Literature DB >> 27170424

Transition to adulthood for young people with intellectual disability: the experiences of their families.

Helen Leonard1, Kitty-Rose Foley1,2, Terri Pikora1, Jenny Bourke3, Kingsley Wong1, Lyn McPherson4, Nick Lennox4, Jenny Downs1,5.   

Abstract

Whilst the transition from school to adult roles can be challenging for any adolescent, for those with an intellectual disability it can present as a particularly difficult time both for the individual and their family. The process may involve coordinated planning, collaboration and decision-making among school staff, families and community agencies. This mixed-methods study utilised information from two cohorts: young people with Down syndrome in Western Australia (n = 190) and young people with intellectual disability (of any cause) in Queensland, Australia (n = 150). The parent-report questionnaires administered in both states comprised two parts: part 1 collected information about the individual with intellectual disability including information on health, functioning and service needs, and about specific transition related issues; and part 2 collected information about the health and well-being of their family. The majority (87 %) of parents said that they were involved in decision-making about transition planning but less than two-thirds (59.5 %) of young people were involved in this process. The three most helpful strategies indicated by parents that assisted with transition planning related to the provision of more information about financial assistance, the school transition program and the building of informal community-based supports. A number of themes emerged from the qualitative data which included parents' views and concerns about the capacity of their young adult to adapt and change to life in adulthood, their difficulty navigating services and programs, issues and challenges around their young person building connectedness, strain on family wellbeing and finances and worry about the longer term future.

Entities:  

Keywords:  Down syndrome; Families; Intellectual disability; Transition

Mesh:

Year:  2016        PMID: 27170424     DOI: 10.1007/s00787-016-0853-2

Source DB:  PubMed          Journal:  Eur Child Adolesc Psychiatry        ISSN: 1018-8827            Impact factor:   4.785


  26 in total

Review 1.  Young adults with intellectual disability transitioning from school to post-school: a literature review framed within the ICF.

Authors:  K-R Foley; P Dyke; S Girdler; J Bourke; H Leonard
Journal:  Disabil Rehabil       Date:  2012-04-03       Impact factor: 3.033

2.  Attitudes towards people with intellectual disability in the UK and Libya: A cross-cultural comparison.

Authors:  Aisha M Benomir; Roderick I Nicolson; Nigel Beail
Journal:  Res Dev Disabil       Date:  2016-01-09

3.  Transitions from school for young adults with intellectual disability: Parental perspectives on "life as an adjustment".

Authors:  Michael D Davies; Wendi Beamish
Journal:  J Intellect Dev Disabil       Date:  2009-09

Review 4.  Issues in caregiving for older people with intellectual disabilities and their ageing family carers: a review and commentary.

Authors:  Assumpta Ryan; Laurence Taggart; Maria Truesdale-Kennedy; Eamonn Slevin
Journal:  Int J Older People Nurs       Date:  2013-03-15       Impact factor: 2.115

5.  Midlife and aging parents of adults with intellectual and developmental disabilities: impacts of lifelong parenting.

Authors:  Marsha Mailick Seltzer; Frank Floyd; Jieun Song; Jan Greenberg; Jinkuk Hong
Journal:  Am J Intellect Dev Disabil       Date:  2011-11

6.  The relationship between quality of life and self-determination: an international study.

Authors:  Y Lachapelle; M L Wehmeyer; M-C Haelewyck; Y Courbois; K D Keith; R Schalock; M A Verdugo; P N Walsh
Journal:  J Intellect Disabil Res       Date:  2005-10

Review 7.  On the road to nowhere? Young disabled people and transition.

Authors:  B Beresford
Journal:  Child Care Health Dev       Date:  2004-11       Impact factor: 2.508

8.  "It's not what you were expecting, but it's still a beautiful journey": the experience of mothers of children with Down syndrome.

Authors:  Divia Pillay; Sonya Girdler; Marie Collins; Helen Leonard
Journal:  Disabil Rehabil       Date:  2012-02-11       Impact factor: 3.033

9.  "I have a good life": the meaning of well-being from the perspective of young adults with Down syndrome.

Authors:  Melissa Scott; Kitty-Rose Foley; Jenny Bourke; Helen Leonard; Sonya Girdler
Journal:  Disabil Rehabil       Date:  2013-11-28       Impact factor: 3.033

10.  Day occupation is associated with psychopathology for adolescents and young adults with Down syndrome.

Authors:  Kitty-Rose Foley; Peter Jacoby; Stewart Einfeld; Sonya Girdler; Jenny Bourke; Vivienne Riches; Helen Leonard
Journal:  BMC Psychiatry       Date:  2014-10-03       Impact factor: 3.630

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  10 in total

1.  Psychiatry, mental health, mental disability: time for some necessary clarifications.

Authors:  Bruno Falissard; Marlène Monégat; Gordon Harper
Journal:  Eur Child Adolesc Psychiatry       Date:  2017-10       Impact factor: 4.785

2.  Transition to adulthood: prospective content in joint parent-youth conversations for young people with intellectual or developmental disabilities (IDD).

Authors:  Richard A Young; Sheila K Marshall; Tim Stainton; Eugene Chi
Journal:  Int J Dev Disabil       Date:  2020-10-07

Review 3.  Variables related to the quality of life of families that have a child with severe to profound intellectual disabilities: A systematic review.

Authors:  N Luitwieler; J Luijkx; M Salavati; C P Van der Schans; A J Van der Putten; A Waninge
Journal:  Heliyon       Date:  2021-06-24

4.  Systematic review of study designs and methods in health transition research for young people with intellectual disabilities.

Authors:  Axel Kaehne; Joann Kiernan; James Ridley
Journal:  Heliyon       Date:  2019-11-19

5.  Measurement of Family Management in Families of Individuals With Down Syndrome: A Cross-Cultural Investigation.

Authors:  Marcia Van Riper; George J Knafl; Maria do Céu Barbieri-Figueiredo; Maria Caples; Hyunkyung Choi; Gert de Graaf; Elysângela Dittz Duarte; Junko Honda; Elena Marta; Supapak Phetrasuwan; Sara Alfieri; Margareth Angelo; Wannee Deoisres; Louise Fleming; Aline Soares Dos Santos; Maria João Rocha da Silva; Beth Skelton; Shelley van der Veek; Kathleen A Knafl
Journal:  J Fam Nurs       Date:  2020-12-04       Impact factor: 3.818

6.  Improving the transition process to independent living for adolescents with profound intellectual disabilities. Experiences of parents and employees.

Authors:  Eirik Roos; Erik Søndenaa
Journal:  BMC Health Serv Res       Date:  2020-12-09       Impact factor: 2.655

7.  Virtual care during the pandemic: Multi-family group sessions for Hong Kong Chinese families of adolescents with intellectual disabilities.

Authors:  Julia Wing Ka Lo; Joyce Lai Chong Ma; Mooly Mei Ching Wong; Monica Lai Tuen Yau-Ng
Journal:  J Intellect Disabil       Date:  2022-03-26

Review 8.  Canadian Resources for Siblings of Youth With Chronic Health Conditions to Inform and Support With Healthcare Management: A Qualitative Document Analysis.

Authors:  Linda Nguyen; Hanae Davis; Samantha Bellefeuille; Jessica Havens; Susan M Jack; Briano Di Rezze; Marjolijn Ketelaar; Jan Willem Gorter
Journal:  Front Rehabil Sci       Date:  2021-10-05

9.  The Relationship between Shoe Fitting and Foot Health of Persons with Down Syndrome: A Case Control Study.

Authors:  César Calvo-Lobo; Ana Ramos García; Marta Elena Losa Iglesias; Daniel López-López; David Rodríguez-Sanz; Carlos Romero-Morales; Ricardo Becerro-de-Bengoa-Vallejo
Journal:  Int J Environ Res Public Health       Date:  2018-05-14       Impact factor: 3.390

Review 10.  Care Coordination Needs of Families of Children with Down Syndrome: A Scoping Review to Inform Development of mHealth Applications for Families.

Authors:  Beth Skelton; Kathleen Knafl; Marcia Van Riper; Louise Fleming; Veronica Swallow
Journal:  Children (Basel)       Date:  2021-06-29
  10 in total

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