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Dame Tariana Turia joins campaign against David Seymour’s euthanasia Bill

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NewsHub 10 March 2019
Family First Comment: DefendNZ is a series of documentaries featuring people with a terminal illness or disability.
The campaign includes the voices of community leaders, like Former Associate Health Minister Dame Tariana Turia. “No one ever said to me ‘I want to be assisted to die’, they want to be assisted to live.” https://www.defendnz.co.nz/ 
#rejectassistedsuicide 
www.protect.org.nz

Dame Tariana Turia has added her voice to those opposing euthanasia in a campaign launched on Sunday.

It comes ahead of a second vote on David Seymour’s End of Life Choice Bill.

Hamilton woman Kylee Black lives with a rare connective-tissue disorder called Ehlers-Danlos Syndrome.

“There is literally a piece of my DNA missing, so there is no cure,” she said.

She features in a campaign called ‘Defend New Zealand’, which raises the concerns of those with terminal illnesses and disabilities about the pressure euthanasia may put on them.

“All of a sudden I feel like well, maybe, I have to make that decision.”

The campaign includes the voices of community leaders, like Former Associate Health Minister Dame Tariana Turia.

“No one ever said to me ‘I want to be assisted to die’, they want to be assisted to live.”

Voices for and against euthanasia have already been heard in a record 37,000 submissions made to Parliament on the End of Life Bill.
READ MORE: https://www.newshub.co.nz/home/politics/2019/03/dame-tariana-turia-joins-campaign-against-david-seymours-euthanasia-bill.html

Anti-euthanasia group launches documentary series
NewsHub 10 March 2019
https://www.newshub.co.nz/home/politics/2019/03/anti-euthanasia-group-launches-documentary-series.html
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What’s happened in Oregon since euthanasia was introduced?

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Oregon 2018 assisted suicide report. A record number of assisted deaths.
Alex Schadenberg blog – Euthanasia Prevention Coalition  3 March 2019
Family First Comment: Hint: It’s not pretty – and sends a clear warning to NZ

The 2018 Oregon annual assisted suicide report is similar to prior years. The report implies that the deaths were voluntary (self-administered), but the information in the report does not address that subject.

According to the 2018 Oregon assisted suicide report.

  • There were 168 reported assisted suicide deaths up from 158 in 2017.  When published, the 2017 report claimed that 143 people died by assisted suicide, 15 fewer than the actual number of death.
  • 168 of 169 people who reportedly ingested lethal drugs in 2018, died from it, one person survived and died of natural causes.
  • 11 of the deaths, the lethal drugs were prescribed in previous years.
  • 3 of the patients were referred for a psychological or psychiatric evaluation.
  • 2 physicians were referred to the Oregon Medical Board for failure to comply with the law.
  • The time of death ranged from 9 minutes to 14 hours. When dying from DCMP2, death took on average 2 hours, with the longest time taking 21 hours.
  • In 2018 one person died 807 days (more than 2 years and 2 months) after requesting assisted death.
  • 43 people received lethal prescriptions, but their “ingestion” status is unknown.
  • There were 249 lethal prescriptions obtained, up from 218 in 2017.
There may be more assisted suicide deaths.

According to the 2018 Oregon report, the ingestion status was unknown in 43 deaths. Last year the report stated that 143 people died by assisted suicide but then revised the report to state that 158 people died by assisted suicide.

When the ingestion status is unknown, it is possible that the person died by assisted suicide. Some or all of these deaths may represent unreported assisted deaths.
Oregon politicians debating expanding the eligibility criteria in the Oregon assisted suicide act.

Recently the Oregon suicide lobby stated that they intend to expand the definitions in the assisted suicide law.

Oregon House Bill HB 2232 proposes to change the definition of terminal from a six month prognosis to:

a disease that will, within reasonable medical judgment, produce or substantially contribute to a patient’s death.

Many people who are not “terminally” ill have a disease that will, within reasonable medical judgement, produce or substantially contribute to death. When considering the OHA inclusion of refusing medical treatment, this new definition enables wide-open assisted suicide.

Oregon Senate Bill SB 0579 enables a physician to wave the 15 waiting period when prescribing lethal drugs for suicide. The current Oregon assisted suicide law requires a 15 day waiting period. SB 0579 states:

Notwithstanding subsection (1) of this section, if the qualified patient’s attending physician has medically confirmed that the qualified patient will, within reasonable medical judgment, die before the expiration of at least one of the waiting periods described in subsection (1) of this section, the prescription for medication under ORS 127.800 to 127.897 may be written at any time following the later of the qualified patient’s written request or second oral request under ORS 127.840.

By waving the 15 day waiting period, a person can be approved for assisted suicide and die the next day.
Oregon Health authority has an expanded definition of terminal.

In December 2017, Fabian Stahle, a Swedish researcher who is concerned about assisted suicide, communicated by email with a representative of the Oregon Health Authority.

Stahle confirmed that the definition of terminal illness, used by the Oregon Health Authority includes people who may become terminally ill if they refuse effective medical treatment.

The responses to Stahle from the Oregon Health Authority also confirmed that there is no effective oversight of the Oregon assisted suicide law.

The yearly Oregon DWD reports are based on data from the physicians who prescribe and carry-out the assisted suicide death and the data is not independently verified. Therefore, we don’t know if the information from these reports is accurate or if abuse of the law occurs.
https://alexschadenberg.blogspot.com/2019/03/oregon-2018-assisted-suicide-report.html?utm_source=Euthanasia+Prevention+Coalition+Contacts&utm_campaign=c16a1cb9ca-EMAIL_CAMPAIGN_2019_03_04_07_06_COPY_02&utm_medium=email&utm_term=0_105a5cdd2d-c16a1cb9ca-157142057

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Twelve Myths About Physician Assisted Suicide and Medical Aid In Dying

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MD Magazine 7 July 2018
Family First Comment: An excellent summary…
#protect
www.rejectassistedsuicide.nz

Introduction
In an age of “alternative facts,” it’s hard to sort out myth from reality when it comes to so-called “medical aid in dying” (MAID), also called physician-assisted suicide (PAS). By whatever label we attach to it, this practice involves a physician’s prescribing a lethal drug for a patient with a putatively terminal illness who is requesting this “service.” Some form of MAID/PAS is now legal in 5 states and the District of Columbia.

People of good conscience, including many physicians, are sharply divided on the ethics of MAID/PAS. Unfortunately, much of the support for this practice is founded on several myths and misconceptions regarding existing MAID laws and practices. Here are 12 of the most common.

1. Everyone has a “right to die,” including a right to take one’s own life, acting alone or with assistance. 
In contrast to “liberties,” rights entail the cooperation or assistance of others.1 Mentally competent people may be at liberty to end their own lives (ie, will not be prosecuted), but there is no recognized right to suicide that involves the cooperation of others. In Washington v Glucksberg (521 US 702 [1997]), the US Supreme Court (USSC) denied that there is a constitutionally protected “right to commit suicide” or a right to PAS. To rule otherwise, the majority held, would force them to “reverse centuries of legal doctrine and practice, and strike down the considered policy choice of almost every state.”

That said, the USSC has held that all competent persons have the right to refuse unwanted or “heroic” measures that merely prolong the dying process.2 Similarly, in Vacco v Quill (521 US 793 [1997]), the USSC held that there is a legal difference between withdrawal of care and provision of a lethal intervention; ie, everyone has a right to refuse medical care, but no one has a “right” to receive a lethal means of ending one’s life.

2. People who request MAID usually do so because they are experiencing severe, intractable pain and suffering.
Most requests for MAID are not made by patients experiencing “untreatable pain or suffering,” as data from Oregon have shown; rather, the most common reasons for requesting medical aid in dying were loss of autonomy (97.2%), inability to engage in enjoyable activities (88.9%), and loss of dignity (75.0%).3

Many patients who request assisted suicide are clinically depressed and could be successfully treated, once properly diagnosed.

3. In states such as Oregon and Washington, where PAS is legal, there are adequate safeguards in place to ensure proper application of the PAS law. 
In Oregon, reporting to the state is done solely by the physician prescribing the lethal drugs, who has a vested interest in minimizing problems. Moreover, if a physician was negligent in making the initial diagnosis or prognosis, there is no way to track this, since, by law, all death certificates will state that the person died of the putative underlying disease. At the same time, the physician is rarely present at the time the patient ingests the lethal drug, so the possibility of abuse—eg, by coercive family members—cannot be adequately assessed.

The Oregon department of human services has said it has no authority to investigate individual death-with-dignity cases,4 and Oregon has acknowledged that its law does not adequately protect all people with mental illness from receiving lethal prescriptions.5 Thus, it is nearly impossible to determine cases in which, for example, terminally ill patients were pressured to end their lives by family members. A study in Michigan Law Review (2008) found that “seemingly reasonable safeguards for the care and protection of terminally ill patients written into the Oregon law are being circumvented…[and that]…the Oregon Public Health Division (OPHD), which is charged with monitoring the law…does not collect the information it would need to effectively monitor the law…OPHD…acts as the defender of the law rather than as the protector of the welfare of terminally ill patients.”6

Kenneth R. Stevens Jr, MD, and William I. Toffler, MD, both of the Oregon Health & Science University, point to other actual or potential abuses in PAS-permissive states, including “physician shopping” to get around safeguards; nurse-assisted suicide without orders from a physician; and economic pressures to use PAS, such as Oregon Medicaid patients being denied cancer treatment but offered coverage for assisted suicide.7Furthermore, an investigative piece by the Des Moines Register revealed that mandatory reporting requirements were not followed by hundreds of doctors in states where MAID/PAS is legal.8

4. In the United States, only people with terminal or incurable illnesses are eligible for PAS.
Most PAS legislation applies to an adult with a terminal illness or condition predicted to have less than 6 months to live. In Oregon and Washington State, nearly identical criteria are interpreted to mean less than 6 months to live—specifically, without treatment. Thus, a healthy 20-year-old with insulin-dependent diabetes could be deemed “terminal” for the purpose of Oregon’s Death With Dignity Act.

So, too, patients refusing appropriate treatment may be deemed “terminal” under current interpretation of the Oregon law. Thus, a patient with anorexia nervosa who refused treatment could be eligible for PAS under Oregon law, even though she could recover with intensive therapy. As Swedish investigator Fabian Stahle observes, “This is in fact an alteration of the traditional meaning of the concept of ‘incurable.’”9

5. Slippery slope arguments against PAS are overblown. In European countries that allow PAS, there is no evidence that patients are being euthanized improperly. 
People with nonterminal illnesses have been legally euthanized at their own request in several countries for nearly 15 years. This has included certain eligible patients who have only psychiatric disorders. In 2002, Belgium, the Netherlands, and Luxembourg removed any distinctions between terminal and nonterminal conditions—and between physical suffering and mental suffering—for legally permitted PAS. Between 2008 and 2014, more than 200 psychiatric patients were euthanized by their own request in the Netherlands (1% of all euthanasia in that country). Among them, 52% had a diagnosis of personality disorder, 56% refused 1 or more offered treatments, and 20% had never even had an inpatient stay (1 indication of previous treatment intensity). When asked the primary reason for seeking PAS/euthanasia, 66% cited “social isolation and loneliness.”

Despite the legal requirement for agreement between outside consultants, for 24% of psychiatric patients euthanized, at least 1 outside consultant disagreed.10-12

The United States has not been immune to the slippery slope, either. For example, in Oregon, a psychiatrist opened a fee-for-service death clinic where, for $5,000, “terminally ill patients who are eligible to take advantage of…Oregon’s suicide law can book a death that might look a lot like a wedding package.”13

6. The method of “assisted dying” now used in Oregon and other PAS-states assures the patient of a quick, peaceful death, without serious complications. 
A peaceful death is by no means guaranteed using current methods of PAS, as a recent piece by Lo pointed out14: “Physicians who support PAD need to consider how to address the potential for adverse outcomes, including longer time to death than expected (up to 24 hours or more), awakening from unconsciousness, nausea, vomiting, and gasping.”

Data collected between 1998 and 2015 showed that the time between ingestion of lethal drugs and death ranged from 1 minute to more than 4 days. During this same period (1998-2015), 27 cases (out of 994) involved difficulty ingesting or regurgitating the drugs, and there were 6 known instances in which patients regained consciousness after ingesting the drugs. However, it is difficult to know the actual rate of drug-induced complications, because in the majority (54%) of cases between 1998 and 2015, no health care professional was present to attend and observe the patient’s death.15

7. “Death with dignity” comes down to the patient’s autonomy and the right of patients to end life on their terms.
In the first place, under current legislation permitting so-called medical aid in dying, the patient is completely dependent on the judgment, authorization, and prescriptive power of the physician—hardly a state of autonomy.1 Moreover, autonomy is just 1 of the 4 “cornerstones” of medical ethics; the others are beneficence, nonmalfeasance, and justice. As Desai and Grossberg observe in their textbook on long-term care:

“The preeminence of autonomy as an ethical principle in the United States can sometimes lead health care providers to disregard other moral considerations and common sense when making clinical decisions…we strongly feel that the role of the medical profession is to understand but not to support such wishes [for physician-assisted death]. Every person’s life is valuable, irrespective of one’s physical and mental state, even when that person has ceased to deem life valuable.”16

8. Doctors who conscientiously oppose PAS are perfectly free to refuse participation in it. 
In theory, the California guidelines state, “[a] healthcare provider who refuses to participate in activities under the act on the basis of conscience, morality or ethics cannot be subject to censure, discipline…or other penalty by a healthcare provider, professional association or organization.”17 However, prior to its PAS law being declared unconstitutional, physicians in California could be compelled to participate in PAS under certain circumstances.

California’s health department regulation requires a state facility to provide PAS. If the request is denied, the patient has a right to a judicial hearing on the matter. If the court determines the patient is qualified, the attending physician must write a prescription for lethal drugs.18 Moreover, there is evidence that physicians are sometimes pressured or intimidated by patients to assist in suicide.7

9. Terminally ill people who request MAID are not suicidal and don’t commit suicide. They are dying and simply want “hastening” of an inevitable death. In contrast, genuinely suicidal people are not dying of a terminal condition, yet they want to die. 
This argument plays fast and loose with language, logic, and law. In fact, it turns ordinary language on its head, thereby eliminating suicide by linguistic fiat. As the American Nursing Association states, “suicide is the act of taking one’s own life,”19 regardless of the act’s context. There may indeed be different psychological profiles that distinguish suicide in the context of terminal illness from suicide in other contexts, but that does not overturn the ordinary language meaning of suicide. Thus, when a terminally ill patient (or any other person) knowingly and intentionally ingests a lethal drug, that act is, incontrovertibly, suicide.

Most suicides occur in the context of serious psychiatric illness. Yet patients who express suicidal ideation in the context of a condition such as major depression rarely want to die; rather, as numerous suicide prevention websites note: “Most suicidal people do not want to die. They are experiencing severe emotional pain, and are desperate for the pain to go away.”20

10. People requesting PAS are carefully screened by mental health professionals to rule out depression. 
Most PAS statutes modeled after the Oregon Death with Dignity statute do not require examination by a mental health professional, except when the participating physician is concerned and decides to do so. Specifically, “[t]he patient is referred to a psychologist or psychiatrist if concern exists that the patient has a psychiatric disorder including depression that may impair judgment.”21

A study of the Oregon law concluded that “[a]lthough most terminally ill Oregonians who receive aid in dying do not have depressive disorders, the current practice of the Death With Dignity Act may fail to protect some patients whose choices are influenced by depression from receiving a prescription for a lethal drug.”21 

In Oregon, 204 patients were prescribed lethal drugs in 2016 under the Death with Dignity statute, yet just 5 patients were referred for psychiatric or psychological evaluation.22 

11. Doctors who participate in PAS are almost always comfortable doing so and rarely regret their decision.
Many doctors who have participated in euthanasia and/or PAS are adversely affected—emotionally and psychologically—by their experiences. In a structured, in-depth telephone interview survey of 38 US oncologists who reported participating in euthanasia or PAS, nearly a quarter of the physicians regretted their actions. Another 16% reported that the emotional burden of performing euthanasia or PAS adversely affected their medical practice.23 For example, 1 physician felt so “burned out” that he moved from the city in which he was practicing to a small town. Similarly, reactions among European doctors suggest that PAS and euthanasia often provoke strong negative feelings.24

12. For terminally ill patients, the only means of achieving death with dignity is by taking a lethal drug prescribed by one’s doctor. 
Just a small minority of persons with a terminal disease seek a physician’s prescription for a lethal drug. It is not clear why self-poisoning confers more dignity to one’s death than more traditional and much more common ways of dying. Many people who are dying choose to “bear with” their pain. Some seek hospice care and—in cases of severe, intractable pain—merit palliative sedation.25

Some choose voluntary stopping of eating and drinking (VSED), which, according to a study involving hospice nurses, results in a more satisfactory death than seen with PAS. In fact, “as compared with patients who died by PAS, those who stopped eating and drinking were rated by hospice nurses as suffering less and being more at peace in the last 2 weeks of life.”26

A form of VSED called “sallekhana” has been practiced in Jainism for centuries and is regarded as an ethical and dignified means of achieving a “natural” death.27

Conclusion
The case for PAS legislation rests on a number of misconceptions, as regards the adequacy, safety, and application of existing PAS statutes. The best available evidence suggests that current practices under PAS statutes are not adequately monitored and do not adequately protect vulnerable populations, such as patients with clinical depression. The American College of Physicians,28 the American Medical Association, the World Medical Association, and the American Nurses Association have all registered opposition to PAS.

It is critical that physicians inform themselves regarding the actual nature and function—or dysfunction—of medical aid in dying legislation. The first step is to recognize and challenge the many myths that surround these well-intended but misguided laws.
https://www.mdmag.com/medical-news/twelve-myths-concerning-medical-aid-in-dying-or-physicianassisted-suicide
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MPs should examine facts on euthanasia, rather than crystal balls

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Stuff co.nz 10 January 2019
Family First Comment: Excellent analysis of the euthanasia issue…
“Vulnerable people are at an unacceptable risk of wrongful death under laws such as these.”
www.Protect.org.nz

OPINION“Prediction is very difficult, especially if it’s about the future,” said the Nobel Prize-winning physicist Niels Bohr. Maryan Street should have heeded this tongue-in-cheek warning when she forecast that the End of Life Choice Bill would become law this year. Prediction is always hard, but it’s near impossible when it’s based on the kind of partial information found in her article.

The stakes are high with this bill, which would legalise euthanasia and assisted suicide, and the public and the MPs who will be voting on it need much better information than Street provided. So let’s look at some of the key issues that MPs might consider.

First, they’re likely to look overseas and see that laws like these are rejected more often than they pass, because most lawmakers look at the evidence and decide these practices are just too risky. Street tells us that Victoria passed an assisted dying law in 2017, but not that similar laws were rejected by South Australia in 2016, Tasmania in 2017, New South Wales in 2017, and the Northern Territories in 2018.

Second, MPs will probably look at the “Sponsor’s Report” on the bill, by ACT leader David Seymour. He suggests limiting the bill to cover terminal illness only, and making it conditional on a public referendum. But it is wrong and misleading to say, as Street does, that his report is “making some critical amendments”, as though these proposals have been accepted. They are simply Seymour’s ideas; only Parliament can change the bill now.

Third, MPs will be looking at how similar laws have worked overseas. For example, in Oregon, which legalised assisted suicide for terminal illness, 55 per cent of patients accessing assisted suicide said one of their reasons was fear “of being a burden on family, friends and caregivers”. This number has been rising steadily over the years, and it should be a concern for a law that is supposed to be based on free choice.

This kind of law can also expand. In Belgium, euthanasia was originally limited to adults, but was extended to children in 2014, although with some limitations. The numbers accessing assisted suicide have also grown steadily in places such as Washington state, with 196 deaths in 2017 compared with 64 in 2009. Street herself notes how disappointed she will be if “grievous and irremediable” medical conditions are no longer eligible for euthanasia and assisted suicide, and if a limited version of the bill is passed it would be surprising if pro-euthanasia campaigners didn’t try to expand the eligibility criteria in future.

There’s much more detail about the evidence, and analysis of the bill, in our submission; in summary, it shows that vulnerable people are at an unacceptable risk of wrongful death under laws such as these.

Lastly, MPs will probably ask themselves what voters think, and realise there is significant public opposition to the bill. While Street mentions that more than 35,000 people made written submissions on the bill, she doesn’t mention reports suggesting that the vast majority of submitters opposed the bill; unofficial estimates put it as high as 90 per cent.

While opinion polls consistently find that a majority of the public supports euthanasia and assisted suicide, it’s odd not to mention submitters’ opposition, especially as submitters have specifically considered this bill and have probably thought about the issue more deeply than someone put on the spot by a polling company’s random call.

It’s only human for our predictions to be coloured by our desires and, as president of the End-of-Life Choice Society (formerly the Voluntary Euthanasia Society), it’s perhaps not surprising that Street’s crystal ball appears to have given her the answer she wanted. But legalising euthanasia and assisted suicide is one of the most consequential issues that Parliament will consider this year, and a bit less crystal ball-gazing and a bit more attention to the facts would do us all a favour.

* Alex Penk is chief executive of the Maxim Institute, an independent research and policy think tank.
https://www.stuff.co.nz/national/politics/opinion/109806944/mps-should-examine-facts-on-euthanasia-rather-than-crystal-balls

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Significant changes to End of Life Choice Bill proposed by David Seymour

By | Recent News

Stuff co.nz 14 December 2018
Family First Comment: David Seymour 1st Rdg:
“There are those in Parl’t who say its worst bill they’ve encountered. I’ve challenged them privately, they know they couldn’t name better one. This bill’s been in public domain since Sep 2015, no critic has laid glove on any aspect..”
Whoops!

Significant changes to the End of Life Choice Bill have been proposed by Act MP David Seymour.

The bill’s strongest supporter in Parliament has suggested limiting legalised euthanasia solely to cases of terminal illness.

He has sought to exclude mental illness and disability from the bill’s provisions, send it to public referendum, and incorporate aspects of a palliative care bill drafted by his loudest critic, National MP Maggie Barry.

Seymour’s concessions are a bid to earn votes from his parliamentary colleagues and allay concerns among the 37,000 who submitted on the End of Life Choice Bill.

The suggested narrowing has drawn both praise and ire – often in equal measure – from advocates and opponents of the prospective law.

The proposed alterations had been met with intrigue by some anti-euthanasia groups including Family First NZ and Right to Life, with Family First national director Bob McCoskrie urging politicians to “move on”.

“[Seymour’s] latest statements should be an indication to politicians that they should give New Zealanders a real Christmas present and move on from the current political push for assisted suicide, and focus on what New Zealanders really need and want – a focus on providing the very best palliative care and support for vulnerable people.”
READ MORE: https://www.stuff.co.nz/national/health/euthanasia-debate/109351644/significant-changes-to-end-of-life-choice-bill-proposed-by-david-seymour

Euthanasia: Lobbyists say David Seymour’s backing down, but is he?
NewsHub 14 December 2018 
Despite lobby groups claiming David Seymour is backing down from his euthanasia bill, he told Newshub he’s more determined than ever to see it become law.
“I’m more in favour of it than ever. I’ve championed this for three years,” he said.

That’s despite National Director of Family First New Zealand Bob McCoskrie claiming Mr Seymour has conceded to his opponents and is backing down from his bill.

“Family First NZ is welcoming ACT MP David Seymour’s significant backdowns on his assisted suicide bill, and says that this indicates just how weak and flawed the bill is,” Mr McCoskrie said on Friday.

Even pro-life group Right to Life New Zealand said it was “delighted that David Seymour has now recognised that the majority of Members of Parliament are opposed to his [bill]”.
But that’s rubbish, according to Mr Seymour, who told Newshub it’s an “absolutely bizarre reaction” from both lobby groups.

He said anyone who’s questioning his commitment to his End of Life Choice Bill is “clearly not really involved in politics because they don’t know much about it – or they may have nefarious motivations.”

The aim of his bill is to legalise voluntary euthanasia in certain circumstances. The explanatory notes say the bill gives “people with a terminal illness or a grievous and irremediable medical condition the option of requesting assisted dying”.

Mr McCoskrie says there’s been “overwhelming opposition to David Seymour’s assisted suicide bill by submitters to the Select Committee”.

According to an analysis of a number of the submissions by the Care Alliance, 92 percent of submissions are against Mr Seymour’s bill.
READ MORE: https://www.newshub.co.nz/home/politics/2018/12/euthanasia-lobbyists-say-david-seymour-s-backing-down-but-is-he.html

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icare – 20 New Zealanders highlight the risks and fallacies of the End of Life Choice Bill.

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icare December 2018
Family First Comment: icare represents a commitment to excellent care to enable good living and good dying. icare is the Care Alliance’s major information campaign featuring short videos of 20 New Zealanders who share their disability, palliative care, medical and legal perspectives highlighting the risks and fallacies of the End of Life Choice Bill.
WATCH THE VIDEO CLIPS HERE https://carealliance.org.nz/icare/
#committedtocare

Like an umbrella, good care shelters a person in adverse conditions, enabling a journey from one place to another that can be shared with others.

icare represents a commitment to excellent care to enable good living and good dying. icare is the Care Alliance’s major information campaign featuring short videos of 20 New Zealanders who share their disability, palliative care, medical and legal perspectives highlighting the risks and fallacies of the End of Life Choice Bill.

WATCH THE VIDEO CLIPS HERE https://carealliance.org.nz/icare/

David Seymour Concedes Opponents’ Euthanasia Concerns Are Correct

By | Media Releases

Media Release 14 December 2018 
Family First NZ is welcoming ACT MP David Seymour’s significant backdowns on his assisted suicide bill, and says that this indicates just how weak and flawed the bill is.

“The backdowns are certainly in contrast to his earlier attacks on our justified concerns, including his statements that There’s just so much scaremongering that doesn’t stand up to evidence and One of the biggest obstacles are MPs who are not in touch with their electorates…and also MPs who may have been coloured by some of the scare-mongering from the other side. There was never any ‘scaremongering’. There was – and continues to be – opposition to this bill based on credible research internationally in jurisdictions that have euthanasia available, and from medical professionals in New Zealand who know the effect such a law would have on their work and on society,” says Bob McCoskrie, National Director of Family First NZ.

“Even if the bill was limited to just the terminally ill, some people will be euthanised on account of a disease they thought they had but did not. Prognosis is an uncertain procedure. Many people know or have heard of a person who, having been given a pessimistic prognosis, has lived for many years to tell the tale. There will be those who decide for euthanasia on the basis of an unduly pessimistic prognosis. There is also concrete evidence from those countries which have authorised euthanasia that the availability and application of euthanasia expands to situations never initially envisaged as indications for it.”

“There has been overwhelming opposition to David Seymour’s assisted suicide bill by submitters to the Select Committee. According to an analysis of a substantial number of the submissions by the Care Alliance, a whopping 92% of submissions are against David Seymour’s bill, and is significantly higher than the already-high 77% opposition during the Health Select Committee’s earlier investigation.”

“The promotion of assisted suicide is a message that will be heard not just by those with a terminal illness but also by anyone tempted to think he or she can no longer cope with their suffering – whatever the nature of that suffering. This is the real risk to young and to vulnerable people, the disabled and elderly people if NZ follows the path of promoting – and allowing – assisted suicide.”

“The latest statements by David Seymour should be an indication to politicians that they should give New Zealanders a real Christmas present and move on from the current political push for assisted suicide, and focus on what New Zealanders really need and want – a focus on providing the very best palliative care and support for vulnerable people, whether they are at the end of their life, or momentarily wishing they were at the end of their life.”
ENDS

Lobby group claims most New Zealanders against euthanasia

By | Recent News

NewsTalk ZB 11 December 2018
Family First Comment: “92% of submissions are against it, UP from 77% during the Health Select Committee’s earlier investigation”!
Once people consider the issue in depth, the opposition is overwhelming.
www.Protect.org.nz

An analysis of public submissions on the End of Life Choice Bill has found a growing number of Kiwis against euthanasia.

A team of volunteers from the Care Alliance, who oppose the bill, have analysed more than 20,000 of the record-breaking 36,000 submissions received.

Secretary Peter Thirkell says their preliminary analysis shows 92 percent of submissions are against it, up from 77 percent during the Health Select Committee’s earlier investigation

“The thing that strikes you is that these are just regular Kiwis for the most part saying what’s important to them. Overwhelmingly, people are quite fearful about
the broader social implications of this bill. That comes through strongly.”

Thirkell says many are concerned about vulnerable people who could be influenced one way or another.

One Christchurch palliative care doctor says she doesn’t support legalising euthanasia.

Doctor Amanda Landers was the former chair of the Kiwi branch of the Australian and New Zealand Society of Palliative Medicine.

She says she had to speak to the initial Health Select Committee when the bill was in its infancy and what she learned concerned her.
READ MORE: https://www.newstalkzb.co.nz/news/national/lobby-group-claims-most-new-zealanders-against-euthanasia/

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Overwhelming Opposition Confirmed On Assisted Suicide Bill

By | Media, Media Releases

Media Release 11 November 2018 
Family First NZ says that the overwhelming opposition to David Seymour’s assisted suicide bill by submitters to the Select Committee is no surprise and was already indicated during the earlier Inquiry by the Health Select Committee.

According to an analysis of a substantial number of the submissions by the Care Alliance, a whopping 92% of submissions are against David Seymour’s bill, and is significantly higher than the already-high 77% opposition during the Health Select Committee’s earlier investigation.

“This is opposition from all walks of life and professional groups across the spectrum. Supporters of assisted suicide have tried to argue that the only opposition comes from ‘religious’ people, but in the recent Inquiry, 82% of submissions opposed to euthanasia contained no reference to religious arguments. Ironically, 208 submissions referred to religious reasoning in supporting euthanasia,” says Bob McCoskrie, National Director of Family First NZ.

“Supporters of Seymour’s bill had their chance to campaign and get people to submit in support of the law change. The fact of the matter is that the support has been found wanting.”

“It is also ironic that ex-MP Maryan Street implied that a record 22,000 responses to her earlier petition meant that it is time to legalise euthanasia. In fact, the message is clearly the exact opposite. New Zealanders want a conversation – but they are opposed to assisted suicide as the solution.”

“The promotion of assisted suicide is a message that will be heard not just by those with a terminal illness but also by anyone tempted to think he or she can no longer cope with their suffering – whatever the nature of that suffering. This is the real risk to young and to vulnerable people, the disabled and elderly people if NZ follows the path of promoting – and allowing – assisted suicide.”

“The politicians should give New Zealanders a real Christmas present and move on from the current political push for assisted suicide, and focus on what New Zealanders really need and want – a focus on providing the very best palliative care and support for vulnerable people, whether they are at the end of their life, or momentarily wishing they were at the end of their life.”
ENDS

What it will take to die: setting a straight path down the ‘slippery slope’

By | Recent News

Stuff co.nz 5 December 2018
Family First Comment: Dr Huhana Hickey, who has multiple sclerosis, is one of many who consider the bill unsafe for the disabled, elderly, and the “easy targets for unscrupulous people”. 
#RejectAssistedSuicide 
www.Protect.org.nz

New Zealand is facing a question of life and death. After taking in the nation’s views on legalised euthanasia, the largest-ever parliamentary tour ended in November. Now, Stuff is laying out the arguments and telling the compelling stories surrounding the End of Life Choice bill.

Armed with alarming anecdotes and evidence from overseas jurisdictions, many arguments for legalising assisted death fall on either side of a divide.

It’s a narrow path to escape a painful death; or a “slippery slope” towards broadly sanctioned killing. But how does the End of Life Choice bill compare?

Dr Huhana Hickey, who has multiple sclerosis, is one of many who consider the bill unsafe for the disabled, elderly, and the “easy targets for unscrupulous people”.

“How do we know that we’re going to keep people who don’t want to be euthanised safe?”

It’s the permissive laws of the Netherland and Belgium, which permit euthanasia of minors and infants, that has Hickey most concerned.

“You can put all the safety measures in place, but the laws have a way of changing over time.

“Once you legislate it, you open the door to amendments, alterations, and the bill becoming, basically, an absolute farce in the end.”

Netherlands and Belgium have liberalised since passing law in 2002, after decades of permitting medically-assisted euthanasia.

Though liberalisation hasn’t happened everywhere. US-state Oregon legalised euthanasia strictly for cases of terminal illness in 1998, and hasn’t changed since. Advocacy to include irremediable conditions is now starting to gain traction two decades later.

The End of Life Choice bill permits assisted dying in a manner similar to Oregon, Canada, and Victoria, Australia – all stricter than European regimes.

Yet Hickey sees demonstrable risks. Belgian prosecutors are now conducting the first criminal investigation into a euthanasia case of a women with autism in 2010.
READ MORE:  https://www.stuff.co.nz/national/health/euthanasia-debate/109071343/what-it-will-take-to-die-setting-a-straight-path-down-the-slippery-slope

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