability Rights in Canada
  • 1961: Vocational Rehabilitation of Disabled Persons Act

  • 1965: The Canada Pension Plan

  • 1976: Council of Canadians with Disabilities

  • 1981: International Year of Disabled Persons

  • 1982: Canadian Charter of Rights and Freedoms

  • 1985: Canadian Human Rights Act

  • 1995: Employment Equity Act

  • 1998: In Unison Report

  • 2010: United Nations Convention on the Rights of Persons with Disabilities

Social Work Practice with Individuals with a Disability

Health and Social Services for Individuals with Disabilities
  • Federal and Provincial Resource Allocation:

    • Provinces and territories design their own health care plans with federal funding support.

    • Must include standardized features but may provide additional benefits.

  • Universality of Equivalent Care:

    • Specialized services often located in urban centres.

    • Jurisdictional disputes between federal and provincial bodies may delay service.

    • Long waiting lists can impede access to services.

  • Income Support:

    • Programs like Canada Pension Plan Disability Benefit require detailed applications.

    • Income support can include specialized housing assistance programs.

Specialized Services
  • Publicly-funded programs cater to specific populations (e.g., Ontario Autism Program)

  • May offer direct services or funding options for individuals.

Educational Services
  • Mainstreaming: Integrates students with disabilities into classrooms based on age, alongside support like aides and individualized education plans (IEPs).

  • Non-Governmental Organizations: Vary in scope and may receive government grants, often initiated by specific interest groups.

Promoting Access to Specialized Care: Health, Rehabilitative, and Social Services
  • Roles of social workers may include:

    • Administering intake and eligibility assessments.

    • Evaluating the individual's level of functioning and psychosocial needs.

    • Engaging in case management and care coordination.

Promoting Access to Educational Services, Employment, and Independent Living
  • Social workers can:

    • Collaborate in educational spaces to implement necessary modifications for students.

    • Support individuals in securing meaningful jobs and ongoing workforce participation through assistance programs.

    • Facilitate independence by involving individuals in critical decision-making and coordinating access to housing and transportation.

Supporting People with Disabilities in Rural or Remote Regions
  • As per 2016 Census data, only 17% of Canadians live in rural areas, affecting resource availability for individuals with disabilities.

  • Rural residents may face significant barriers in accessing care, education, and transportation.

  • Individualized funding models can be beneficial in rural contexts.

  • Social workers in these regions should leverage networking and communication technologies with urban peers for ongoing development.

Addressing Poverty: Access to Income Support
  • Individuals with disabilities face higher poverty rates compared to those without.

  • In 2012, median income for individuals with disabilities was significantly lower (approx. $10,000) than that of non-disabled peers.

  • Social workers may assist individuals and their families in applying for eligible income support programs and advocate for policy reforms.

Fostering Quality of Life
  • Quality of life is a multifaceted concept, including:

    • Interpersonal relations

    • Social inclusion

    • Personal development

    • Physical, material, and emotional well-being

    • Self-determination and rights

  • Social workers address oppression and marginalization, promoting life satisfaction and community participation.

Supporting the Transition to Adulthood
  • The transition to adulthood for youth with disabilities encompasses multiple factors (health care, education).

  • Institutional settings provide support for effective transitioning while addressing psychosocial goals.

  • Social workers assist youth in managing health care, honing independent living skills, and participating in community activities.

Addressing Caregiver Well-Being
  • Caregivers often endure:

    • Financial strain

    • Employment difficulties

    • Relationship stress

    • Emotional distress

  • Support strategies include:

    • Respite care

    • Counseling and therapy

Social Work Practice Guidelines
  • Recognize interaction between impairments and environments.

  • Challenge ableism and stereotypes related to disability.

  • Foster partnerships with individuals and their families.

  • Consider the individual’s entire life course in practice.