Erratum to Family decision making: Benefits to persons with developmental disabilities and their family members, [Intellectual and Developmental Disabilities, 46, 2, (2008) 93-105, DOI: 10.1352/0047-6765(2008)46[93:FDMBTP]2.0.CO;2];Family decision making: Benefits to persons with developmental disabilities and their family members

Intellectual and Developmental Disabilities

Volumn 46, Issue 2, 2008, Pages 93-105

  Neely Barnes, Susan ^a   Carolyn Graff, J ^b   Marcenko, Maureen ^c   Weber, Lisa ^d  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^b and Fellow Transcultural Nursing Society Scholars   (United States)

^c UNIVERSITY OF WASHINGTON   (United States)

^d Washington State Division of Developmental Disabilities   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BEHAVIOR; CAREGIVER; CASE MANAGEMENT; CONSUMER; DECISION MAKING; FEMALE; HUMAN; MALE; MENTAL DEFICIENCY; MIDDLE AGED; MULTIVARIATE ANALYSIS; PSYCHOLOGICAL ASPECT; SOCIAL SUPPORT;

ADULT; AGED; CAREGIVERS; CASE MANAGEMENT; CONSUMER PARTICIPATION; CONSUMER SATISFACTION; DECISION MAKING; FEMALE; HUMANS; MALE; MENTAL RETARDATION; MIDDLE AGED; MULTIVARIATE ANALYSIS; POWER (PSYCHOLOGY); SOCIAL SUPPORT;

EID: 46449121074     PISSN: 19349556     EISSN: None     Source Type: Journal    
DOI: 10.1352/1934-9556(2008)46[ii:E3]2.0.CO;2     Document Type: Erratum

References (48)

1. Ashbaugh, J. W. (2002). Down the garden path of self-determination. Mental Retardation, 40, 416-417.
2. Bambara, L. M. (2004). Fostering choice-making skills: We've come a long way but still have a long way to go. Research and Practice for Persons With Severe Disabilities, 29, 169-171.
3. Caldwell, J. (2006). Consumer-directed supports: Economic, health, and social outcomes for families. Mental Retardation, 44, 405-417.
4. Caldwell, J., & Heller, T. (2003). Management of respite and personal assistance services in a consumer-directed family support programme. Journal of Intellectual Disability Research, 47, 352-366.
5. Dunst, C. J., & Trivette, C. M. (1993). Empowering case management practices: A family-centered perspective. In C. J. Dunst, C. M. Trivette, & A. G. Deal (Eds.), Supporting and strengthening families: Vol. 1. Methods, strategies, and practices (pp. 187-196). Cambridge, MA: Brookline Books.
6. Dunst, C., Trivette, C., & Deal, A. (1988). Enabling and empowering families: Principles and guidelines for practice. Newton, MA: Brookline Books.
7. Dykens, E. M. (2005). Happiness, well-being, and character strengths: Outcomes for families and siblings of persons with mental retardation. Mental Retardation, 43, 360-364.
8. Essex, E. L., Seltzer, M. M., & Krauss, M. W. (1999). Differences in coping effectiveness and well-being among aging mothers and fathers of adults with mental retardation. American Journal on Mental Retardation, 104, 545-563.
9. Everson, J. M., & Zhang, D. (2000). Person-centered planning: Characteristics, inhibitors, and supports. Education and Training in Mental Retardation and Developmental Disabilities, 35, 36-43.
10. Freedman, R. I., Griffiths, D., Krauss, M. W., & Seltzer, M. M. (1999). Patterns of respite use by aging mothers of adults with mental retardation. Mental Retardation, 37, 93-103.
11. Fujiura, G. T. (1998). Demography of family households. American Journal on Mental Retardation, 103, 225-235.
12. Grinnell, R. M. (1997). Social work research and evaluation: Quantitative and qualitative approaches (5th ed). Itasca, IL: Peacock Publishers.
13. Halle, J. W. (1995). Innovations in choice-making research: An editorial introduction. Journal of the Association of Persons with Severe Handicaps, 20, 173-174.
14. Hastings, R. P., & Taunt, H. M. (2002). Positive perceptions in families of children with developmental disabilities. American Journal on Mental Retardation, 107, 116-127.
15. Hayden, M. F., & Goldman, J. (1996). Families of adults with mental retardation: Stress levels and need for services. Social Work, 41, 657-667.
16. Hayden, M. F., & Heller, T. (1997). Support, problem-solving/coping ability, and personal burden of younger and older caregivers of adults with mental retardation. Mental Retardation, 35, 364-372.
17. Heller, T. (2000). Supporting adults with intellectual disabilities and their families in planning and advocacy: A literature review. Physical & Occupational Therapy in Geriatrics, 18, 59-73.
18. Heller, T., Miller, A. B., & Hsieh, K. (1999). Impact of a consumer-directed family support program on adults with developmental disabilities and their family caregivers. Mental Retardation, 48, 419-427.
19. Heller, T., Miller, A. B., Hsieh, K., & Stern, H. (2000). Later-life planning: Promoting knowledge of options and choice-making. Mental Retardation, 38, 395-406.
20. Herman, S. E. (1991). Use and impact of a cash subsidy program. Mental Retardation, 29, 253-258.
21. Herman, S. E. (1994). Cash subsidy program: Family satisfaction and need. Mental Retardation, 32, 416-421.
22. Hodges, V. G., Burwell, Y., & Ortega, D. (1998). Empowering families. In L. M. Gutierrez, R. J. Parsons, & E. O. Cox (Eds.), Empowerment in social work practice: A sourcebook (pp. 146-162). Pacific Grove, CA: Brooks/Cole.
23. Human Services Research Institute. (2005, February). Adult family survey: Final report 2003-2004 data. Cambridge, MA: Author.
24. Kim, H. W., Greenberg, J. S., Seltzer, M. M., & Krauss, M. W. (2003). The role of coping in maintaining the psychological well-being of mothers of adults with intellectual disability and mental illness. Journal of Intellectual Disability Research, 47, 313-327.
25. Kim, K. M., White, G. W., & Fox, M. H. (2006). Comparing outcomes of persons choosing consumer-directed or agency-directed personal assistance services. Journal of Rehabilitation, 72, 32-43.
26. Kincaid, D., & Fox, L. (2002). Person-centered planning and positive behavioral support. In S. Holburn & P. M. Vietze (Eds.), Person-centered planning: Research, practice, and future directions (pp. 29-49). Baltimore: Brookes.
27. Kroll, T., Beatty, P., & Bingham, S. (2003). Primary care satisfaction among adults with physical disabilities: The role of patient-provider communication. Managed Care Quarterly, 11, 11-19.
28. Law, M., Hanna, S., King, G., Hurley, P., King, S., & Kertoy, M. et al. (2003). Factors affecting family-centred service delivery for children with disabilities. Child: Care, Health, & Development, 29, 357-366.
29. Little, R. J. A., & Rubin, D. B. (1987). Statistical analysis with missing data. New York: Wiley.
30. Lustig, D. C. (2002). Family coping in families with a child with a disability. Education and Training in Mental Retardation and Developmental Disabilities, 37, 14-22.
31. Mary, N. L. (1998). Social work and the support model of services for people with developmental disabilities. Journal of Social Work Education, 34, 247-260.
32. McCutcheon, A. L. (1987). Latent class analysis. Newbury Park, CA: Sage.
33. Meyers, J. C., & Marcenko, M. O. (1989). Impact of a case subsidy program for families of children with severe developmental disabilities. Mental Retardation, 27, 383-387.
34. Muthén, L. K., & Muthén, B. O. (2004). Mplus: Statistical analysis with latent variables user's guide. Los Angeles: Author.
35. Neely-Barnes, S. L. (2005). Consumer choice in developmental disability services: Assessing the impact on quality of life indicators (Doctoral Dissertation, University of Washington, Seattle, 2005). Dissertation Abstracts International, 66, 2725
36. Neely-Barnes, S. L., & Marcenko, M. O. (2004). Predicting impact of childhood disability on families: Results from the 1995 National Health Interview Survey Disability Supplement. Mental Retardation, 42, 284-293.
37. O'Brien, C. L., & O'Brien, J. (2002). The origins of person-centered planning: A community of practice perspectives. In S. Holburn & P. M. Vietze (Eds.), Person-centered planning: Research, practice, and future directions (pp. 3-27). Baltimore: Brookes.
38. O'Brien, C. L., O'Brien, J., & Mount, B. (1997). Person-centered planning has arrived...or has it?. Mental Retardation, 35, 480-483.
39. Orsmond, G. I., & Seltzer, M. M. (2000). Brothers and sisters of adults with mental retardation: Gendered nature of the sibling relationship. American Journal on Mental Retardation, 105, 486-508.
40. Parish, S. L., Seltzer, M. M., Greenberg, J. S., & Floyd, F. (2004). Economic implications of caregiving at midlife: Comparing parents with and without children who have developmental disabilities. Mental Retardation, 42, 413-426.
41. Ptacek, L. J., Sommers, P. A., Graves, J., Lukowicz, P., Keena, E., & Haglund, J. et al. (1982). Respite care for families of children with severe handicaps: An evaluation of parent satisfaction. Journal of Community Psychology, 10, 222-227.
42. Schafer, J. L., & Graham, J. W. (2002). Missing data: Our view of the state of the art. Psychological Methods, 7, 147-177.
43. Schwartz, C. (2005). Parental involvement in residential care and perceptions of their offspring's life satisfaction in residential facilities for adults with intellectual disability. Journal of Intellectual & Developmental Disability, 30, 146-155.
44. Scorgie, K., & Sobsey, D. (2000). Transformational outcomes associated with parenting children who have disabilities. Mental Retardation, 38, 195-206.
45. Seltzer, M. M., & Krauss, M. W. (1989). Aging parents with adult mentally retarded children: Family risk factors and sources of support. American Journal on Mental Retardation, 94, 303-312.
46. Stainton, T., & Besser, H. (1998). The positive impact of children with an intellectual disability on the family. Journal of Intellectual and Developmental Disability, 23, 57-70.
47. Stancliffe, R. J. (1995). Assessing opportunities for choice making: A comparison of self and staff reports. American Journal on Mental Retardation, 99, 418-429.
48. Stancliffe, R. J. (2000). Proxy respondents and quality of life. Evaluation and Program Planning, 23, 89-93.