Latest Event Updates

Report from Radio NZ on Equality Network presentation

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Screen Shot 2017-08-02 at 10.34.18 AM.pngGood coverage from Radio NZ on the presentation of the Equality Network‘s Election Statement.

It is essential that the issue of reducing inequality remains forefront with an election breathing down our necks. Any inaction on concrete and committed longterm planning to reduce inequalities will continue to have long-reaching impacts for those who live in the harshest of conditions in Aotearoa.

It is essential to keep the pressure up.

Image: Screenshot of Radio NZ page

Presentation at the launch of Equality Network Election Statement

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Debbie Leyland_UCANDebbie Leyland spoke on the step of Parliament voicing endorsement of the Election Statement launched by the Equality Network. Attached is the text of Debbie speech.

“We believe it is possible for all New Zealanders to enjoy a decent life, one where everyone thrives. But we recognise that big imbalances of income and wealth have been deeply destructive and unfair. They corrode our social fabric and limit the life chances of hundreds of thousands of New Zealanders. Combined with other inequalities – such as those of gender and ethnicity – they damage lives and deepen disadvantage.” Equality Network, Election Statement 2017

My name is Debbie Leyland. I am 53 years old and I am on a benefit. I am also the co-founder, coordinator and spokesperson for UCAN – United Community Action Network, and I am on the steering group of the Equality Network – both of which are voluntary roles.

Every week  after i pay rent power and bills I am left with $70 a week.

The sad thing is, among my friends I’m considered rich.

My $70 covers my weekly food, transport, medication and doctor’s fees. It’s really hard.

Most weeks I’m also helping out my family – putting $10 into my daughter or son’s account, or buying them a top up card or whatever they need.

My daughter has carpal tunnel syndrome which affects her hands so she can’t work. She has an 8-month old baby. Her and her partner are on a benefit, and they are left with just $102  a week after power and rent, to support two adults. and my 8 month old grandchild – $102.  for food and everything else including nappies.

A few weeks ago my daughter was over here, and I found some money under the bed. I asked her what we should buy as a treat, and we both said peaches! It was like we’d won lotto. Who can afford to buy fruit? No one that I know. I haven’t seen a full fruit bowl, in the house of anyone I know, for years.

We bought some cauliflower the other day and we were in heaven, it was like Christmas. I’d love to be able to fill my cupboards with fresh vegetables and food so when my family come I could feed them a really wholesome meal. My fridge is empty. I’ve got a can of baked beans and a can of tomatoes. I haven’t bought a block of cheese for months. It’s too expensive.

I’m on the invalid’s benefits because I suffer from Post Traumatic Stress Disorder due to things that happened during my childhood. I suffer from depression and anxiety. It’s very difficult but I’m at a level now where I’m well and I can maintain my life. But sometimes I can’t afford my medication, because I don’t have enough money, and then I become really unwell.

I feel like being on a benefit has impacted on my life hugely. The saddest thing for me is the reaction when I’m working out in the community. There’s a lot of people who, when you say you are a beneficiary, think you are either a bludger, or lazy, or whatever. The second part is the financial restraints – it is nearly impossible to live on that amount of money. People frame being on the benefit as a choice. I didn’t wake up and think “I’m going to go on the benefit and live in complete poverty for the rest of my life.” I didn’t ask to be here.

Every day I have to make choices. Do I go to the doctor or do I feed the kids? It’s an ongoing battle. I used to go out and about, and now I don’t.  The last time I actually went out with my friends was 2 and a half years ago. I can’t do things that people take for granted like going out as a family for dinner, or going out to entertainment. It’s really hard.

It was my granddaughter’s birthday the other day, and I just didn’t have enough money to buy her a present or even to go out to Porirua to see her.  I just had to ring her and say happy birthday. I’d like to be able to take my daughter or grandchildren for a walk through the town belt but they can’t afford the train fare from Porirua, and i can’t afford to get out there. Being on the benefit really creates distance within families.

Being on a benefit and being in a Housing Corp house creates a community of fear. If something happens in my house, nothing ever gets done. After the big earthquake, my bedroom door fell off. They haven’t come to fix that. The toilet upstairs leaks, my windows have mould all over them and I have to wash them every few days. You can’t lock the front door – it’s been like that for about a year. I had my granddaughter over here 2 weeks ago, and she kicked a ball through the window. I rang housing corp and they sent someone over to board up the window. It’s been three weeks and they still haven’t fixed it. But you don’t want to kick up too much fuss because there’s a constant worry that they might throw you out.

I hate going to WINZ. There’s nothing more humiliating than having to go to WINZ and ask a complete stranger for money. It’s horrible. When I went to WINZ to get some help with a washing machine, my appointment was at 2 o’clock, but I didn’t get to see my case manager until 3.30. People think that if you are on the benefit your time is not important and you have nothing better to do. What about the people who have to pick up their kids from school? My local WINZ in Kilburnie has moved to Newtown, so if you need assistance or a grant or medicine you have to walk to Newtown. That has affected so many people. We just don’t go now. It’s too far to walk.

I’m asking the Government to increase benefits.  By increasing the benefit and providing fairer income support it would mean that I could actually partake in society. I could spend more time with my family,  I would be able to eat a healthy diet. I could go to the doctor when I need to. I could have some dignity.

Getting special or an emergency benefit for example a food grant, as cash would make life so much easier.  It would mean I could buy veggies at the Newtown market, cheap Indian grains at places like the Spice Market, and shop around for cheap heaters that I want.  Plus, the cards that WINZ gives you are only valid for three days. So in the middle of winter when it’s pouring with rain, you have to walk in the rain to the shops and back with your shopping – all because your card can’t be used on the bus and you don’t have spare money. It’s a real struggle.

I think that that’s why the Equality Network is so important, it keeps these issues at the forefront of what is going on. That’s why I’m involved. It gives a voice to people that don’t have any. I want people to realise that beneficiaries are human beings and that decisions made in parliament affect all of us. It’s tragic to think that we’ve gone from Joseph Savage, who set up social welfare so all citizens could have a decent quality of life, to this – where we are living on crumbs, and having to feel grateful. I ask the Government to be brave and act with courage. To support people like myself to have a decent quality of life.

Thank you.

An invitation to the Health Funding Crisis Forums

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EventPhotoHelp make Health Funding an Election issue

Join the greatest health minds and activists to make health funding a key election issue. and United Community Action Network [UCAN] invite you to Health Funding Crisis Forums on Saturday 1st July from 10 am – 3.30 pm.

Our main forum will be held in Christchurch. It will be streamed online to events in Auckland, Wellington, any self-hosted events and online for those who can’t attend an event or where there isn’t one yet. (Want to host an event in your town?)

The pre-election budget is out and the smoke and mirrors around health funding has cleared.

Without action, more Kiwis are going to miss out on the mental and physical health care they need, when they need it.

That’s where you come in.

We’ve invited the most active community groups, workplace and health activists to work on a grassroots election plan.

Campaigning has made mental health a key election issue. We need to keep the pressure up and make physical health funding a key election issue as well.

At the forum, you’ll:

  • Hear about the latest research on unmet need and health underfunding,
  • How campaigning made mental health a key election issue, and
  • Learn how to get your story in the media, or
  • Discover how our new health and safety laws can fix unsafe workloads.

We’ll provide lunch. You’ll provide the energy.

For more information visit:

RSVP here before June 23 for catering purposes.

What are your top three election priorities?

At the conference, we’ll be announcing three health pledges we want all parties, candidates and politicians to commit to in this election. We’re crowd-sourcing the asks and need your help to develop them.

If you or your organisation will struggle with travel costs, please let know. They have a small fund to help.

We look forward to seeing you there.

Nāku noa, nā.
Simon Oosterman Campaign Coordinator
027 526 8704

Pat Bolster & Debbie Leyland
On behalf of UCAN
United Community Action Network

Action Groups work jointly on Child Poverty

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UCAN, United Community Action Network’s Health Charter has received endorsement from the Child Poverty Action Group (CPAG).

CPAG, an independent charity established in 1994, has maintained a robust focus on the elimination of poverty for the children of Aotearoa. Doctors, teachers, academics, healthcare workers and many other committed people contribute to the body of research and reportage that CPAG produces.

Approximately three hundred thousand children live in poverty in Aotearoa. If you add to this the older siblings, parents, extended family and whanau, the burden of poverty escalates. The long term impacts of poverty are widely documented: the tragic loss of potential of the children; increased difficulty in accessing affordable physical and mental healthcare; the increase in incidence of domestic violence; poorer educational outcomes; limited access to decent accommodation; and the tailspin of homelessness. This is an avoidable situation. There needs to be a willingness to engage, innovate, and reduce the impacts of these situations for the benefit of all.

CPAG states “child poverty could be eliminated completely. It’s all about Choice.” UCAN agrees, and this unfolding disaster is a failure of political policy and loss of values based politics.

UCAN spokesperson, Debbie Leyland, says, “These conditions need to be considered as the escalating crisis that it is. It’s brilliant, but also a tragedy, that organisations like CPAG are active and necessary. They are essential in these times to document and report the struggles of the most vulnerable among us. There is something seriously broken in New Zealand.”


Child Poverty Action Group (CPAG) Press Release.

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Please see the press release from Child Poverty Action Group(CPAG) who have published this endorsement of the UCAN Health Charter. We thank CPAG for their ongoing commitment and advocacy to improving the health and wellbeing of children, and the families they live within, in Aotearoa.

CPAGSupport for UCAN NZ Health Charter

Child Poverty Action Group (CPAG) supports and endorses the Health Charter by the United Communities Action Network New Zealand (UCAN) that says “everyone deserves the right to health”.

UCAN, an organisation formed four years ago, believes that the right to health is, “being denied to many in Aotearoa-New Zealand, through poor access to health services, an unfair economic and education system that strongly favours the wealthy over the poor.”

CPAG agrees that much of the poor health among children in New Zealand is attributable  to  “inadequate and unhealthy housing, poor living environments that alienate vulnerable sections of the community.”

The link between poverty and poor mental and physical health among children, whose opportunities to thrive are compromised, is very real. Professor Innes Asher, Health Spokesperson for CPAG says that “poverty and unhealthy housing and inadequate basic health care are the drivers behind many of the thousands of children admitted to hospital each year with preventable diseases.

“Comprehensive effective policies are needed to change this grim situation which results in large numbers of children, many of whom are babies, becoming very sick and who often suffer lifelong damage.”

CPAG says that UCAN promoting the right to healthcare that is not met with a cost barrier is a commendable effort, and aligns with the United Nations Convention on the Rights of the Child, which New Zealand ratified 24 years ago.

CPAG notes with great concern that over half a million New Zealanders cannot afford to see their GPs.  We are asking that the Government extends the zero fees scheme for free access to General Practice to include all children up to their 18th birthdays.

This would be one of the measures needed toward a goal of halving the number of hospital admissions for preventable illness among children – which is currently around 40,000 annually.

The UCAN Health Charter (2016) also supports everyone having the right to affordable, safe and healthy housing.

CPAG hopes that there will be a greater commitment by the New Zealand Government to ensuring that every family has access to an affordable, healthy home. Instituting a rental Warrant of Fitness to ensure that a minimum standard is met and that homes are made to be safe, dry, and insulated would be a step toward ensuring better health for all children of low-income families.

Follow this link to download a pdf version of the UCAN Health Charter. Ends




Not settling for seconds, people demand better.

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slide03When we posted the Kurow Cure, by Professor Don Matheson, last month we thought it may gather a bit of interest. We were quite unprepared for the massive interested it generated in a short space of time. The post itself was shared over 300 times via social media sites.

It seems obvious to us that there is a increasing number of individuals, community organizations, and professional bodies who are deeply disturbed at the degradation of our national health service, and who are looking for practical and equitable alternatives.

It is impressive to see this active engagement at a community level by organisations such as the PSA, NZNO [Shout out for Health], E tū, among others, have embarked on a national roadshow, from tip to tip of both islands, to talk directly with communities on the impact of an estimated $1.8 billion missing from the national health budget.

Screen Shot 2017-03-20 at 8.20.11 PMAround the launch of this campaign, the Yes We Care campaign announced in a press release the mind-blowing results of a survey of 6000 health professionals.  A massive 90% felt our health system was underfunded to the point that it lacked appropriate staffing and resources meaning that timely health care was not accessible, or available, when needed.

Screen Shot 2017-03-20 at 8.03.42 PMThe UCAN Health Charter continues to striking accord as well. There have been number of endorsements to date, of which we will make public shortly. It is very exciting for UCAN to be invited to forums, professional bodies and hui to present the Charter to interested parties. For example we ubderstand the UCAN Health Charter will be discussed at the Equality Network Hui in Wellington in March.


The Kurow Cure: worth another crack

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We are thrilled to be able to present this article by Professor Don Matheson, with illustrations by the awesome Bob Kerr, as presented to the Fabian Society.

With thanks and acknowledgements to those mention above.

Please enjoy this thoughtful read.


An address to the Fabian Society of New Zealand

Don Matheson

88 years ago a mass migration of economic refugees was occurring in Kurow, North Otago as desperate families moved into the area in search of work from the Waitaki hydroelectric dam. Some even brought their own spades, in case the government did not have enough for them. In fact there was not enough work and an informal settlement formed of desperately poor, unemployed families, on the banks of the river. The local school roll shot from 30 to 300. Andrew Davidson, the local teacher, Gervan McMillan, the local doctor, and Arnold Nordmeyer, the local minister, came together and built a health and its determinants response to the poverty that they saw. It was called the ‘Kurow Cure’ – a scheme based on the concept of justice rather than charity.

Bob Kerr, our Mt Victoria artist, has created these images of that discussion in his work, The Three Wise Men of Kurow. His work summarizes the key concepts behind the health response they envisaged:It must aim at the prevention of disease

It must make provision for income loss

It must provide all the facilities for the diagnosis and treatment of disease

The service must be based on the principle of the patient’s free choice of doctor

It must include the adequate provision for research in all matters relating to health

It should be free, it must be complete and it must meet the needs of all the people

So the concept of a free, universal and comprehensive health service for all New Zealanders was born and incubated in Kurow. It became the blueprint for the Social Security Act of 1938, one of the first internationally recorded expression of what today sits within the United Nations Sustainable Development Goals. It is known as Universal Health Coverage, which has been developed by World Health Organisation and the World Bank – with a lot less clarity but the same intent as the Kurow Cure.

So what happened?

In this discussion I will explore what has happened to this vision of health service provision, 80+ years later, especially the last idea, that:

  • It should be free, it must be complete and it must meet the needs of all the people

Many aspects of the social security act transformed the health and life chances of generations of New Zealanders, especially free hospital care. However free primary health care for all did not become a reality. This particular provision proved controversial right from the start.

Medical resistance1

For the next 60 years, attempts by governments to introduce free health care were effectively and passionately blocked by the Medical Profession, then called the New Zealand branch of the British Medical Association (BMA). It was seen as an affront to their right to charge their own fees, and the thin end of the wedge of “socialized medicine”.slide10

Many of the members had come to New Zealand to get away from the NHS. It was also strongly argued that the state should not interfere in the special relationship between the doctor and the patient – both the relationship with the doctor’s wallet and, more broadly, on ‘his’ ability to do the right thing for the patient.

80 years later, the protagonists in this conflict appear to be changing sides.

The NZMA with its 2011 statement on health equity, comes close to repeating McMillan’s mantra, backing accessible care and greater attention to the social determinants of health.

The government, on the other hand, as we have seen by the feedback to the draft NZ Health Strategy, had to be cajoled by the health sector and professional groups to give greater emphasis to health equity.

Changes in the health sector

But the sector ain’t what she used to be. From the 1970s onwards this ‘special’ three-way relationship, between the medical professional providing primary health care, the state and the public, began to change. The formation of group practices, the concept of teamwork with nurses, the introduction of contracts, the appearance of professional ‘managers’ within general practice settings, have all pushed the provision of general practice towards a more complex model of care.

Medical influence on the sector has not entirely dissipated, but evolved into new forms. The MBChB2 leadership for now is being replaced by the MBChB/ MBA3, and soon the MBA. On its own. The obstructive industrial position of the BMA around user charges has been absorbed into new medical corporate entities, IPA4s, which have further evolved into PHO5s. Even more ‘disruptive’, is the recent arrival of medical care companies into the sector, such as Nirvana Health group, Green Cross Health and others springing out of PHOs. These are increasingly shaping the sector – and changing its politics with the dilution of medical power – adding multiple partners to this professional – state marriage and the imperative to deliver a return on investment for shareholders.

So although the equity word is used freely within medical professional circles, the control of the primary health sector is shifting to a series of semi corporate, corporate, and international business entities.

Have we made any progress?

So what progress have we made on bringing free care to those who need it 80 years on?

Various attempts by successive governments have been made to improve primary health care access, including the creation of group practices and trials of capitation in the 70s and 80s. Helen Clark’s first attempt to introduce medical contracts in the late 80s was an attempt to control fees charged to patients. But with a change in government, it was not till the 1997 coalition agreement between National and NZ First that free under six care was successfully introduced.

The early 2000s saw the introduction of enrolment and capitation as a system wide contracting instrument for PHC funding, a sector wide discussion on the meaning and drivers of inequity, and a large injection of government funding into the sector. This funding effectively halved the number of people having difficulty accessing care and, at one stage, had NZ leading world rankings in primary care physician satisfaction ratings.

The 2010s have seen free care for under 6s extended to after-hours care and in 2015 zero fees for under 13s were introduced in New Zealand.

Free care is a no brainer. There is ample evidence that out of pocket payments, particularly for poorer and sick people, adversely impact on their health. Since the Rand study of the 1970s, it has been consistently shown that, faced with increased user charges, people use services less, irrespective of the severity of their condition. This is bad for people and bad for the effective use of health services.

How well are these current instruments working?

According to the New Zealand Health Survey, the answer is not very well. Almost one million New Zealanders report difficulty accessing primary health care services, the majority because of the cost barrier, closely followed by service availability.

The number of conditions appearing in hospitals, which could have been more appropriately treated in primary care, is increasing, with persisting higher rates for Maori, Pacific and people on low incomes.

Even capitation, the funding instrument vital to the delivery of a population approach, has not been applied in an equitable fashion. The introduction of near universal capitation has also not lived up to its policy intent, and is now an instrument that could be making health equity worse. Maori are much less likely to be on a capitation register, with some 10% of Māori currently unregistered. The implications of this, in the age of the Medical Home, is that the community with the greatest need are likely to remain, or become, the medically homeless.

Why do  inequalities persist?

Some of the reasons that the policy solutions such as PHOs, DHBs and capitation have so far failed to take equity seriously are worth exploring.

Primary health organisations

The policy of the PHO policy intent was to pursue equity, represent community views and aspirations, and lead a coordinated population health approach. But these organisations have rapidly morphed into provider dominated organisations. They have been consolidated to the point that they have, with some exceptions, lost any relationship with discrete populations, and have weak accountability to communities. PHOs have struggled in many cases to be more than a GP funding post box. Although they are now much bigger they have yet to demonstrate being better than smaller PHOs . Many are focused on buying practices and some are busy plotting the overthrow of their DHB with the talk of fund holding and social investment. Moving the sector towards a population equity focus has disappeared as a priority for many PHOs.

District health boards

The situation for district health boards (DBHs) is more complex. Some in the last decade did take their population health responsibilities seriously, began to invest in their communities, with a measureable improvement in health access for the most vulnerable, and the added bonus of reduction in unnecessary hospitalization. Some even went as far as investing in housing. With the financial squeeze of the global financial crisis, the DHBs have become increasingly brain dead, with an obsessive focus on their end of year financial result, disinvesting in community services, and focusing on Minister defined targets that were reset on a very narrow set of activities that belied the complexity of the organizations they were meant to guide.

A recent Treasury report6 shows that over the last five years most DHBs have shifted financial resources meant for primary care and community services into the hospitals, in attempts to make ends meet. At the same time they have shifted some hospital functions into the community. This amounts to a significant shift in financial resources in the opposite direction to their own planned intent, the policy intent of their organizations under the NZ Health and Disability Act. It has contributed to the failure to address equity of access at the community level. It is also a failure of the existing governance and oversight structures that such a high level of shifting costs onto the community has not been called out.

Having said that, the DHBs and their predecessors, the hospitals, have maintained free access for the whole population, and consistently done this since their inception. While the primary health care sector has failed to achieve equity of access, the hospitals have been much more successful in this regard. This includes effectively fighting off a neoliberal rush of blood to the head in the 1990s when the government of the day attempted to introduce user charges.

Of course the economists, managers, funders and planners all think this is mad. Why would we have access barriers to the front gate and least expensive part of the system, then have free rein for the rest, up to the most expensive offering? It does not make, economic, system, or efficiency sense. However from an equity perspective, it is the continuously open doors of our hospitals that have softened the impact of an inequitable primary health care system for generations of New Zealanders.

The way forward

So what are the lessons learned from the time of the Kurow Cure? The strongest structures in the health sector from an equity perspective and low access barriers remain the public hospital system. It has become part of our culture, or our “socialist streak” in the words of the current prime minister. We have failed consistently to introduce a similar public service culture into the primary health care sector. This sector was built on a small professionally led business model, and is fast becoming a large corporate model, with its focus on shareholder value rather than health equity.

Going forward, my belief is that the institutional instruments such as DHBs, PHOs, and capitation could all be effectively used to reduce health inequalities. But the overall intent is lacking.

At the highest level, the concept of the right to health within a national constitution would help maintain this strategic focus. This would help drive the cultural change required to shift the bureaucracies toward a better balance of economic and human values.

Within the health sector, the revised NZ Health Strategy generally has a much weakened focus on health equity, and is intending to take us into new territory with its emphasis on “social investment”.

The hope here is that with the financialisation of services to the poor, the actuaries and the quants with their algorithms from the insurance world will achieve what the doctors, PHOs, DHBs etc have so far failed to do.

On a more positive note, the strategy does state an intent to promote people-led service design, including for high-need priority populations. This would be a major reversal to recent trends, where community and Maori primary health care initiatives have struggled to survive, overwhelmed by the mismatch between the growing needs of their communities and the resources made available.

At the technical level, what is required is more effective governance and management within some of the existing instruments.

The capitation formula should encompass more of the fragmented funding streams, and have much stronger pro equity bias. VLCA 7should be enhanced, and universalised to all practices, and used to lower access – effective financial incentives should be available for practices that are providing free care. Currently the capitation formula amounts are based on a person’s age. Health needs are greater for Maori, Pacific and low income people, and the formula should be reflecting this.

Free care for under 6s and free care for under 13s now have cross party political currency and should go further to free care for people with chronic conditions, then free care for the elderly.

The availability of primary care services to the highest needs populations needs to be increased. This will require state investment in infrastructure, provision directly, or through community providers.

Fixing the two system holes – the transfer of government resources meant for the community to the hospitals and the failure to enrol the populations with the high needs into the capitation system should be made the highest priority of the system.

Resisting user pays and privatisation

On a broader level, what is it about our hospitals that have enabled them to effectively resist the countervailing forces of user pays and privatisation? Can we replicate these in the further development of the primary health care system? Can we build a sustainable, powerful sector that is patient-centred, values professional leadership, and resists erosion of its social justice focus? We need to harness the protective effect of a strong professional group or groups within the sector that can shape the primary care institutions and maintain a focus on equity.

The Kurow Cure yet to heal

In conclusion, the Kurow Cure as a vision of health care delivery has stood the test of time. A health system built on the concept of social justice vs charity or flawed market mechanisms is as relevant today as it was in the Waitaki riverbed in the 1930s. It is an embarrassment that 80 years later we still have families living in tents and a politically-led public discourse dehumanising the poor.

I’m confident we as a people, and the people of the health system, can do better.


1. Michael Belgrave, ‘Primary health care – Improving access to health care, 1900s–1970s’, Te Ara – the Encyclopedia of New Zealand, (accessed 26 November 2016)
2. A medical degree
3. A business degree
4. Independent practitioners association
5. Primary health organisations
6. Analysis of District Health Board Performance to
30 June 2015. The Treasury, New Zealand Government, June 2016
7. Very Low Cost Access

An open letter to DHB Board members – 2016 elections

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This text is from a speech presented by Professor Don Matheson at the launch of the 2016 UCAN Health Charter to the prospective Capital and Coast District Health Board (CCDHB) Board candidates in the 2016 election cycle.

An open letter to DHB Board members.

This letter comes from a network called UCAN that is supporting action being taken to ensure everyone in New Zealand enjoys the right to health.

One area that Boards can make a difference is Primary Care.

We recommend you eliminate access inequalities (increase availability, acceptability, and decrease price barriers) to primary health care services in your DHB area.

This will require differential investment to promote equity of access, by strengthening the primary care providers whose focus is on the provision of care and improved access for people on low incomes, Māori, Pacific, refugees and those with chronic illnesses, including mental illness.  These providers may be mainstream general practices, Maori, NGO, or publicly provided services. 

In strengthening primary care provision in the Board’s area, support models of care that are responsive to and respectful of the diversity of the Board’s community.  One size does not fit all, and a single organisation outside of the public sector, monopolising primary health care provision in the Board’s area is to be avoided.

The DHB can fund this by stopping the current leakage and underspend that for a number of years has been shifting the Board’s resources from the community and primary care to the Board’s provider arm and the hospital. See this report for the situation in your Board. (Analysis of District Health Board Performance to 30 June 2015, Published June 2016, The Treasury, New Zealand Government)

In addition, we recommend you act collectively with other Boards and the Minster to address the national funding mechanism (base capitation formula, Very Low Cost Access, Services to Improve Access) so practices have money available to subsidise fees for patients who currently are struggling to access services. The current capitation formula is not adjusted to meet the high needs found in deprived areas, those on low incomes irrespective of where they live, or amongst Maori and Pacific populations.


The UCAN Charter for Health

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screen-shot-2016-09-12-at-8-22-26-amUCAN believes all people have a right to health.

That right is being denied to many in Aotearoa/ New Zealand, through poor access to health services, an unfair economic and education system that strongly favours the wealthy over the poor, inadequate and unhealthy housing, poor living environments that alienate vulnerable sections of the community. We have not met our Treaty obligations.

We believe as a nation we can and must do better than this.

The UCAN Charter for Health 2017

Everyone’s right to the health care they need

Free primary medical care available in every community.   One million people have an unmet need for primary medical care. The cost of care is the biggest barrier, including the cost of drugs. There is low availability of primary medical care services, particularly in deprived areas. Barriers are bigger for those with chronic conditions, especially mental illness. A primary health care approach with a focus on equity and social justice is required across the health system.

Everyone’s right to a living income

Support a living wage and income for all, including beneficiaries. The gap between the rich and the poor is rapidly growing in New Zealand and this is bad for our health. More and more New Zealanders in work don’t get paid enough to meet their needs, to eat healthy food, and live dignified and healthy lives. Just to survive, many are left with no time for leisure or opportunity to participate in society.  In addition, poverty is health damaging reality for many beneficiaries, and especially for 28% of our children who live in poverty.

Everyone’s right to a home

Support affordable, safe and healthy housing. We are failing as a nation to adequately house our children and other vulnerable groups. They are exposed to housing conditions that damage their health and are not fit to live in. You need a Warrant of Fitness for a car, but not a house.   People with severe mental illness are often living in substandard temporary housing with insecure tenure. They have been betrayed by a failed market model for housing provision.

Everyone’s right to take part in our society

Support community centres, drop in centres, with free internet connectivity and public transport. We are denying more and more groups the right to actively take part in our society. More people are working are working longer hours, leaving less time for involvement in their communities. We used to house people with severe mental illness in asylums. This role has shifted to the community, but the social contract that community support would be there, has been broken.

Everyone’s right to a safe environment

Support improved access to healthy food, water and air. Regulate and tax foods full of sugar, fat and salt. Ban advertising of unhealthy foods and alcohol. Protect our water and the air we breathe from contamination.. Exposure of children to foods that are harmful to their health, and unrestricted marketing of unhealthy products are now leading causes of later illness. Our water and the air we breathe needs to be protected from contamination, as does the physical environment from which they are generated.

Everyone’s right to education

Support accessible educational opportunities for all. Student loans, unequal and unfair outcomes for children from poor communities, reduced educational opportunities for the elderly and beneficiaries are all opportunities lost.

Questions and Answers

What does a “Right” mean?

An entitlement that humans have by the fact of being human, such as the right to life and the right to be free from torture or degrading treatment. The highest attainable standard of health is a fundamental right of every human being. Health is a reflection of a society’s commitment to equity and justice. Health and human rights should prevail over economic and political concerns.

 Can the country afford free health care?

Improved access to primary health care will reduce inappropriate use of hospitals, and help to keep health care costs down overall. Healthier people in the community also has an economic benefit.

What is Primary Health Care?

The main ideas are; that health care is focused on health needs; involves an enduring personal relationship between health workers and the community, particularly for those people with a chronic illness; is comprehensive (not just one illness) continuous (no barriers for patients needing care in both hospitals and the community) and person centred; responsibility for the health of everyone in the community at all stages of life; tackles the determinants of ill-health; and people are partners in managing their own health and that of their community.

Primary Health Care is a social justice and pro equity approach to health care described in the World Health Organisation’s Alma Ata Declaration of 1978 and updated by WHO in 2008. It encompasses primary medical care, hospital care, public health and the wider determinants of health.

Can the country afford a Living Wage?

A living wage has been shown to improve the economy of a country. People are a country’s greatest asset, and our children are our future. Addressing child poverty through supporting a living wage and income is a wise investment in the future.

Can the country afford decent housing?

Housing is not a cost to the economy- it is an asset, an essential piece of infrastructure, as important, if not more so, as a road, or a bridge, or an airport. Once built it has a monetary value, outside of its contribution towards nurturing the next generation.

Can the country afford education that achieve fair outcomes for all?

Like housing, education increases rather than decreases, the overall wealth of the community. Barriers to educational opportunities do not make sense – at any age.

Does the country have enough money for this?

Many of these features will have low cost or even improve the economy. The country has enough wealth to provide for all its citizens if that is made a priority. Currently the country’s wealth is poorly distributed and the provision of basic rights for all citizens is a low priority. The economy has a profound influence on people’s health. Economic policies that prioritise equity, health and social well‐being can improve the health of the people as well as the economy.

Does the UCAN Charter cover all the important issues?

The UCAN charter covers the issues its supporters see as most important at this time. There are a number of other important issues (the right to education, the protection of the planet from global warming) that we support, but are the subject of action led by other groups.


The Devastating Effects of Health Care Cuts

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United Community Action Network (UCAN)

The Devastating Effects of Health Care Cuts 

“Two tragic events in Wellington’s southern suburbs of Newtown and Kilbirnie calls attention to the devastating consequences of inadequate health funding, including the ongoing health funding cuts, for mental health consumers”, says spokesperson, Debbie Leyland, from the Wellington based health advocacy group, United Community Action Network (UCAN).

“The recent death in the Kilbirnie supported accommodation facility, Mahora House, highlights the dangers caused by continual cuts to health-based funding from Capital and Coast District Health Board (CCDHB) to community based health services” Leyland states.

Mahora House was established in 1985 to support people who were being ‘deinstitutionalised’ from long-term mental health facilities and moving into community-based settings. In 2013 CCDHB 2013 withdrew funding from Mahora House. In March 2016 a resident at Mahora house was fatally assaulted by another resident.

This event follows a similarly tragic event in 2009 at Te Menenga Pai, otherwise known as Mansfield House. The murder of one resident and conviction and imprisonment of another was a traumatic experience for residents, staff, friends and whanau. The Coroner’s investigation found that Mansfield House was chronically short staffed and frequently had an occupancy rate beyond capacity. The report was critical of the role of the CCDHB in its support of a facility with such high need. The Coroner stated that if the controlling health authority, in this case CCDHB, “devolves its responsibilities” to another service then it must continue to ensure ongoing audits ensure that care is delivered appropriately.

“Will an investigation into the recent tragedy at Mahora House present similar findings from the events of 2009? Did the DHB heed the warnings from the Coroner’s report?”, asks Leyland. “The CCDHB has a mandated role to improve, promote, and protect the health of people and communities and to reduce health disparities”

In 2010 the Minister of Health instructed the CCDHB to commence a policy of clawing back savings of $60 million in a three year period. The CCDHB CEO Ken Whelan resigned stating then that he could not “cut costs any further without undermining patient care”. Many of these ‘savings’ came from restructuring funding streams to community based services, ultimately forcing many to merge, reduce the services offered, or to close. Some of the service losses in the Wellington southern suburbs have been advocacy and Midwifery services and drop-in and activity centres.

UCAN calls on the CCDHB to halt all plans to reduce funding to any community-mental health focused services and for an investigation to assess the impacts of the loss of services that have supported the health and well-being of some of the most marginalised and vulnerable within our communities. Are these on-going cuts making inequalities worse? UCAN feels the answer is yes.

“Tragedies hit harder in small communities” says Leyland, “It’s no longer health, it’s Hell”.