In the referendum on assisted dying in which it was voted in by a decisive majority (65%) in 2020, I voted against it.
This was primarily because much of the argument in support seemed to me to centre on difficulties in accessing palliative care, including in hospices.
My view was that the priority was to improve accessibility to palliative care. I would have felt better if palliative care access had been improved but sadly it has further deteriorated to the point of crisis and tipping point.
Understanding palliative care and hospices
Palliative care is a branch of medicine regulated by the Medical Council. It improves the quality of life of patients and that of their families who are facing challenges associated with life-threatening, including terminal, illness. When a person receives a terminal diagnosis, they can choose to receive hospice care.
Annually hospice services in New Zealand provide palliative and holistic wrap around care to over 10,000 people who die, as well as another 9,000 living with terminal illness, and their whΔnau.
Although hospices are not statutory health authorities, everything they provide is free of charge. Roughly there is a 50:50 split between government funding and hospice fundraising. Hospice New Zealand is the national representative organisation of these 32 hospices.
Hospice health professionals include doctors, nurses, therapists (physical, occupational and speech) and social workers. Consequently, even more so than hospitals, they are labour intensive.
Hospices provide medical care designed for the end of a personβs life. The purpose of this care is to improve the quality of the life that these patients have left. It includes pain and other symptom relief, along with emotional, psychosocial, and spiritual help for both patients and their families.
Hospice care operates at four levels depending on circumstances β routine home care, continuous home care, general inpatient care, and respite care.
Most patients under hospice care are able to stay in their own homes, with brief admissions to hospice for respite or to adjust pain medication.
Hospice funding crisis reaches tipping point
Unfortunately, despite the invaluable work for the terminally ill that only they as institutions can provide, the funding crisis that hospices face has reached a tipping point.

Tina McCafferty, Chief Executive of Totara Hospice highlights tipping point of funding crisis
This was brought to the fore by Kathryn Ryanβs Radio New Zealand Nine to Noonprogramme (6 June):Β Hospice funding crisis.
The focus was on one of the largest hospices, TΕtara Hospice, which services the communities of South and South-East Auckland. Β It has had to formally advise Health Minister Simeon Brown that it is planning to reduce services next month.
This action comes after years of warnings from hospices that their funding was unsustainable. This was reinforced by a recent report by the MartinJenkins consultancy which concluded that for the first time the hospice sector wonβt be able to raise enough money to break even.
Expanding the tipping point
Radio New Zealandβs coverage of the funding tipping point continued three days later on Morning Report in a thorough piece by health journalist Ruth Hill:Β Collapse of hospices could cost taxpayers millions.

Ruth Hill reports on the plight of hospices
Hill reported the hospices warning that funding shortfalls were putting their critical services at risk. Already they were only available to one out of three New Zealanders who were dying. She provided individual examples of this sorry state of affairs.
The Governmentβs scuttling of the pay equity claim for hospice nurses also had a negative impact. Hospice New Zealand chief executive Wayne Naylor noted that hospice nurses were currently paid up to 35% less than Health New Zealand nurses. He said:
That was a real out-of-the-blue sideswipe for hospices and hospice nurses in particular, to have our pay equity claim, which was almost completed, just stop.
Hospices were being forced to consider two unpalatable alternatives. Naylor described it this way:
That then falls back on community to provide more money to support their local hospice. The alternative is that hospices have to make some staff redundant so that they can increase the salaries of other staff, and that leads to a reduction in services.

Simeon Brown claims Health NZ has sufficient funding for hospices
Minister Brown has said that Health New Zealand had enough funding for hospice care. However, Naylor reported that the organisation had told Hospice New Zealand something quite opposite to the Minister:
They told us they had no more funding, that they have no contingency that they can call upon, and the people with whom we met said they had no authority to allocate funding from anywhere else. So essentially itβs a no to funding from Health NZ right now.
Ruth Hill also tellingly cites the MartinJenkins report which that the 28 partially publicly-funded hospices are returning at least $1.59 in health benefits for every dollar of taxpayer money received, including fewer emergency departments and hospital admissions or rest home stays.
What is to be done
Simeon Brown maintains that he and his government value the services hospices provide. What they provide is as core to the public health system as the services provided in our general practices and public hospitals.
Further, many (probably most) of the terminally ill are people who have invested in the public health system for much longer than those who sit around the cabinet table.
They have done their bit to ensure their health system has been funded for the benefit not just for themselves and their families.
It has also for hugely many more others that are unknown to them. It is only reasonable that hospice care should be available for them in their final weeks or months.
It is not just a question of the hospice service being sufficiently funded. It should not have to be financially dependent on charity to survive, let alone function.
This is fundamentally wrong. Being dependent on charity only makes sense if governments are so cynical to factor into their calculations that the terminally ill donβt amount to many votes and not for very long!
It also makes sense if governments are so short-sighted that they canβt see the financial return of investing in hospice care!
If hospice care being dependent on charity does make sense, then the words βdisgraceβ and βscandalβ have no meaning.
Ian Powell was Executive Director of the Association of Salaried Medical Specialists, the professional union representing senior doctors and dentists in New Zealand, for over 30 years, until December 2019. He is now a health systems, labour market, and political commentator living in the small river estuary community of Otaihanga (the place by the tide). First published at Otaihanga Second Opinion
Well Said IAN.
I could not put it better myself.
It is just more of the under funding by stealth the National party and Act use to make our health system dysfunctional .
Difficult for me to take seriously anything written by Ian Powell given his pro-left background, heβs biased before putting pen to paper.
Dont be afraid of facts
I voted against the assistered dying Bill as it makes more sence to invest in early Detection of Cancer. Some years ago i launced a petition to lower the bowel cancer age 45 and lower for anyone with family history of bowel cancer to save lives .Way too many people are detected with bowel cancer at stage 4 where only 10 out 100 live 5 years or more after diagnosis .Australia bowel screening age is from 45 years of age where a our health minister just lowered it to 58 from age 60 .While scrapping pilots for free bowel screening for Maori and people of pacific Island descent from age 50 .Both these populations are 70 percent more likely to develop bowel cancer from age 50 than non Maori . The Government could save alot of money with early Detektion.ie reduced spending on Chemotherapy ,radation ,illuostomys and reversals ie thats when you get your arse back to get arse Peter Marra bowel cancer free for 5 years