Urge D.C. Council Members to Reject Fatally Flawed Assisted Suicide Bill B21-38

[Editor’s Note: Disability rights advocates in the District of Columbia are part of a diverse coalition of people from disability, minority, medical provider and faith communities working to oppose the assisted suicide bill currently before the D.C. Council and scheduled for a vote on Tuesday, November 1st. Below is an announcement that came from the D.C. coalition over the weekend, including ways you can help, especially by mobilizing your friends and colleagues in D.C.]

At 11 AM on Tuesday, November 1, 2016, the D.C. City Council will hold its initial vote on B21-38, the so-called “Death with Dignity 2015” bill. This bill would legalize assisted suicide in the District of Columbia.

This bill discriminates against racial minorities, the poor, the sick, the elderly and individuals with disabilities. It limits both choice and autonomy for patients, and pressures them to make decisions they otherwise should never have to make.  It drives wedges between doctors and their patients, caregivers and family members.  It places government bureaucrats and insurance companies as potentially key decision makers on whether a person will receive the medical treatment their life may well depend on or whether those patients will simply be offered suicide drugs.

Over the past three weeks our coalition has grown in size and volume as grassroots organizations across the District, church organizations, as well as representatives from the Hispanic community, have joined in demanding that their elected officials reject this fatally flawed legislation.  Our voice is being heard on B21-38.

Over the next few days, our coalition has several opportunities to show the DC Council where their constituents stand on this issue:

  • On Sunday, October 30 at 3 pm, DC area churches will hold an inter-faith prayer service on the steps of the Wilson Building: 1350 Pennsylvania Avenue, N.W.  Please consider joining us for an hour of prayer and unity against assisted suicide.
  • On Monday, October 31, DC Council offices will be open and accepting phone calls to hear where DC residents stand on this issue.  In meetings with councilmembers, they and their staff have indicated they want to hear from DC residents, particularly those in Wards 5, 7 and 8.  If you have friends in those wards willing to make calls, please share the below contact information, and please keep those calls going into the offices. (Click here to find talking points.)
  • On Tuesday, November 1, we will be gathering at the Wilson Building (1350 Pennsylvania Avenue, N.W.) as visible show of support for those councilmembers who have stood against this legislation and to help confirm in the minds of those councilmembers still considering their positions that B21-38 is a fatally flawed bill that is #wrong4DC.  Please join us outside of Room 500 as early as you can.

If you cannot join us for these events, you can still play a role.  You can:

  • Send a letter to your council member through our website
  • Tweet at @councilofdc using the #wrong4DC
  • Call your council member using the information found here
  • Call Mayor Muriel Bowser at (202) 727-2643 and ask her to be prepared to veto the bill

Thank you for all you’ve done and all that we will do together over the next two weeks to defeat B21-38.

Action Alert: Urge the AMA to Reaffirm Opposition to Assisted Suicide

[Editor’s Note: Thanks to the Patients Rights Action Fund for the information in this urgent alert!]

For decades, the official position of the American Medical Association (AMA) has been to oppose the legalization of assisted suicide (Policy 140.952, Policy 270.965).   The AMA will have an interim meeting to discuss its policy on assisted suicide Nov. 12-15, at Walt Disney World Swan/Dolphin, Orlando, Florida. At its July 2017 annual meeting, the AMA will consider taking a “neutral” position, which would essentially send a green light to the states that legalizing assisted suicide is acceptable to physicians who are among our most important allies in opposing such a public policy. It is imperative that the AMA retain and affirm its current position. 

Please send your own letter and ask your doctors to send a letter as well.

Who to contact:

Dr. Andrew W. Gurman, MD, Andrew.gurman@ama-assn.org
AMA President
330 N Wabash, Ste 43482
Chicago IL 60611-5885
312.464.5618 ph
312.464.4094 fx

Bette Crigger, PhD, bette.crigger@ama-assn.org
Secretary, Council on Ethical and Judicial Affairs
American Medical Association
330 N Wabash, Ste 43482
Chicago  IL 60611-5885
312.464.5223 ph
312.224.6911 fx

What to Say:

(Select one or more of the following statements and re-word or add your own thoughts.)

The AMA should retain its longstanding position in opposition to the legalization of assisted suicide because:

  • Medical professionals should focus on the true nature of their profession – to provide care and comfort to patients – instead of becoming a source of lethal drugs. I would not want my doctor to have this power and suggest it to me as an “option.”
  • Will the government and profit-driven insurance companies do the right thing – pay for treatment costing thousands of dollars – or the cheap thing – pay for lethal drugs costing hundreds of dollars? Patients in Oregon and California have been denied payment for treatment and offered lethal drugs instead.
  • Assisted suicide is a recipe for elder and disability abuse. A relative who is an heir to the patient’s estate or an abusive caregiver can pick up the lethal drugs and administer them without the patient’s knowledge or consent. There is no oversight and no witnesses are required once the lethal drugs leave the pharmacy.
  • Everyone knows someone who has been misdiagnosed or outlived a terminal diagnosis.
  • Wanting to die because of depression is treatable. Millions of people are living proof.
  • Everyone agrees that dying in pain is unacceptable, and it is also unnecessary.   A patient in pain should be referred to a palliative care specialist or find a new doctor.
  • Oregon is proof that general public suicides rise once assisted suicide is promoted as a “good.”
  • My family member could die from taking lethal drugs and I wouldn’t know about it until he/she is dead — no family notification is required in advance.

Australia: Liz Carr speaks about euthanasia and assisted suicide (youtube)

Liz Carr is a British activist, actor, comedian, essayist (there’s also a musical added to her resume, but more about that at another time).

Debate on euthanasia and assisted suicide has kicked up again in Australia. Liz made this video to make the case against legalizing it there – or anywhere, really – including the USA. The video embedded is captioned.

John Kelly: Movies Can Send A Dangerous Message About Suicide and Disability

As we have been covering since spring, here, here, here and here, disability rights advocates around the country, the UK, Australia, and New Zealand held protests against the movie “Me Before You” for its hateful message that some disabled people are better off dead.

John shares the same disability as the fictional Will in the movie, who has everything in his life he would want, except that he is a quadriplegic. So he kills himself, and leaves his girlfriend money so that she might “live boldly.”

After helping to organize four June protests against the movie, two at his local cinema, he wrote this opinion piece in July for his local neighborhood paper, the Fenway News. Now, as some legislatures are considering assisted suicide bills, it’s worth reminding people that cultural attitudes reflected in film can influence what people believe about disability and how people react to disability.

‘Me Before You’ Paints Dangerous Picture of Disabled Life

Every evening for the past month, you’ve been able to watch me get euthanized at the Regal Fenway Stadium 13. Not to worry, it’s my choice, and neither fantastic wealth nor mutual love with a beautiful woman dissuade me.

This is the outline of the movie Me Before You, in which the audience gets plenty of laughs along the way as I—in the movie, my name is Will (Sam Claflin)—teach Louisa (Emilia Clarke), hired by my parents to cheer me up, to love life and soon enough, to love me. And when I/Will stay true to my desire to die, audiences have a good cry. Some theaters even supply patrons with Kleenex.

I use the first person because it’s my disability, shared with fictional Will, that is on the chopping block. Our disability is iconic, a powerful eliciter of suicidal urgings. I was talking by telephone to a reporter a few months ago, trying to explain why disability rights groups oppose legalized assisted suicide, when she blurted out, “I know I would want it if I was ever paralyzed from the neck down.” She didn’t notice when I told her those words are used to describe me.

Some percentage of people who see me think they would rather be dead, and a few have told me so directly. People get to have their opinions, of course, but this prejudice is broadcast again and again. So we defend our lives. In 2005, we protested the Oscar winner for Best Picture Million Dollar Baby, which along with Best Foreign Picture The Sea Inside presented disabled characters clamoring for death. I heard that some audiences cheered when Clint Eastwood’s Frankie murdered Hilary Swank’s Maggie.

Thanks to social media, this time around we’ve been able to organize multiple protests, across the US and in Britain and Australia, against the “better dead than disabled” message of Me Before You. Over the first four weekends of June, groups of disabled people and allies gathered outside the Regal Fenway 13 and Boston Common 19 to hand out flyers and hold a banner calling the film a “disability snuff movie.” The fallback line for suicide proponents, which we heard occasionally during our actions, is “choice,” as in every (disabled) individual should have the right to choose.

But the “choice” presented in Me Before You belongs solely to the screenwriter and author of the book by the same name, JoJo Moyes. From observing a couple of disabled family members, Moyes said “qualityof-life was very high in my mind.” She told another interviewer, “At what point does the quality become meaningless? At what point do you give someone the right to decide for themselves?”

I object to being told that my life is “meaningless,” and think JoJo Moyes is a bigot. Unfortunately for me and disabled people, the bigot wrote a book that sold millions and got made into a Hollywood movie.

Moyes constructed everything in Will’s life to be as wonderful as could be—except for that quality-of-life-killing disability. Moyes has Will tell Louisa at the end of the book that his death will free her. “I don’t want you to be tied to me, to my hospital appointments, to the restrictions on my life. I don’t want you to miss out on all the things that someone else could give you.”

Will’s death is presented as a sacrifice of sorts, a death that gives life. Will leaves Louisa a lot of money so that she can go forth and “live boldly.” That phrase, used without irony, is the tag line of the movie. Living boldly, it seems, is for the nondisabled.

Like Will, I was depressed two years after my injury, but it was the peer support and solidarity of other disabled people that got me through that time. I shudder to think of newly injured people hearing about this movie. I want them to learn, as I did, that we all have the ability to adjust to circumstances as long as we are provided with love, support, and opportunities.

We disabled people proclaim that suicidal people, disabled or not, deserve the same suicide-prevention services as teenagers, the only target of most states’ anti-suicide programs.

It was heartening at our protests to receive so much support from moviegoers and passersby. People took pictures of us, decided to ditch the film after talking to us, and a few even passed out flyers with us. As one young couple said leaving the Fenway theaters, “you were right, it was terrible!”

John Kelly is a longtime East Fens resident and disability rights advocate. He founded Neighborhood Access Group (NAG) in 2000 and is now director of Second Thoughts Massachusetts: Disability Rights Advocates against Assisted Suicide.

For the online version of this article, go to page 4 here. The article includes a photo entitled “Protestors gather outside the Fenway Regal Cinema” and depicting about 14 protesters, including at least 5 wheelchair users, gathered outside a theater with a banner and signs.

John Kelly’s Testimony Opposing New Jersey Assisted Suicide Bill A2451

[Editor’s Note: John Kelly lived in New Jersey in his younger years and traveled back there to testify on October 6, 2016 in opposition to the latest assisted suicide bill, A2451. His oral testimony is below, and his full written testimony is here.]

Chair Burzichelli, Vice Chair Lagana, Members of the Committee:

My name is John Kelly, and I am the New England Regional Director for Not Dead Yet, the national disability rights group that has long opposed euthanasia and assisted suicide. I am also the director of Second Thoughts Massachusetts, Not Dead Yet’s Massachusetts affiliate.

We are concerned that this bill is before the Appropriations Committee. It suggests that cost-containment really is a major factor behind the push for assisted suicide laws. So when in the state of Oregon, Barbara Wagner and Randy Stroup received letters from Oregon Medicaid denying coverage for prescribed chemotherapy. The letters did, however, offer to cover the negligible cost of assisted suicide. Because assisted suicide will always be the cheapest treatment, its availability will inevitably affect medical decision-making. This will actually end up constraining choice.

A2451 threatens you, every single resident of New Jersey, because all of us are vulnerable to misdiagnosis. “Terminally ill” is defined as:

“Terminally ill” means that the patient is in the terminal stage of an irreversibly fatal illness, disease, or condition with a prognosis, based upon reasonable medical certainty, of a life expectancy of six  months or less.”

When it comes to life and death, there is no such thing as “reasonable medical certainty.” Of the millions of misdiagnoses every year, many are terminal misdiagnoses. We know this because of the thousands of people who “graduate” from hospice each year. Every year in Oregon, people have lived longer than their six-month terminal diagnosis.

Every year in New Jersey, it is estimated that 1/10 people over the age of 60 are abused, almost always by adult children and caregivers. Although “self administration” is touted as one of the key “safeguards”, in about half of Oregon program deaths, there is no evidence of consent or self-administration in the death. If the drugs were administered by others without consent, no one would know. The request form constitutes a virtual blanket of legal immunity covering all participants in the process.

Assisted suicide laws inevitably take the lives of innocent people through mistakes, coercion, and abuse. Please reject this bill.