Homepage, News

New Zealand’s euthanasia bill is a step into the unknown for disabled people

By Wendi Wicks, The Guardian, 14th November 2019

“How can any MP be able to agree to a measure that endangers a whole community that they are not a member of?”

MPs have voted for a public referendum on the euthanasia bill, asking the vague question, “do you support this bill?”

“It’s to be hoped that the population at large can do a sound job, but that depends on the quality and range of information they get. MPs had a huge range of sound, factual information. But judging from their voting record, many clearly disregarded heaps of it.”

“Yes, there are many individual stories both for and against this bill. All deserve respect because telling them takes effort. But there’s more to good law than basing it on individual stories. It’s about the collective impact on our community. It should be good, safe law for all. That’s what MPs are there to do but didn’t.”

“The opposition we express is consistently based on concerns that society is full of negative, biased and discriminatory attitudes and behaviours, so that people think disabled lives are less worthy. Given this attitude as a basis, the state provides really limited support for us to live well. So it’s disturbing when laws are put up that mean the state will provide the means to die, not live. But that’s where we are now. We aren’t dead yet and we don’t want state-sanctioned death support.”

“A friendly QC commented on my vulnerability to the law thus: “You’re toast.” Me and how many other disabled people?”

Read the full article here.

Homepage, News

MP Alfred Ngaro tables amendment to uphold principles of The Treaty of Waitangi in the euthanasia bill

There is no cookie cutter situation in a world with legalised euthanasia. Every patient is different, bringing their own concerns, views, background and support systems with them in any health decision they make. Integral to this is the patient’s cultural background.

Currently, nothing in the bill requires a medical practitioner, when dealing with Maori, to be culturally competent and carry out assessments in a way that considers Maori culture. Previously, David Seymour has said that cultural considerations and competencies are a serious issue, but has also stated it’s for the people to choose. MP Alfred Ngaro points out that such action is dismissive of real concern about the inequities Maori people face in the current health system. If this isn’t addressed in the euthanasia bill, the system won’t allow for the complexities of Maori language and culture, in assessing cases of euthanasia. Alfred Ngaro has tabled an amendment to the euthanasia bill to address this, by including a part on cultural considerations. This will ensure a practical commitment to uphold the principles of the Treaty of Waitangi is cemented in law.

Watch MP Alfred Ngaro’s speech here.

Homepage, News

‘No-one is beyond help’: Why euthanasia should never be an option

By Danielle Gibbs, Stuff.co.nz, 10 July 2019

We live in a world where things are not perfect. How can we say, “it’s okay for you to die, your life is intolerable” when we don’t always have the means to provide the full support a person needs to live?
We need more support for vulnerable people, such as the disabled and mentally ill, that is based on the individual’s needs. There should not be a set standard…

We need to start thinking that prevention is always better than cure.
We need to tell society that it’s okay to need help. It doesn’t mean you are weak. It means you know your limits and capabilities. Asking for help is a strength.

Read the full article here.

Homepage, News

Disabled man feeling pressured to “ask” for euthanasia

By Alex Schadenberg , Euthanasia Prevention Coalition, 21st June 2019

To all those who say that things are working well in Canada, and to all those who say that the law can create a ring-fence around assisted death that protects the disabled, we say, ‘Read this true story’:

“I was contacted by man with a disability, who was telling me how he was feeling pressured to ask for euthanasia. After explaining his concerns he sent me this email comment:
I am living in the advanced stages of quadriplegia, now 33 years along. I am feeling the suggestive influence from my nursing care, regarding euthanasia. They use indirect pressure by speaking about other patients who have chosen the path of assisted death, unsolicited from me. I am worried about Canadian laws, so anti-life, and I don’t ever want to end my life. I didn’t choose when I was born, and I won’t choose when I die. Another thing that concerns me is as these evil laws progress against the vulnerable like myself, when will this newfound right to die become the duty or obligation to die? I can see it coming…

People talk about “freedom, choice and autonomy” without realizing how these concepts only apply to euthanasia in theory. In reality, it is the doctor or nurse practitioner who decides if you should die by euthanasia and many doctors and nurse practitioners judge the equality of people with significant disabilities.”

Read the full article here.

We need to take heed of what is happening in countries like Canada – despite what proponents of assisted death such as Stephanie Green might be saying, all is not well in Canada. We still have a chance not to make the same mistake as Canada. Vote ‘no’ to the End of Life Choice Bill.

Homepage, News

1000 Kiwi doctors sign letter against euthanasia

By Simon Collins, NZ Herald / Newstalk ZB, 23rd June 2019

One thousand doctors have signed a letter saying they “want no part in assisted suicide”. They have urged politicians and policy-makers to let them focus on saving lives and care for the dying, rather than taking lives, which they deemed unethical – whether legal or not.

“We believe that crossing the line to intentionally assist a person to die would fundamentally weaken the doctor-patient relationship which is based on trust and respect,” the letter reads.
“We are especially concerned with protecting vulnerable people who can feel they have become a burden to others, and we are committed to supporting those who find their own life situations a heavy burden.”
Finishing, they said: “Doctors are not necessary in the regulation or practice of assisted suicide. They are included only to provide a cloak of medical legitimacy.

Read the full article here.

Homepage, News

The euthanasia debate: Death is not a black-and-white issue

By Dr Amanda Landers, Stuff.co.nz, 24th June 2019

In reading social media pages, I have realised there are many misconceptions that have taken root in our community which need weeding out. One of these misconceptions is that euthanasia and withdrawing medical intervention is one and the same.

The answer to bad deaths is not euthanasia. The answer is a better understanding of basic medical ethics, of palliative medicine, of what happens to the body when it is dying, and how to care for  someone at the end of life.

Read the full article here.

Homepage, News

Newshub Nation Interview with anti-euthanasia advocate Vicki Walsh

Vicki Walsh was diagnosed with terminal brain cancer 8 years ago, and has so far defied the predictions. She discusses the effect her prognosis and treatment had on her, as well as how legalised euthanasia could have affected her.

I was actually suffering, I believe, from depression and exhaustion and the shock of finding out you’re dying. All those things were combined. Any one of those things would be quite difficult to deal with, let alone having them all at once.

Read the article here.

Homepage, News

Disability Commissioner incredibly concerned about the euthanasia bill in New Zealand

Euthanasia is legal in Canada and a visiting expert says its very patient-driven, but our Disability Commissioner is concerned the Bill doesn’t protect the most vulnerable. Watch the debate from TV1, Breakfast, here:

The euthanasia debate is heating up as the End Of Life Choice Bill has its second reading in Parliament.

The euthanasia debate is heating up as the End Of Life Choice Bill has its second reading in Parliament. Euthanasia is legal in Canada and a visiting expert says its very patient-driven, but our Disability Commissioner is concerned the Bill doesn't protect the most vulnerable.

Posted by Breakfast on Sunday, 23 June 2019
Homepage, News

Why I changed my mind on euthanasia

By Chris Ford, Newsroom, May 27 2019

Chris Ford explains why he’s now firmly in the ‘no’ camp on the voluntary euthanasia legislation.

The way in which society views disabled people is still largely negative and any introduction of euthanasia laws might further diminish our standing in the eyes of wider New Zealand society.

Wouldn’t the legislation be an effective weapon in a time of economic austerity when spending on social services would be even tighter than it is now? One could imagine that deeper future cuts to health and disability services, for example, would see many more disabled people placed under even greater pressure by both government and wider society to feel worthless and a burden.

Read the full article here.

Homepage, News

Claire Freeman’s incredible story

In a powerful interview on TVNZ Sunday, Claire Freeman describes the car accident that left her paralysed as a teenager and how, after multiple suicide attempts, she received medical advice to pursue assisted suicide overseas.

Had assisted suicide been available in NZ, Claire says it’s likely she would have taken her life. Claire has now turned her life around and she’s determined to save the lives of other vulnerable people.

Watch the interview here.

You can learn more about Claire and her eligibility under the End of Life Choice Bill at www.defendnz.co.nz/claire