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“I am no longer alone”: Evaluation of the first North American camp for youth living in families with Huntington's disease

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  • Kavanaugh, Melinda S.
  • Cho, Chi
  • Maeda, Hotaka
  • Swope, Chandler

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  • Kavanaugh, Melinda S. & Cho, Chi & Maeda, Hotaka & Swope, Chandler, 2017. "“I am no longer alone”: Evaluation of the first North American camp for youth living in families with Huntington's disease," Children and Youth Services Review, Elsevier, vol. 79(C), pages 325-332.
    • Handle: RePEc:eee:cysrev:v:79:y:2017:i:c:p:325-332
    DOI: 10.1016/j.childyouth.2017.06.029
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    References listed on IDEAS

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    1. Forrest Keenan, Karen & van Teijlingen, Edwin & McKee, Lorna & Miedzybrodzka, Zosia & Simpson, Sheila A., 2009. "How young people find out about their family history of Huntington's disease," Social Science & Medicine, Elsevier, vol. 68(10), pages 1892-1900, May.
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    Cited by:

    1. Dare, J. & Marquis, R. & Wenden, E. & Gopi, S. & Coall, D.A., 2020. "The impact of a residential camp on grandchildren raised by grandparents: Grandparents’ perspectives," Children and Youth Services Review, Elsevier, vol. 108(C).
    2. Nagl-Cupal, Martin & Prajo, Natasa, 2019. "It is something special: How children and their parents experience a camp for young people who care for a parent with a severe physical illness," Children and Youth Services Review, Elsevier, vol. 107(C).

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