PARENTS` EMOTIONAL SUPPORT DURING THE INTEGRATION PROCESS OF CHILDREN WITH SPECIAL EDUCATIONAL NEEDS

Authors

  • Laura Elena Nastasa Faculty of Psychology and Educational Sciences, Transilvania University of Brasov
  • Mihaela Cimpu School Center for Inclusive Education of Brasov
  • Anca Daniela Farcas Faculty of Medicine, Iuliu Hatieganu University of Medicine and Pharmacy of Cluj- Napoca

Keywords:

emotional support, emotional intelligence, support group,

Abstract

Parents of children with disabilities may be in a great deadlock and the way they
react is very different from one person to another. Thus, various emotional states
and reactions may occur, such as shock, confusion, anxiety, uncertainty,
frustration, distrust of diagnosis, denial, anger, fury, despair, negotiation, fear,
self-blame, accusation of destiny and / or the others, isolation, rejection,
depression, acceptance, resignation, and struggle. Often these emotions are not
recognized and expressed, which creates multiple difficulties that can be
overcome by improving human relationships in a supportive psychotherapeutic
intervention. This research aims at identifying their needs and emotional states.
The results obtained highlight the need to implement support groups for these
parents, groups that focus on the development of emotional abilities and on the
most effective strategies for maintaining constructive interpersonal relationships
in the process of integration of children with special educational needs.

References

Bailey, D. B., Golden, R. N., Roberts, J., & Ford, A. (2007). Maternal depression and

developmental disability: Research critique. Mental Retardation and Developmental

Disabilities Research Reviews, 13(4), 321–329.

Baker, B. L., Blacher, J., & Olsson, M. B. (2005). Preschool children with and without

developmental delay: Behavior problems, parents’ optimism and well-being. Journal of

Intellectual Disability Research, 49(8), 575–590.

Blacher, J., & Baker, B. L. (2007). Positive impact of intellectual disability on families.

American Journal on Mental Retardation, 112(5), 330–348.

Bourke-Taylor, H., Pallant, J. F., Law, M., & Howie, L. (2012). Predicting mental health

among mothers of school-aged children with developmental disabilities: The relative

contribution of child, maternal and environmental factors. Research in Developmental

Disabilities, 33(6), 1732–1740.

Brotheridge, C.M., Lee, R.T. (2003). Development and validation of the Emotional Labour

Scale. Journal of Occupational and Organizational Psychology, 76, 365-379.

Browne, D. T., Rokeach, A., Wiener, J., Hoch, J. S., Meunier, J. C., & Thurston, S. (2013).

Examining the family-level and economic impact of complex child disabilities as a function

of child hyperactivity and service integration. Journal of Developmental and Physical

Disabilities, 25(2), 181–201.

Carnevale, F. A., Alexander, E., Davis, M., Rennick, J., & Troini, R. (2006). Daily living with

distress and enrichment: The moral experience of families with ventilator-assisted children

at home. Pediatrics, 117(1), 48–60.

Caruso, D. R., & Salovey, P. (2012). The emotionally intelligent manager – how to develop

and use the four key emotional skills of leadership. Bucharest: Business Tech International

Press.

Chu, K. H.-L., & Murrmann, S. K. (2006). Development and validation of the Hospitility

Emotional Labor Scale. Tourism Management, 27, 1181 - 1191.

Dabrowska, A., & Pisula, E. (2010). Parenting stress and coping styles in mothers and fathers

of pre-school children with autism and Down syndrome. Journal of Intellectual Disability

Research, 54(3), 266–280.

Dembo, T. (1984). Sensitivity of one person to another. Rehabilitation Literature, 45, 90–95.

Ekas, N. V., Lickenbrock, D. M., & Whitman, T. L. (2010). Optimism, social support, and

well-being in mothers of children with autism spectrum disorder. Journal of Autism and

Developmental Disorders, 40(10), 1274–1284.

Emerson, E., Hatton, C., Llewellyn, G., Blacker, J., & Graham, H. (2006). Socio-economic

position, household composition, health status and indicators of the well-being of mothers

of children with and without intellectual disabilities. Journal of Intellectual Disability

Research, 50(12), 862–873.

Emerson, E., McCulloch, A., Graham, H., Blacher, J., Llwellyn, G. M., & Hatton, C. (2010).

Socioeconomic circumstances and risk of psychiatric disorders among parents of children

with early cognitive delay. American Journal on Intellectual and Developmental

Disabilities, 115(1), 30–42.

Farrugia, D. (2009). Exploring stigma: Medical knowledge and the stigmatisation of parents

of children diagnosed with autism spectrum disorder. Sociology of Health & Illness, 31(7),

–1027.

Featherstone, H. (1980). A difference in the family: Living with a disabled child. New York:

Penguin.

Francis, A. (2012). Stigma in an era of medicalisation and anxious parenting: How proximity

and culpability shape middle-class parents’ experiences of disgrace. Sociology of Health &

Illness, 34(6), 927–942.

Gill, J., & Liamputtong, P. (2011). Being the mother of a child with Asperger’s syndrome:

women’s experiences of stigma. Health Care for Women International, 32(8), 708–722.

Glidden, L. M., & Jobe, B. M. (2006). The longitudinal course of depression in adoptive and

birth mothers of children with intellectual disabilities. Journal of Policy and Practice in

Intellectual Disabilities, 3(2), 139–142.

Green, S. E. (2007). We’re tired, not sad: Benefits and burdens of mothering a child with a

disability. Social Science & Medicine, 64(1), 150–163.

Greer, F. A., Grey, I. M., & McClean, B. (2006). Coping and positive perceptions in Irish

mothers of children with intellectual disabilities. Journal of Intellectual Disabilities, 10(3),

–248.

Hardman, M. L., Drew, C. J., & Egan, M. W. (1996). Human Exceptionality: society, school,

and Family. Boston: Allyn and Bacon.

Jones, J., & Passey, J. (2005). Family adaptation, coping and resources: Parents of children

with developmental disabilities and behavior problems. Journal on Developmental

Disabilities, 11, 31–46.

Lightsey, O. R., & Sweeney, J. (2008). Meaning in life, emotion-oriented coping, generalized

self-efficacy, and family cohesion as predictors of family satisfaction among mothers of

children with disabilities. Family Journal, 16(3), 212–221.

Manning, M. M., Wainwright, L., & Bennett, J. (2011). The double ABCX model of

adaptation in racially diverse families with a school-age child with autism. Journal of

Autism and Developmental Disorders, 41(3), 320–331.

McManus, B. M., Carle, A., Acevedo-Garcia, D., Ganz, M., Hauser-Cram, P., & McCormick,

M. (2011). Modeling the social determinants of caregiver burden among families of children

with developmental disabilities. American Journal on Intellectual and Developmental

Disabilities, 116(3), 246–260.

Montes, G., & Halterman, J. S. (2007). Psychological functioning and coping among mothers

of children with autism: A population-based study. Pediatrics, 119(5), 1040–1046.

Muir-Hutchinson, L. (1987). Working with professionals. Exceptional Parent. 17(5), 8–10.

Nastasa, L.E. (coord).(2015).Counseling the family in a deadlock - a psychological and

educational approach. Bucharest: Ed. Eikon.

Nastasa, L.E., & Mindu, S. (2016). Emotional support for teachers who interact with disabled

children’s families. Bulletin of the Transilvania University of Brasov. Series VII: Social

Sciences – Law. 9 (59), 2, 53-64.

Nastasa, L.E., Stroe, E., & Sandu, M. (2017). Managing emotions of specialists who interact

with the social services beneficiaries in M. Milcu, M. Stevens & I. Dahl. Modern Research

In Health,Education And Social Sciences. From Evaluation To Intervention. (pp. 217-226).

Bucuresti: Ed. Universtara.

Olsson, M. B. (2008). Understanding individual differences in adaptation in parents of

children with intellectual disabilities: A risk and resilience perspective. International

Review of Research in Mental Retardation, 36, 281–315.

Olsson, M. B., Larsman, P., & Hwang, P. C. (2008). Relationships among risk, sense of

coherence, and well-being in parents of children with and without intellectual disabilities.

Journal of Policy and Practice in Intellectual Disabilities, 5(4), 227–236.

Plant, K. M., & Sanders, M. R. (2007). Predictors of care-giver stress in families of

preschool-aged children with developmental disabilities. Journal of Intellectual Disability

Research, 51(2), 109–124.

Reichman, N. E., Corman, H., & Noonan, K. (2008). Impact of child disability on the family.

Maternal and Child Health Journal, 12(6), 679–683.

Resch, J. A., Benz, M. R., & Elliott, T. R. (2012). Evaluating a dynamic process model of

wellbeing for parents of children with disabilities: A multi-method analysis. Rehabilitation

Psychology, 57(1), 61–72.

Rodger, S., & Mandich, A. (2005). Getting the run around: Accessing services for children

with developmental co-ordination disorder. Child: Care, Health and Development, 31(4),

–457.

Ruiz-Robledillo, N., & Moya-Albiol, L. (2014). Emotional intelligence modulates cortisol

awakening response and self-reported health in caregivers of people with autism spectrum

disorders. Research in Autism Spectrum Disorders. 8, 1535–1543.

Ryan, S., & Runswick-Cole, K. (2008). Repositioning mothers: Mothers, disabled children

and disability studies. Disability & Society, 23(3), 199–210.

Schutte, N. S., Malouff, J. M., Hall, L. E., Haggerty, D.,J., Cooper, J. T., Golden, C. J., &

Dornheim, L. (1998). Development and validation of emotional intelligence. Personality

and Individual Differences, 25, 167–77.

Seligman, M., & Darling, R.B. (1989). Ordinary families, special children. New York:

Guilford Press.

Seligman, M., & Seligman, D.A. (1980). The professional`s dilemma: learning to work with

parents. Exceptional Parent. 10(5), 511–513.

Singer, G. H. S., & Floyd, F. (2006). Meta-analysis of comparative studies of depression in

mothers of children with and without developmental disabilities. American Journal on

Mental Retardation, 111(3), 155–169.

Smith, L. E., Seltzer, M. M., Tager-Flusberg, H., Greenberg, J. S., & Carter, A. S. (2008). A

comparative analysis of well-being and coping among mothers of toddlers and mothers of

adolescents with ASD. Journal of Autism and Developmental Disorders, 38(5), 876–889.

Totsika, V., Hastings, R. P., Emerson, E., Lancaster, G. A., & Berridge, D. M. (2011). A

population-based investigation of behavioral and emotional problems and maternal mental

health: Associations with autism spectrum disorder and intellectual disability. Journal of

Child Psychology and Psychiatry, 52(1), 91–99.

Trute, B., Benzies, K. M., Worthington, C., Reddon, J. R., & Moore, M. (2010). Accentuate

the positive to mitigate the negative: Mother psychological coping resources and family

adjustment in childhood disability. Journal of Intellectual and Developmental Disability,

(1), 36–43.

Trute, B., Benzies, K., & Worthington, C. (2012). Mother positivity and family adjustment in

households with children with a serious disability. Journal of Child & Family Studies,

(3), 411–417.

Trua, C. (2012). The management of emotions in education. Antecedents and strategies.

Brasov: Transilvania University Press.

Yirmiya, N., & Shaked, M. (2005). Psychiatric disorders in parents of children with autism: A

meta-analysis. Journal of Child Psychology and Psychiatry, 46(1), 69–83.

Ylven, R., Bjorck-Akesson, E., & Granlund, M. (2006). Literature review of positive

functioning in families with children with a disability. Journal of Policy and Practice in

Intellectual Disabilities, 3(4), 253–270.

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Published

2018-12-21