Showing posts with label death with dignity legislation. Show all posts
Showing posts with label death with dignity legislation. Show all posts

Thursday, September 26, 2019

Wisconsin lawmakers introduce legislation that would legalize physician-assisted suicide

By: Brittany Lewis

MADISON, Wis. (CBS 58) -- State lawmakers have introduced legislation that gives terminally ill patients the option to have doctors help them end their lives.

"I think it is immoral to keep those people suffering the last days of their life," said State Senator Fred Risser, D - Madison.

Sen. Risser says the first time he introduced the legislation was in 1993 and he believes people's opinions on the topic have changed since then.

The End-of-Life Options Act (LRB 1624-1) would allow mentally capable, terminally ill adults with less than six months to live the ability to end life on their own terms.

The Executive Director for Wisconsin Right to Life says she has concerns there aren't safeguards in place for people who think this is the best alternative.

"It's not a doctor's job to take life, it's not a doctor's job to assist in the killing of someone at the end of life," says Heather Weininger, Executive Director for Wisconsin Right to Life. "What they should be doing is providing comfort care to those people. That's what they should be doing."

Sen. Risser says the bill is being circulated among lawmakers to see what kind of support it receives.

 Full Article & Source:
Wisconsin lawmakers introduce legislation that would legalize physician-assisted suicide

Wednesday, April 25, 2018

End of Life Options Act stalls in Legislature

Roger Kligler, a retired physician from Falmouth and a volunteer with the national organization Compassion & Choices, speaks on the subject of medical aid in dying to about 60 people gathered at the Northampton Friends Meetinghouse on Monday, October 16, 2017. Kligler was introduced by John Berkowitz, right, coordinator of the Pioneer Valley Death with Dignity Action Group, one of the sponsors of the talk. Gazette File  Photo
Despite the Massachusetts Medical Society dropping its opposition to the bill, the state’s End of Life Options Act failed to make it to a vote before the legislative session ended.

While supporters of the bill are disheartened by the action, those opposed to the act say the bill got what it deserved.

The Legislature’s Joint Committee on Public Health referred the bill for further study late last month. The bill was the fifth such bill filed by its chief House sponsor, Rep. Louis Kafka, D-Stoughton. Supporters of the bill call these “death with dignity” laws, while opponents call them “physician-assisted suicide.”

State Rep. Stephen Kulik, D-Worthington, said he was disappointed to learn the bill was to be studied further, ending its path for this legislative session.

“I’ve sponsored this bill for a number of years and I felt that this session it perhaps had a better chance than ever, largely because the Massachusetts Medical Society, which represents physicians, changed its position,” Kulik said. “I felt that it was a positive step for this bill and its prospects, but the committee decided to send it to a study once again.”

In the latest bill, introduced Jan. 18, 2017, patients looking to qualify for medically assisted death would need to have less than six months to live, make the request orally and in writing, have two physicians sign it, and have a mental health professional ensure the patient is making the decision in sound mind. After a 15-day waiting period, the patient would be given the drugs to take if they choose.

The act did not require health care providers to participate and allowed them to opt out without facing punishment.

The Massachusetts Medical Society announced in December that it had rescinded its opposition to “the act of a physician writing a prescription for a lethal dose of medication to be used by an adult with a terminal illness at such time as the patient sees fit.”

At the same time, the society adopted a position of “neutral engagement, which allows the organization to serve as a medical and scientific resource as part of legislative efforts that will support shared decision-making between terminally ill patients and their trusted physicians.”

Kulik and state Rep. John Scibak, D-South Hadley, were sponsors of the bill. Both are stepping down this year, but said they are hopeful the bill will pass in the future.

“When one looks at an organization that is as powerful and well respected as the Massachusetts Medical Society having taken a position absolutely opposed last session and now in support this session, I think there is definitely the possibility of things changing in a subsequent session,” Scibak said.

John B. Kelly, director of Second Thoughts, a grassroots group in Boston, said the bill “got what it deserved.”

“The committee listened to everyone with a stake in this and that especially includes disability rights advocates, because we brought forward objections that are really unanswerable,” Kelly said. “The bill does not just apply to people who are terminally ill but to people who are mistakenly judged to be terminal.

“People talk a lot about choice, but it’s no choice if you are not terminal. It’s no choice if your insurance company is denying you treatment, and people think they have the power in their hands but insurance companies decide who and what treatment they will cover.”

Florence resident Chris Palames, who is executive director of Independent Living Resources, called the bill’s failure to make it out of committee “terrific.” Opposing the act, Palames said there were unintended consequences many were unaware of and that the first thing that needed to be dealt with was “our broken health care system as a whole.”

“Once people have an assurance that they can live with dignity, then you can start making those decisions in a way that really addresses the concerns of all the communities that would be affected by that kind of legislation,” he said. “I and lots of my good friends and colleagues in the world of disability advocacy are very pleased.”

John Berkowitz, director of Pioneer Valley Death With Dignity, said he was dismayed and disappointed by the bill’s failure.

“We are going to go back and try and build a stronger and more vocal groundswell of support throughout the state, so that when this bill is re-introduced in January of the next session there will be a different outcome, and next year the bill will pass the joint health care committee, and hopefully will be passed by the whole Legislature,” Berkowitz said.

Voters turned down a “death with dignity” ballot initiative in 2012 by a margin of 51 to 49 percent. Northampton’s City Council unanimously approved a resolution last fall calling on the Legislature to pass the act. Amherst Town Meeting passed a similar measure in November by a supermajority.

Full Article & Source:
End of Life Options Act stalls in Legislature

Friday, January 12, 2018

'Death with dignity' devalues disability

By Mike Volkman, Commentary

The debate over assisted suicide continues. A bill has not passed in New York yet, but it keeps getting reintroduced every session in the legislature. Its proponents everywhere keep using a catchphrase, "death with dignity," to describe it. They even use it as a title for it.

The main points of their argument for why we need to legalize assisted suicide is that there are incurable diseases that will end up killing people anyway, and those diseases cause intractable pain. They say they have a right to choose when and how they die, so they should have the freedom to make that choice. It is a quick and easy argument.

It's not so simple. Doctors are not perfect and don't know everything. It is impossible to make an accurate prediction with how much time a person has left. The late Ted Kennedy was told he had months, but he hung on for several years. Insurance companies deny treatments based on many factors, but in states that now allow assisted suicide they are more willing to pay for lethal doses when they are prescribed. If people are making choices based on economic factors, that is coercion, not freedom.

Another major factor that it is deeply ingrained in Western cultures is that people are better off dead than being disabled. You can find references to studies on the Not Dead Yet website and blog that show how common it is for people to choose to die not because they are in intractable pain, but because something changed in their circumstances and they acquired a disability. Nobody ever expects this to happen, and when it does they are confronted with fears they have had their whole lives. Those fears are reinforced by the most respected institutions in society: family, government, the schools, religious teachings, medicine, architecture, the arts, and the press, just to name a few. People are seriously scared of the idea that they might need some help in order to stay independent.

What does it mean to die with dignity? Or the opposite, what is death without dignity or with indignity? There is no legal definition. It is a phrase people like to use with the hope that it is sufficient and accepted. Remember the bit George Carlin did in 1992 about euphemisms? They hide the truth.

Legislative bodies should come up with legal definitions for the term. They should specify what constitutes dignified ways of dying. When they come to define what are undignified ways of dying, the challenge is how to do it without describing circumstances that go with disability. Because if they can't get around that, then it makes one thing perfectly clear.

That one thing is that it is in the interests of the state to protect all lives except those of people with disabilities. If the presence of a disability, whether it is from birth or from later acquisition, makes it justifiable to place a value judgment on a person for a life-or-death decision, that makes an entire class of people subject to a double standard. That is state-sponsored bigotry allowing up to one sixth of the population to be discarded and unprotected.

Afraid of needing help? Imagine living in a world in which no one was willing to provide it. Afraid of tubes? Imagine a time when they weren't invented. Today's tubes make life much more bearable and livable for those of us who use them. Like me.

Choice is free when people and states do all that they can to help us live better.

Mike Volkman of Albany is a longtime disability rights advocate. He is a member of the board of Not Dead Yet.
 
Full Article & Source:
'Death with dignity' devalues disability

Saturday, April 22, 2017

Gov. LePage says he'll veto "death with dignity" legislation

AUGUSTA, Maine - Republican Gov. Paul LePage says he'll veto legislation that would allow doctors to prescribe medication that a patient may self-administer to hasten death.

The Legislature's health and human services committee on Wednesday is set to decide whether to recommend bills sponsored by Republican Sen. Roger Katz and Democratic Rep. Jennifer Parker.

The Maine Medical Association is not yet taking a position on the legislation because its members are divided.

Opponents say the bills would spur elder abuse and exploitation.

Supporters say the legislation protects against such abuse and that medications cannot treat all pain.

So-called assisted suicide is legal in Washington D.C. and six states, including Vermont.

The nonprofit Death with Dignity Political Fund says 25 states are considering similar bills this year.

Full Article & Source:
Gov. LePage says he'll veto "death with dignity" legislation