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The views and opinions expressed in our blog series are those of the authors and are not necessarily supported by CareSearch, Flinders University and/or the Australian Government Department of Health.
Due to advances in medicine, people with physical disabilities are living longer. While end-of-life care should be readily accessible for this group, the care needs of people with significant physical disabilities arguably adds an additional layer of complexity to such care. Dr Ruth Walker from Flinders University discusses end-of-life care needs for adults with long-standing physical disability and the new research she is involved in to explore the specific needs of people with physical disabilities who are at the end-of-life, as well as the needs of their families and the support staff who help care for them.
Health care professionals agree that the quality of care provided in the emergency department for dying patients and their families is often not as good as it needs to be. Dr Tracy Giles of Flinders University explains how her research into the experiences of family members will help to identify what is working well already and areas of care that need improvement, and how you can become involved.
The pattern of disease, dying and death has changed dramatically in Australia over the last century. In Australia alone almost 160,000 people die every year. Of these at least 120,000 are expected deaths, meaning that access to palliative care could be of great benefit to both the individuals and their families. But ensuring access to quality palliative care for all who need it is not without its challenges. This is why a group of researchers sought funding from National Health and Medical Research Council (NHMRC) for the Centre of Research Excellence in End-of-Life Care (CRE-ELC).
At CareSearch we acknowledge and respect the Kaurna people, the traditional custodians whose ancestral lands on which CareSearch located.
Naa Marni? This greeting in Kaurna language translates to ‘Are you all good?’
I recall once walking through a university corridor on my way to give a tutorial, and overhearing some students complaining that they couldn't understand why they had to spend so much time in their course on Aboriginal Health. I was quite shocked by this, because to me the reason was obvious – Aboriginal and Torres Strait Islander people die at least 10 years earlier than non-indigenous Australians. How had they missed this vital point?
One of the key goals of the Close the Gap campaign for Indigenous health equality is to reduce the gap in life expectancy and healthcare access between Aboriginal and Torres Strait Islander peoples and the non-indigenous Australian population.