Narratives Published on the Internet by Parents of Children With Autism: What Do They Reveal and Why Is It Important?

Focus on Autism and Other Developmental Disabilities

Volumn 19, Issue 1, 2004, Pages 35-43

  Fleischmann, Amos ^a  

^a ACHVA ACADEMIC COLLEGE   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84993790937     PISSN: 10883576     EISSN: None     Source Type: Journal    
DOI: 10.1177/10883576040190010501     Document Type: Article

References (29)

1. Boyce, G., Behl, D., Mortensen, L., & Akers, J. (1991). Child characteristics, family demographics and family processes: Their effects on the stress experienced by families of children with disabilities. Counseling Psychology Quarterly, 4, 273—288.
2. Bruner, J.S. (1990). Acts of meaning. Cambridge, MA: Harvard University Press.
3. Bruner, J.S. (1996). The culture of education. Cambridge, MA: Harvard University Press.
4. Dale, M. (1996). Working with families of children with special needs: Partnership and practice. London: Routledge.
5. DeMeyer, M. (1979). Parents and children with autism. New York: Wiley.
6. Eysenbach, G., & Till, J.E. (2001). Ethical issues in qualitative research on Internet communities. British Medical Journal, 323, 1103—1105.
7. Faulkner, R.A., Klock, K., & Gale, J.E. (2002). Qualitative research in family therapy: publication trends from 1980 to 1999. Journal of Marital and Family Therapy, 28, 69—74.
8. Fleischmann, A. (2001, August). Coping among parents of an autistic child. Paper presented at the conference of the Association for Research on Learning and Instruction, Fribourg University, Switzerland.
9. Freeman, N., Perry, A., & Factor, D. (1991). Child behaviors as stressors—replicating and extending the use of the CARS as a measure of stress: A research note. Journal of Child Psychology and Psychiatry and Allied Disciplines, 32, 1025—1030.
10. Gergen, M. (1988). Narrative structures in social explanation. In C. Antaki (Ed.), Analyzing everyday explanations: A casebook of methods (pp. 94—112). London: Sage.
11. Gray, D., & Holden, W. (1992). Psychosocial wellbeing among the parents of children with autism. Australia and New Zealand Journal of Developmental Disabilities, 18, 83—93.
12. Hunt, P. (2000). Futures for children’s literature: Evolution or radical break? Cambridge Journal of Education, 30, 111—119.
13. Huws, J.C., Jones, R., & Ingledew, D.K. (2001). Parents of children with autism using an email group: A grounded theory study. Journal of Health Psychology, 6, 569— 584.
14. Hyden, L.C. (1997). Illness and narrative: A critical review. Sociology of Health and Illness, 19, 48—69.
15. Jones, R., Zahl, A., & Huws, J.C. (2001). First-hand accounts of emotional experiences in autism: A qualitative analysis. Disability & Society, 16, 393—401.
16. Labov, W. (1972). The transformation of experience in narrative syntax. In W. Labov (Ed.), Language in the inner city: Studies in the Black English vernacular (pp. 354— 396). Philadelphia: University of Pennsylvania Press.
17. Labov, W. (1982). Speech actions and reactions in personal narrative. In D. Tannen (Ed.), Analyzing discourse: Text and talk (pp. 219—247). Washington, DC: Georgetown University Press.
18. Lainhart, J.E. (1999). Psychiatric problems in individuals with autism, their parents and siblings. International Review of Psychiatry, 11, 278—299.
19. Liwag, M. (1989). Mothers and fathers of autistic children: An exploratory study of family stress and coping. Philippine Journal of Psychology, 22, 3—16.
20. Midence, K., & O’Neill, M. (1999). The experience of parents in the diagnosis of autism: A pilot study. Autism, 3, 273—285.
21. Moes, D., Koegel, R., Schreibman, L., & Loos, L. (1992). Stress profiles for mothers and fathers of children with autism. Psychological Reports, 71, 1272—1274.
22. Pennebaker, J.W., & Seagal, J.D. (1999). Forming a story: The health benefits of narrative. Journal of Clinical Psychology, 55, 1243—1254.
23. Piven, J., Chase, G., Landa, R., & Wzorek, M. (1991). Psychiatric disorders in the parents of autistic individuals. Journal of the American Academy of Child and Adolescent Psychiatry, 30, 471—478.
24. Piven, J., & Palmer, P. (1999). Psychiatric disorder and the broad autism phenotype. American Journal of Psychiatry, 156, 557— 564.
25. Pugach, M.C. (2001). The stories we choose to tell: Fulfilling the promise of qualitative research for special education. Exceptional Children, 67, 439—454.
26. Sarbin, T.R. (1986). The narrative as a root metaphor for psychology. In T. R. Sarbin (Ed.), Narrative psychology (pp. 3—21). New York: Praeger.
27. Siegel, B. (1997). Coping with the diagnosis of autism. In D. J. Cohen & F. R. Volkmar (Eds.), Handbook of autism and pervasive developmental disorders (pp. 745—766). New York: Wiley.
28. Tarakeshwar, N., & Pargament, K.I. (2001). Religious coping in families of children with autism. Focus on Autism and Other Developmental Disabilities, 16, 247—260.
29. Wehman, T. (1998). Family-centered early intervention services: Factors contributing to increased parent involvement. Focus on Autism and Other Developmental Disabilities, 13, 80—87.