From Palliative Care Australia Stories about living, dying and Palliative Care
24 May 2020
What do you when you’re 35 years old and in palliative care during COVID-19? You dance, of course. Why? “Because you can’t choose what happens to you in life but you can choose how you […]
7 May 2020
The richness of the Bear Cottage culture has made it possible for me to transition to providing online Zoom music therapy sessions with an ease which has taken me by surprise. Working from home, as […]
26 August 2019
Back in 2017 Lorna Hurst shared her very personal story with Palliative Matters about her son Sam’s bowel cancer diagnosis, treatment and death at just 17 years-of-age. Lorna has now generously agreed her to share […]
18 July 2019
Sarah Williams wanted what so many of us already have — an education and to be married with a family of her own. Instead, she died from cancer at 33 before having the chance to legally marry […]
19 June 2019
Briony Lyle will share insights from her extraordinary life with late husband, professional golfer Jarrod Lyle, at the Oceanic Palliative Care Conference this September. From their high school days in Shepparton, Victoria to the world […]
3 June 2019
An innovative new resource kit has been developed in NSW to help local Aboriginal communities feel more welcome in palliative care settings and start inclusive and culturally appropriate conversations about end of life planning. “Into […]
6 December 2018
In the lead up to this holiday season, Palliative Care Australia (PCA) hosted the third Dying to Talk online art competition which asked participants to create a piece of art that demonstrates what matters most to them during the holiday season. With a record of 125 entries submitted, artworks were created by artists all around the country.
17 October 2018
“Disability is not a deficit within the person, but shows up the deficits in our culture and society that does not fully accept, encourage and celebrate humanity, no matter what it looks like. The unique and distinctive abilities of this amazing group of children can act as an inspiration for all of us, to encourage each other.”
13 October 2018
When Max was diagnosed with Batten Disease, we had no idea what his future held. All we knew was that our little boy was going to die.
12 September 2018
We sometimes find ourselves on a long and difficult journey. Whether we are a patient, carer, family member or friend, illness takes a toll on everyone involved. Often people reach out to help us but often we don’t accept support, even when we need it. To help change this situation, Andrea Grindrod from La Trobe University is encouraging families and the community to work together.