JCPSLP Vol 18 no 2 July 2016

References Anderson, K. L., Balandin, S., & Stancliffe, R. J. (2014). Australian parents’ experiences of speech generating device (SGD) service delivery. Developmental Neurorehabilitation , 17 (2), 75–83. Anderson, K. L., Balandin, S., & Stancliffe, R. J. (2016). “It’s got to be more than that”: Parents and speech- language pathologists discuss training content for families with a new speech generating device. Disability and Rehabilitation: Assistive Technology , 11 (5), 375–384. Blackburn, C., & Read, J. (2005). Using the Internet? The experiences of parents of disabled children. Child: Care, Health and Development , 31 (5), 507–515. Disability Reform Council. (2015). National Disability Insurance Scheme: A framework for information, linkages, and capacity building . [On-line policy document]. Retrieved from Framework.pdf Eastin, M. S. (2001). Credibility assessments of online health information: The effects of source expertise and knowledge of content. [Electronic resource]. Journal of Computer-Mediated Communication , 6 (4). doi:10.1111/j.1083-6101.2001.tb00126.x Eysenbach, G., Yihune, G., Lampe, K., Cross, P., & Brickley, D. (2000). MedCERTAIN: quality management, certification and rating of health information on the Net . Paper presented at the Proceedings of the AMIA Symposium, 230–234. [Electronic resource]. Retrieved from Fox, S. (2006). Online health search 2006 . Pew Internet & American Life Project. Retrieved from http://www. Fox, S., & Duggan, M. (2013). Health online 2013 . Pew Internet & American Life Project. Retrieved from http:// Greenberg, L., D’Andrea, G., & Lorence, D. (2004). Setting the public agenda for online health search: A white paper and action agenda. [Electronic resource]. Journal of Medical Internet Research , 6 (2), e18. doi:10.2196/ jmir.6.2.e18

Kate Anderson is a researcher and lecturer in disability and inclusion at Deakin University, Melbourne, Australia. Paul Andres is an occupational therapist and AAC consultant at Prentke-Romich Deutschland, in Germany. Zaidman-Zait, A., & Jamieson, J. R. (2007). Providing web-based support for families of infants and young children with established disabilities. Infants & Young Children , 20 (1), 11–25. Hallgren, K. A. (2012). Computing inter-rater reliability for observational data: An overview and tutorial. Tutorials in Quantitative Methods for Psychology , 8 (1), 23. Hemsley, B., Dann, S., Palmer, S., Allan, M., & Balandin, S. (2015). “We definitely need an audience”: Experiences of Twitter, Twitter networks and tweet content in adults with severe communication disabilities who use augmentative and alternative communication (AAC). Disability and Rehabilitation , 37 (17), 1531–1542. Kunst, H., & Khan, K. S. (2002). Quality of web-based medical information on stable COPD: Comparison of non- commercial and commercial websites. Health Information & Libraries Journal , 19 (1), 42–48. Porter, A., & Edirippulige, S. (2007). Parents of deaf children seeking hearing loss-related information on the internet: The Australian experience. Journal of Deaf Studies and Deaf Education , 12 (4): 518–529. Rice, R. E. (2006). Influences, usage, and outcomes of Internet health information searching: Multivariate results from the Pew surveys. International Journal of Medical Informatics , 75 (1), 8–28. Roche, M. I., & Skinner, D. (2009). How parents search, interpret, and evaluate genetic information obtained from the internet. Journal of Genetic Counseling , 18 (2), 119–129. Spink, A., & Jansen, B. J. (2004). A study of web search trends. Webology , 1 (2), 4.

Correspondence to: Dr Kate Anderson Deakin University email:


JCPSLP Volume 18, Number 2 2016

Journal of Clinical Practice in Speech-Language Pathology

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