Australian Young Onset Dementia Special Interest Group (YOD-SIG)

About YOD-SIG

The Australian Young Onset Dementia Special Interest Group (YOD-SIG) is a national network committed to research, policy, and clinical care to improve outcomes for people with young onset dementia and their families.

Our group includes nearly 100 people living with young onset dementia, care partners, researchers, clinicians and service providers, and is working to foster and improve collaboration and information sharing across sectors.

Our principal activities include:

  • Developing resources
  • Delivering education activities
  • Conducting collaborative research
  • Advocating for improved care and support
  • Providing expert advice on topics of importance for people with young onset dementia and their families

Executive Committee

A/Prof Adrienne Withall
(Immediate Past Co-Chair)

View Biography

A/Prof Jade Cartwright
(Immediate Past Co-Chair)

View Biography

A/Prof Nathan D’Cunha
(Co-Chair)

View Biography

Naomi Moylan 
(Co-Chair)

View Biography

Nicholas Lawlis (Communications Chair)

 

Michelle Chiu 

Dr Fiona Bright, PhD

A/Prof Elissa Burton

Associate Professor of Healthy Ageing, Curtin University’s School of Allied Health. Co-domain lead, Dementia and Ageing Domain, Curtin enAble Institute. Harken Fellow, Brightwater Research Centre.

View biography
View blog

Naomi Folder

 

Rebecca (Becky) Layton 

 

 

 



Our Webinars

Watch our latest webinar: Let us Grow: Life, Creativity and Connection

For more YOD-SIG webinars, please visit the ADNeT YouTube Channel or view our webinar resources page.


Our Research

The YOD-SIG is a member of the Joint Solutions Project Consortium, led by the Young People in Nursing Homes National Alliance, and further including The Eastern Cognitive Disorders Clinic (ECDC), and Dementia Australia. The Joint Solutions project is funded by the Australian Department of Social Services (DSS) and will map the services required by people living with young onset dementia (YOD) and their families from diagnosis to end of life care, and identify the programs best placed to provide support.

The YOD-SIG was engaged to conduct research to understand the experiences and needs of people with YOD, their families, and the people who work with them. The data will be used by the Joint Solutions Consortium to inform development of a fully described system of care for YOD, along with a road map of responsibilities that outlines services that should be available along the disease pathway.

The final research report and findings of a rapid review of models of care and pathways for people with young onset dementia can be viewed below. The infographic provides a summary of the main research findings and recommendations for a gold-standard pathway of care for people with YOD. An accessible version of the report is also being prepared and will be available shortly.

Our Newsletters

You can read the YOD-SIG newsletters here.

Newsletter Highlights

Dementia Support Australia and the Australian Frontotemporal Dementia Association are working in partnership to develop and run a nationwide network of proactive groups called Carer Conversations. Designed for carers who are supporting someone living with frontotemporal dementia (FTD), the groups are an opportunity for you to meet with other carers either face to face or virtually. You can read a case study from participants here.


Join YOD-SIG

If you would like to join YOD-SIG, please fill out this New Members form.