Wednesday, February 16, 2011

Alleged internet suicide predator pleads not guilty in the death of Nadia Kajouji, but waves his right to a trial.

Mark Drybrough
William Melchert-Dinkel (48), the former Minnesota nurse, has waved his right to a trail, but also pled not guilty to assisting the suicides of Canadian teen Nadia Kajouji (18), and Mark Drybrough (32) of Coventry England.

Nadia Kajouji
Melchert-Dinkel failed to get the charge of assisted suicide dropped when a Minnesota judge refused to accept the arguement that this was a case of freedom of speech.

Melchert-Dinkel has admitted to being involved in the deaths of Carlton University student Nadia Kajouji and Mark Drybrough from the UK, but he has pled not guilty to assisting their suicide deaths.

Instead of facing a three week trial, Melchert-Dinkel has decided to opt for a rarely used Minnesota provision that gives the judge seven days to review the case and then the judge decides whether or not he is guilty of the crime.

The following is the article in the Ottawa Citizen by Lee Greenberg:

Melchert-Dinkel
Nurse waives right to trial in suicide case

The trial of a Minnesota nurse accused of assisted suicide in the death of a Carleton University student took another unexpected turn Tuesday, when William Melchert-Dinkel announced he will waive his right to a trial.

Melchert-Dinkel, who has admitted to prowling online suicide chat rooms and coercing depressed people into killing themselves, was scheduled to appear at a three-week trial in April.

Instead, he is employing a rarely used Minnesota legal provision. A judge will Thursday review the prosecution’s case against Melchert-Dinkel and decide within seven days whether the 48 year old Minnesotan is guilty of two counts of assisted suicide.

By entering the unusual motion, known as a Lothenbach plea, Melchert-Dinkel waives his right to cross-examine prosecution witnesses, to compel his own witnesses to testify and his right to testify on his own behalf.

He is still nevertheless pleading not guilty.
“We neither think witnesses are necessary nor do we think a trial in any way benefits my client,” said Terry Watkins, Melchert-Dinkel’s lawyer.

“There’s not a disagreement basically with the facts in this case so a trial based on stipulated facts would be much more efficient and much more effective and would be in the best interests of both my client and the government.”
Melchert-Dinkel, a father of two teenage daughters, lives in the picturesque town of Faribault, Minnesota, about an hour south of Minneapolis. State authorities began investigating the troubled former nurse after a British grandmother complained in 2008 he was encouraging depressed online chatroom participants into suicide.

Celia Blay pointed Minnesota police to the case of Mark Drybrough, a 32-year old Briton, who hanged himself in 2005 after corresponding with Melchert-Dinkel.

Police later learned of the 2008 suicide of Nadia Kajouji, a Brampton teen and first-year Carleton University student who was befriended by Melchert-Dinkel and coaxed into a false suicide pact. The aging, overweight man was posing as a 20-something woman when he asked Kajouji to kill herself in front of a webcam while he watched.
“If you go ... any kind of home improvement store — get yellow nylon rope about eight feet or about 3.5 meters and about one-inch thick or about three centimetres that is all you need and look around apartment for somewhere to hang from,” he told Nadia during one chat session. “I can help you with the cam when you need to.”
When he learned of a police investigation into the issue, Melchert-Dinkel checked into a state hospital and claimed to be suffering from an “addiction” to suicide chat rooms.

He told police he formed “10 or 11” false suicide pacts with people over the world and compared his preoccupation with hunting human game, telling detectives he enjoyed “the thrill of the chase.”

Ottawa police told Kajouji’s mother they decided against charging Melchert-Dinkel because there was no evidence he directly caused her suicide.

That decision perplexed legal scholars, who said Canada’s suicide provision does not require such causality.

Minnesota police says the charges are the first in recent memory. State law punishes anyone who “intentionally advises, encourages, or assists” suicide with up to 15 years imprisonment and up to a $30,000 fine.

Links to information about the Melchert-Dinkel case.

Bill to clarify that assisted suicide is prohibited in Idaho unanimously passes in the Idaho Senate Affairs Committee.

The bill to clearly define assisted suicide as prohibited in Idaho has unanimously passed in the Idaho Senate Affairs Committee.

The Idaho Spokesman Review stated:
Legislation to outlaw physician-assisted suicide in Idaho has cleared the Senate State Affairs Committee, which just voted to send SB 1070 to the full Senate with a recommendation that it pass. The bill was sponsored by pro-life groups who worked with the Idaho Medical Association, in order to protect physicians making appropriate patient-care decisions for dying patients or following those patients' living wills or advance care directives.

Ken McClure, IMA lobbyist, told the committee, “Under current law, it is not at all clear whether assisted suicide is a crime or not.” It's not currently a part of Idaho's standards for patient care, he said, and doctors don't want it to be. “This law gives a physician the assurance that if proper medical care is being given, he or she is safe from prosecution,” McClure told the senators.

The bill makes it a felony to assist in a suicide, plus revokes the licenses of physicians who do so. It also authorizes court injunctions against anyone “reasonably believed to be about to violate” the new law.

Interesting Op-ed by PR Guy for Hawaii Death with Dignity Society

Stephen Drake, the research analyst for the disability rights group Not Dead Yet has done a great analysis of the recent comments by Scott Foster, the communications director for the Hawaii Death with Dignity group. Drake always does a great analysis, and he always looks into the archives for more information.

Drakes comment is work reading.

Interesting Op-ed by PR Guy for Hawaii Death with Dignity Society

Well, whatever else you can say about Scott Foster, Communication Director at the Hawaii Death with Dignity Society, he churns out an op-ed pretty quickly. Like lots of communications folks, he regurgitates stuff he's written elsewhere, but every once in awhile he introduces some new gem and there are several items of interest in his op-ed in the Star Advertiser after the defeat of the assisted suicide bill last week.

Foster wants a "better" debate - an ironic request from an assisted suicide zealot who exploited the tragic attempted murder-suicide in late 2009. Robert Yagi attempted to kill his wife with a flare gun loaded with shotgun shells. It was unsuccessful. However, Yagi succeeded in killing himself a short time later when police sent him home after being charged with attempted murder, left alone in his home. Like "Conflation and Con Jobs," Foster jumped on this incident to promote legalized assisted suicide, making the bizarre case that an attempted murder of a woman who didn't want to die somehow would have been prevented by a "death with dignity." Draw that reasoning up on a chalkboard and it would have a striking similarity to some of Glenn Beck's exercises in fantastical "logic."

The first "gem" in Foster's op-ed is that he comes very close to "speaking" Derek Humphry's "unspoken argument" - that an aging population and rising health care costs are powerful hidden motivations in supporting assisted suicide. Here's what Foster says:

I remain convinced that the well-organized opposition to DwD legislation in Hawaii and elsewhere is more about money and God than about our solving the many challenges associated with an aging population, the resulting end-of-life issues, or the out-of-control cost of health care in our state and nation. If you wonder where all that money is going, according to the U.S. Department of Health & Human Services Office of Research, Development, and Information: "Medicare provides 64 percent of total health expenditures for beneficiaries in their last year of life ..." and the numbers for private insurance and out-of-pocket expenditures are similar. Despite the smoke and mirror arguments about "compassion," as it is, there's big money in death for many in the health care industry and DwD seems to threaten the status quo. (Emphasis added.)

It's fascinating, really. If you read that carefully, what Foster is saying is "assisted suicide will save money." After you look beyond "the smoke and mirror arguments about 'compassion'" (to use Foster's words) you see what Foster and the rest are really betting on.

Another interesting aspect of this op-ed is his attack on the chair of the Committee that held the hearings on the assisted suicide bill. Pro-assisted suicide advocates normally portray physicians as absolutely trustworthy professionals who would never abuse or expand killing beyond what an assisted suicide statue allows. That doesn't mean that Foster wants one to run a hearing on assisted suicide:

It is also clear that an M.D. should not be chairing health committees. It's an inherent conflict of interest.

There's a contradiction there - trust a doc with your life but not your legislation? Seriously, though, I doubt that Foster would object to the hearing being chaired by a pro-euthanasia doctor.

For anyone interested, there's been a fairly heated exchange between myself and another commenter at the newspaper site. I wouldn't be surprised if the other person was Foster himself, since he or she uses the same tired old arguments and fantasy scenarios about husbands who murder their wives.

Check out the comments in the Star Advertiser.

Tuesday, February 15, 2011

Assisted Suicide is Not Legal in Montana; Clarification Needed

The Montanans Against Assisted Suicide and for Living with Dignity put an important update on their website concerning the status of Senator Hinkle's Bill SB 116, the Elder Abuse Prevention Act. There is confusion in Montana related to the Montana Supreme Court - Baxter decision, which did not legalize assisted suicide but gave physicians, if prosecuted, a potential defense of consent.

Please read the update:

On February 10, 2010, the Senate Judiciary Committee defeated and tabled SB 167, which would have legalized physician-assisted suicide in Montana. Despite this defeat, some assisted suicide proponents are encouraging doctors and others to engage in assisting and/or causing suicide, claiming that the practice is legal under Baxter v. State.

Under Baxter, doctors are given a potential defense to a homicide charge, which may or may not succeed. Baxter did not overrule prior case law imposing civil liability for doctors and others who cause another person’s suicide, typically in a hospital or jail setting. Under Baxter, doctors and others can still be held criminally and civilly liable for causing another person’s suicide.

Historically, the movement to legalize assisted suicide and euthanasia has had a eugenic component, which seems to be the case here. Legalization is, regardless, a recipe for elder abuse, which Baxter completely overlooked. Baxter also overlooked statistics from Oregon showing a positive correlation between legalization of assisted suicide and an increased rate of other violent suicides. Montana already has one of the highest suicide rates in the country. Montana does not need even more suicide.

Senator Hinkle’s bill, SB 116, is a short simple bill that seeks to return Montana to the status quo of 47 other states in which assisted suicide is clearly not allowed. SB 116 is needed because, with Baxter, the law is convoluted; Montanans, especially our older citizens, are not protected.

References:
The Hinkle Report: Link
SB 116 at a glance: Link Elder Abuse At a Glance

Monday, February 14, 2011

Why Safe Voluntary Euthanasia is a Myth

The following article is written by Australian Dr. Brian Pollard who is a retired anaesthetist and palliative care physician, who founded and directed the first full-time palliative care service in a teaching hospital in Sydney Australia at Concord Hospital in 1982 and directed it for five years. He is author of The Challenge of Euthanasia (Little Hills Press, 1994).

The article was printed in Quadrant online:

Why Safe Voluntary Euthanasia is a Myth

The criminal law in Australia holds that the intentional taking of human life is a major criminal offence. This accords with the United Nations Universal Declaration of Human Rights, to which Australia is a signatory, which declares that the right to the integrity of every person’s life is equal, inherent, inviolable, inalienable and should be protected by law.

Since the intentional taking of human life is the specific aim of every euthanasia law, such a law would be unique in the following critically important ways:

• it would intend to subvert the existing law
• it would fail to respect the principle that all are equal before the law
• it would fail to respect the principle that all human lives have equal value, and
• it would attempt to gain legal recognition for the concept of life not worth living.

This would present an impossible task, if honesty were to prevail. It would have to rely on such things as asserted but non-existent human rights, shades of deceit, inexact definitions and words or clauses allowing loose interpretations, rather than objectivity and precision.

The push for legalised medically assisted death in Australia has now increased to the point where bills are before several state parliaments and another is before the Commonwealth parliament to reverse the previous overturning of the Northern Territory legislation. I have analysed most of the previous failed bills and noted their weaknesses. Rather than debate the pros and cons of the social role of euthanasia, I believe that MPs, who have sole responsibility for making safe laws, should direct their attention to ensuring that draft euthanasia bills cannot imperil the lives of innocent people who do not wish to die.

It is evident that the authors of those bills have not read any of the extensive literature on this subject because they invariably include, as so-called safeguards, provisions which are known not to work in practice. A common feature of those who advocate euthanasia bills is their touching faith that certain things will happen, just because the draft prescribes them. If that were true, no crime would ever be committed because all crime is currently forbidden by some law.

In 1958, Yale Kamisar, an American professor of law in this field, wrote a seminal paper in which he listed these basic difficulties: ensuring that the person’s choice was free and adequately informed; physician error or abuse; difficult relationships between patients and their families and between doctors and their patients; difficulty in quarantining voluntary euthanasia from non-voluntary; and risks resulting from this overt breach of the traditional universal law protecting all innocent human life. All these problems still exist and others have been added, such as the critical role of depression in decision-making and the evolution in the moral basis for requesting death from the relief of severe suffering in the terminally ill to reliance on respect for personal autonomy. Some of these will be discussed below.

Definitions are often vague or at odds with ordinary meanings. For example, in place of “terminal illness” one may find “incurable illness”. Many illnesses are literally incurable but do not necessarily cause death or shorten life. Pain and suffering are both highly subjective experiences; neither can be measured or compared between persons, while suffering is often due to social causes rather than medical. According to the drafts, both have to be simply accepted as the person describes them, even when this may raise serious doubt. And, as most now allow, if the symptoms are said to make life “intolerable”, even though it is recognised that what one person finds intolerable others can bear, that claim has only to be made to be incontestable. The situation then will have become virtually one of death on demand.

All bills require the doctor to be “satisfied” that the patient’s request was freely made, though no one could ever know with certainty about coercion from sources of which he was totally unaware. But would coercion be likely? Brian Burdekin, a former Human Rights Commissioner, reported that in his experience, “The most vulnerable were the most likely to be abused and the most likely to be coerced.” Subtle degrees of coercion would be almost impossible to detect.

If a well person asks for death he will be referred for counselling. If a sick person asks, he is as likely to be supported in his “exercise of personal autonomy”. And what of autonomy in the presence of severe illness, especially terminal illness, with its frequent association with depression and unrelieved pain, which powerfully hinder careful evaluation of issues? More importantly, no matter what the patient decides, in every case it will be the doctor’s decision that determines whether euthanasia actually proceeds. Leon Kass, a lawyer and prolific author in this area, wrote that, in view of the totality of the impediments to clear reasoning in such patients, “the ideal of rational autonomy, so beloved of bioethicists and legal theorists, rarely obtains in actual medical practice”.

Doctors are experienced in persuading patients to follow their legitimate advice concerning treatment options, to the point where some have been heard to say, “I can get my patients to do anything I want.” Their power, relative to that of the patient, is large even when there is no intention to manipulate. Euthanasia draft bills require doctors to inform patients about the medical details of their illness and future alternatives. Since such discussions will usually occur in private, one could never know whether such information was accurate, adequate, non-coercive and impartial. If the doctor’s personal view was that euthanasia was appropriate for a patient, we may be sure some would not be deterred from advocating it.

A lot of publicity has lately been given to the fact that some 85 per cent of respondents to opinion polls favour legalised euthanasia. This refers to the Morgan poll which has been using this question for many years: “If a hopelessly ill patient in great pain with absolutely no chance of recovering asks for a lethal dose, so as not to wake again, should the doctor be allowed to give the lethal dose or not?” It is not hard to see why many respondents, whose understanding of the complex matter of euthanasia is unknown, might agree to such an emotionally charged question. Given that repeated polls have shown that most Australian doctors have not received adequate training in palliative care, and sometimes none at all, should anyone be surprised that too often pain is poorly managed? Against that background, the poll question may be truthfully reworded, “If a doctor is so negligent as to leave his patient in pain, severe enough to drive him to ask to be killed, should the doctor be able to compound his negligence by killing the patient, instead of seeking expert help?” The community would be appalled to know how few doctors who must care for dying patients are able to deal with severe pain effectively. The only remedy for this situation will be to introduce mandatory levels of competence in palliative care training in all medical schools. In the meantime, legalising euthanasia will lead inevitably to many needless deaths. Australia has about half the palliative care specialists it needs, all of whom are in cities or big towns.

Too often, draft bills for euthanasia only require the doctor to obtain expert psychiatric advice if he “suspects” the patient is “not of sound mind”, that is, has impairment of competence, which is not the key issue. The literature of psychiatry contains abundant evidence that the sustained wish to die is associated, in a large number of the seriously ill, with depression, which alters mood and inhibits the ability to reason coherently. Not to require consultation by a psychiatrist experienced in the treatment of dying patients whenever a sustained wish to die is encountered, is a negligent omission, especially as such depression is often difficult to diagnose. A published retrospective review of the Northern Territory legislation in its short life showed that relevant psychiatric evidence had been withheld and treatable depression was missed in four of the seven patients whose lives were taken under its provisions. The demoralising combination of depression or despair, anxiety and fear associated with a desire to die, can usually be treated with a mix of empathy, psychotherapy and medication.

The usual superficial approach to this problem is in stark contrast to the following advice from expert psychiatrists: “No request for hastened death can be understood without first attempting to understand the psychological landscape within which the request arises.” One advised, “Never kill yourself when you are suicidal—you are not yourself then.” Accordingly, it has been suggested that the need for better training in the detection of profound psychological disturbance in these patients is as great as that for the relief of severe pain. Even in the Netherlands, there is awareness of past failings, as the former health minister from 1994 to 2002, Mrs Borst-Eilers, commented in 2009, “The government’s move [to legalise euthanasia] was a mistake, we should have first focused on palliative care.”

Wherever voluntary euthanasia is practised, legally or not, non-voluntary is also found, including in Australia. Many find this difficult to credit because, whatever their failings, doctors surely would not take life without any request. In fact, they do it because it seems logical. Once euthanasia for patients who are suffering and ask to be killed is regarded as providing them with a benefit, it will appear, at least to some, that it would be wrong to withhold that benefit from others who suffer as much, but who, for some reason, cannot ask. In their eyes, this would be a matter of compassion. Because the same rationale can be the justification for euthanasia for both groups, the extension of one to the other must be regarded as inevitable and so will be uncontrollable. The Dutch have long since given up trying to prevent non-voluntary euthanasia.

Bills require the doctor to notify the coroner, following euthanasia. Since he will be its sole author, the chief actor and the sole survivor of the event, what chance is there that the doctor will include anything he would not wish the coroner to know?

Some may have found the earlier reference to deceit too strong, but it was not. At length, the draft bill must somehow directly confront the present law which outlaws euthanasia. So, the doctor is required by the bills to certify the death as due to the underlying illness, that is, to lie (though falsifying a death certificate is currently a punishable offence), and the death is not to be regarded, for the purposes of the Act, as any form of homicide, even though it was unquestionably homicide. Truth must yield to weasel words for these bills to succeed.

After euthanasia, the doctor may not be subject to any civil or criminal action, nor to any penalty or loss of privilege by any professional body. With only a few exceptions, medical associations throughout the world hold that euthanasia is forbidden to doctors because it is unethical, that is, morally wrong. Australian state governments establish boards and tribunals to regulate medical practice and they all regard medical life-taking as deserving of deregistration because those doctors are no longer fit to practise, on ethical grounds. These clauses in the bills are included without the consent or authority of the regulators, who regard them as necessary to protect patients against attacks on their lives, in recognition of their genuine human rights. Just now, when it is being more widely recognised that there is a need for more emphasis on ethics in many areas of moral significance, the supporters of euthanasia want to dispense with them altogether. It may be wondered what benefits the community can expect to gain from having unethical doctors.

When all euthanasia draft bills so far put before state parliaments over many years are reviewed, it can be observed that they go to extreme lengths to shield the doctor from the effects of current law, no matter what he or she may have done negligently or by omission, while including many opportunities for endangering the lives of patients who did not want their life ended. In justice, it is the vulnerable who need protection, not the powerful. This danger is exactly what all the large committees of inquiry into the consequences of legalising euthanasia have predicted in their published reports, even those which included some members who were in favour of euthanasia. No other reasoned conclusion was available to them after extensive oral and written evidence had been taken from a wide range of community and professional sources. Every law to permit euthanasia will be inherently and unavoidably unsafe.

Sunday, February 13, 2011

Assisted suicide: Annual report raises more questions than answers

Dr. Kenneth Stevens, the leader of physicians for Compassionate Care in Oregon, wrote a Guest Column that was printed in Oregon Live on Friday, February 11, 2011

Dr Stevens examines the Annual Report on assisted suicide by the Oregon Public Health Division and he explains that their are more questions than answers concerning the assisted suicide statute in Oregon.

The Column states:
The doctor-assisted suicide information released by the Oregon Public Health Division for the past year raises more questions than answers.

Why was the report compiled and released before all of the information for the year was available? All prior years' reports were released in March, allowing sufficient time for the receipt of information from prescribing doctors for the prior year. Although the new report lists 65 deaths, there are likely to be others who died of doctor-assisted suicide in 2010 for whom the prescribing doctors' reports had not been received as of Jan. 7.

The report mentions that there is no further information about 15 patients who had received prescriptions under the law in 2010. Why was the report prepared and released so hastily rather than with more accurate and complete information?

The report did reveal, however, that two patients who attempted to take the supposedly lethal drugs did not die. The reports' sparse information states that one person regained consciousness within 24 hours and died of the underlying illness five days later, a second person regained consciousness three days after ingestion of the drugs and died of the underlying illness three months later. Vomiting was reported in both people. These drugs are not easy to take and swallow; they are very bitter and foul-tasting.

Why did the report not provide more information regarding these two unsuccessful suicides? Why did the report fail to detail why these two people chose not to repeat the overdose?

Perhaps the two patients found the experience less pleasant than promoters of doctor-assisted suicide led them to believe. The individuals and their family and friends probably had a harrowing time dealing with those unsuccessful suicides.

It seems strange to live in a society where a failed suicide is considered to be unsuccessful and an accomplished suicide is considered a success.

Why did only one of the 65 people reported to have taken their lives with the drugs have a psychiatric or psychological referral? Researchers at Oregon Health & Sciences University reported in 2008 that 25 percent of patients requesting doctor-assisted suicide were considered to be depressed. There continues to be no protection for depressed patients in the process.

Why, according to the state's report, was a doctor present for only six people when the drugs were taken and when death occurred? Why are Oregon's doctors distancing themselves from the final fatal act? Is it because of the significant personal emotional toil that occurs when doctors prescribe lethal drugs?

The report lists that there was "unknown information" for 50 to 70 percent of deaths for the following categories: whether the doctor was present when the drugs were ingested, if there were complications, if emergency services were called, and the time between ingestion to unconsciousness and to death.

When such a substantial proportion of important information is unknown and with much incomplete information, how are we to know what is really happening with doctor-assisted suicide in Oregon?

The state's report appears to be perfunctory and does little to relieve the concerns regarding the dangers of doctor-assisted suicide in Oregon.

Kenneth R. Stevens is a Sherwood physician.

Thursday, February 10, 2011

Bill to legalize assisted suicide defeated in the Montana Judiciary Committee

Congratulations to everyone who worked in coalition to successfully defeat Senator Anders Blewett's bill SB 167 by a vote of 7 - 5 in the Montana Senate Judiciary Committee. SB 167 would have legalized assisted suicide in Montana.

Senator Greg Hinkle's - Elder Abuse Prevention Act - Bill SB 116, will reverse the Baxter court decision and prohibit assisted suicide in Montana will go to a vote soon.

I was told that the majority of the Montana Senators oppose assisted suicide, but many of them are unsure of where Montana citizens stand on the issue of assisted suicide.

A few Montana Senators have suggested that they oppose assisted suicide but thought that it was acceptable to maintain the status quo.

The fact is that the Status quo is unacceptable because Compassion & Choices, formerly the Hemlock Society, has been lying to Montana physicians by stating that they could prescribe a lethal dose for their patients without fear of prosecution. In other words, because Compassion & Choices is encouraging doctors to take the law in their own hands, that it is absolutely necessary for Montana legislators to support Senator Hinkle's Bill SB 116.

Finally, the news article from CNBC suggested that the Montana Governor may not sign the Hinkle bill into law. The fact is that everytime the Governor usurps the role of the House and Senate, he does so at a political cost. Bill SB 116 needs to be supported in order to protect Montana citizens from elder abuse.

The Montanans against Assisted Suicide and for Living with Dignity are working to get more people to write letters and call their Legislators.

A pro-assisted suicide article entitled: Bill to set rules for doc-assisted suicide fails was published today on CNBC

Now that the Blewett bill has been defeated in Montana, and a similar bill was also unanimously defeated in the Senate Health Committee in Hawaii last week, with a focused hard working effort, it is likely that the bills to legalize assisted suicide in New Hampshire and Vermont will likely also be defeated this Spring.

Wednesday, February 9, 2011

Euthanasia and Assisted suicide debate in Quebec

Deborah Gyapong has written an update concerning the euthanasia debate in Quebec. Gyapong, who writes for the Canadian Catholic News, interviewed Linda Couture, the director of Vivre dans la Dignite (Living with Dignity). Couture has done an excellent job at building a coalition against euthanasia and assisted suicide in Quebec.

The reality is that the Quebec government committee continues to favour presentations that support euthanasia, even though the majority of the presentations have opposed euthanasia.

By the way, it appears that the Quebec committee is thinking about turning a blind-eye to euthanasia by establishing guidelines that will favour Belgium style Euthanasia. Couture is correct when she states that the people of Quebec really don't support euthanasia.

The article by Deborah Gyapong stated:

Quebec holds hearings on assisted suicide during “Suicide Prevention Week”

­As Quebec marked Suicide Prevention Week (Jan 30­ - Feb 5), the Select Committee on Dying with Dignity held hearings here testing support for legalized euthanasia and assisted suicide.

The irony did not escape Linda Couture, who directs Living with Dignity, a grassroots, non-religious organization that has been monitoring the hearings as the committee travels across Quebec. Living with Dignity is also marshaling opposition from a wide range of groups and individuals to any changes to the law or its enforcement.

On Jan 30, Couture had received a copy of a press release from Marguerite Blais, the Quebec minister responsible for seniors, who kicked of Suicide Prevention Week by expressing alarm over the high rates of suicide among the elderly and criticizing the belief that suicide is a normal response to growing older.

Couture said Blais has made as eloquent a plea as any she has heard that suicide is never a normal or acceptable response to age or illness.

“How could a medicalized suicide be acceptable?” Couture asked. “There’s something missing. I don’t get it.”

The Select Committee composed of Members of Quebec’s National Assembly (MNAs) has been holding public hearings in cities across Quebec since September. Couture said she has attended most of them. The committee wraps up its hearings at the end of February and will then work on a written report.

On Feb 1, Ottawa Hospital Palliative Care chief Dr. Jose Pereira told the committee that legalized euthanasia and assisted suicide “places people at risk.”

“In Oregon, for example, where depression has to be excluded, we know that people with a depression are more likely to ask for assisted suicide or euthanasia,” he said. “That's very well-known.”

He added that in Oregon, one in six people who received assisted suicide were found to have untreated depression.

“My brother-in-law committed suicide last year, and it was a very difficult time for our family,” he said. “And, looking back, we feel it was a depression that wasn't treated. And, so, people with depression do ask for assisted suicide and do commit suicide.”

Pereira, who has worked in Switzerland where assisted suicide is allowed, said he observed the rules change over time. At first assisted suicide was only supposed to apply to those who are terminally ill, at the end of life and suffering.

Yet within two years, there was a campaign to allow assisted suicide for those “in long-term care facilities and nursing homes, for people who were elderly and felt that they didn't want to live anymore.”

Joan Lusignan, a private citizen in her eighties, testified the Special Committee had her worried. “What will our children and future generations think of a government that on one hand spends large sums of our money and effort to help prevent the escalating rate of suicides among young people in Quebec, but at the same time allows other people to help them commit suicide?”

The problem of suicide doesn’t just affect one person, it haunts the whole family for generations,” she said.

Couture said she is worried about how political the process has become. She noted how the MNAs tend to zero in on the five or six hard cases of individuals whose stories seem to recur over and over at the hearings.

“They really get stuck on the individual stories, the exceptions,” Couture said. “We don’t build a law on exceptions like that. We can’t afford to do that.”

Most of the MNAs’ questions, especially for those who identified themselves as religious, raised the hard cases of those suffering from terminal illness who clearly want death.

They asked why they think they can impose their religious views on others who disagree.

Couture said that line of questioning is typical.

There have been 300 or so testimonies presented to the Select Committee so far. Most of them---about 80 per cent---have been made by individuals. The rest are have been made on behalf of groups. Couture estimates they have been about two to one against legalizing euthanasia or assisted suicide.

But reports have said the presentations are about 50/50, she said.

The committee has also said it is not numbers they are interested so much as the “quality” or the emotional appeal of the presentation, especially from individual citizens, Couture said.

Yet emotionally touching stories of those who pitched in as a family to take care of dying parents and spouses “don’t seem to touch them,” she said.

The process has been set up to test the tolerance level for assisted suicide in those exceptional cases, said Couture, but she warned the province better “think twice” about introducing a new bureaucracy that might require two doctors signing off to kill patients when “one million people like me don’t have a family doctor.”

The province did not expect the level of response, she said. If politicians go ahead and “smuggle” in euthanasia and assisted suicide under euphemism like “medical aid in dying” she believes Quebeckers will find it unacceptable and rise up.

Assisted Suicide: the Precautionary Principle and the Tasmanian Premier

By: Paul Russell - is the director of Hope Australia.
HOPE Australia

precautionary principle — n: the precept that an action should not be taken if the consequences are uncertain and potentially dangerous (World English Dictionary )
Paul Russell

The commitment of newly appointed Tasmanian Premier Lara Giddings to supporting a euthanasia and assisted suicide agenda in that state’s parliament would seem to elevate the issue to a new alert level in the Apple Isle. The Labor/Green alliance forged by her predecessor, David Bartlett, with Greens leader, Nick McKim will, no doubt, be honoured in the next few months by the introduction of yet another euthanasia bill.

This leaves me to wonder at the enduring nature (or lack of) and consideration given to the two inquiries conducted by the Tasmanian Parliament on euthanasia and assisted suicide in the last decade or so. In 1998 the Community Development Committee’s Inquiry into the Need for Legislation in Tasmania on Voluntary Euthanasia for the Terminally Ill rejected euthanasia as a bad idea in clear and emphatic terms. In 2009, the committee set up to examine McKim’s own Dignity with Dying Bill rejected his approach also.

While the 2009 inquiry dealt specifically with the bill in question, it inescapably echoed the findings of the earlier inquiry. The 1998 inquiry, it should be said (to this writer at least) is a document worthy of being read by anyone interested in the issue. Certainly, for the current Tasmanian Parliament, it should be on every MPs reading list.

Consider Finding #8: The Committee found that the codification of voluntary euthanasia legislation could not adequately provide the necessary safeguards against abuse.

Remember, this is a general comment about euthanasia – not about a particular euthanasia bill. In that context and by reflection on the failure of recent bills here and overseas and also upon the mounting data showing the rates of abuse from jurisdictions where euthanasia is practiced, the statement is clearly true in an absolute sense.

Euthanasia legislation can never be made safe from abuse. Safeguards, so-called, can never provide certainty. (As Wesley Smith once observed, safeguards are really only included so as to make legislators (and all of us into the bargain) feel somewhat at ease about legislating for killing.)

Interesting that the 2009 inquiry should then make the following observation: The Dying with Dignity Bill 2009 has been described as containing insufficient safeguards or for having too many safeguards to enable a sufferer seeking assistance to end their life. (finding #2)

How is it that a bill could be simultaneously criticised for having too many or too few safeguards? We can understand insufficient safeguards in terms of the finding of the earlier inquiry, but what are we to make of the counter-claim by some that McKim’s bill contained too many?

South Australian Green MLC, Mark Parnell gives us a clue in his speeches on his failed attempts in the SA Upper House in 2009 and 2010:
One of the dilemmas that we have got is that we want safeguards, but we do not simply want to put obstacles in the way of people so that they cannot ever use it. We have got to get the balance right.” (2009)

“I know that some people will not be happy until enough hurdles are put in place to make the laws unworkable, and that is always the tension in law reform like this. We want safeguards. We want strong safeguards, but the safeguards need to have a purpose behind them, and the purpose needs to be the prevention of misuse or abuse.” (2010)

“In terms of some of the comments that other members made, the Hon. Ann Bressington, as she did last time, has sympathy and support for some of the concepts in voluntary euthanasia and, in particular, the people in the terminal phase of a terminal illness. That might be something that we need to revisit: whether the eligibility criteria is simply too broad for members of parliament to accept, but that will be a decision for another day.” (2010)
Parnell has a dilemma: not enough safeguards would mean that his bill would fail to attract enough votes to pass. Too many safeguards would render his bill ineffective in terms of its stated aims. His suggestion that ‘we have got to get the balance right’ would seem to be a denial of the reality that drafting a bill that would prevent abuse is an impossibility. The inexhaustible variations to personal circumstances and diagnoses alone should tell us that; let alone the vagaries of human nature.

So, considering safeguards as points on a line, we could observe that moving toward fewer safeguards increases the risk of abuse while swinging back towards more safeguards, while certainly decreasing risk, can never remove risk entirely.
Paul Russell & Alex Schadenberg
at Tasmanian Parliament.

This would seem to be an argument for the status quo; that is: a firm no to euthanasia. But on our line the starting or ‘zero point’ is not a place where no risk exists. As Parnell also acknowledges, euthanasia already exists; with and without consent. It is merely, therefore, only a point where we have not legislated to create an opportunity for abuse, pure and simple.

It strikes me, therefore, that the precautionary principle should apply in the upcoming debate in Tasmania. It should fall to the Premier, or to whomever it is that sponsors the new bill, to prove beyond doubt that no risk of abuse exists in their model of legislation. The use of this principle is an accepted standard across the globe in many spheres of activity (such as environmental protection and drug approval), why not in matters of life and death? There should always be a higher burden of proof upon those who want to usher in change than upon those who argue for the status quo.

Tuesday, February 8, 2011

Six countries, Six defeats

Dr. Peter Saunders, the Campaign Director of the Care Not Killing Alliance in the UK and a speaker at the upcoming Third International Symposium on Euthanasia and Assisted Suicide that will be in Vancouver BC on June 3 - 4, 2010, yesterday published an article about the fact that euthanasia and assisted suicide bills are being defeated everywhere.

His article titled: Six countries, Six defeats was published one day before the bill in Hawaii was unanimously defeat in the Health Committee in Hawaii and his article didn't report the massive defeat of the euthanasia bill in Western Australia by 24 to 11 in September 2010.

Those people who think that the legalization of euthanasia and assisted suicide are inevitable, need to examine the reality.

Saunders comments are also important because assisted suicide bills are now being debated in Montana, Vermont, New Hampshire, Hawaii, and in Quebec a government committee is receiving input from its citizens concerning the concept of turning a blind-eye to the laws in Canada that prohibit euthanasia.

Peter Saunders wrote:
Last November I reported on the overwhelming defeat in the Scottish Parliament of Margo Macdonald’s End of Life Assistance (Scotland) Bill by the margin of 85 to 16.

MSPs were persuaded that any weakening of the law to allow euthanasia or assisted suicide would put vulnerable people under pressure to end their lives.

This was not an isolated incident. In January 2010, an ‘Oregon Style’ assisted suicide bill was defeated in the US state of New Hampshire by a vote of 242 to 113.

On 21 April the Canadian parliament defeated Bill C-384, a bill that would have legalized euthanasia and assisted suicide by a vote of 228 to 59.

In November a bill that would have legalized euthanasia in South Australia was defeated by a vote of 12 to 9.

The pace of rejection of similar bills has continued into 2011.

On 19 January, in a preliminary reading, the Knesset (Israeli House of Representatives) rejected a law proposal that would have allowed terminally ill patients to self-administer drugs that would cause them to die.

NK Chaim Oron (Meretz), who initiated the law titled 'Death by Prescription,' proposed that a dying patient who is able and of legal age should receive, upon request, a prescription for a lethal dose of a sedative. Only 16 MKs voted for the law, while 48 voted against it.

On 20 January the European Court of Human Rights (ECHR) ruled that while there is a ‘human right’ to suicide, the state has no obligation to provide citizens with the means to commit suicide. The court found Article 2 of the European Convention on Human Rights, guaranteeing the right to life, particularly persuasive.

‘The Court notes that the vast majority of member States place more weight on the protection of an individual’s life than on the right to end one’s life and concludes that the States have a broad margin of appreciation in that respect,’ explained Grégor Puppinck, the director of the European Center for Law and Justice in a press release about the decision.

The court therefore concluded that states have no direct responsibility to help their citizens commit suicide by providing lethal drugs and also ruled that respect for the right to life compels the state to prevent a person from committing suicide if such a decision is not taken freely and with full knowledge

And just last night the French Senate rejected proposals to legalise assisted suicide and euthanasia, by 170 votes to 142. Francois Fillon, the French prime minister, had spoken out strongly against the proposals.

The pace of rejection of such legislation is exceeded only by the frenetic rate at which pro-euthanasia groups are desperately bringing forward new bills.

But it’s not working because parliamentarians and judges who consider the matter carefully are not being fooled by emotive arguments, hard cases and misinformed public opinion.

In a democratic society there are limits to human autonomy. The law is there primarily to protect vulnerable people and public safety will always trump the demands of determined individuals backed by pressure groups who want to undermine existing laws.

As Lord Falconer’s discredited Commission on Assisted Dying moves into its third month trying to craft a justification for changing the law in the UK one hopes that British parliamentarians are reading their newspapers and learning from the wisdom of jurisdictions all around the world.

Hawaii Legislature scuttles assisted suicide

Great news.

Yesterday the Senate Health Committee in Hawaii unanimously rejected Bill SB 803, a bill that would have legalized assisted suicide. SB 803 was sponsored by Hawaii Senator Ige.

The article that was published today by CNBC:

A Hawaii legislative panel on Monday unanimously voted down a bill that would have legalized physician-assisted suicide for the terminally ill, ending the possibility that it would become law this year.

The Senate Health Committee dropped the issue following 4½ hours of testimony overwhelmingly against the proposal.

Dozens of car-accident survivors, elderly care providers and disabled Hawaii residents told state lawmakers they shouldn't allow terminally ill, competent adults to receive medication to end life. The bill prohibited mercy killings and lethal injections.

A much smaller group of people testified that they should be able to decide their fate.

Kevin Inouye spoke from his wheelchair about how he thought about killing himself for five years following a car wreck, and he said he would have lied to doctors to make it happen if the law had allowed him to.

"All I thought about was killing myself. I had no hope," said Inouye, who wore a yellow sticker saying, "No doctor prescribed death." "As soon as my situation got a little bit better and I learned to live with my disabilities, I wanted to live again."

Others, such as Marcia Linville, who went through two hip replacements and couldn't walk for eight months, said she deserves the right to end her own life if the time comes.

"As much as I want to live, when the time comes, if I want to die, that is also my choice — nobody else's," she said.

Health Committee Chairman Josh Green, a Big Island emergency room doctor, said he was swayed by the vast majority of testifiers who opposed the bill.

"For an issue of this magnitude, I believe we need to have much more agreement as a community," said Green, D-Milolii-Waimea. "So for now, we need to find other ways to support those dealing with end-of-life decisions with the greatest possible compassion and respect."

Many opponents of assisted suicide said people who are sick, injured or depressed aren't able to make competent life-or-death decisions for themselves.

"We do not need a law that is presented to people when they are vulnerable, sick and unable to think clearly," said Kim Howard, who has been a quadriplegic for 20 years but still paints art by holding a brush in her mouth.

Hawaii last heard assisted suicide proposals in 2005 and 2007, when the legislation failed to make it out of committee as it did Monday.

Conference Opposes Euthanasia, Honors 'Italy's Terri Schiavo'

Conference on Second Anniversary of Eluana Englaro's Death by Dehydration in Rome

On Wednesday, February 9th, pro-life and anti-euthanasia leaders are gathering in Rome to remember the death of Eluana Englaro, who is often referred to as "Italy's Terri Schiavo" for the many similarities between the ways they were unjustly killed. The one-day conference will also raise awareness and support for an Italian anti-euthanasia bill that is circulating in the Italian Parliament.

Eluana Englaro, who was cognitively disabled, died on February 9, 2009 of dehydration, after her father, Beppino Englaro, was successful in having her fluids and food removed. The case was widely publicized as Italian politicians took opposing sides in the matter, and many advocates from Terri Schiavo's late father, Bob Schindler, to the Vatican, pleaded for her life to be spared.

"There are many similarities between Terri's and Eluana's cases: both boiled down to a family member and the courts trying to end their lives, and being opposed by other family members, national politicians and the Church," said Joseph Meaney, Acting Director of HLI's Rome office, and one of the presenters at the conference. "Eluana's case has national and regional significance, as Italian legislators are trying to pass an anti-euthanasia bill. Euthanasia advocates are also busy throughout the European Union trying to expand this grisly practice, which is already sadly legal in several member nations."

Human Life International, Italia Christiana and Militia Christi are co-sponsoring the one-day conference at the prestigious Roma Cavour Conference center.

Wednesday, February 2, 2011

Oregon citizen wants assisted suicide for people with Alzheimer's

Rodger Winn, an Oregon citizen, wrote an article promoting the extension of assisted suicide laws to people with Alzheimer's that he titled: A matter of choice

Winn is proposing that the answer to people with Alzheimer's is to give them a lethal dose.

Since when is it a matter of choice for people who cannot ask for assisted suicide, and what happens when the person is unable to "self-administer" the lethal dose themselves. Well, self-administer is really a misnomer in Oregon because it has been defined as "to ingest" and because there is no witness required at the time of death. To ingest could mean that you swallow or that it is absorbed throught your IV.

I wonder if Winn would say that there is no fear of a slippery slope in Oregon?

Link to Winn's letter that was published on Oregon Live on Saturday, January 29, 2011.

A bill to legalize assisted suicide introduced in New Hampshire - again

House Bill HB 513 FN was introduced by Representative Charles Weed, Representative Parkhurst, and Representative Vaillancourt.

The bill is slightly amended from the bill that was defeated in New Hampshire in January 2010 by a vote of 242 to 113. Once again, the bill is an "Oregon style" bill that claims to have tight safeguards, where in fact the safeguards are an illusion.

The 2010 assisted suicide bill was a recipe for elder abuse. The current bill has similar problems.

The sponsors of the assisted suicide bill have pushed it into the Health, Human Services and Elderly Affairs committee rather than the Judiciary committee. The new strategy for the suicide lobby is to promote their bills as health care bills rather than amendments to criminal law. The suicide lobby believes that politicians are more likely to accept assisted suicide if it is defined within a medical model rather than a legal model.

Assisted suicide legalization bills have been introduced in Montana, Hawaii, and New Hampshire. Vermont Governor, Peter Shumlin, has promised to have an assisted suicide bill introduced in Vermont.

Assisted Death, Palliative Care And Human Rights

An article by Kim Barnhardt in the Canadian Medical Association Journal discusses an article written by Mary Shariff, from the faculty of law at the University of Manitoba. The article is basically stating that the issue of assisted suicide must be viewed within the context of human rights. Based on a human rights model, the legalization of euthanasia and assisted suicide should not be considered in Canada until palliative care is adequately and equally developed.

This is a very strong arguement considering the fact that Quebec is considering turning a blind-eye to acts of euthanasia, even though they are not a leader in palliative care and many of their citizens lack access to good palliative care.

The result would be that people would be given the choice between suffering or dying, in other words choice would simply be an illusion.

The article stated:
The issues of assisted death and palliative care in Canada should be discussed in the context of human rights, states a commentary published in CMAJ (Canadian Medical Association Journal).

While the topic of assisted death has been a recent discussion in Canada, we cannot address until the issue of equal access to palliative care has been resolved. In Canada, at least 70% of residents lack access to palliative care and for those who do have access, it is inequitable.

"The equalization of palliative care must occur before legalization of assisted suicide, otherwise, there runs the very real risk that a decision to request assisted death is not fully consenting because of the lack of meaningful choice in the ability to alleviate pain and distress," writes Mary Shariff, Assistant Professor, Faculty of Law, University of Manitoba.

She cites articles 12 the United Nations Universal Declaration of Human Rights, the right to enjoy the highest attainable standard of health as requiring that the scope of the Canadian palliative care system be fully optimized before assisted death is legalized.

"The decisions surrounding our policies on health care must be considered in the broader context of the express commitments and aspirations that we have made as a country. If our tax dollars fall short of providing integrated end-of-life care to all Canadians equally, then our legislators ought to acknowledge and incorporate that fact before moving forward with the legalization of assisted death," concludes the author.

Source:
Kim Barnhardt
Canadian Medical Association Journal

The report from the Parliamentary Committee on Palliative and Compassionate Care will soon be released. It is important for all Canadians that the recommendations from this all-party ad-hoc committee be implemented.

Tuesday, February 1, 2011

Parents of dying baby simply want to bring their baby home

By Alex Schadenberg

The family of Baby Joseph Maraachli have been told that their baby will not survive. Baby Joseph requires a breathing tube and the hospital is demanding that the breathing tube be removed, while the Maraachli family have asked that a tracheotomy be done to enable the family to bring Joseph home where he would die in their arms. Why is the hospital and the courts denying the Maraachli family an opportunity to allow their child to die naturally on their terms?

Yesterday, LifeSiteNews asked me for comments concerning the case of Baby Joseph Maraachli. I stated to LifeSiteNews that:
“I have no idea why the London Health Sciences Centre would be putting such a legal and emotional burden upon the Maraachli family. If there are complications related to the tracheotomy, well, the child is supposedly dying anyway.”

“The fact is that this family is living through an emotionally draining experience and all they want to do is love their son with the time that he may have left. Why must the hospital impose their plan of death upon the family?”
Today I received a phone call from Joseph's father, Moe Maraachli. After speaking to Mr Maraachli I can only say that my heart goes out to their family and I hope that a resolve will come to their case soon.

The facts of the case:
Baby Joseph Maraachli has been at the Victoria Hospital in London, Ontario, since mid-October when his parents, Moe and Sana Maraachli of Windsor, found he had difficulty breathing and was losing all color in his face.

Doctors discovered that he suffers from “severe and progressively deteriorating neurological problems,” in the words of a Windsor Star reporter, that there is no hope for recovery.

The doctors petitioned the consent and capacity board to have the breathing tube, the enables Joseph to breath, removed.

The Maraachli family have asked that instead of removing the breathing tube that a tracheotomy be done to allow the family to bring Joseph home where he would die in the loving arms of his family, without choking to death.

The consent and capacity board sided with the doctors which is not surprising considering the fact that Ontario's consent and capacity board almost always side with the doctor.

The Maraachli family is challenging the decision of the consent and capacity board to the Ontario Superior Court.

Eight years ago the Maraachli's daughter died from similar complications; she had a tracheotomy done and died at home. The Maraachli's want Joseph to also have the opportunity to die at home.

My response:
Since when has our society denied the parents of a supposedly dying child the right to allow the child to die at home on their terms.

This is a devastatingly sad case, that has been exasperated by the unnecessary legal battle that is totally based on the question of who has the right to decide.

In a health care system that we are being constantly told, is out of money, why are they expending tax payers dollars to bring a family to court, who simply want to bring their baby home?

Assisted Suicide? “I was afraid to leave my husband alone again with doctors and nurses”

This was a letter I recently found in the Hawaii Free Press concerning one persons experience with assisted suicide in Oregon.
Dear Editor,

Hello from Oregon.

When my husband was seriously ill several years ago, I collapsed in a half-exhausted heap in a chair once I got him into the doctor's office, relieved that we were going to get badly needed help (or so I thought).

To my surprise and horror, during the exam I overheard the doctor giving my husband a sales pitch for assisted suicide. 'Think of what it will spare your wife, we need to think of her' he said, as a clincher.

Now, if the doctor had wanted to say 'I don't see any way I can help you, knowing what I know, and having the skills I have' that would have been one thing. If he'd wanted to opine that certain treatments weren't worth it as far as he could see, that would be one thing. But he was tempting my husband to commit suicide. And that is something different.

I was indignant that the doctor was not only trying to decide what was best for David, but also what was supposedly best for me (without even consulting me, no less).

We got a different doctor, and David lived another five years or so. But after that nightmare in the first doctor's office, and encounters with a 'death with dignity' inclined nurse, I was afraid to leave my husband alone again with doctors and nurses, for fear they'd morph from care providers to enemies, with no one around to stop them.

It's not a good thing, wondering who you can trust in a hospital or clinic. I hope you are spared this in Hawaii.

Sincerely,
Kathryn Judson, Oregon

Oregon records do not track elder abuse

Montana Senator Greg Hinkle wrote a letter to the editor that was published in the online edition of the Missoulian paper. The letter was posted on Monday, January 31, 2011.

This is what Senator Hinkle wrote:
Oregon records do not track elder abuse

Stephen Speckart (guest column, Jan. 18) is correct that elder abuse is my major concern with legalizing aid in dying, better known as assisted suicide and euthanasia. He is, however, completely uninformed when it comes to Oregon’s records, which he claims demonstrate that none of the people who used Oregons law were abused. These records don’t even talk about abuse.

Legalizing assisted suicide is, regardless, inherently abusive. This is because it allows heirs and others who will benefit from a person’s death to pressure and abuse that person to cut short his or her life. This is why I have proposed the Elder Abuse Prevention Act, which will remove the uncertainty created by the Baxter decision and clearly prohibit aid in dying.

For more information, please read my report to the Legislature describing why assisted suicide creates new paths of abuse, especially for older people. My report can be viewed here.

Copies of the Oregon and Washington after-death reporting forms are attached to the appendix. They do not mention elder abuse.

To learn about my bill at a glance, please go here.

Sen. Greg Hinkle,
Thompson Falls

Dehydrating Aruna Shanbaug - Killing or Letting Die?

By Alex Schadenberg
Executive Director - Euthanasia Prevention Coalition

Aruna, a nurse, experienced a serious cognitive disability when she was strangled with a chain and raped in 1973. She has been living in what has been described as an unresponsive state for 38 years.

What is significant is that Shanbaug is not dying. She is a human person who is in an incredibly vulnerable condition. She is not requiring medical treatment, but rather she continues to live as long as she is fed. This is similar to the case of Terri Schiavo.

There are a few serious points in these cases.

To dehydrate Shanbaug to death is euthanasia. 

Shanbaug is not otherwise dying and the action and intention in removing Shanbaug's feeding tube is to cause her death by dehydration. She would die of dehydration and not natural causes. To provide hydration and nutrition to a person with a cognitive disability, who cannot receive it in any other manner, should be defined as normal care. It is not excessive, extraordinary, or burdensome and it is able to be done, with minimal training, by anyone.

This is not a case of letting Shanbaug die. If she were dying of a medical condition and experiencing end of life symptoms that indicated that continuing her feeding would provide no further benefit, then discontinuing feeding is not the cause of the death, but rather the acceptance of the limits of life.

When society decides that killing people by dehydration, which should be called euthanasia by dehydration, is acceptable, then society will have agreed that the most vulnerable in our society have lost their right to protection and are able to killed by others. There are many people in this condition already and there are many more people in similar conditions who would soon be deemed to be "better off dead."

It is very concerning that the courts are being petitioned to have Shanbaug dehydrated to death by a person who is not a family member or a friend from years before, but rather by Pinki Varani, a woman who wrote a book about Shanbaug.

The life of Schanbaug is being defended by the officials at the Mombai hospital, where she had worked 38 years before, and where she currently lives.

Ms Virani has stated that the court needs to consider the medical definition of death. If people with cognitive conditions are labelled as dead, then the meaning of life will be altered to a man-made definition. Who else will be defined as already dead?

Finally, what is the intention of Ms Virani. She wrote a book about Shanbaug and now she is petitioning the court to dehydrate her to death. Is this a case where she thinks she can make more money on the sequel?

A few years ago, the United Nations declaration on the rights of people with disabilities stated that people with disabilities had a right to be fed. Scanbaug has a right to be fed.

Society needs to stop considering who should live and who should die and instead society needs to focus on how to provide the best care possible for the living and how to ensure that all human beings are being treated with equality and dignity.

The case of Aruna Shanbaug is heart wrenching.