Bibliography on Disability and Mothering
Compiled by Cynthia Lewiecki-Wilson
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Amundson, Ron. “Against Normal Function.” Studies in History and Philosophy of Biological and Biomedical Sciences 31.C (2000): 33-53. Print.
---. “Disability, Ideology, and Quality of Life: A Bias in Biomedical Ethics.” Quality of Life and Human Difference. Ed. David Wasserman, Robert Wachbroit, and Jerome Bickenbach. Cambridge: Cambridge UP, 2005. 101-24. Print.
Asch, Adrienne. “Disability, Bioethics, and Human Rights.” Albrecht, Seelman, and Bury 297-326. Print.
---. “Prenatal Diagnosis and Selective Abortion: A Challenge to Practice and Policy.” American Journal of Public Health 89.11 (1999): 1649-57. Print.
---. “Why I Haven’t Changed My Mind about Prenatal Diagnosis: Reflections and Refinements.” Parens and Asch 234-60. Print.
Asperger, Hans. “‘Autistic Psychopathy’ in Childhood.” Autism and Asperger Syndrome. Ed. Uta Frith. New York: Cambridge UP, 1991. 37-92. Print.
Aston, Maxine. Aspergers in Love: Couple Relationships and Family Affairs. London: Jessica Kingsley, 2003. Print.
Atkinson, Dorothy. “Research and Empowerment: Involving People with Learning Difficulties in Oral and Life History Research.” Disability and Society 19.7 (2004): 691-702. Print.
Atkinson, Dorothy, et al. Good Times, Bad Times: Women with Learning Difficulties Telling Their Stories. Kidderminster, UK: BILD, 2000. Print.
Atkinson, Dorothy, et al. Witnesses to Change: Families, Learning Difficulties and History.” Kidderminster, UK: BILD, 2005. Print.
Atkinson, Dorothy, and Jan Walmsley. “Using Autobiographical Approaches with People with Learning Difficulties.” Disability and Society 14.2 (1999): 203-16. Print.
Atkinson, Dorothy, Mark Jackson, and Jan Walmsley. Research and Empowerment: Involving People with Learning Difficulties in Oral and Life History Research. Kidderminster, UK: BILD, 1997. Print.
Autism Diva. “Conferences, Culture, Communication, Ages, Aegis and Diagnosis.” Autism Diva. Mar. 2005. Web. 30 Aug. 2008.
Barker, Linda T., and Vida Maralani. Challenges and Strategies of Disabled Parents: Findings from a National Survey of Parents with Disabilities. Berkeley: Through the Looking Glass, 1997. Print.
Barnes, Colin, and Geoff Mercer. Disability. Cambridge: Polity, 2003. Print.
Bérubé, Michael. Life as We Know It: A Father, A Family, and an Exceptional Child. NY: Pantheon, 1996. Print.
Biklen, Douglas, et al. Autism and the Myth of the Person Alone. New York: New York UP, 2005. Print.
Birke, Lynda. Feminism and the Biological Body. New Brunswick: Rutgers UP, 2000. Print.
Bogdan, Robert, and Steven Taylor. Inside Out: The Social Meaning of Retardation. Toronto: U Toronto P, 1982. Print.
---. “The Judged, Not the Judges: An Insider’s View of Mental Retardation.” American Psychologist 31 (1976): 47-52. Print.
Boorse, Christopher. “Health as a Theoretical Concept.” Philosophy of Science 44 (1977): 542–73. Print.
Boston Women’s Health Course Collective. The New Our Bodies, Ourselves: A Book By and For Women. New York: Simon, 1992. Print.
Bould, Sally. “Familial Caretaking: A Middle-Range Definition of Family in the Context of Social Policy.” Journal of Family Issues 14.1 (1993): 133-51. Print.
Bowman, James E. “Genetic Screening and Public Policy.” Phylon 38.2 (1977): 117-42. Print.
Boyd, Susan. From Witches to Crack Moms: Women, Drug Law, and Policy. Durham: Carolina Academic P, 2004. Print.
Brady, Wilfrid. “The Mental Health Act.” Australian Children Limited 1 (1962): 345. Print.
Breggin, Peter. Toxic Psychiatry. New York: St. Martin’s, 1993. Print.
Brigham, Lindsay, et al. Crossing Boundaries: Change and Continuity in the History of Learning Disability. Kidderminster, UK: BILD, 2000. Print.
Browner, Carole H., and Nancy Ann Press. “The Normalization of Prenatal Diagnostic Screening.” Conceiving the New World Order: The Global Politics of Reproduction. Ed. Ruth Ginsberg and Rayna Rapp. Berkeley: U California P, 1995. Print.
Brownworth, Victoria A. “Introduction.” Restricted Access: Lesbians on Disability. xi-xxii. Print.
Brownworth, Victoria A., and Susan Raffo, eds. Restricted Access: Lesbians on Disability. Seattle: Seal P, 1999. Print.
Brueggemann, Brenda Jo. Lend Me Your Ear: Rhetorical Constructions of Deafness. Washington: Gallaudet UP, 1999. Print.
Bryan, Alison, Teresa Blankmeyer-Burke, and Steven Emery. Human Fertilisation and Embryology Bill: Genetic Selection and the Deaf Community. Slideshare, 2006. Web. 2008.
Buchanan, Allen, et al. From Chance to Choice: Genetics and Justice. Cambridge: Cambridge UP, 2000. Print.
Cassiman, Shawn A. Everyday Resistance among Poor Disabled Single Mothers. Diss. U Wisconsin, 2008. Ann Arbor: UMI, 2008. Print.
Chamberlin, Judi. “The Ex-Patients’ Movement: Where We’ve Been and Where We’re Going.” Journal of Mind and Behavior 11.3-4 (1990): 323-36. Print.
Charo, R. Alta, and Karen H. Rothenberg. “‘The Good Mother’: The Limits of Reproductive Accountability and Genetic Choice.” Women and Prenatal Testing: Facing the Challenges of Genetic Technology. Ed. Karen H. Rothenberg and Elizabeth J. Thomson. Columbus: Ohio State UP, 1994. 105-30. Print.
Cho, Mike, Mike Cohen, and Seetla Sistla. “What is a ‘Normal’ Phenotype?” Bioethics for Developmental Biologists. Ed. Scott F. Gilbert and Emily Zackin. Sunderland, MA: Sinauer, 2006. Web. Aug. 2004.
Clare, Eli. Exile and Pride: Disability, Queerness, and Liberation. Cambridge, MA: South End P, 1999. Print.
Cocks, Errol, et al, eds. Under Blue Skies: The Social Construction of Intellectual Disability in Western Australia. Perth: Centre for Disability Research and Development, Faculty of Health and Human Sciences, Edith Cowan U, 1996. Print.
Coleborne, Catharine, and Dolly MacKinnon, eds. Madness in Australia: Histories, Heritage and the Asylum. St Lucia, QLD: U Queensland P, 2003. Print.
“Couple ‘Choose’ to have Deaf Baby.” BBC News. BBC News, 8 Apr. 2002. Web. 25 Aug. 2008.
Corker, Mairian, and Tom Shakespeare, eds. Disability/Postmodernity: Embodying Disability Theory. London: Continuum, 2002. Print.
Couser, G. Thomas. “From Conflicting Paradigms: The Rhetorics of Disability Memoir.” Lewiecki-Wilson and Brueggemann 190-97. Print.
---. Recovering Bodies: Illness, Disability, and Life Writing. Madison: U Wisconsin P, 1997. Print.
Davis, Lennard J., ed. The Disability Studies Reader. 2nd ed. New York: Routledge, 2006. Print.
Davis, Lennard J. “The End of Identity Politics and the Beginning of Dismodernism: On Disability as an Unstable Category.” Lennard Davis 231-42. Print.
Davis, N. Ann. “Invisible Disability.” Ethics 116 (2005): 153-213. Print.
Dax, Eric. Asylum to Community: The Development of the Mental Hygiene Service in Victoria, Australia. Melbourne: F.W. Cheshire, 1961. Print.
Dekker, Martijn. “On Our Own Terms: Emerging Autistic Culture.” Autistic Culture, 2006. Web. 30 Aug. 2008.
Deleuze, Giles. Pure Immanence: Essays on a Life. Trans. A. Boyman. New York: Zone Books, 2005. Print.
Disabled Peoples’ International Europe. “Disabled People Speak on the New Genetics.” DPI Europe Position Statement on Bioethics and Human Rights. 2000. Web. 2008.
Dolmage, Jay, and Cynthia Lewiecki-Wilson. “Refiguring Rhetorica: Linking Feminist Rhetoric and Disability Studies.” Rhetorica in Motion: Researching Feminist Rhetorical Methods and Methodologies. Eds. Eileen Schell and Kelly Rawson. Pittsburgh: Pittsburgh UP, forthcoming. Print.
Dowling, Monica, and Linda Dolan. “Families with Children with Disabilities—Inequalities and the Social Model.” Disability and Society 6.1 (2001): 21-35. Print.
Dragonas, Thalia. “Whose Fault Is It? Shame and Guilt for the Genetic Defect.” Ed. Elizabeth Ettorre. Before Birth: Understanding Prenatal Screening. Aldershot, Eng.: Ashgate, 2001. Print.
Dubowitz, Victor. “Disorders of the Lower Motor Neuron: The Spinal Muscular Atrophies.” Muscle Disorders in Childhood. 2nd ed. London: Saunders, 1995. Print.
Duden, Barbara. Disembodying Women: Perspectives on Pregnancy and the Unborn. Cambridge: Harvard U, 1993. Print.
Edwards, Steven D. “Disability, Identity and the ‘Expressivist Objection”’ Journal of Medical Ethics 30 (2004): 418-20. Print.
Elman, Julie Passanante. “Medicalizing Edutainment: Enforcing Disability in the Teen Body,
1970-2000.” Diss. George Washington U, 2008. Print.
Estabrook, Arthur H. The Jukes in 1915. Carnegie Institution of Washington. 1916. Disability History Museum. Web. 2009.
Etchegary, Holly, et al. “The Influence of Experiential Knowledge on Prenatal Screening and Testing Decisions.” Genetic Testing 12.1 (2008): 115-24. Print.
Ewald, François. “Insurance and Risk.” Burchell, Gordon, and Miller 197-210. Print.
Fausto-Sterling, Anne. “The Bare Bones of Sex: Part 1—Sex and Gender.” Signs: Journal of Women in Culture and Society 30. 2 (2005): 1491-1527. Print.
---. Sexing the Body: Gender Politics and the Construction of Sexuality. New York: Basic Books, 2000. Print.
Ferguson, Philip M. “Mapping the Family: Disability Studies and the Exploration of Parental Responses to Disability.” Albrecht, Seelman, and Bury 373-95. Print.
Fineman, Martha Albertson. The Autonomy Myth: A Theory of Dependency. New York: New Press, 2004. Print.
Finger, Anne. Past Due: A Story of Disability, Pregnancy and Birth. Berkeley: Seal Press, 1990. Print.
Fletcher, Agnes. “Making it Better? Disability and Genetic Choice” Designer Babies: Where Do We Draw the Line? London: Hodder and Stoughton, 2002. Print.
Foucault, Michel. Abnormal: Lectures at the College de France, 1974-1975. Trans.
Graham Burchell. New York: Picador, 1999. Print.
---. “The Birth of Biopolitics.” Michel Foucault: Ethics, Subjectivity and Truth. Ed. Paul Rabinow. New York: New Press, 2003. Print.
---. Discipline and Punish. Trans. Alan Sheridan. New York: Vintage, 1977. Print.
---. Ethics: Subjectivity and Truth (Essential Works of Foucault, 1954-1984, Vol. 1). Trans. and Ed. Paul Rabinow. New York: New Press, 2006. Print.
---. The History of Sexuality. Volume 1. An Introduction. 1978. Trans. Robert Hurley. New York: Random House, 1983. Print.
---. “Society must be defended.” Lectures at Collège de France, 1975–1976. Ed. Mauro Bertani and Alessandro Fontana. Trans. David Macey. New York: Picador, 2003. Print.
---. “The Subject and Power.” Michel Foucault: Beyond Structuralism and Hermeneutics. Ed. Hubert Dreyfus and Paul Rabinow. Chicago: U Chicago P, 1997. Print.
Frank, Arthur. The Wounded Storyteller: Body, Illness, and Ethics Chicago: U Chicago P, 1995. Print.
Fraser, Nancy, and Linda Gordon. “A Genealogy of Dependency: Tracing a Keyword of the U.S. Welfare State.” Signs 19.2 (1994): 309-36. Print.
Garland-Thomson, Rosemarie. Extraordinary Bodies: Figuring Physical Disability in American Culture and Literature. New York: Columbia UP, 1997. Print.
---. “Integrating Disability, Transforming Feminist Theory.” Lennard Davis 257-73. Print.
Garrison, Michelle M., et al. “Mental Illness Hospitalizations of Youth in Washington State.” Archives of Pediatrics and Adolescent Medicine 158.8 (2004): 781-85. Print.
Gentner, Dedre, and Michael Jeziorski. “The Shift from Metaphor to Analogy in Western Science.” Metaphor and Thought. 2nd ed. Andrew Ortony, ed. Cambridge: Cambridge UP, 1979. 447-80. Print.
“Gene Testing.” Human Genome Project Information. Human Genome Project Information, n.d. Web. May 2008.
Gignac, Monique A.M., and Cheryl Cott. “A Conceptual Model of Independence and Dependence for Adults with Chronic Physical Illness and Disability.” Social Science and Medicine 47.6 (1998): 739-53. Print.
Goddard, Henry. The Kallikak Family: A Study of the Heredity of Feeble-mindedness. 1912. New York: Macmillian. 1925. Print.
Godwin, Louise, and Catherine Wade. Kew Cottages Parents’ Association: The First Fifty Years. Melbourne: Kew Cottages Parents’ Association, 2007. Print.
Goffman, Erving. Stigma: Notes on the Management of Spoiled Identity. New York: Simon, 1986. Print.
Goggin, Gerard, and Christopher Newell. Disability in Australia: Exposing a Social Apartheid. Sydney: U New South Wales P, 2005. Print.
Goode, David. A World Without Words: The Social Construction of Children Born Deaf and Blind. Philadephia: Temple UP, 1994. Print.
Gordon, Linda. Women, the State, and Welfare. Madison: U Wisconsin P, 1990. Print.
Gordon, Meg, Linda Rosenman, and Monica Cuskelly. “Constrained Labour: Maternal Employment When Children Have Disabilities.” Journal of Applied Research in Intellectual Disabilities 20.3 (2007): 236-46. Print.
Gottlieb, Eli. The Boy Who Went Away. New York: St. Martin’s, 1997. Print.
Graves, Heather Brodie. “Marbles, Dimples, Rubber Sheets, and Quantum Wells: The Role of Analogy in the Rhetoric of Science.” Rhetoric Society Quarterly 28.1 (1998): 25-48. Print.
Green, Sara Eleanor. “We’re Tired, Not Sad”: Benefits and Burdens of Mothering a Child with Disability.” Social Science and Medicine 64.1 (2007): 150-63. Print.
Greenspan, Stanley I., and Serena Wieder. Engaging Autism: Using the Floortime Approach to Help Children Relate, Communicate and Think. Cambridge: Da Capo Press, 2006. Print.
Groce, Nora Ellen, and Jonathan Marks. “The Great Ape Project and Disability Rights: Ominous Undercurrents of Eugenics in Actions.” American Anthropologist 102.4 (December 2000): 818-22. Print.
Gross, Alan. The Rhetoric of Science. Cambridge: Harvard UP, 1990. Print.
Grover, Chris, and Linda Piggott. “Disabled People, the Reserve Army of Labour and Welfare Reform.” Disability and Society 20 (2005): 705-17. Print.
Hacking, Ian. “How Should We Do the History of Statistics?” Burchell, Gordon, and Miller 181-96. Print.
---. The Social Construction of What? Cambridge: Harvard UP, 1991. Print.
Haddon, Mark. The Curious Incident of the Dog in the Night-Time. New York: Doubleday, 2003.
Hallowell, Nina. “Doing the Right Thing: Genetic Risk and Responsibility.” Sociology of Health and Illness 21.5 (1999): 597-621. Print.
Haraway, Donna. Modest₋Witness@Second₋Millennium.FemaleMan₋Meets₋OncoMouse: Feminism and Technoscience. New York: Routledge, 1997. Print.
---. Primate Visions: Gender, Race, and Nature in the World of Modern Science. 1990. New York: Routledge, 1999. Print.
Hayles, N. Katherine. How We Became Posthuman: Virtual Bodies in Cybernetics, Literature, and Informatics. Chicago: U of Chicago P, 1999. Print.
Hayward, Anna. “‘Alien’ Parenting: Experiences of a Mother with Asperger’s Syndrome.” Disability Pregnancy and Parenthood International 34 (Apr 2001): 3-5. Print.
Hirsch, Sherry, et al., eds. Madness Network News Reader. San Francisco: Glide, 1974. Print.
Hollander, Joanne. “Resisting Vulnerability: The Social Reconstruction of Gender in Interaction.” Social Forces 49 (2002): 474-96. Print.
Holmes, Steven. “Radio Talk About TV Anchor’s Disability Stirs Ire in Los Angeles.” New York Times. New York Times, 23 Aug. 1991. Web. 25 Aug. 2008.
Hoopmann, Kathy. All Cats Have Asperger Syndrome. London: Jessica Kingsley, 2006. Print.
Howlin, Patricia, Simon Baron-Cohen, and Julie Hadwin. Teaching Children with Autism to Mind-Read: A Practical Guide for Teachers and Parents. Chichester, UK: Wiley, 1999. Print.
Hubbard, Ruth. “Abortion and Disability: Who Should and Who Should Not Inhabit the World.” Lennard Davis 93-103. Print.
Huet, Marie-Helene. Monstrous Imagination. Cambridge: Harvard UP, 1993. Print.
Hughes, Bill, and Kevin Paterson. “The Social Model of Disability and the Disappearing Body: Towards a Sociology of Impairment.” Disability and Society 12 (1997): 325–40. Print.
Jacobson, Denise Sherer. The Question of David: A Disabled Mother’s Journey Through Adoption, Family, and Life. Berkeley: Creative Arts, 1999. Print.
Johnson, Kelley, and Rannveig Traustadóttir, eds. Deinstitutionalization and People with Intellectual Disabilities: In and Out of Institutions. London: Jessica Kingsley, 2005. Print.
Jones, Maxwell. The Therapeutic Community: A New Treatment Method in Psychiatry. New York: Basic, 1953. Print.
Judge, Cliff, and Fran van Brummelen. Kew Cottages: The World of Dolly Stainer. Melbourne: Spectrum, 2002. Print.
Kallianes, Virginia, and Phyllis Rubenfeld. “Disabled Women and Reproductive Rights.” Disability and Society 12.2 (1997): 203-21. Print.
Kanner, Leo. “Autistic Disturbances of Affective Contact.” Nervous Child 2 (1943): 217-50. Rpt. in Classic Readings in Autism. Ed. Anne M. Donnellan. New York: Teacher’s College, 1985. 11-52. Print.
Kenen, Regina. “The Human Genome Project: Creator of the Potentially Sick, Potentially
Vulnerable and Potentially Stigmatized?” Ed. Ian Robinson. Life and Death under High Technology Medicine. Manchester, UK: Manchester UP, 1994. Print.
Kent, Deborah. “Somewhere a Mockingbird.” Parens and Asch 57-63. Print.
King. Deborah K. “Multiple Jeopardy, Multiple Consciousness: The Context of a Black Feminist Ideology.” Signs 14.1 (1988): 42-72. Print.
Kittay, Eva Feder. Love’s Labor: Essays on Women, Equality and Dependency. New York: Routledge, 1999. Print.
Kleege, Georgiana. Sight Unseen. New Haven: Yale UP, 1999. Print.
Knipfel, Jim. Slackjaw: A Memoir. New York: Berkeley Books, 1999. Print.
Kudlich, Catherine. “Modernity’s Miss-Fits: Blind Girls and Marriage in France and America, 1820-1920.” Women on Their Own: Interdisciplinary Perspectives on Being Single. Ed. Rudolph M. Bell and Virginia Yans. 201-218. Print.
Kuusisto, Stephen. Planet of the Blind: A Memoir. New York: Delta, 1998. Print.
Lacom, Cindy. “Revising the Subject: Disability as ‘Third Dimension’ in Clear Light of Day and You Have Come Back.” NWSA Journal 14.3 (2002): 138-54. Print.
Landsman, Gail. “Does God Give Special Kids to Special Parents? Personhood and the Child with Disabilities as Gift and as Giver.” Layne 133-165. Print.
---. “Reconstructing Motherhood in the Age of Perfect Babies.” Signs 24.1 (1998): 69-99. Print.
Leiter, Valerie, et al. “The Consequences of Caring: Impacts of Mothering a Child with Special Needs.” Journal of Family Issues 25.3 (2004): 379-403. Print.
Lewiecki-Wilson, Cynthia, and Brenda Jo Brueggemann, eds. Disability and the Teaching of Writing: A Critical Sourcebook. Boston: Bedford/St. Martin’s, 2008. Print.
Lewis, Suzan, Carolyn Kagan, and Patricia Heaton. “Dual-earner Parents with Disabled Children: Family Patterns for Working and Caring. Journal of Family Issues 21 (2000): 1031-60. Print.
Lewis, Bradley. “A Mad Fight: Psychiatry and Disability Activism.” Lennard Davis 339-52. Print.
Linton, Simi. Claiming Disability: Knowledge and Identity. New York: New York UP, 1998. Print.
---. “From Reassigning Meaning.” Lewiecki-Wilson and Brueggemann. 174-81. Print.
Lippman, Abby. “Prenatal Testing and Screening: Constructing Needs and Reinforcing Inequities. American Journal of Law and Medicine 17.1-2 (1991): 15–50. Print.
Little, Joseph. “Analogy in Science: Where Do We Go from Here?” Rhetoric Society Quarterly 30.1 (2000): 69-92. Print.
Lloyd, Arthur. Payment by Results: Kew Cottages First 100 Years 1887-1987. Melbourne: Kew Cottages and St. Nicholas Parents’ Association, 1987. Print.
Lockhart, Charles. Gaining Ground: Tailoring Social Programs to American Values. Berkeley: U of California P, 1989. Print.
Longmore, Paul, and Lauri Umanski, eds. The New Disability History: American Perspectives. New York: New York UP, 2001. Print.
Lorde, Audre. “Breast Cancer: Power Versus Prosthesis.” Tuana and Tong 420-429. Print.
Magaña, Sandra, Susan L. Parish, and Shawn A. Cassiman. “Policy Lessons from Low-income Mothers with Disabilities. Journal of Women Politics and Policy 29 (2008): 181-206. Print.
Mairs, Nancy. Ordinary Time: Cycles in Marriage, Faith, and Renewal. Boston: Beacon, 1993. Print.
---. “Sex and Death and the Crippled Body: A Meditation.” Disability Studies: Enabling the Humanities. Eds. Sharon Synder, Brenda Jo Brueggemann, and Rosemarie Garland-Thompson. New York: MLA, 2002. 156-70. Print.
---. Waist-High in the World: A Life Among the Non-Disabled. Boston: Beacon P, 1996.
Manning, Corinne. Bye-Bye Charlie: Stories from the Vanishing World of Kew Cottages. Sydney, Australia: U of New South Wales P, 2008. Print.
Marcus, Neil. Storm Reading. Adapted for the stage by Rod Lathim, Neil Marcus, and Roger Marcus. Storm Reading Video Production, 1996. Print.
Martin, Teran, and Paul S. Davies. “Changes in the Economic and Demographic Characteristics of SSI and DI Beneficiaries between 1984-1999.” Social Security Bulletin 65.2 (2004). Web. 2009.
Mayes, Susan Dickerson, Susan L. Calhoun, and Dana L. Crites. “Does DSM-IV Asperger’s Disorder Exist?” Journal of Abnormal Child Psychology 29.3 (2001): 263-271. SpringerLink, Web. 2009.
McKeever, Patricia, and Karen-Lee Miller. “Mothering Children Who Have Disabilities: A Bourdieusian Interpretation of Maternal Practices.” Social Science and Medicine 59.6 (2004): 1177-91. Print.
McRuer, Robert. Crip Theory: Cultural Signs of Queerness and Disability. New York: New York UP, 2006. Print.
Michalko, Rod. The Difference that Disability Makes. Philadelphia: Temple UP, 2002. Print.
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Mintz, Susannah B. Unruly Bodies: Life Writing by Women with Disabilities. Chapel Hill: U North Carolina P, 2007. Print.
Montgomery, Cal. “Critic of the Dawn.” Ragged Edge Online. Ragged Edge Online, 2001. Web. 2008.
Moraga, Cherríe. Heroes and Saints and Other Plays. Albuquerque: West End P, 1994. Print.
---. The Hungry Woman and Heart of the Earth. Albuquerque: West End P, 2001. Print.
---. The Last Generation: Prose and Poetry. Boston: South End, 1993. Print.
---. Loving in the War Years: lo que nunca pasó por sus labios. 1983. Boston: South End P, 2001. Print.
---. Waiting in the Wings: Portrait of a Queer Motherhood. Ithaca: Firebrand, 1997. Print.
---. Watsonville: Some Place Not Here/ Circle in the Dirt: el pueblo de East Palo Alto. Albuquerque: West End P, 2002. Print.
---. “A Xicanadyke Codex of Changing Consciousness.” Sing, Whisper, Shout, Pray! Feminist Visions for a Just World. Eds. M. Jacqui Alexander, et al. Canada: Edgework, 2003. 91-102. Print.
Morgan, Kathryn. “Contested Bodies, Contested Knowledges: Women, Health, and the Politics of Medicalization.” Sherwin 83-121. Print.
Morris, David B. “Narrative, Ethics, and Pain: Thinking With Stories.” Narrative 9.1 (2001): 55-77. Print.
Morris, Jenny. Encounters with Strangers: Feminism and Disability. London: Women’s Press, 1996. Print.
---. Pride Against Prejudice: Transforming Attitudes to Disability. London: Women’s Press, 1991. Print.
Nelson, Hilde Lindemann, ed. Stories and Their Limits: Narrative Approaches to Ethics. New York: Routledge, 1997. Print.
Novas, Carlos, and Nikolas Rose. “Genetic Risk and the Birth of the Somatic Individual.” Economy and Society 29.4 (2000): 485–513. Print.
O’Brien, Ruth. Bodies in Revolt: Gender, Disability, and a Workplace Ethic of Care. New York: Routledge, 2005. Print.
Okin, Susan Moller. Justice, Gender, and the Family. New York: Basic, 1989. Print.
Oliver, Michael. The Politics of Disablement. London: Macmillan, 1990. Print.
---. Understanding Disability: From Theory to Practice. London: Macmillan, 1996. Print.
Olkin, Rhoda. What Psychotherapists Should Know about Disability. New York: Guilford, 1999. Print.
O’Neill, Jasmine. Through the Eyes of Aliens: A Book about Autistic People. London: Jessica Kingsley, 1999. Print.
Padden, Carol. “From the Cultural to the Bi-cultural: The Modern Deaf Community.” Parasini 79-98. Print.
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Parens, Erik, and Adrienne Asch, eds. Prenatal Testing and Disability Rights. Washington: Georgetown UP, 2000. Print.
Parish, Susan L., Sandra Magaña, and Shawn A. Cassiman. “It's Just That Much Harder: Multi-Layered Hardship Experiences of Low-Income Mothers with Disabilities.” Affilia 23 (2008): 51-65. Print.
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Pokempner, Jennifer, and Dorothy. E Roberts. “Poverty, Welfare Reform, and the Meaning of Disability.” Ohio State Law Journal 62 (2001): 425-64. Print.
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Price, Margaret. The Rhetoric of Madness: Psychosocial Disability and Academic Discourse. U of Michigan P, forthcoming. Print.
Price, Janet and Margrit Shildrick. “Bodies Together: Touch, Ethics, and Disability.” Corker and Shakespeare 62-75. Print.
Priestley, Mark, ed. Disability and the Life-course: Global Perspectives. Cambridge, UK: Cambridge UP, 2001. Print.
Prince-Hughes, Dawn. Songs of the Gorilla Nation: My Journey Through Autism. New York: Three Rivers, 2004. Print.
Purdy, Laura. “Reproductive Risk: Can Having Children Be Immoral?” Reproducing Persons: Issues in Feminist Bioethics. Ithaca: Cornell UP, 1996. Print.
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Rapley, Mark. The Social Construction of Intellectual Disability. Cambridge: Cambridge UP, 2004. Print.
Rapp, Rayna. “Chromosomes and Communication: The Discourse of Genetic Counseling.” Medical Anthropology Quarterly 2.2 (1988): 143-57. Print.
---. “Refusing Prenatal Diagnosis: The Meanings of Bioscience in a Multicultural World.” Anthropological Approaches in Science and Technology Studies, Special Issue: Science, Technology, and Human Values. 23.1 (1998): 45-70. Print.
---. “Risky Business: Genetic Counseling in a Shifting World.” Schneider and Rapp 175-89. Print.
---. Testing Women, Testing the Fetus: The Social Impact of Amniocentesis in America. New
York: Routledge, 1999. Print.
Rapp, Rayna, and Faye Ginsburg. “Enabling Disability: Rewriting Kinship, Reimagining Citizenship.” Public Culture 13.3 (2001): 533-56. Print.
Read, Janet. Disability, the Family and Society: Listening to Mothers. Buckingham,UK: Open UP, 2000. Print.
Rivera y Carlo, Roberto. “Targeting the Disabled.” Boundless Webzine. Boundless, 2002. Web. May 2003.
Roberts, Dorothy. Shattered Bonds: The Color of Child Welfare. New York: Basic, 2002. Print.
Rodas, Julia Miele. The Satellite Syndrome: Disability in Victorian Literature and Culture. Diss. The Graduate Center of the City University of New York, 2003. Print.
---. “Misappropriations: Hugh Stuart Boyd and the Blindness of Elizabeth Barrett/Browning.” Victorian Review 33.2 (2007): 103-18. Print.
---. “Tiny Tim, Blind Bertha, and the Resistance of Miss Mowcher: Charles Dickens and the Uses of Disability.” Dickens Studies Annual 34 (2004): 51-97. Print.
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