Category: News

Tell us about accessing specialist healthcare in WA

Long waits, high fees, travel, referral problems and difficulty finding a specialist can all affect whether you get the care you need.

HCCWA is gathering experiences from Western Australians to help inform our submission to a Federal Parliamentary inquiry into access to and affordability of medical specialists.

Who should respond?
Anyone in WA who has tried to access a medical specialist in the past five years.

What do we want to hear about?
Costs, waiting times, availability, referrals, travel and what happened when you could not access care.

How long does it take?
About 3 to 5 minutes.

Share your experience in our survey and you’ll be helping to improve specialist care access across Western Australia.

Digital Health Consumer Panel: Australia-wide EOI

Paid national digital health consumer opportunity: Join the National Consumer and Carer Digital Health Panel

Expressions of interest close 26 September 2026. Click here to apply.

Consumers and carers from across Australia are invited to apply for a paid opportunity to help shape national work on digital health.

Health Consumers’ Council WA is convening the National Consumer and Carer Digital Health Panel on behalf of Sparked.

Sparked is a national collaboration working to improve how health information is recorded and exchanged across Australia. It is led by CSIRO’s Australian e-Health Research Centre and delivered in partnership with the Australian Government Department of Health, Disability and Ageing, the Australian Digital Health Agency and HL7 Australia.

The Consumer and Carer Digital Health Panel will bring together consumers and carers from states and territories across Australia to give consumers and carers an opportunity to be at the table and contribute directly to national digital health initiatives.

Expressions of interest close 26 September 2026.

What is the National Consumer and Carer Digital Health Panel?

The National Consumer and Carer Digital Health Panel will bring consumer and carer perspectives into national conversations about the future of digital health in Australia.

Panel members will elevate the consumer voice in national digital health initiatives.

The panel is being convened by Health Consumers’ Council WA on behalf of Sparked.

Sparked brings together consumers, clinicians, health services, governments, researchers and technology organisations to develop and support nationally consistent digital health standards.

CSIRO describes Sparked as Australia’s Fast Healthcare Interoperability Resources, or FHIR, accelerator. Its work aims to help health information move more safely, seamlessly and meaningfully across Australia’s healthcare system.

Why does digital health matter for consumers and carers?

Your health information can move through many different parts of the healthcare system.

You might see a GP, have pathology or imaging, attend a specialist appointment and receive treatment through a hospital or another health service.

For those services to work together effectively, the digital systems behind them need to be able to exchange and understand health information.

National digital health standards help make this possible.

CSIRO says these standards can support better sharing of information between healthcare systems and make it easier for information to move with a person between different points of care.

But digital health should also reflect what consumers and carers need from the healthcare system.

That is where the National Consumer and Carer Digital Health Panel comes in.

Who should apply?

Expressions of interest are being sought from consumers and carers across Australia who have an interest in digital health and experience of digital health projects in their state or territory.

You may have been involved in a project such as the implementation of an electronic medical record system in a hospital or health service.

The focus is on bringing consumer and carer experience into the work.

Applicants are being sought from states and territories across Australia.

What will panel members do?

Panel members will participate in five half-day workshops between November 2026 and June 2027.

The workshops will provide an opportunity for consumers and carers to share their experiences, perspectives and priorities in their interactions with digital health, and contribute directly to national digital health initiatives.

Most workshops will be held online.

There is also the possibility of one in-person session.

How much will panel members be paid?

Panel members will receive $418 for each workshop.

There will be five half-day workshops in total.

What is Sparked?

Sparked is a national collaboration working to improve how health information is recorded and exchanged across Australia.

As noted above, it is a collaborative partnership between CSIRO’s Australian e-Health Research Centre, the Australian Government Department of Health, Disability and Ageing, the Australian Digital Health Agency and the non profit data standards organisation HL7 Australia.

Its community includes consumers, clinicians, researchers, governments, health services and software vendors.

More than 1,500 people had contributed to Sparked by June 2026, according to CSIRO.

The National Consumer and Carer Digital Health Panel provides a dedicated way for consumer and carer perspectives to contribute to this broader work.

Opportunity at a glance

Opportunity: National Consumer and Carer Digital Health Panel

Who: Consumers and carers from across Australia with relevant digital health experience

What: This panel gives consumers and carers an opportunity to be at the table and contribute directly to national digital health initiatives

Commitment: Five half-day workshops

Dates: November 2026 to June 2027. First meeting to be held on 5 November 2026

Format: Mainly online, with the possibility of one in-person session

Payment: $418 per workshop

Expressions of interest close: 26 September 2026

How to apply

If you are a consumer or carer with experience of digital health projects and would like to contribute to national digital health work, complete the Expression of Interest form.

Expressions of interest close 26 September 2026.

Apply for the National Consumer and Carer Digital Health Panel through the online Expression of Interest form.

Vale Nadeen Laljee-Curran

We are very sad to share the news that our colleague Nadeen Laljee-Curran passed away after being diagnosed with cancer in 2024 on Friday 17 July 2026.

Pictured L-R: Rachel Seeley, Nadeen Laljee-Curran

Nadeen has been involved in some way or other with Health Consumers’ Council since she joined the team as a Master of Public Health student in 2017. She was a stand-out, dedicated intern and after doing a couple of short-term roles in the team she took on the role of Cultural Diversity Engagement Lead in January 2020. Little did we know what the year had in store.

Her work at HCC enabled Nadeen to combine the lessons learned from her own personal experience with the health system, her unwavering determination to become a mother, her passion for social justice, and her academic learning, to play her part in improving health services to be more inclusive, more fair, and more person centred.

Nadeen’s talents and qualities were called on in unprecedented ways when COVID arrived in March 2020. Despite navigating her own health challenges and her need to socially distance – she switched quickly to doing her work from home championing the voices and rights of people from multicultural backgrounds.

As we all learned about Zoom, and how to stay connected with loved ones and essential services, Nadeen pored over the papers being published by public health experts, monitored social media chatter, and had many in-depth discussions with other consumers who were deeply engaged. It was clear there was a thirst for information in the community.

So Nadeen set up a community of interest and worked with others to run a series of presentations for people and organisations in the community to help them get informed about the virus, the public health measures, and provide feedback to government. She delivered sessions online and in person – socially distanced and masked. We heard lots of feedback that both the content of these presentations – that Nadeen took so much care over – and how they were presented – in Nadeen’s warm and credible way – “genuinely eased panic” for many people in the community.

This is just one of the many projects Nadeen led at HCC that played a part in making healthcare fairer for everyone in WA. She also played a role in gathering community feedback on people’s attitudes to organ and tissue donation, people’s experiences of ambulance services, and gathering feedback from people from culturally and linguistically diverse communities about their information needs about cancer treatment, resulting in a series of targeted resources being developed.

Nadeen was a strong and capable advocate for consumer rights – and we were all infected by her jubilation when the new Assisted Reproductive Technology and Surrogacy Act was passed in December last year. This is something Nadeen had consistently and passionately championed for years.

As a team mate, colleague and friend, Nadeen brought fun, kindness and rigour to our work and everyone in the HCC family misses her enormously. Nadeen’s legacy will live on through HCC as we honour her passion for social justice, and her commitment to elevating voices that often go unheard.

Nadeen is survived by her husband Jason, and daughter Maya. The HCCWA team will organise an opportunity for people in the HCCWA community to gather and celebrate Nadeen’s life in the coming weeks.

Meeting with WA’s incoming Chief Health Officer: Why consumer voices matter in public health

Health Consumers’ Council WA (HCCWA) meets with WA’s incoming Chief Health Officer to strengthen consumer partnership in public health

Public health decisions affect every person in Western Australia. They influence disease prevention, environmental health, food safety, health equity, emergency preparedness and the policies that shape healthier communities. That is why we welcomed the opportunity to meet with Western Australia’s incoming Chief Health Officer, Dr Clare Huppatz.

HCCWA Executive Director, Clare Mullen spoke with Dr Huppatz’s on her vision for public health in WA, including ideas for involving health consumers, carers, families and communities across the broad range of portfolios under Dr Huppatz’s responsibility.

The recent consumer consultation on the WA Preventative Health Strategy is one of the pieces of work that Dr Huppatz is responsible for – but her responsibilities are much wider than that. The CHO responsibilities include

  • reducing the inequalities in public health of disadvantaged communities
  • promoting and improving public health and wellbeing and to prevent disease, injury, disability and premature death
  • facilitating the provision of information to decision-making authorities about public health risks and benefits to public health
  • monitoring trends in the health status of the WA community and representing Western Australia on national committees, including Australian Health Protection Principal Committee.
  • Food hygiene and environmental health

Dr Huppatz is a senior public health doctor with extensive regional, national and international experience. She has worked across regional Australia, including the Kimberley and Goldfields, where she played a part in bringing the “Squeaky Clean Soap Aid” program to the Kimberley, Pilbara, Midwest and Goldfields – to tackle the barrier of affordable soap which has now seen over 1.4m bars of soap provided to the WA community. This is a major contributor to good hygiene, which in turn can help to reduce a range of diseases that are impacted by environmental health.

Dr Huppatz is keen to partner with consumers and the ‘two Clares’ discussed a range of options. As the independent peak body representing health consumers in Western Australia, HCCWA believes better health outcomes are achieved when the people most affected by decisions are involved in shaping them.

Dr Huppatz has a long list of stakeholders to talk with in coming weeks and months – as well as a huge amount of reform to oversee. From the WA Preventative Health Strategy to tackling health inequities and improving community wellbeing, the Chief Health Officer’s role touches many aspects of everyday life. Building strong partnerships between government, communities and health consumers is essential to creating a healthier, fairer Western Australia.

It was a productive discussion, especially so early in her tenure. We look forward to supporting Dr Huppatz, the Chief Health Officer, and her team to ensure the public are at the heart of public health.

HCCWA’s Diversity Dialogues Forum 2026

Older people from multicultural communities and their access to, and experience of, healthcare

Older people from culturally and linguistically diverse communities can face significant barriers when accessing healthcare in Western Australia. These barriers extend beyond language differences and include difficulties navigating the health system, digital exclusion, transport, cultural understanding, trust, trauma, and limited awareness of available services.

To better understand these experiences, Health Consumers’ Council WA (HCCWA) convened a Diversity Dialogues forum bringing together community leaders, healthcare professionals, researchers, service providers and consumers. Participants shared lived experience, professional insights and practical examples of the challenges older people encounter when seeking healthcare and aged care.

Across diverse communities, participants consistently identified common issues. These included difficulties accessing information and services, limited cultural responsiveness within healthcare settings, challenges using digital systems such as MyGov and My Aged Care, and the importance of building trust through long-term community relationships.

The discussion also highlighted practical solutions already being implemented across Western Australia. Community-led navigation services, culturally responsive education, Care Finder programs and stronger partnerships between community organisations and health services were identified as important approaches to improving access and health outcomes.

The findings reinforce the importance of involving multicultural communities in the planning, design and delivery of healthcare services. They also demonstrate that improving equitable access requires both system-level change and ongoing collaboration with the communities most affected.

About Diversity Dialogues

Diversity Dialogues is an ongoing initiative of Health Consumers’ Council WA that brings together consumers, community organisations, healthcare providers and policymakers to explore issues affecting culturally and linguistically diverse communities.

The forums provide an opportunity to share lived experience, identify barriers to healthcare, and develop practical recommendations that can improve health services across Western Australia.

Key Findings

Read the in-depth report here.

1. Healthcare systems are often difficult to navigate

Participants described healthcare and aged care systems that can be difficult to understand, particularly for people who migrated to Australia later in life or who have limited English proficiency.

Common barriers included:

  • complex forms and eligibility processes
  • difficulty using MyGov and My Aged Care
  • limited awareness of available services
  • uncertainty about how to access support

Many participants emphasised that services may exist, but understanding how to access them remains a significant challenge.

2. Language and communication remain significant barriers

Participants discussed how language barriers affect every stage of healthcare.

Challenges included:

  • limited English proficiency
  • low literacy in any language
  • complex medical terminology
  • translated information that does not reflect cultural context
  • interpreter availability and quality

Some participants also described concerns about privacy when interpreters come from small local communities.

These communication barriers may contribute to misunderstanding, delayed care and reduced confidence in healthcare services.

3. Trust is essential for good healthcare

Many participants explained that trust strongly influences whether people seek healthcare.

Past experiences of conflict, displacement, trauma or negative interactions with institutions can influence how some older people engage with Australian healthcare services.

Participants noted that trust often develops through long-term relationships with healthcare professionals and trusted community organisations rather than through single appointments.

4. Cultural understanding influences healthcare experiences

Participants shared examples where cultural practices or expectations had been misunderstood within healthcare settings.

Examples included:

  • differing expectations about family involvement in care
  • culturally appropriate food during hospital stays
  • differing understandings of ageing and illness
  • differing expectations about consultation length

Participants suggested that greater cultural understanding could improve communication, person-centred care and consumer experience.

5. Digital exclusion is becoming a healthcare barrier

As healthcare increasingly relies on digital systems, many older consumers experience additional barriers.

Participants highlighted difficulties using:

  • MyGov
  • My Aged Care
  • online appointment systems
  • SMS verification
  • email-based communication

Without practical support, digital systems may unintentionally reduce access for older people with limited digital literacy.

6. Social isolation increases health risks

Participants described social isolation as an important contributor to poorer health outcomes.

Examples included:

  • delayed assistance following falls
  • reduced access to appointments
  • fewer opportunities to receive health information
  • increased loneliness

Community organisations highlighted the importance of regular outreach and trusted relationships to reduce isolation.

Community-led solutions

The forum highlighted several initiatives already improving access for multicultural communities across Western Australia.

These included:

  • Care Finder services
  • community health navigation
  • digital literacy programs
  • culturally responsive community education
  • seniors’ support programs
  • intergenerational community initiatives

Participants emphasised that community-led approaches help build trust and support people to navigate complex healthcare systems.

Recommendations

The discussions identified several opportunities to improve healthcare access for older people from multicultural communities.

These include:

  • Increase cultural responsiveness across health and aged care services.
  • Improve representation of culturally and linguistically diverse consumers in health service planning and decision-making.
  • Expand community-led navigation and Care Finder services.
  • Improve access to face-to-face assistance with digital health systems.
  • Increase awareness of available health and aged care services through trusted community organisations.
  • Strengthen partnerships between health services and multicultural communities.
  • Ensure culturally appropriate food, communication and care are recognised as components of quality healthcare.
  • Continue investing in community-led mental health education and culturally appropriate support.

What this means for Western Australia

The experiences shared during this forum demonstrate that improving healthcare access for older people from multicultural communities requires more than translation services alone.

Participants described the importance of trust, culturally responsive care, accessible information, community leadership and meaningful partnerships.

Many of the barriers identified are interconnected. Addressing them will require collaboration between consumers, community organisations, healthcare providers and government.

By listening to lived experience and working alongside multicultural communities, Western Australia has an opportunity to create a more equitable, accessible and person-centred health system.

It is also worthwhile considering that improvements to help older people from multicultural communities would benefit everyone in WA, for example trust, accessible information and meaningful partnerships make healthcare fair for all.

Acknowledgements

Health Consumers’ Council WA thanks the forum panellists, participants and community organisations who generously shared their knowledge, lived experience and practical insights.

The experiences documented in this report reflect the views shared during the forum and are intended to inform ongoing discussion, collaboration and continuous improvement across Western Australia’s health system.

About Health Consumers’ Council WA

Health Consumers’ Council WA is the independent peak body representing health consumers across Western Australia. HCCWA works alongside consumers, carers, communities, clinicians and policymakers to improve access, equity, safety and person-centred care across the health system.

Join our eNews and let’s make healthcare fair for all!

* indicates required

National recognition for HCCWA’s advocacy for Western Australian health consumers

Health Consumers’ Council WA recognised as a national nominated finalist for consumer advocacy

Health Consumers’ Council WA (HCCWA) is proud to have been recognised as a finalist in the 2026 Consumers’ Federation of Australia Consumer Advocacy Award.

The award recognises outstanding consumer advocacy that creates meaningful change for people across Australia. The 2026 award was presented during the Australian Competition and Consumer Commission’s National Consumer Congress in Sydney.

Congratulations to Super Consumers Australia, whose Take Your Super Back campaign received this year’s award for helping thousands of Australians affected by the Shield and First Guardian superannuation collapses understand their rights and seek compensation.

HCCWA was honoured to stand alongside nationally respected consumer organisations including CHOICE and the Owners Corporation Network and Australian Consumers Insurance Lobby.

While every organisation works in a different area of consumer advocacy, they share a common goal of ensuring people are heard, informed and treated fairly.

For HCCWA, this recognition reflects the importance of independent health consumer advocacy in Western Australia.

Every year we support people to navigate complex healthcare experiences, amplify consumer voices in policy and service design, and work alongside communities, clinicians and decision makers to improve the safety, quality and fairness of our health system.

Our advocacy is shaped by the experiences of Western Australians. Individual stories help identify broader patterns, which can lead to lasting improvements that benefit entire communities.

Being recognised alongside Australia’s leading consumer advocacy organisations reinforces the value of independent, consumer-led advocacy and encourages us to continue working towards a health system that is safe, equitable and centred on people.

We congratulate Super Consumers Australia on their well-deserved achievement and thank every consumer, carer, volunteer, consumer representative, member, partner and supporter who helps make our work possible.

Together, we can continue making healthcare fair for all.

Help shape fairer healthcare in WA

Whether you’ve shared your healthcare experience, volunteered as a consumer representative, attended one of our workshops, supported our advocacy or worked alongside us, you are part of this achievement.

If you would like to help improve healthcare in Western Australia, we’d love you to get involved.

Join our movement for fairer healthcare in WA.

Join our eNews and let’s make healthcare fair for all!

* indicates required

What Aboriginal and Torres Strait Islander consumers say makes GP care culturally safe

What is culturally safe GP care? New research from Aboriginal and Torres Strait Islander consumers

A new paper, “Towards assessment of culturally safe general practitioners: co-designing with Aboriginal and Torres Strait Islander peoples’ perspectives, the Calgary–Cambridge guide and clinical yarning”, published in the Australian Journal of Primary Health on 25 May 2026, puts Aboriginal and Torres Strait Islander consumer voices at the centre of the conversation about cultural safety in general practice.

The research was carried out in Queensland across four sites, including three Aboriginal Medical Services and one mainstream general practice, spanning regional, rural and very remote communities. A total of 131 Aboriginal and Torres Strait Islander people took part through surveys, interviews and group processes. The work was guided by an Aboriginal Community Reference Group to ensure the findings reflected community perspectives.

This research matters because cultural safety is often discussed in policy or training settings, but less often defined by consumers themselves.

What Aboriginal and Torres Strait Islander consumers said matters most

Participants were clear about what they expect from a GP consultation. The priorities people identified were not theoretical; they were grounded in what really helps people feel respected, understood and confident about their care.

The most important attributes were:

  • knowing how to diagnose and treat disease properly
  • explaining things clearly, using basic words
  • greeting people respectfully
  • not stereotyping Aboriginal people
  • listening carefully

Other highly ranked elements included recognising what matters to the patient, not interrupting, being polite and respectful, creating a welcoming environment, and providing enough time for the appointment.

These findings show that culturally safe care is not something separate from everyday practice but is built through how care is delivered and whether people feel heard and taken seriously.

What does culturally safe care look like in a GP appointment?

Consumers said they want GPs who get clinical care right, use plain language, listen without interrupting, speak respectfully and as an equal, and avoid assumptions.

Participants also described the importance of privacy, comfort, and having enough time in appointments. Cultural safety also sits in the environment, including how welcoming the service feels, whether privacy is maintained, and whether people feel comfortable in the space.

What consumers want to see change

Consumers are asking for consistent, high-quality clinical care, clear communication, genuine listening, respectful interactions, freedom from stereotyping, and adequate time, privacy and follow-up.

There was also a strong message about consent. Participants wanted control over who is involved in their care and how information is shared, including during consultations, procedures and examinations.

Participants also valued continuity of care. Seeing the same GP over time, not having to repeat their story, and having follow-up on results and referrals all contributed to feeling safe and supported.

Important findings about culture and identity

Participants had mixed views about being asked about Country, Mob or cultural identity. For some, this was helpful. For others, it was intrusive or distressing, particularly where identity had been questioned or where people were disconnected from family or community. The paper recommends allowing these conversations to develop over time, rather than making them a standard opening question.

The research also goes further in challenging routine identification processes in general practice. It highlights that asking people to identify as Aboriginal or Torres Strait Islander in a standard administrative way can create fear of stereotyping, mistrust and disengagement. It points to the need for safer systems, where identity can emerge over time through relationships and where access to supports does not depend on a process that can cause harm.

What this means for general practice

The authors recommend strengthening existing GP consultation approaches by embedding relational practices such as respectful greeting, listening and clear communication, and integrating elements of social yarning into standard practice.

The paper also challenges commonly taught approaches. It shows that practices such as asking about Country, using silence, or trying to find common ground should not be assumed to be culturally safe for everyone. These approaches need to be used carefully and in response to the individual.

Where to next

Suggested future work includes testing the proposed consultation model in real settings and developing tools to assess cultural safety from a consumer perspective. This research was conducted in specific Queensland communities, and further work is needed across different regions and communities.

Why this matters in Western Australia

This paper provides clear direction based on what Aboriginal and Torres Strait Islander consumers have said themselves.

The key message is straightforward, people want care that is clinically sound, clearly explained, respectful, and free from judgement or stereotyping.

For services, this means reviewing how care is delivered and making practical changes that reflect these expectations.

Further reading & reference

Training for healthcare professionals

The insights in this article reflect what Aboriginal and Torres Strait Islander consumers have shared with HCCWA over many years. They also inform the content of our Aboriginal Patient Advocacy Training, where we work with community workers, advocates and health professionals to turn these insights into practical skills. Visit our training and events page to register for our next training session, or contact us to find out more.

Further reading

Brumpton K, Evans R, Sen Gupta T, Ward R (2026) Towards assessment of culturally safe general practitioners: co-designing with Aboriginal and Torres Strait Islander peoples’ perspectives, the Calgary–Cambridge guide and clinical yarning. Australian Journal of Primary Health, 32, PY25245. doi:10.1071/PY25245

ABSTRACT
Background. Cultural safety is a key component of quality general practice for Aboriginal and Torres Strait Islander peoples; however, few tools exist to assess this from the patient’s perspective. This study aimed to explore the qualities of a general practitioner (GP) that support culturally safe consultations, as described by Aboriginal and Torres Strait Islander peoples, and to examine how these align with two consultation models: the Calgary–Cambridge Guide and clinical yarning. Methods. A mixed methods approach was used, including a survey, qualitative interviews and a modified nominal group technique (mNGT). Participants were Aboriginal and Torres Strait Islander peoples who had previously engaged with general practice care. Data were both described and analysed thematically. Results. In total, 131 Aboriginal and Torres Strait Islander peoples participated (70 in the survey and interview; 43 in mNGT to validate the findings; and 18 in three separate mNGTs to rate desirable attributes of a GP). Participants identified several qualities underpinning a safe GP consultation. Within the top five attributes in the mNGT were universal skills – clinical competence, avoidance of jargon and attentive listening – alongside welcoming patients with a greeting and avoiding stereotyping. Although there was strong emphasis on respectful, individualised care, preferences varied significantly, highlighting the limitations of a generic approach to consultation skills. Some findings challenged core assumptions regarding clinical yarning and elements of cultural safety training. Conclusion. We propose a refined, integrated consultation model that enhances the Calgary– Cambridge Guide with relational elements of the social yarn, particularly during initiation of the consultation. This integrated model, grounded in Aboriginal and Torres Strait Islander peoples’ perspectives yet familiar to GPs and academics, offers a promising foundation for culturally safe practice and assessment, with potential applicability across other diverse populations.

Keywords: Aboriginal and Torres Strait Islander health, Australia, Calgary–Cambridge guide, clinical yarning, cultural safety, equity, general practice, Indigenous health care.

WA Winter Readiness Insights

Clare Mullen | Executive Director

 Winter is coming here!

While I never watched a full episode of Game of Thrones, I’m familiar with the ominous warning that “winter is coming…”

If you’re involved in the health system as a consumer or community representative, then you’ll know that health services in the south of the state are battening down the hatches to prepare for the increase in people who get sick at this time of year.

But we know from our discussions with WA community members that people don’t want to get sick if they can help it. Getting sick during winter isn’t inevitable and we know that every time you get a group of health consumers in a room, people sharing their knowledge is powerful.

So while we couldn’t easily get almost 200 people together in a room, we’ve gathered views from 200 of you about how you stay well and if you’re stepping up your efforts as winter approaches. Here’s what you told us…

First up – you care about your health

Everyone does something to protect their health usually. With the most selected options being:

  • Wash hands
  • Get vaccinated
  • Eat as healthily as possible
  • Stay in touch with family and friends
  • Get some regular exercise

Getting regular check ups with your GP and sleeping well scored highly too.

Next – most of us are doing something extra to prep to avoid winter bugs

More than three quarters of respondents think about taking extra measures – including:

  • Getting vaccinated
  • Maintaining strong hygiene like hand-washing and using masks
  • Avoiding higher-risk environments during peak season
  • Staying home and keeping your distancewhen unwell
  • Building overall health and immunity
  • Paying attention to air quality and ventilation

Most of our respondents plan to get vaccinated if they’re eligible

More than 80% of respondents plan to get vaccinated and know where to go to get it done, with about 7% of respondents unsure. Among the people who say they’re not planning to get vaccinated, about 5 people express concern about the risks of vaccination, with another 7 people commenting on how they’ve experienced cold/flu-like illnesses after previous vaccinations.

We can all play our part in reaching the community target which gives us all the best chance of staying safe. At the time of writing we’re already over half way towards these targets – but there’s still a way to go. You can check out progress at the WA Health site here: https://access.health.wa.gov.au/immunisation

Finally, we want clear, accessible public health information in places where we already go

Many people who responded to our survey shared it would be helpful if getting vaccinated was as easy as possible. So it’s great to see the WA Government rolling out flu vax clinics across community settings including at the footy – check out this link to see the upcoming dates: https://www.wa.gov.au/government/media-statements/Cook%20Labor%20Government/-More-WA-footy-fans-to-roll-up-their-sleeves-as-flu-clinics-extended-20260521

People also said they want strong public health messaging and transparency – if you haven’t already, check out the WA Health website which has links to your nearest place to get vaccinated, as well as more information about what to expect.

Survey information

We shared a link to a MS Forms survey between 06/03/26 and 09/06/26. The link was shared with HCCWA networks via email and social media. It was also shared on Reddit in r/Perth. There were 191 respondents. Over three quarters of respondents belong to a group that is known to experience health inequities. Almost a quarter of respondents were between 35-44, and over one tenth of respondents were 75 or over.

Employment opportunities, join the team!

A great time to join HCCWA and play your part in improving health outcomes and strengthening the voice of health consumers in WA.

We have a number of opportunities to join the HCCWA team at the moment. Some of these jobs are open for recruitment now, others will come on board in the coming days. Please share these roles with people in your networks who might be great additions to the HCCWA team.

These roles have become available after some internal changes, and the availability of some fixed term funding from the WA Government.

To enquire about any of these roles, email jobs@hconc.org.au – to apply, follow the instructions for each of the jobs.

To see all the roles visit our employment page under the ‘About Us’ menu.

Why consumer representatives matter more than ever in WA healthcare

What we heard in 2026

In March and April, we ran two workshops and brought together thirteen people at different stages of their consumer representation journeys. What they shared was honest, thoughtful and consistent with what we have heard over many years of running this training.

People come to this work because something happened to them or to someone they love, and they want it to mean something changes for the next person. They want to understand the system well enough to push back on it. They want to contribute in a way that is heard and respected, not just invited in and then overlooked.

“our perspectives and experiences are so valuable and give services and systems the information they can’t get anywhere else”

We have put together a full summary of both workshops, including what participants told us about the value of lived experience, the realities of consumer representative roles, the importance of diversity and who is still missing from these spaces, and what makes participation meaningful rather than tokenistic.

Why this matters beyond the training room

Consumer representatives play a specific and important role in systems change. They bring the perspectives of people who use services into the places where decisions are made. They help ensure that what the health system understands about what is working, what is missing and what needs to change is grounded in real life, not just data and projections.

HCCWA’s role is to make sure the people stepping into those roles feel ready: informed, supported and clear that their experience is a form of expertise. That has been our commitment for 34 years and this training is one of the places where that commitment shows up in practice

A training built for the long haul

This is not a one-off workshop or a box to tick before someone is assigned to a committee or a working group or a seat at an executive table. It is a space where people with lived and learned experience of health services can explore what consumer representative work actually involves, think about whether and how they want to contribute, and build confidence to do that well. The content covers the shape of the WA health system and where consumer voices can fit within it. It is honest about the challenges: the risk of tokenism, the emotional weight of bringing personal experience into formal spaces, the patience required when change is slow. And it is grounded, always, in the belief that people who use health services hold knowledge the system cannot get from anywhere else.

It has been delivered face to face, fully online, and now in both formats because we have learned that different options open the door for different people. In 2026, two people who couldn’t make the Saturday in-person session came back and attended the Tuesday evening online session instead. That is what genuine accessibility looks like: not just saying people are welcome, but making sure there is more than one way in.

Over three decades of consumer voices: the training that keeps people ready

Since 1994, Health Consumers’ Council WA has stood alongside people who use health services across WA. Throughout that time, one thread has run consistently through our work: helping people understand that their experience matters, that their voice belongs in the room, and that they have something real to contribute to making the health system better.

Our Introduction to Consumer Representation training is one of the ways we do that. The current iteration of this training goes back to 2019, but this commitment goes back much further. The format has evolved; the purpose has not.

Read the full 2026 workshop summary report or get in touch with us at engagement@hconc.org.au if you are interested in consumer representation opportunities or want to know when our next session is running.

Health Consumers’ Council WA
www.hccwa.org.au