The BNPCC Hub

Welcome to the BNPCC Hub!

The Hub is an online space to support the work of the Brisbane North Palliative Care Collaborative.

This page no longer requires a login-to access. Sensitive documents are restricted with a member-only password. Please contact Caroline if you do not remember the password.

Welcome to the BNPCC Hub!

The Hub is an online space to support the work of the Brisbane North Palliative Care Collaborative.

This page no longer requires a login-to access. Sensitive documents are restricted with a member-only password. Please contact Caroline if you do not remember the password.

  • PallConsult Educators' Muster – End-of-life care skills registration closes 1 May

    PallConsult delivers Educators' Muster events for clinicians who undertake clinical educator and facilitator roles in work areas that support patients in the last 12 months of life. These two-day events foster collaboration, share strategies and facilitate effective mentoring for frontline nursing, QAS and allied health clinicians across community, aged care and acute care settings.

    The program is designed around sharing train-the-trainer principles, ensuring that educators gain the knowledge and confidence to cascade training within their local services.

    Muster 1: Metro North Registrations close Friday, 1 May 2026

    PallConsult delivers Educators' Muster events for clinicians who undertake clinical educator and facilitator roles in work areas that support patients in the last 12 months of life. These two-day events foster collaboration, share strategies and facilitate effective mentoring for frontline nursing, QAS and allied health clinicians across community, aged care and acute care settings.

    The program is designed around sharing train-the-trainer principles, ensuring that educators gain the knowledge and confidence to cascade training within their local services.

    Muster 1: Metro North Registrations close Friday, 1 May 2026

  • MASS PCEP First Nations Consumer Resources Project

    supporting image

    [From MASS PCEP]

    The Medical Aids Subsidy Scheme (MASS) has partnered with the First Nations Health Office to review and develop consumer resources for the Palliative Care Equipment Program (PCEP). We are now seeking feedback from prescribers and consumers to further edit and finalise the resources.


    Resources include handouts about: MASS PCEP and Continence Aids, Daily Living and Mobility Aids, Home Oxygen, Syringe Drivers (pumps). The documents have been drafted with input from several external stakeholders.


    Each document has been developed in line with the governing MSH procedure - PR2023-342 Metro South Health Delivering Health Literate Services. The documents are written in the Easy English (low literacy, English as a second language) and Plain English (grade 7-9 reading level) writing styles.

    The team are now seeking feedback from prescribers and consumers to further edit and finalise the resources.

    Feedback to be provided by 30 April 2026.

    Survey (click)

    Please contact Simone Dullaway, MASS PCEP Clinical Advisor, for more information: MASS-PCEP@health.qld.gov.au.

    [From MASS PCEP]

    The Medical Aids Subsidy Scheme (MASS) has partnered with the First Nations Health Office to review and develop consumer resources for the Palliative Care Equipment Program (PCEP). We are now seeking feedback from prescribers and consumers to further edit and finalise the resources.


    Resources include handouts about: MASS PCEP and Continence Aids, Daily Living and Mobility Aids, Home Oxygen, Syringe Drivers (pumps). The documents have been drafted with input from several external stakeholders.


    Each document has been developed in line with the governing MSH procedure - PR2023-342 Metro South Health Delivering Health Literate Services. The documents are written in the Easy English (low literacy, English as a second language) and Plain English (grade 7-9 reading level) writing styles.

    The team are now seeking feedback from prescribers and consumers to further edit and finalise the resources.

    Feedback to be provided by 30 April 2026.

    Survey (click)

    Please contact Simone Dullaway, MASS PCEP Clinical Advisor, for more information: MASS-PCEP@health.qld.gov.au.

  • Research grant opportunity: Childhood dementia

    New National Health and Medical Research Council (NHMRC) grant opportunity:

    A Targeted Call for Research (TCR) is a one-time request for grant applications designed to stimulate research in a particular area that will benefit the health of Australians or address a specific health issue. This TCR aims to accelerate research that transforms the diagnosis, care and therapeutic landscape for children with dementia and their families.

    The proposed objectives of this grant opportunity are to:

    • Develop rapid diagnostic pathways to improve screening and diagnosis. This includes improving clinician awareness, creating standardised protocols, and enabling timely access to treatment and support through

    New National Health and Medical Research Council (NHMRC) grant opportunity:

    A Targeted Call for Research (TCR) is a one-time request for grant applications designed to stimulate research in a particular area that will benefit the health of Australians or address a specific health issue. This TCR aims to accelerate research that transforms the diagnosis, care and therapeutic landscape for children with dementia and their families.

    The proposed objectives of this grant opportunity are to:

    • Develop rapid diagnostic pathways to improve screening and diagnosis. This includes improving clinician awareness, creating standardised protocols, and enabling timely access to treatment and support through rapid diagnostic approaches.
    • Design and evaluate evidence-based multidisciplinary care frameworks for children diagnosed with dementia. This should include rehabilitation therapies, symptom management strategies for pain, sleep, communication, mobility and behavioural issues, as well as integrated palliative care approaches. Education for healthcare professionals and carers on managing complex symptoms should also be considered.
    • Advance therapeutic developmentand health system readiness through translational research that will uncover disease mechanisms and identify novel therapeutic targets. This should also include building capacity in the healthcare sector to increase access to disease modifying treatments for affected children. The research should also address systemic barriers such as education, referral pathways and care coordination with the aim to develop evidence-based guidelines to standardise and reduce variation in care.
    • Improve psychosocial and family support by developing and testing interventions that address the mental health, grief and wellbeing of families and carers. Research should focus on scalable models for psychological support and care coordination to reduce caregiver burden and strengthen family resilience.


    See https://www.grants.gov.au/Go/Show?GoUuid=f0036c4b-600e-4b4d-8bb9-de234b721ac6 for more information

  • Help decide delirium research priorities

    Delirium is:

    • a sudden change to a person’s mental state that can be related to the effects of illness, injury, having surgery, medicines, or withdrawal from drugs or alcohol.
    • a medical condition, which is often not recognised and needs urgent medical care.
    • a temporary condition that develops quickly over hours or days but can last a few days or weeks. 
    • different from dementia which occurs more gradually and for a longer time, but both can happen at the same time.  
    • more common in older people and people living with dementia but can affect anyone.

    People with delirium can find it

    Delirium is:

    • a sudden change to a person’s mental state that can be related to the effects of illness, injury, having surgery, medicines, or withdrawal from drugs or alcohol.
    • a medical condition, which is often not recognised and needs urgent medical care.
    • a temporary condition that develops quickly over hours or days but can last a few days or weeks. 
    • different from dementia which occurs more gradually and for a longer time, but both can happen at the same time.  
    • more common in older people and people living with dementia but can affect anyone.

    People with delirium can find it hard to: 

    • deal with the symptoms, such as seeing or hearing things that are not there.
    • trust the people caring for them.
    • manage emotions.  
    • communicate their needs.  
    • make decisions.  
    • care for themselves.

    Delirium can be frightening. It can lead to slower recovery from illness, and longer hospital stays.

    What matters most to you

    In our first survey, which closed in September 2025, we invited patients, carers, and healthcare staff to tell us what questions about delirium they thought were most important for research to answer. Thank you to everyone who contributed and shared their questions.

    A total of 186 people took part in the first survey and submitted 513 questions. We carefully reviewed all the questions and combined them into 40 summary questions. Our research team then undertook a detailed review of published evidence to confirm which questions have not been answered by research yet.

    Now, we need your help to decide which of these summary questions are the most important to you. Your input will guide future delirium research priorities.


    Why is this study important?

    Understanding what people think are the most important topics for delirium research can help us improve the care and wellbeing of people with delirium.


    Who should take part in this study?

    • People who have had delirium.
    • People who have cared for someone with delirium, e.g. family members
    • People with health conditions that increase the risk of delirium (e.g. people living with frailty or dementia, cancer), and their carers or family members.
    • Healthcare staff caring for people with or at risk of delirium (e.g. doctors, nurses, allied health professionals)


    You must live in Australia or New Zealand and be aged 18 years or older to take part in this questionnaire.


    How can I take part in the study?

    If you would like to take part in the study, please complete our survey. The survey should take 10 – 15 minutes to complete. By submitting your responses, you consent to participate.

    If you would like to be involved in the next stage of the study, we will request some contact details at the end of the survey. Your information will be kept safe on a password-protected drive that only the project team can use, and we will delete them once the study is complete.

    Access survey here


    See more information: https://www.delirium.org.au/research-priorities

  • CarerHelp resources and free online sessions

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    [From CarerHelp]

    Resources

    Carer Information Kits and Rural Carer Kits back in stock! These kits provide core information to prepare families for end of life caring.

    Order your Kits now at Order resources - Resources

    We are also delighted to share our new ‘Caring in Aged Care Homes’ page and resources with you. Please take some time to explore these resources as they will help families who are considering transitioning to an Aged Care Home.

    Free online sessions

    We are also offering free online sessions for families caring for someone nearing the end of life. Led by experienced

    [From CarerHelp]

    Resources

    Carer Information Kits and Rural Carer Kits back in stock! These kits provide core information to prepare families for end of life caring.

    Order your Kits now at Order resources - Resources

    We are also delighted to share our new ‘Caring in Aged Care Homes’ page and resources with you. Please take some time to explore these resources as they will help families who are considering transitioning to an Aged Care Home.

    Free online sessions

    We are also offering free online sessions for families caring for someone nearing the end of life. Led by experienced health professionals, these sessions cover a range of topics and are designed to meet carers where they are on their journey. Carers can find out more and self-register here.

    Upcoming dates include:

    Preparing for caring as illness advances

    • April 21 at 11am
    • May 12 at 11am

    Preparing for the last weeks

    • April 21 at 1pm
    • May 12 at 1pm

    Living beyond loss: Finding your way through grief

    • April 28 at 2pm
    • May 26 at 2pm

  • palliAGED Introduction modules refreshed

    [from palliAGED]

    The palliAGED Introduction Modules have been co-designed with industry and re-aligned to the strengthened Aged Care Quality Standards. The refreshed modules now also consider all aged care settings, the roles of the interprofessional care team including family and carers, and present interactive 10-minute learning activities on a range of topics that connect to practice.

    What’s new?

    • Same trusted content, but with more practical tips and evidence-based resources
    • Realistic scenarios for Support at Home and Residential Aged Care
    • Consideration for cultural safety, role clarity, and self-care embedded throughout

    Easy access via the palliAGED website, no cost, and a certificate

    [from palliAGED]

    The palliAGED Introduction Modules have been co-designed with industry and re-aligned to the strengthened Aged Care Quality Standards. The refreshed modules now also consider all aged care settings, the roles of the interprofessional care team including family and carers, and present interactive 10-minute learning activities on a range of topics that connect to practice.

    What’s new?

    • Same trusted content, but with more practical tips and evidence-based resources
    • Realistic scenarios for Support at Home and Residential Aged Care
    • Consideration for cultural safety, role clarity, and self-care embedded throughout

    Easy access via the palliAGED website, no cost, and a certificate of completion once you are done.


    Explore modules: https://www.palliaged.com.au/Supporting-Services/palliAGED-Products/palliAGED-Introduction-Modules

  • Health professionals invitation- Paediatric palliative care Eldership Project

    [From Quality of Care Collaborative Australia (QuoCCA)]

    As a health care professional working in the context of paediatric palliative care in Australia or New Zealand - your voice matters!

    So, if you could ask a pioneer in paediatric palliative care one question about their experiences, what would you ask?

    To respond, please undertake a brief survey as part of the research project Honouring the Past and Looking to the Future of Paediatric Palliative Care (PPC) in Australia: Stories of Pioneers.

    In joining the conversation:

    • Share your ‘one question’ (or perhaps you have more than one!)
    • Leave your details if

    [From Quality of Care Collaborative Australia (QuoCCA)]

    As a health care professional working in the context of paediatric palliative care in Australia or New Zealand - your voice matters!

    So, if you could ask a pioneer in paediatric palliative care one question about their experiences, what would you ask?

    To respond, please undertake a brief survey as part of the research project Honouring the Past and Looking to the Future of Paediatric Palliative Care (PPC) in Australia: Stories of Pioneers.

    In joining the conversation:

    • Share your ‘one question’ (or perhaps you have more than one!)
    • Leave your details if you’d like to hear the outcome of this project
    • Your involvement will take around 20 minutes

    After the survey closes, we will –

    • Gather your questions
    • Use these to inform the interview guide for pioneers in PPC
    • Interview pioneers in PPC in Australia and New Zealand

    The project will culminate in a book of pioneer narratives designed to create intergenerational learning between pioneers, current and future PPC practitioners. Most importantly, the wisdom of pioneers will continue to shape compassionate care for children and families. More information about the study is available in the attached Participant Information Statement.

    Take the survey now via this link: https://qsurvey.qut.edu.au/jfe/form/SV_2m0mPWEjbhw7x0G.

    The survey closes by Friday 17 April 2026.

    This project is being led by Principal Investigator Dr Leigh Donovan. For any queries, please contact leigh@collaboraide.com

    Please share across your networks to help understand what it is you wish to ask your pioneer PPC colleagues!

  • Dearly Departed: death in life- Exhibition at SLQ

    New exhibition at the State Library Queensland looks at Death

    Free exhibition
    Until 23 August 2026

    9am – 5pm Monday to Friday
    10am – 5pm Saturday and Sunday

    slq Gallery, level 2

    [From website]

    Death is a universal experience. It will come to us all. Yet the way we confront, discuss, experience and ultimately reckon with death, and the realities of dying, varies enormously. Culturally diverse traditions and practices around death offer unique insights into how communities around the world honour and mourn their loved ones, shaping vastly different experiences and understandings of life’s final chapter.

    Throughout the 20th century

    New exhibition at the State Library Queensland looks at Death

    Free exhibition
    Until 23 August 2026

    9am – 5pm Monday to Friday
    10am – 5pm Saturday and Sunday

    slq Gallery, level 2

    [From website]

    Death is a universal experience. It will come to us all. Yet the way we confront, discuss, experience and ultimately reckon with death, and the realities of dying, varies enormously. Culturally diverse traditions and practices around death offer unique insights into how communities around the world honour and mourn their loved ones, shaping vastly different experiences and understandings of life’s final chapter.

    Throughout the 20th century, death became a quiet taboo; something rarely spoken of, despite touching every life. Positioned at the powerful intersection of history, art and emotion, Dearly Departed encourages audiences to reflect on what it means to live well, die well and honour those who came before us. It reframes death not as an ending, but as a profound and enduring part of Queensland’s living story.

    Innovative, accessible, and deeply human, Dearly Departed: death in life invites visitors into a bold exploration of mortality across Queensland’s past, present and future. Through rich historical insight, evocative artistic interpretation and interactive design, the exhibition sparks meaningful conversation about life, death and the memories we hold.

    Drawing on the State Library’s rich collections of objects and stories, the exhibition explores how social, cultural, spiritual, historical and political forces have shaped Queenslanders’ attitudes to death and dying – then and now.

    Join us as we rediscover how confronting death helps us better understand life itself.

    Content note

    This exhibition features images, videos, and objects associated with death and dying. These can evoke emotions, memories, or personal reflections. Visitors are encouraged to move through the space at their own pace and to take breaks whenever needed. This exhibition contains photographs, videos and recordings of people who have since passed, including Aboriginal and Torres Strait Islander peoples.


    For more information visit the SLQ Dearly Departed webpage: https://www.slq.qld.gov.au/dearlydeparted

  • Palliative Care Australia highlights gaps for under 65's

    [Press release from Palliative Care Australia]

    Younger Australians with life-limiting illness are being left without the basic support they need to die at home, with thousands each year missing out on vital support to help them stay out of hospital safely.

    Palliative Care Australia (PCA), together with Parliamentary Friends of Palliative Care co-convenors Senator Kerrynne Liddle and Senator Raff Ciccone, today gathered advocates, clinicians and peak bodies from across the country at Parliament House to highlight the issue and call for urgent, coordinated reform.

    PCA CEO Camilla Rowland said age should not determine the level of care and support someone

    [Press release from Palliative Care Australia]

    Younger Australians with life-limiting illness are being left without the basic support they need to die at home, with thousands each year missing out on vital support to help them stay out of hospital safely.

    Palliative Care Australia (PCA), together with Parliamentary Friends of Palliative Care co-convenors Senator Kerrynne Liddle and Senator Raff Ciccone, today gathered advocates, clinicians and peak bodies from across the country at Parliament House to highlight the issue and call for urgent, coordinated reform.

    PCA CEO Camilla Rowland said age should not determine the level of care and support someone receives at the end of life.

    “People under 65 are falling between the cracks of the NDIS, aged care and health systems,” Ms Rowland said. “If people don’t qualify for the NDIS or aged care systems, there is no clear pathway to access basic support at home, and people are left navigating complex processes at the most vulnerable time in their lives.”

    A keynote address from Fiona Hassmann of the Peace of Mind Foundation brought the human impact into sharp focus, drawing on her lived experience supporting her partner through terminal illness and now working with families facing similar challenges.

    “There is no system built for people under 65 who are dying… the safety net is not a net at all, it is a series of gaps,” Ms Hassmann said.Her address highlighted how, when supports do align across disability, health and palliative care, people can die at home with dignity, but for most families this remains the exception rather than the norm.

    PCA Chair Dr Peter Allcroft said a significant cohort of Australians are missing out on essential support. “This is not a marginal issue. It is a systemic failure that is causing real harm to individuals and families,” Dr Allcroft said.

    “Each year, thousands of Australians with advanced life-limiting illness go without the practical support they need, like personal care and help at home – support that is fundamental to dignity and quality of life.”

    PCA estimates that up to 10,000 Australians under 65 with advanced life-limiting illness, including children and adolescents (and people in rural and remote locations), are unable to access the functional support required to remain safely at home.

    Without this support, many face extended hospital stays or are forced into early entry to residential care, outcomes that are distressing for individuals and families, and place additional pressure on the health system. Speakers from across the sector, including lived experience, clinical care and national peak bodies, highlighted ongoing challenges including delays in accessing support, inconsistent NDIS decisions, and confusion about which system is responsible for care.

    The group is calling for coordinated national action, including:

    • A clear commitment by all governments that filling this service gap is a priority, with national leadership from the Australian Government
    • Jointly funded trials across multiple locations to test the size and support needs of this cohort
    • Better coordination between disability and palliative care services, with clearer roles and responsibilities across systems
    • Faster and more flexible access to support for people at a very challenging time.

    Participants also reinforced the need for this issue to be prioritised in an updated National Palliative Care Strategy Implementation Plan.

    “This is about ensuring people can die with dignity, in the place of their choosing, with the support they need,” Ms Rowland said. “For too many younger Australians, that is not currently possible.”

  • CPCRE Lunch & Learn: Research for Beginners: Generating research ideas, formulating a research question, how to do a great literature search (23 Apr)

    [From CPCRE]

    The CPCRE Lunch & Learn Education for April:

    "Research for Beginners: Generating research ideas, formulating a research question, how to do a great literature search"


    Thursday 23 April 2026
    12.00 - 13:00 hours
    (Queensland time)


    To be presented by Professor Phillip Good, Clinical Research Program Leader, CPCRE; Director of Palliative Care, St Vincent's Private Hospital Brisbane.

    The CPCRE Research for Beginners online session aims:

    • To promote the value and importance of palliative care research,
    • To contribute to the development of palliative care researchers in Queensland, to enable them to build high quality research studies that will add to

    [From CPCRE]

    The CPCRE Lunch & Learn Education for April:

    "Research for Beginners: Generating research ideas, formulating a research question, how to do a great literature search"


    Thursday 23 April 2026
    12.00 - 13:00 hours
    (Queensland time)


    To be presented by Professor Phillip Good, Clinical Research Program Leader, CPCRE; Director of Palliative Care, St Vincent's Private Hospital Brisbane.

    The CPCRE Research for Beginners online session aims:

    • To promote the value and importance of palliative care research,
    • To contribute to the development of palliative care researchers in Queensland, to enable them to build high quality research studies that will add to the body of evidence and knowledge for palliative care practice.


    Who should register?

    • Health professionals of all disciplines who have an interest in undertaking research particularly in palliative or end of life care.
    • Clinicians of all disciplines working in any health setting are encouraged to register and attend.
    • Targeted toward knowledge level of Medical Officers, Senior Nurses and Allied Health Professionals.
    • Health students of any discipline are welcome to register.

    REGISTER HERE for this free online education session

Page last updated: 13 Jul 2026, 02:24 PM