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    Caring for a child with severe intellectual disability in China: The example of Rett syndrome

    189278_189278.pdf (489.4Kb)
    Access Status
    Open access
    Authors
    Lim, Faye
    Downs, Jennepher
    Li, Jianghong
    Bao, Xinhua
    Leonard, Helen
    Date
    2013
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Lim, Faye and Downs, Jenny and Li, Jianghong and Bao, Xinhua and Leonard, Helen. 2013. Caring for a child with severe intellectual disability in China: The example of Rett syndrome. Disability and Rehabilitation. 35 (4): pp. 343-351.
    Source Title
    Disability and Rehabilitation
    ISSN
    0963-8288
    Remarks

    This is an Author's Original Manuscript of an article published by Taylor & Francis in the journal Disability and Rehabilitation 2013, available online at <a href="http://www.tandfonline.com/10.3109/09638288.2012.715720">http://www.tandfonline.com/10.3109/09638288.2012.715720</a>

    URI
    http://hdl.handle.net/20.500.11937/12411
    Collection
    • Curtin Research Publications
    Abstract

    Purpose: Rett syndrome is one of several genetic disorders known to cause severe intellectual and physical disability, mostly in girls. Girls affected by Rett syndrome appear to develop normally in the first 6 months of life, after which the usual clinical presentation comprises regression of communication and hand skills, the appearance of hand stereotypies and impaired gait. Intellectual disability affects more than 1.5% of the population of children in developing countries yet we know little about the daily lives and support services available for them and their caregivers. Method: This qualitative study explored the daily experiences of 14 mothers and one grandmother caring for a child with Rett syndrome in China via telephone interviews. Results: Participants reported a lack of education, rehabilitation and support services available to them. Limited access to information reduced families’ capacity to adequately meet the needs of their child. These gaps were further exacerbated by discrimination and perceived stigma from some members of the community. Conclusions: Additional support services and educational programs at the governmental level can improve the quality of life of persons with an intellectual disability and their families and programs involving community participation in the care of people with disabilities may help to address discrimination.

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