Skip to main content
Resource details

Australian family carer responses when a loved one receives a diagnosis of Motor Neurone Disease

"Our life has changed forever”

Margaret O'Connor, Samar Aoun, Lauren Breen

22.1.2018

View Publication

Summary

This paper analyses qualitative data from a large Australian survey of family carers of people with Motor Neurone Disease (MND), to ascertain their experiences of receiving the diagnosis. Documenting the experiences of family carers of people with MND in receiving their diagnosis, this study seeks to inform and improve the ways in which diagnosis is communicated.

Related Publications

  • Add your research

    Is something important missing from the Research Library? Share your research or suggest research by another author using our submission form. For more information about how to create an account click here and for more information about how to upload a publication to the research library click here.

    My Research
  • How to use the Research Library

    Find out more about how to find a resource on the Carer Knowledge Exchange Research Library here.

    FAQs