The Psychological and Social Impact of Chronic Illness and Disability, 8th Edition
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Copyright Dedication Contributors Foreword Preface Acknowledgments Springer Publishing Resources I: Historical and Cultural Perspectives on Illness and Disability Chapter 1: History of Treatment Toward Persons With Disabilities in America and Abroad Chapter 2: Societal Attitudes and Myths About Disability: Improving the Social Consciousness Chapter 3: History of Treatment Toward Persons With Psychiatric Disabilities Chapter 4: Disability Identity and Disability Culture Chapter 5: Recognizing, Understanding, and Constructively Responding to Ableism Chapter 6: The Evolution of Laws and Policies in the United States and Their Impact on Disabled People
II: The Personal Impact of Disability Chapter 7: Psychosocial Adaptation to Chronic Illness and Disability: A Primer for Counselors Chapter 8: Theories of Adjustment and Adaptation to Disability Chapter 9: Vulnerabilities, Abuse, and Psychosocial Disparities of Women With Disabilities Chapter 10: Sexuality and Disability Chapter 11: Ableist Microaggressions Chapter 12: Quality of Life and Psychosocial Adaptation to Chronic Illness and Disability
III: Family Issues in Illness and Disability Chapter 13: Family Adaptation Across Cultures Toward Loved Ones With Disability Chapter 14: Giving Parents a Voice: Challenges Experienced by Parents of Children with Disabilities Chapter 15: Psychosocial Counseling Aspects of Grief, Dying, and Death Chapter 16: Psychosocial Issues for Family Caregivers
IV: Specific Trauma and Stigmatized Populations Chapter 17: Living With Substance use Disorder: From Stigma to Recovery Chapter 18: Culturally Competent Service Provision: Considerations for Supporting Veterans and Family Reintegration Chapter 19: Responding Well to Individuals Experiencing Abuse and Relationship Violence Chapter 20: Immigrants, Refugees, and Asylum Seekers: The Psychosocial Cost of War on Civilians Chapter 21: Key Concepts and Techniques for an Aging Population of Persons with Disabilities
V: New Directions, Issues, and Perspectives Chapter 22: Interventions to Improve the Well-Being of People with Disabilities and Chronic Illness Chapter 23: Users of Assistive Technology: The Human Component Chapter 24: Religion and Disability Chapter 25: Social Justice, Oppression, and Disability Counseling Chapter 26: The Impact of Social Media Influence on Mental Health Chapter 27: Reflections and Considerations
VI: Personal Perspectives My Experience as a Deaf Woman Fires Are not Drills My Story of Becoming Blind Multiple Sclerosis: Not Just Surviving but Thriving Chris and His Mother: Hope and Home Karen—My Daughter Forever Living in Spite of Multiple Sclerosis Surviving Amyotrophic Lateral Sclerosis: A Daughter’s Perspective My Life With a Disability: Continued Opportunities Experiencing Sexuality as an Adolescent With Rheumatoid Arthritis My Life With Muscular Dystrophy: Lessons and Opportunities Life Lessons Taught to Me by My Disability
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Chapter 9: Vulnerabilities, Abuse, and Psychosocial Disparities of Women With Disabilities
Copyright Dedication Contributors Foreword Preface Acknowledgments Springer Publishing Resources I: Historical and Cultural Perspectives on Illness and Disability Chapter 1: History of Treatment Toward Persons With Disabilities in America and Abroad Chapter 2: Societal Attitudes and Myths About Disability: Improving the Social Consciousness Chapter 3: History of Treatment Toward Persons With Psychiatric Disabilities Chapter 4: Disability Identity and Disability Culture Chapter 5: Recognizing, Understanding, and Constructively Responding to Ableism Chapter 6: The Evolution of Laws and Policies in the United States and Their Impact on Disabled People
II: The Personal Impact of Disability Chapter 7: Psychosocial Adaptation to Chronic Illness and Disability: A Primer for Counselors Chapter 8: Theories of Adjustment and Adaptation to Disability Chapter 9: Vulnerabilities, Abuse, and Psychosocial Disparities of Women With Disabilities Chapter 10: Sexuality and Disability Chapter 11: Ableist Microaggressions Chapter 12: Quality of Life and Psychosocial Adaptation to Chronic Illness and Disability
III: Family Issues in Illness and Disability Chapter 13: Family Adaptation Across Cultures Toward Loved Ones With Disability Chapter 14: Giving Parents a Voice: Challenges Experienced by Parents of Children with Disabilities Chapter 15: Psychosocial Counseling Aspects of Grief, Dying, and Death Chapter 16: Psychosocial Issues for Family Caregivers
IV: Specific Trauma and Stigmatized Populations Chapter 17: Living With Substance use Disorder: From Stigma to Recovery Chapter 18: Culturally Competent Service Provision: Considerations for Supporting Veterans and Family Reintegration Chapter 19: Responding Well to Individuals Experiencing Abuse and Relationship Violence Chapter 20: Immigrants, Refugees, and Asylum Seekers: The Psychosocial Cost of War on Civilians Chapter 21: Key Concepts and Techniques for an Aging Population of Persons with Disabilities
V: New Directions, Issues, and Perspectives Chapter 22: Interventions to Improve the Well-Being of People with Disabilities and Chronic Illness Chapter 23: Users of Assistive Technology: The Human Component Chapter 24: Religion and Disability Chapter 25: Social Justice, Oppression, and Disability Counseling Chapter 26: The Impact of Social Media Influence on Mental Health Chapter 27: Reflections and Considerations
VI: Personal Perspectives My Experience as a Deaf Woman Fires Are not Drills My Story of Becoming Blind Multiple Sclerosis: Not Just Surviving but Thriving Chris and His Mother: Hope and Home Karen—My Daughter Forever Living in Spite of Multiple Sclerosis Surviving Amyotrophic Lateral Sclerosis: A Daughter’s Perspective My Life With a Disability: Continued Opportunities Experiencing Sexuality as an Adolescent With Rheumatoid Arthritis My Life With Muscular Dystrophy: Lessons and Opportunities Life Lessons Taught to Me by My Disability
DOI:
10.1891/9780826151117.0009
Authors
- Harley, Debra A.
- Jordan, Carol E.
Abstract
The purpose of this chapter is to discuss issues of abuse, vulnerabilities, and intimate partner violence (