Links to Commonwealth Budget 2002-03: information of relevance to Indigenous health and well being

Federal Treasurer Peter Costello delivered his seventh Commonwealth Budget on Tuesday evening, 14 May 2002. The following links provide information on the Budget and its implications for Indigenous health and well being. They include statements by various ministers, and comments by peak Indigenous bodies before and after the release of the Budget.

Full Budget details
Full Commonwealth Budget details are available at the official Budget website.

Health and Ageing Portfolio Budget 2002 – 2003
2002-03 Portfolio Budget Statements for the Health and Ageing Portfolio are available on the Commonwealth Department of Health and Ageing website. Part C discusses the performance of individual outcomes within the Department, and includes Outcome 7: Aboriginal and Torres Strait Islander Health (PDF – 194KB).

Further details regarding the Health and Ageing Portfolio Budget are available on the following web pages:

Health Budget Ageing Budget
Health Budget at a glance
Health Budget index
Health media releases
Health fact sheets
Ageing Budget at a glance
Ageing Budget index
Ageing media releases
Ageing fact sheets

Information on the future of the Pharmaceutical Benefits Scheme (PBS) (Health fact sheet No.1: Securing the future of the Pharmaceutical Benefits Scheme) receives special attention and is accompanied by a series of answers, by Minister Kay Patterson, to questions regarding the PBS.

Immigration, Multicultural and Indigenous Affairs Portfolio Budget 2002-03
2002-03 Portfolio Budget Statements (PDF – 1.5MB) for the the Immigration and Multicultural and Indigenous Affairs Portfolio are available on the Department’s website.

Part C of the document includes sections on the following:

  • Sound and well-coordinated policies, programs and decision making processes in relation to Indigenous affairs and reconciliation;
  • Aboriginal and Torres Strait Islander Commission;
  • Aboriginal Hostels Limited;
  • Australian Institute of Aboriginal and Torres Strait Islander Studies;
  • Indigenous Business Australia;
  • Indigenous Land Corporation; and
  • Torres Strait Regional Authority

Indigenous Affairs statements released on May 14 include:

Indigenous Affairs statements by other Ministers include:

National Aboriginal Community Controlled Health Organisation (NACCHO)
Prior to the delivery of the Budget, NACCHO raised concerns regarding the impact of proposed changes to the PBS.

Short sighted approach to medicines (9 May 2002)

Aboriginal and Torres Strait Islander Commission (ATSIC)
ATSIC Chairman Geoff Clark has released a background brief outlining ‘ATSIC’s budget, its role and its capacity and responsibility to provide services’ and a statement regarding ATSIC-specific funding for the 2002-03 financial year.

ATSIC Budget background
2002-03 Budget holds the line (media release)

Recipients of the 2002 Puggy Hunter Aboriginal Health Scholarships are announced

The first recipients of the Puggy Hunter Scholarships for Indigenous students in medicine and nursing were recently announced by Federal Health Minister Kay Patterson in Melbourne.

Speaking at the 5th Wonca World Rural Health Conference (1 – 3 May 2002), Senator Patterson announced that the first round of scholarships had been awarded to five medicine and three nursing students. She described the scholarships as:

‘… a lasting tribute to Dr Hunter and will go part of the way to addressing the under-representation of Aboriginal and Torres Strait Islander people in health professions. The recipients of this award have demonstrated both a commitment to leadership in the health sector and a desire to work in the Aboriginal and Torres Strait Islander communities. These skills are essential for developing a generation of skilled Aboriginal and Torres Strait Islander health professionals to continue the work that Dr Hunter tirelessly dedicated his life to.’

National Aboriginal Community Controlled Health Organisation (NACCHO) Chairperson, Ms Pat Anderson, also highlighted the importance of addressing the shortage of Aboriginal health professionals:

‘The scholarships are a testimony to the late Dr Hunter’s life-long campaign for Aboriginal health. As the [former] NACCHO Chairperson, he was passionately committed to achieving change by empowering Aboriginal people through increasing Aboriginal community control of their health services… The advantages of a strong Aboriginal workforce are obvious. Aboriginal workers in the health profession are more likely to return and provide health care in their home communities. They don’t face the kind of cross-cultural problems of many outsiders. And they can serve as health advocates for their communities, making sure that governments deliver effective and appropriate health policies… They also are important role models for young people in their community. The existence of qualified and successful professionals can be a much needed boost to the ambitions and hopes of young Aboriginal people.’

Funding of $1.23 million over five academic years (2002 – 2006) will provide at least 44 undergraduate scholarships to train Aboriginal health workers and Indigenous students in medicine and nursing. This will include:

  • 10 undergraduate Indigenous medical scholarships;
  • 10 undergraduate Indigenous nursing health scholarships;
  • 12 Aboriginal health worker scholarships for completion of Vocational Educational Training sector courses; and
  • 12 Advanced Tertiary Diploma level Aboriginal health worker training scholarships or articulation into other tertiary level health courses.

The funding will provide students with $10,000 per annum over the term of their enrolment. In addition, it is proposed to provide up to $5 000 per annum to each student as a disadvantage supplement.

Details of the successful applicants for 2002

Nursing students:

  • Emily Hunter, 3rd year student in 2002 at Notre Dame University, Broome Campus;
  • David B Baker, 3rd year student in 2002 at Australian Catholic University, Brisbane;
  • Inawantji Scales, 1st year student in 2002 at the Northern Territory University in Darwin, and the first girl from the Pitjantjatjara Lands to complete year 12.

Medical students:

  • Kiarna Adams, 3rd year student in 2002 at University of WA;
  • Sarah-Jane Gibbons, 3rd year student in 2002 at Newcastle University;
  • Bradley Murphy, 3rd year student in 2002 at James Cook University;
  • Tanya Keane, 4th year student in 2002 at Newcastle University;
  • Olivia O’Donoghue, 5th year student in 2002 at Adelaide University.

For further information:

OATSIH website: http://www.health.gov.au/internet/wcms/publishing.nsf/Content/health-oatsih-welco.htm
NACCHO website: http://www.naccho.org.au/Scholorships.html

NSW Aboriginal Vascular Health Program

The following summary is reproduced with permission of the Program Manager, Margaret Scott.

NSW Aboriginal Vascular Health Program

Suggested citation: Scott M (2002, 13 November) NSW Aboriginal Vascular Health Program. Australian Indigenous HealthBulletin, 2(4), Brief report 3. Retrieved [access date] from http://www.healthinfonet.ecu.edu.au/html/html_bulletin/bull_24/bulletin_brief_reports_cvd.htm

Artist : Bronwyn Bancroft

Overview

The Aboriginal Vascular Health Program was established in July 2000 and is responsible for supporting implementation of the components of the NSW Aboriginal Health Strategic Plan which relate to diabetes, diseases of the circulatory system and renal disease. The NSW Aboriginal Health Strategic Plan (1999) is an initiative under the NSW Aboriginal Health Partnership and the NSW Aboriginal and Torres Strait Island Health Agreement jointly developed by the Aboriginal Health & Medical Research Council(AHMRC), the NSW Department of Health(DOH), the Office of Aboriginal and Torres Strait Islander Health (OATSIH)and the Aboriginal and Torres Strait Islander Council (ATSIC).

The Aboriginal Vascular Health Program is committed to working within the NSW Aboriginal Health Partnership Framework at both state and local levels. An Aboriginal Vascular Health Working Group with representation from the AH&MRC, OATSIH and the NSW Health Department oversees the development and implementation of the program.

Program aim

To work in collaboration with relevant organisations and service providers to improve the provision of high quality prevention and care services and programs to promote the vascular health of Aboriginal and Torres Strait Islander people in New South Wales.

Objectives

  • To facilitate implementation of the components of the NSW Aboriginal Health Strategic Plan which relate to diabetes and diseases of the circulatory system
  • To improve standards of clinical care for Aboriginal people with or at risk of vascular disease ensuring a more consistent approach, support for chronic disease self-management and reduction in hospitalisation for preventable complications
  • To play a key role in facilitating the development of local Chronic and Complex Care projects in relation to cardiovascular disease in Aboriginal people as part of implementation of the NSW Government Action Plan for Health
  • To provide input into implementation of related strategies of the Aboriginal Health Strategic Plan which are pertinent to the delivery of a continuum of prevention and care for Aboriginal people in relation to chronic disease
  • To facilitate and support the implementation of local initiatives aiming to improve the provision of prevention and care programs to the Aboriginal community
  • To facilitate a more coordinated approach to Aboriginal health by directly linking with other related Aboriginal health strategies as appropriate

Reasons for adopting a vascular health approach

The Program has adopted a broad vascular health approach (including diabetes, heart disease, stroke, hypertension and kidney disease) rather than a single disease or body part approach because of the common risk conditions which place Aboriginal people at greater risk for these diseases, and the common approaches needed to prevent and manage these conditions in Aboriginal communities.

It is well known that Aboriginal and Torres Strait Islander people experience excess morbidity and mortality from diseases of the circulatory system; heart, stroke and vascular disease are the biggest cause of excess deaths in Indigenous Australians. Compared with the non-Indigenous population, Aboriginal and Torres Strait Islander populations experience :

  • rates of diabetes which are 2 to 4 times higherrates of heart,
  • stroke and vascular disease which are 2 times higher
  • rates of renal disease which are 10 to 15 times higher;
  • deaths from heart disease at twice the rate, within the 25-64 age groups this rises to 7-10 times higher.

The social and environmental circumstances in which many Indigenous Australians live create risk conditions eg poverty, poor housing, inadequate food supply which predispose them to the development of chronic diseases and the uptake of risk behaviours which may lead to physiological risk factors for chronic disease. (See Fig 1.)

The range of biological and behavioural factors which are common to and increase a person’s risk of developing diabetes, heart, stroke and vascular disease include the following:

Behavioural risk factors

  • Smoking
  • Physical inactivity
  • Poor diet and nutrition
  • Excessive alcohol use

Physiological/metabolic risk factors

  • Elevated lipids (high blood fats)
  • Hypertension (high blood pressure)
  • Hyperglycaemia (high blood sugar)
  • Overweight and central obesity

When several risk factors coexist, the risk of vascular disease is multiplied and having one of these chronic diseases can predispose to another, for example cardiovascular disease is a common complication of diabetes. Many national and state reports and initiatives recommend that a joint approach to chronic vascular disease is likely to be more effective and more efficient.

Advantages of a broad vascular disease approach

Due to the shared risk factors, primary and secondary prevention messages relating to health and lifestyle across the major health issues (ie diabetes, circulatory, renal diseases) are virtually the same. Integration of vascular risk prevention programs and clinical management interventions enables greater efficiency of effort with potentially greater health outcomes. Also a holistic approach is more in keeping with Indigenous concepts of health and illness than a separate body parts or single disease approach. It is anticipated that a coordinated and strategic whole of person approach should over time impact the delay in onset and reduced numbers of adverse health outcomes in vascular disease in Aboriginal people in NSW.

Program guiding principles

  • Implementation through state and local Aboriginal Health Partnerships
  • Adoption of a social model of health
  • Recognition that self-determination and empowerment are central
  • Congruence with national and state strategic directions in health
  • Strategies developed within a primary health care framework
  • A broad chronic disease(vascular) approach
  • Ensuring Aboriginal community support and involvement
  • Ensuring cultural appropriateness of strategies and programs
  • Focus on patient centred services
  • Adoption of an holistic approach
  • Prevention as a priority, with a whole of life course approach
  • Support for chronic disease self-management
  • Utilisation of a capacity building approach
  • Inter-sectoral collaboration to modify identified determinants of health and achieve consistency and synergy of effort
  • Optimum utilisation of all available resources
  • Ensuring transparency and accountability

Current program initiatives

The AVHP has developed a comprehensive Strategic Framework (see Fig 2) and is implementing a broad range of interrelated projects with funds allocated in 2000/2001 and 2001/2002 through Aboriginal Statewide Enhancement Funds. From July 2002 the AVHP has been recurrently funded.

Aboriginal vascular health demonstration site projects

A series of demonstration site Aboriginal vascular health projects has been funded throughout the state, commencing in April 2001. The projects are developed and implemented through local partnerships with service providers and communities to establish programs and models of care to improve the prevention and management of vascular disease in local Aboriginal people. All projects have a strong emphasis on working collaboratively with mainstream and Aboriginal Community Controlled Services to provide the best services possible utilising locally available resources. Aboriginal health workers are working in a range of designated roles; training and support is being provided to increase knowledge and skills in prevention, early detection and management of chronic diseases. The projects are being closely monitored and evaluated to gather evidence and develop a better understanding of effective systems and models of care.

In 2001 projects were funded in 8 Area Health Services (Central Coast, Hunter, South Western Sydney, Western Sydney, Macquarie, Illawarra, Mid-Western, New England) and 3 correctional sites serviced by Corrections Health Service (Broken Hill, Tamworth, Grafton).

In 2002 additional projects are being funded in Mid North Coast, Northern Rivers, Greater Murray, South Eastern Sydney, Far West, Wentworth and 3 additional Correctional Centres (Emu Plains, Mannus, Ivanhoe).

Vascular health project objectives

The projects aim to:

  • improve prevention, early identification, early intervention and ongoing care for Aboriginal people with or at risk of vascular disease
  • increase primary health care utilisation by Aboriginal people
  • promote greater coordination and continuity of care for those with established disease, with an emphasis on community based care and support for disease self-management
  • reduce preventable hospital admissions for complications of vascular disease
  • promote improved environmental and community support for disease prevention and health improvement

Key features of all projects:

  • project development and implementation through local Aboriginal Health Partnerships and with relevant local services providers and other stakeholders
  • recruitment and training of designated Aboriginal Vascular Health Workers
  • close integration with the Chronic and Complex Care Cardiovascular projects in local Area Health Services
  • close monitoring and evaluation
  • a central focus on improved access to early detection of disease and risk, referral for care improved coordination of services and provision of evidence based care and support for disease self-management

Aboriginal vascular health network

A key strategy of the NSW Aboriginal Vascular Health Program has been the establishment of a network for all health professionals involved in work related to Aboriginal vascular health. The AVHN has a wide range of membership including: Aboriginal and non-Aboriginal health professionals, clinicians, and staff from relevant non-government organisations such as Aboriginal Community Controlled Health Services, National Heart Foundation of Australia, Diabetes Australia, and Australian Kidney Foundation. The AVHN aims to provide a support and information and resource dissemination system for those working in Aboriginal chronic disease in NSW. A quarterly bulletin Vascular Health Matters is distributed to members to share information on the NSW Aboriginal Vascular Health projects, other AVHP activities, available resources, funding opportunities, conferences and current programs being conducted around NSW and Australia. All interested health professionals are welcome to join the network.

Aboriginal vascular health resource catalogue

To increase information on available resources, the NSW Aboriginal Vascular Health Program has developed a comprehensive catalogue which includes a description of education and training resources available for cardiovascular disease, diabetes, renal disease, public health and project development which are relevant for Aboriginal and Torres Strait Islander communities. Information on relevant web-sites and available training is also provided.

Aboriginal vascular health workforce development

A strategy to build the capacity of the Aboriginal Health Workforce in the prevention and management of vascular disease is being implemented. A workshop training manual about Aboriginal people and kidney disease Check your kidneys has been produced and similar manuals in cardiovascular disease and diabetes are underway. Other resources will be developed over time according to identified need.

Check your kidneys – training manual

The Check your kidneys training manual was developed in partnership with the Centre for Kidney Research at the Children’s Hospital Westmead and was piloted across the state. The purpose of the training is to increase awareness and knowledge of kidney disease in Aboriginal people and to create an opportunity for health workers and health services to identify steps which can be taken to address kidney disease in their home, community and workplace roles. The training has a strong emphasis on prevention across the continuum of life.

Research initiatives

Improving prevention and care of diabetes and related disease in the Aboriginal community of Wagga Wagga (NHMRC Grant)

This collaborative research initiative involves the implementation and evaluation of an Australian version of a model of systematic diabetes care (Staged Diabetes Management) which has demonstrated significant health improvements following its introduction into American Indian Health Services. The project is being conducted in collaboration with the Riverina Medical and Dental Aboriginal Corporation in Wagga Wagga, NSW.

Models of chronic disease self-management for Aboriginal vascular disease

Specific focussed projects developing and testing appropriate and effective models of disease self-management for Aboriginal people with established vascular disease have been funded in the Illawarra Aboriginal Medical Service at Wollongong and Daruk Aboriginal Medical Service at Mt Druitt.

Aboriginal vascular health indicators framework

A framework is under development to monitor progress in Aboriginal vascular disease prevention and management in NSW. The initial focus will be on measuring changes in local capacity to address prevention and management issues.

Program evaluation

A 12 month evaluation of the AVHP commenced in August 2002 to assess the appropriateness and effectiveness of the overall program strategic approach and of individual project initiatives of the Program. The evaluation has a strong participatory and capacity building approach.

On the web

The Aboriginal Vascular Health Program can be viewed on the NSW Department of Health internal website which also contains details of the 9 demonstration site vascular health projects. Address: http://internal.health.nsw.gov.au/public-health/crcp/ceb/projects/projects.html

Program contacts

For more information about the Aboriginal Vascular Health Program contact:

Margaret Scott
Program Manager Aboriginal Vascular Health Program
Centre for Research and Clinical Policy
NSW Health
LMB 961, N Sydney 2059
Email: mscot@doh.health.nsw.gov.au
Tel: 02 9391 9853
Fax: 02 9391 9556

To join the Aboriginal Vascular Health Network or obtain a copy of the Aboriginal Vascular Health Resources Catalogue forward contact details to:

Samantha O’Connor
Project Officer
Aboriginal Vascular Health Program
Centre for Research and Clinical Policy,
NSW Health,
LMB 961, N Sydney 2059,
Tel: 02 9391 9571
Fax: 02 9391 9556
Email: socon@doh.health.nsw.gov.au

Indigenous palliative care needs study 2002

The Commonwealth Department of Health and Ageing has initiated a national scoping study into the needs of Aboriginal and Torres Strait Islander peoples in the area of palliative care. The study is being done by consultants Kate Sullivan and Associates and will be conducted throughout 2002.

The primary aim of the study is to identify the palliative care services available to Aboriginal people and Torres Strait Islanders, find out how well these services work and whether they can be improved, and determine whether there are areas where needs are not being met. This information will be used to inform and improve the Commonwealth’s National Palliative Care Strategy, and identify areas where resources are most needed. The formal objectives of the scoping study are to identify:

  1. Existing activities in palliative care for Aboriginal and Torres Strait Islander peoples at Commonwealth,State/Territory and community levels, including mainstream programs, which incorporate Indigenous components as well as Indigenous-specific activities.
  2. Areas that could be enhanced or developed under the National Palliative Care Strategy at Commonwealth, State/Territory and community levels.
  3. The particular needs of Aboriginal and Torres Strait Islander peoples for palliative care, taking into account the diversity of Aboriginal and Torres Strait Islander communities and the different needs of rural, remote and metropolitan communities.
  4. Spiritual and cultural practices that relate to death and examine the extent to which these are being implemented in a culturally sensitive way, taking into account the diversity of settings and cultural beliefs.

The project recognises that Aboriginal and Torres Strait Islander communities’ experience of loss and grief is profoundly affected by socioeconomic disadvantage, high death rates, and past policies which have caused separation and loss. It also recognises the central place of family and of the land, and that cultural and spiritual beliefs are particularly important in providing appropriate palliative care services to Aboriginal people and Torres Strait Islanders.

The scoping study is overseen by a Steering Committee which includes Indigenous members from the Congress of Aboriginal and Torres Strait Islander Nurses and the Aboriginal and Torres Strait Islander Research Agenda Working Group. The team of consultants, headed by Kate Sullivan, also includes Indigenous researchers and interviewers with specialist skills and experience in working with Indigenous communities.

The project is being conducted in four parts. The first (stages 1-3), which will be completed in April 2002, includes a literature review and scoping study, conducted by telephone. A series of questions have been developed for state and regional agencies, service providers, and community organisations, to gather information about palliative care services in their regions. The aim of the phone survey is to find out who is doing what (including provision of appropriate training) to enable the Steering Committee and consultants to decide which communities should be visited later in the research.

The second part (stages 4-5, May-June 2002) will focus on methodology development and partnership development with the communities in which the consultants wish to undertake field work. Relevant ethics committees and community organisations will be asked to review the methodology.

Field work will be conducted during stages 6-7 of the project (July-October 2002). The purpose of the field work will be to record from the perspective of Aboriginal and Torres Strait Islander people their experience of existing palliative care services and the unmet needs they identify. The field work will include rural and remote areas and some metropolitan centres where services are often not appropriate to Aboriginal and Torres Strait Islander needs. The field work will be conducted by male and female team members and will provide for remuneration for local Aboriginal and/or Torres Strait Islander assistance. A question sheet will be posted to community organisations in selected communities that cannot be visited.

The final part, stages 8-9, will be the reporting phases. There will be several rounds of reporting and the final report will be in two parts – a detailed report for the Commonwealth Department of Health and Ageing, and a short ‘plain English’ report which will be made available to all communities and organisations that have participated in the study. It is expected that reporting will be finalised by March 2003.

Information about the study and the consultants can be obtained from http://member.telpacific.com.au/ksa/. A newsletter will be posted on the website and distributed to participating communities and organisations.

The consultants are keen to hear from people who are providing palliative care services to Indigenous people, and are particularly interested in examples that are considered good practice.

Kate Sullivan can be contacted at (02) 9810 5755 or 1800 810 575.

Australian Indigenous HealthInfoNet gives keynote address at the national Aboriginal Health Information Symposium in Ottawa, Canada

Professor Neil Thomson, Director, and Bronwyn Gee, Manager presented a keynote address on ‘a model of knowledge management for Aboriginal health’ at the national Aboriginal Health Information Symposium held in Ottawa, Canada on 11-13 February.

The topic was of particular relevance to the National Aboriginal Health Organization (NAHO), as effective knowledge management has been recognised as critically important in addressing its mandate of improving and promoting the health of Canada’s Aboriginal Peoples and communities.

The presentation included a demonstration on how the HealthInfoNet attempts to address the needs of the variety of potential users of Australian Aboriginal and Torres Strait Islander Indigenous health knowledge and information.

Neil outlined how the HealthInfoNet researches and develops introductory material and detailed overviews of specific health conditions and topics, regularly updated summaries of Aboriginal and Torres Strait Islander health status, and brief answers to frequently asked questions. He stressed that:

‘It is important that knowledge and other information provided to users is both authoritative and current. Dissemination of knowledge and other information via the Internet provides the potential to be totally up-to-date.’

Bronwyn and Neil also conducted a HealthInternet café on the Tuesday and Wednesday of the symposium. This provided delegates with an opportunity of getting some hands-on guidance on specific topics. The café also demonstrated how the Australian Indigenous HealthInfoNet could be used as a model for a comprehensive site for Canadian Aboriginal health.

The opportunity to participate at this symposium was an enlightening experience, with Bronwyn and Neil attending many thought-provoking and challenging sessions including ‘Don’t be on the other side of the digital divide: an overview of current health information initiatives impacting Aboriginal Peoples’ by Ms Ceal Tournier, First Nations Centre Governing Committee, NAHO.

They were able also to consider similarities and differences between the HealthInfoNet and Canadian initiatives, and explore various ways to use health knowledge and information to inform and strengthen the health care system for Indigenous people, and thus contribute to improvements in health and wellbeing.

Acknowledgment to NAHO for their permission to use these photos

Harkness Fellowship examining Indigenous Australians’ access to kidney transplantation

Dr Alan Cass, a PhD student at the Menzies School of Health Research and researcher at the Cooperative Research Centre for Aboriginal and Tropical Health, has been awarded a Harkness Fellowship to continue his research in the United States. He will undertake a cross-national study of the barriers facing Indigenous Australians and Native Americans with end-stage renal disease (ESRD) who need a kidney transplant. He is a clinical nephrologist at the Royal Darwin Hospital and a member of the ‘Sharing the True Stories’ team looking at the impact of miscommunication in the delivery of health care to Indigenous patients with ESRD. His PhD explores health inequalities in Australia, with a focus on renal disease.

Nine Harkness Fellowships are awarded each year to scholars in Australia, New Zealand and the United Kingdom to allow them to spend up to 12 months in the US. The Fellowships are managed by the Commonwealth Fund, a private foundation that supports independent research on health and social issues. The Fund’s goals are to improve access to health care for disadvantaged groups and to improve quality of care. It aims to build a network of policy-oriented health care researchers and to stimulate innovative thinking on health policy and practice in the United States and other industrialised countries.

Native Americans, like Indigenous Australians, have very high rates of renal disease and receive relatively few transplants, the most effective treatment for ESRD. A successful transplant confers a better quality of life, a longer life expectancy and results in lower costs than does the alternative, long-term dialysis.

Similar factors may well influence transplantation for both Native Americans and Indigenous Australians. Social determinants-poverty, lack of education and other disadvantage-play an important part, but cultural issues also profoundly affect how Indigenous people relate to the health care system.

Dr CASs will use US databases pertaining to dialysis and renal transplantation. He will examine how people have interacted with the system and whether they have had access to transplants. He plans to use the data to document any disparities and then to interview service providers, policy makers and, of course, Native Americans themselves, to discover whether or not there are systemic barriers to access.

The predominant aim of his research is to develop strategies that will help improve equity in access to transplantation for Indigenous Australians.

Alan CASs MBBS FRACP Grad. Dip. Clin. Epidemiology
PhD student, Menzies School of Health Research
Nephrologist, Royal Darwin Hospital

James Cook University: maternal health education program for health workers

Jenny Darr, Hanni Gennat, Jacinta Elston, Lynore Geia, Adrian Miller, Vicki Saunders.

It has been acknowledged by both community stakeholders and government that Aboriginal and Torres Strait Islander women are in the high-risk group for complications at any stage of pregnancy1. Infant mortality rates for Aboriginal and Torres Strait Islanders remain unacceptably high, with prematurity and low birth weight still prevalent especially in remote areas2.

Earlier recruiting of Aboriginal and Torres Strait Islander pregnant women into antenatal programs is essential, as maternal nutrition, substance abuse, high blood pressure and infections are all important risk factors for low birth weight babies. The anecdotal experience by Aboriginal and Torres Strait Islander women is commonplace.

In order to meet the demand of providing adequate services and programs, the health workforce must be trained. Aboriginal and Torres Strait Islander participation in the workforce is essential and should not be an optional add-on for any Indigenous community. Aboriginal and Torres Strait Islander Health Workers have been recognised through numerous government and community reports as being central to the provision of health services for Indigenous people, and invaluable in the role of cultural and health brokers3, 4. Aboriginal and Torres Strait Islander Health Workers provide culture-specific knowledge, access, and an ability to liaise with Indigenous communities about their interactions with the health care system.

Today, throughout all States and Territories there is an expansive network of Aboriginal and Torres Strait Islander Health Workers, employed in either Aboriginal Medical Services or by State/Territory Health Departments. Their scope of practice and career paths as health professionals within the broader health field has been slow since the creation of the Aboriginal and Torres Strait Islander Health Worker role.

A major objective of this education program offered through James Cook University, School of Public Health and Tropical Medicine, is to increase the number of skilled Aboriginal and Torres Strait Islander Health Workers in maternal health, to help address the unacceptably high levels of Aboriginal and Torres Strait Islander perinatal mortality and morbidity, through improving access to and appropriateness of obstetric services especially in under-serviced rural and remote areas.

The National Centre for Maternal Health Education for Aboriginal and Torres Strait Islander Health Workers has an innovative program entitled ‘Maternal Health for Aboriginal and Torres Strait Islander Health Workers’. The Program provides theoretical knowledge and clinical skills enabling Aboriginal and Torres Strait Islander Health Workers to better manage maternal health care within their communities.

The Royal Australian College of Obstetrics and Gynaecology (RACOG, now RANZCOG) established a pilot program in 1990 with funding from the Federal Government (DEETYA) to provide a Skills Transfer (Maternal Health Education) Program for 12 Aboriginal Health Workers, in Broome, Western Australia. The Aboriginal and Torres Strait Islander Health Studies unit in the School of Public Health and Tropical Medicine (SPHTM) at James Cook University taught the skills transfer program.

This early collaboration developed into the current partnership between RANZCOG, the SPHTM at James Cook University, Kimberly Aboriginal Medical Service Corporation (KAMSC) and the teaching hospitals involved in the program. A Commonwealth grant in 1997 saw an injection of financial resources enabling the partners to increase the numbers of courses on offer each year and the number of sites where teaching occurs. This improved access for Aboriginal and Torres Strait Islander Health Workers whose ability to study was limited by family, community and work commitments.

The Maternal Health Education Program is aimed at transferring both practical skills and knowledge to female Aboriginal and Torres Strait Islander Health Workers, allowing them to practically contribute to the obstetric care of Aboriginal and Torres Strait Islander women during their antenatal, labour and post natal terms. The course has been designed to provide the experienced health worker with a solid foundation in both theoretical background and clinical experience. It aims to optimise the management of normal pregnancy and the early identification of at-risk pregnancy. It is now offered to both experienced and non-experienced health workers.

The Maternal Health Education Program is delivered in block mode comprising a two-week theoretical component with face-to-face delivery of lectures and a clinical placement, consisting of an additional two weeks within an appropriate tertiary level maternity hospital.

The program examines current maternal health epidemiological patterns and includes an examination of various maternal health programs and their comparative impact. The curriculum includes a basic knowledge of female anatomy and obstetric anatomy and physiology; the principles of normal pregnancy and antenatal care, the recognition and management of high risk and abnormal pregnancy, and management of the puerperium. Other topics include: the recognition of onset of labour, management of out-of-hospital deliveries, communicating effectively with hospital staff, abnormal palpation and the use of foetal Doppler and stethoscope.

A variety of teaching techniques are used to achieve these learning objectives. These include small group learning sessions and clinical skill laboratories using mannequins and case studies. Teaching aids such as videos and mock case studies help reinforce the theoretical content. Nutrition, sexual health, breast feeding, risk factors for high-risk pregnancy, and post-natal care at home and hospital, are subjects delivered by guest lecturers with particular expertise in these topics. During each block guest lecturers who work or reside in the community where the block is being delivered are identified and invited to lecture on specific subjects. This enables a local community perspective and flavour to be fostered within particular sessions inclusive of the objectives that have been outlined in curriculum.

The content is delivered in such a way that it aims to contextualise Indigenous worldviews and experiences within the western medical setting, as appropriate for maternal health. Consequently, the students participate more effectively in the learning process.

The structural design of the program content enables students to follow a logical pathway in basic maternal health care. It exposes students to technical terminology and practices of maternal medicine whilst being delivered in the context of Indigenous learning. The topics are sequenced from pre-conception to antenatal care and then on to postnatal care and are delivered in the context of the physiological processes that would occur in a normal pattern of pregnancy. Additionally, the course structure is designed to address those factors such as nutrition, sexually transmitted infections, substance misuse, and other factors that contribute to high-risk pregnancies which are prevalent amongst Aboriginal and Torres Strait Islander mothers.

The clinical component of the course is designed to cement the knowledge acquired during the theoretical component by immersing health workers in a clinical hospital setting. This ensures student learning by hands-on, practical experience within a major tertiary (teaching) maternity hospital. This is further reinforced by the clinical assessment, which requires the student to attain specific skills while on placement. During clinical placement, students are exposed to a variety of ward areas within the hospital to experience and attain a wide range of skills. The students are required to complete a Clinical Experience Record that demonstrates they have observed and conducted a range of appropriate clinical and program activities whilst on placement.

Many factors impact on the ability of the graduates to successfully apply the skills and knowledge attained during the course. There is some anecdotal evidence that the program is contributing to increased antenatal attendance and at an earlier stage in pregnancy at several sites around Australia5. This experience includes several Aboriginal Community Controlled Health Organisations who have established dedicated Maternal and Child health programs utilising the skills and knowledge of staff that have successfully completed the program.

The course has had national uptake. There has also been an increase in hospital sites participating in the clinical phase of the program to accommodate the increased number of students in the course. The hospitals include: The Townsville Hospital (Townsville, QLD), Royal Darwin Hospital (Darwin, NT), King Edward Hospital (Perth, WA), Nepean Hospital (Penrith, NSW), and King George V Memorial Hospital for Mothers and Babies (Sydney, NSW). A range of tertiary hospital sites are utilised to expose Aboriginal and Torres Strait Islander Health Workers to the treatment and care that the majority of high-risk Indigenous mothers and babies experience in these hospital settings.

The Maternal Health Education program featured as part of the recommendation in a report to the Victorian Aboriginal Community Controlled Health Organisation (VACCHO) and the Victorian Department of Human Services6. The report recommended that the James Cook University Maternal Health Education Program be made available to all female Aboriginal and Torres Strait Islander Health Workers involved in maternal and child health care. VACCHO emphasised that the course is Aboriginal owned and recommended that Aboriginal and Torres Strait Islander Health Workers who are employed to provide maternity services, undertake this training.

In 1997, a new course, Basic Ultrasound Skills for Indigenous Health Workers in Remote Locations was written as a partnership between SPHTM, RANZCOG and the Australasian Society of Ultrasound Medicine. The course was designed to provide female Aboriginal Health Worker in rural and remote settings with limited access to sonographers, skills in maternal ultrasonography. The ultrasound course is skill specific and is only intended to assist Health Workers to identify a normal pregnancy via ultrasonography. The course emphasises that any abnormal findings should be referred to a doctor. Since the commencement of this course a total of nine students have been trained in maternal ultrasound skills. All of the ultrasound students are currently based in rural or remote communities. Indigenous women appear already to be attending the antenatal clinic earlier often in the hope of having an ultrasound examination. It has also become apparent that the partners of the pregnant women are also attending the ultrasound examination, which was previously unheard of in this community7.

Health Worker Profile

Heather Lee successfully undertook her Health Worker training at Townsville TAFE, and the Maternal Health Education Program in 1999, also in Townsville. Heather completed the clinical component of the course at Kirwan Hospital for Women (now The Townsville Hospital) and stated that this experience was good. She has since been working at Townsville Aboriginal and Islander Health Service (TAIHS) as the Coordinator/Health Worker of Mum’s and Babies Clinic. Heather has always had an interest in the medical field and her experiences as a birthing partner for friends and family led her to pursue studies so that she could formally provide health assistance to the Indigenous population.

In the Mum’s and Babies Clinic Heather finds that she utilises her maternal health training on a daily basis and the program has grown successfully since her employment in this position. Heather says that being able to provide holistic and culturally appropriate care to Aboriginal and Torres Strait Islander women has improved their health and wellbeing and she enjoys being part of this important team.

When asked whether she thought her training had been of benefit to her employer, Heather said she thought her training had helped to generate an increasing client base to the Mum’s and Babies clinic, which has an atmosphere where everyone feels comfortable and safe to attend. Heather feels that her maternal health training has improved the quality of the service that she provides as she is able to discuss women’s issues with clients in a safe environment and feels confident about giving them information that they can easily understand.

Heather believes that all of the Townsville community, particularly those who attend the clinic (and their families and partners) have benefited from her training and has helped to break down barriers between non-indigenous and indigenous people. This unique Mum’s and Babies clinic has been funded for a two-year period by Rio Tinto, and provides an important service. Unfortunately at this point in time, TAIHS has been unable to secure future funding for this successful program.

Ms Heather Lee – Coordinator of Mum’s and Babies Clinic at TAIHS

References

    1. NHMRC. (2000). Standards of Antenatal Care.

 

    1. Commonwealth of Australia. (May 2000). Health is life: Report on the Inquiry into Indigenous Health House of Representatives Standing Committee on Family and Community Affairs. Canberra. Family and Community Affairs. pp 4.

 

    1. Commonwealth of Australia. (May 2000). Health is life: Report on the Inquiry into Indigenous Health House of Representatives Standing Committee on Family and Community Affairs. Canberra. Family and Community Affairs. pp 97-98.

 

    1. William, A. and Cadet-James, Y. (2000). The role of tertiary education in strengthening Indigenous health. Brisbane. Centre for Indigenous Health Education and Research, University of Queensland.

 

    1. Aboriginal and Torres Strait Islander Health Studies. (May 2001). Internal Report on the Maternal Health Education Program for Aboriginal and Torres Strait Islander Workers. Townsville. School of Public Health and Tropical Medicine, James Cook University. pp 44.

 

    1. Campbell, S. (2000). From Her to Maternity. A report to the VACCHO members and the Victorian Department of Human Services about maternity services for the Aboriginal women of Victoria. Melbourne. Department of Human Services, Victorian Government. pp 33.

 

  1. Kohlenberg, C. (1998). Report on the review of the pilot scheme. Penrith. Ultrasound skills transfer project, Nepean Hospital

Patricia Fagan: new senior medical advisor at the Office for Aboriginal and Torres Strait Islander Health added

In October 2001, Patricia (Trish) Fagan was appointed as senior medical advisor (SMA) at the Office for Aboriginal and Torres Strait Islander Health (OATSIH). She brings to the position a wealth of experience in Indigenous health. The Australian Indigenous HealthInfoNet asked Trish to submit a brief article to the HealthBulletin regarding her recent appointment. She has provided an informative piece that explains OATSIH’s primary objectives, the role of the SMA within the Office, her own background in Indigenous health, and what she hopes to contribute as SMA at OATSIH.

About OATSIH

The Office for Aboriginal and Torres Strait Islander Health (OATSIH) was established in the mid 1990s when responsibility for Aboriginal and Torres Strait Islander health at a Commonwealth level moved from the Aboriginal affairs to the Health portfolio (OATSIH is located in the Department of Health and Ageing).

Since its beginning, the Office has developed its vision to reduce the gap in health status between Indigenous and non-Indigenous Australians through strengthening primary health care for all Aboriginal and Torres Strait Islander people. Support for Indigenous specific community-controlled services and the improvement of functional access to general health services are priorities. The Office supports strategies to reform existing health systems and improve the infrastructure, workforce and information systems on which comprehensive primary health care rests. It aims to address specific health issues and to enhance the evidence base that underpins health interventions. In addition, OATSIH seeks ways to maximise whole-of-government responses across all levels of government and jurisdictions to achieve improvements in Aboriginal and Torres Strait Islander health.

The Office is organised around three broad streams of activity: health and community strategies, program planning and development, and workforce, information and policy. Within these streams, current activities include:

  • the primary health care access program (PHCAP) directed at improving access to primary health care through supporting mechanisms to increase community-control, reforming existing health system structures, and increasing the available resources within selected PHCAP sites;
  • initiatives directed at improving access of Aboriginal and Torres Strait Islander peoples to general health programs (for example, the Medicare Benefits Schedule and the Pharmaceutical Benefits Scheme);
  • consultation on a draft National Strategic Framework for the Aboriginal and Torres Strait Islander health workforce
  • assisting the Minister’s National Aboriginal and Torres Strait Islander Health Council in its task to consult on and finalise a second National Aboriginal and Torres Strait Islander Health Strategy;
  • the development of policy frameworks in the areas of chronic disease and maternal and child health; and
  • support for the work of the Research Agenda Working Group in its task to develop a strategic ‘roadmap’ to facilitate and guide initiatives, nationally, in Aboriginal and Torres Strait Islander health research.

The breadth and depth of activity is impressive.

The role of SMA at the Office

The senior medical advisor (SMA) position is important in linking the Office and other areas of the Department of Health and Ageing, in particular those areas concerned with medical professional activity. The SMA facilitates liaison with outside organisations (such as medical schools, universities and research institutions) and maintains communication with medical and other health professionals and organisations in the Indigenous health field. Within the Office, and in collaboration with other staff, the SMA provides clinical and public health expertise, and guidance for policy development work. There is considerable room to move within the position, with scope to take on projects of interest and to allow one’s particular experience and talents to be utilised.

My background in Indigenous health

With Queensland Health in far north Queensland

I arrived in the Office from far north Queensland (FNQ) in October 2001, having worked for some years for Queensland Health as a community women’s health program manager. I established an outreach women’s general practitioner service for remote area Aboriginal and Torres Strait Islander women (now operating under the auspices of the Royal Flying Doctor Service (Qld) as the Rural and Remote Women’s Health Program). In FNQ, this service is supported by visiting district mobile women’s health teams (comprising registered nurse and health worker), an accredited training program, comprehensive information systems, and access to specialist services. This well-women’s program has increased women’s access to a skilled women’s health practitioner and to appropriate reproductive health and well-women’s screening services. It has resulted in 200-300 per cent improvement in cervical screening participation rates over the course of the 1990s (albeit from a very low base). Importantly, all elements of this program continue today.

Other activities during my time in FNQ included:

  • the establishment of the breast screening service in Cairns;
  • overseeing the feasibility study that explored options for the provision of breast screening to remote area women in FNQ; and
  • the development of the medical aspects of a sexual assault service. Since1993, the Cairns-based sexual assault service has provided a female medical officer to attend adult women immediately following sexual assault.

I worked also for ‘The Well Person’s Health Check’ project as the sexual health physician for the first 18 months of its operation, and was involved in the implementation of an important initiative that has introduced screening for domestic violence in Queensland Health facilities (the Queensland Domestic Violence Initiative). I was a member also of the FNQ Community Corrections (Parole) Board up to October 2001, building on an early interest in Indigenous prison health that arose from clinical visits to prisons in Sydney during the 1980s.

With the Redfern Aboriginal Medical Service in Sydney

Prior to my time in Queensland, I was privileged to work in Sydney at the Aboriginal Medical Service (AMS) in Redfern for nine years. I started work at Redfern as a young(ish!!) medical officer having recently returned from post-graduate clinical training (with an emphasis on women’s and children’s health) in England. I returned to Australia in order to work at the Redfern AMS and, indeed, I had to wait six months (for the departure of Dr Archie Kalokerinos) before they could take me on. Working at Redfern was grand – a great clinical experience within a pretty cohesive community.

It was a tremendously steep learning curve:

  • interacting across cultures (with bemused and tolerant teachers);
  • operating in a multidisciplinary health care team;
  • participating in intersectoral action in health service provision; and
  • working in an organisational structure that fostered community-control and made community development a reality for many individuals and satellite communities.

After five years as a full-time general practitioner within the AMS I took on a more public health role, working only part-time in the clinic. Over the following few years, I completed a Master of Public Health and was involved in much project work at Redfern. These projects included writing submissions (such as: Far West Children’s Home at Manly, asbestos mining at Baryulgil, drug and alcohol treatment programs in the inner city, prison health, etc.), development of health promotion programs (HIV, breast-feeding, diabetes, immunisation), and the conduct of research (mental health problems presenting to Indigenous primary health care services in NSW – the subject of my masters thesis).

How I hope to contribute to OATSIH’s vision

The OATSIH has come far since its establishment. There have been gains – but the strengthening of primary health care remains a continuing challenge and core business for a department of health. At a broader level (than health alone can achieve), it is critical to improve the environment into which many Aboriginal and Torres Strait Islander children are born. I hope to contribute to this vision during my time in OATSIH, in particular through:

  • strengthening OATSIH’s links across the Department and with medical professionals/organisations involved in Indigenous health; and
  • the carriage of projects that will benefit from my medical and public health experience (across a diverse range of Aboriginal and Torres Strait Islander health settings – in urban and remote locations, and within both the community-controlled and government health sectors).

Dr Patricia Fagan FAFPHM, DCH, DRCOG
Senior Medical Advisor
The Office for Aboriginal and Torres Strait Islander Health
Department of Health and Ageing
Patricia.Fagan@health.gov.au

Sharing an Aboriginal aged care quality assessor’s journey

The following report has been reproduced from The Standard with kind permission of the author, Noela Baigrie.

‘Elders have always played a critical role in maintaining the health of Indigenous nations. They are living libraries, repositories of the oral traditions for their nations. They remember the old ways, old ceremonies, songs to sing for gathering the plants, medicines to use that will cure their people. In the face of environmental degradation and excessive agricultural use of the land, this foundation has been shaken to its core’ (L.A. Colomeda & E.R.Wenzel, 1999. ‘Medicine Keepers: Issues in Indigenous Health’ ).

My first recollection of caring was the nurturing role of my Grandmother and Mother. It was through these influences that my passion for caring was awakened. My Grandmother and Mother encouraged and guided me into truly understanding and accepting the dual role of embracing and choosing the best from both cultures. It is my true passion and desire to care for my old people and that has enabled me to apply my skills to develop best practice models for Indigenous aged care facilities.

My career in nursing commenced in 1967 and by 1997 I was the Director of Nursing at Jimbelunga Indigenous Nursing Centre. In my 30 years as a registered nurse I have found that one of the greatest opportunities for improvement lies within the true identification and assessment of the needs of Indigenous aged peoples in Australia.

In July 2000 I was sponsored to undertake training as an aged care quality assessor. I could see that the achievement of my registration as an aged care quality assessor was another milestone in my journey and passion for caring for my old people. When I successfully completed my quality assessor training and was placed on the Quality Society’s Register as an aged care assessor, another part of my dreaming was realised.

When the Aged Care Standards Agency in Western Australia contacted me about my availability to undertake an audit in the Kimberley’s, my initial response was one of shock. After this instinctive reaction had passed there was a tingle of excitement and an even greater surge of honour and pride that came with the privilege of being selected as the first Indigenous aged care assessor to conduct an aged care audit in Australia.

The challenge facing me was not being able to follow in anyone’s footsteps and not having an Indigenous mentor or role model was quite daunting. This was overcome through the positive and real support and encouragement provided by: Alan Litschner, a colleague and dear friend; Michael Menso from the Systems 3 Group; and Suzanne Leavesley, State Manager, Aged Care Standards and Accreditation Agency WA. My thanks and appreciation must go to these remarkable people.

My auditing journey commenced with a day’s flight from one side of the country to the other and this not only moved me geographically but tossed me right out of my comfort zone. My long flight gave me, not only the opportunity to ponder this adventure, it provided me with the chance to reflect upon the influences of my Grandmother and Mother that led me to follow my dreams in aged care. It was during this journey I realised that they would be happy to see this achievement for our people. This thought gave me the courage and strength to positively participate in one of the greatest challenges in my working life.

In my journey toward the facility being audited I experienced mixed emotions about the history of Indigenous aged care within this country. These feelings were shared with my fellow auditors Christine Martin and Jenny Pike. Through our sharing of experiences during this journey Jenny and Christine provided me with confidence that the aged care auditing system was positively focused and flexible in the assessment of Indigenous aged care facilities.

Upon reaching the facility I was encouraged and delighted to observe my elders receiving high quality care in a safe and comfortable environment that was culturally acceptable and suitable. The harmonious environment of the facility was underpinned by the cooperation and positive interaction between all levels of the management and staff.

Another prominent feature of my observations related to the encouragement of residents and staff to retain and use their tribal language. This was music to my ears! This was further reinforced through discussions with other people from the area as they were delighted to see one of their own people assessing one of their own facilities.

Another memorable aspect was the positive and constructive spirit in which the facility greeted and interacted with me. Whilst the facility management and staff may have experienced some minor apprehensions about my visit, these were quickly dispelled and I delighted in the positive interaction with the team at this facility.

From an auditor’s perspective one can appreciate that the implementation of the Aged Care Standards could be viewed as a potentially arduous exercise. It is extremely pleasing to have been exposed to one of the success stories.

In summary, I can only say that the opportunity to undertake this audit was initially intimidating, however it quickly transformed into one of the most memorable and pleasant experiences of my career. My true thanks has to be extended to Christine & Jenny for their support, encouragement and mentoring during the audit. It was truly wonderful to meet and to work with two such practised auditors who gladly shared their understanding and knowledge with me.

I look forward to my next opportunity to audit with the Agency

It is hoped that all readers of this article will appreciate and recognise the right of Indigenous aged care facilities within Australia to maintain their true spirit, purpose and individual sense of identity.

Thank you for allowing me to share my story with you.

Noela Baigrie
Principal Advisor
Sharing Solutions
Queensland

Please feel free to provide me with reader feedback by email: noelab@sharingsolutions.com.au or ph: 0407 200 888

Dr Arnold ‘Puggy’ Hunter (1951 – 2001) recipient of 2001 Human Rights Medal

The late Dr Arnold ‘Puggy’ Hunter has been named by the Human Rights and Equal Opportunity Commission as the recipient of the Human Rights Medal 2001.

Dr Hunter fought uncompromisingly for human rights for the Aboriginal community. Upon his untimely and recent death, tributes to Dr Hunter poured in from around Australia -click here to view the obituary by Professor Neil Thomson from the HealthInfoNet and obituaries from Indigenous groups, federal politicians, medical boards and associations.

Dr Hunter helped establish the East Kimberley Aboriginal Medical Service in 1982, and served as Chairman of the Kimberley Aboriginal Medical Services Council for many years.

In 1991, Puggy was elected as inaugural Chairperson of NACCHO (the National Aboriginal Community Controlled Health Organisation), the peak national advisory body on Aboriginal health.

As Chairperson of NACCHO, Puggy worked tirelessly to strengthen and expand the crucial roles of Aboriginal community-controlled health services. He played a critical role in government responses to Indigenous health, including the negotiation of health framework agreements in every State and Territory.

Puggy also made a major contribution to ensuring that Medicare services and the Pharmaceutical Benefits Scheme benefits were more equitably provided to Indigenous people, particularly those living in remote parts of the country.

He was Deputy Chair of the National Aboriginal and Torres Strait Islander Health Council, the principal advisory body to the Minister for Health and Aged Care. Puggy was also a Chairman of the Aboriginal and Torres Strait Islander Working Group of the National Public Health Partnership, and a member of the National Rural Health Alliance and the Public Health Association of Australia.

Puggy was also a respected and successful ATSIC Regional Councillor in the Kullarri region from 1993 to 1996, and was involved in numerous voluntary community-based organisations

In recognition of his ‘exceptional contribution to the advancement of human well-being’, Puggy was awarded an honorary doctorate by James Cook University in April 2001.

The recent awarding of the Human Rights Medal acknowledges Dr Hunter’s ‘unwavering commitment over many years to improving Aboriginal health in the face of hostility, disruption to his family, financial hardship and his own health.’

His family accepted the award on his behalf with both pride and sadness. His daughter, Renee, said her father had one wish for himself and other Aboriginal men – to live to 50 years of age. He died about a week after his 50th birthday celebrations earlier this year. Ms Hunter says her father worked tirelessly for the betterment of Aboriginal health but shirked recognition. ‘He always said that “no don’t worry about putting me in these awards” because everyone always wanted to nominate him for awards’, she said. ‘But he said “no, no that’s alright”. So he was one of the people who was a real quiet achiever, who really worked very hard and got a lot of things put into place, and who helped a lot of Aboriginal people.’