Seattle Elder Law Attorney Discusses What Lawyers Should Be Telling Clients About “Death With Dignity” Act

Margaret Dore has been doing strong work exposing the pitfalls and logical fallacies that are embedded in the framework of Washington State’s “Death With Dignity” law. She does so from the perspective of a lawyer who specializes in Elder Law.

Recently, the King County Bar Association published her analysis of the newly-passed assisted suicide legislation in Washington State, titled “What Do We Advise Our Clients?

Here is the brief description of Ms. Dore given in the article:

Margaret Dore is a Seattle attorney admitted to practice in 1986. She is the immediate past chair of the Elder Law Committee of the ABA Family Law Section. She is a former chair of what is now the King County Bar Association Guardianship and Elder Law Section.

Readers here might also want to know that she authored and submitted an amicus brief in support of the Montana attorney general’s appeal of a lower court decision legalizing assisted suicide.

Below is the entire article from Ms. Dore, reproduced in accordance with the guidelines listed by the publication:

May 2009 Bar Bulletin

‘Death with Dignity’:

What Do We Advise Our Clients?

By Margaret Dore

A client wants to know about the new Death with Dignity Act, which legalizes physician-assisted suicide in Washington.1 Do you take the politically correct path and agree that it’s the best thing since sliced bread? Or do you do your job as a lawyer and tell him that the Act has problems and that he may want to take steps to protect himself?

Patient “Control” is an Illusion

The new act was passed by the voters as Initiative 1000 and has now been codified as Chapter 70.245 RCW.

During the election, proponents touted it as providing “choice” for end-of-life decisions. A glossy brochure declared, “Only the patient — and no one else — may administer the [lethal dose].”2 The Act, however, does not say this — anywhere. The Act also contains coercive provisions. For example, it allows an heir who will benefit from the patient’s death to help the patient sign up for the lethal dose.

How the Act Works

The Act requires an application process to obtain the lethal dose, which includes a written request form with two required witnesses.3 The Act allows one of these witnesses to be the patient’s heir.4 The Act also allows someone else to talk for the patient during the lethal-dose request process, for example, the patient’s heir.5 This does not promote patient choice; it invites coercion.

Interested witness

By comparison, when a will is signed, having an heir as one of witnesses creates a presumption of undue influence. The probate statute provides that when one of the two required witnesses is a taker under the will, there is a rebuttable presumption that the taker/witness “procured the gift by duress, menace, fraud, or undue influence.”6

Once the lethal dose is issued by the pharmacy, there is no oversight. The death is not required to be witnessed by disinterested persons. Indeed, no one is required to be present. The Act does not state that “only” the patient may administer the lethal dose; it provides that the patient “self-administer” the dose.

“Self-administer”

In an Orwellian twist, the term “self-administer” does not mean that administration will necessarily be by the patient. “Self-administer” is instead defined as the act of ingesting. The Act states, “‘Self-administer’ means a qualified patient’s act of ingesting medication to end his or her life.”7

In other words, someone else putting the lethal dose in the patient’s mouth qualifies as “self-administration.” Someone else putting the lethal dose in a feeding tube or IV nutrition bag also would qualify. “Self-administer” means that someone else can administer the lethal dose to the patient.

No witnesses at the death

If, for the purpose of argument, “self-administer” means that only the patient can administer the lethal dose himself, the patient still is vulnerable to the actions of other people, due to the lack of required witnesses at the death.

With no witnesses present, someone else can administer the lethal dose without the patient’s consent. Indeed, someone could use an alternate method, such as suffocation. Even if the patient struggled, who would know? The lethal dose request would provide an alibi.

This situation is especially significant for patients with money. A California case states, “Financial reasons [are] an all too common motivation for killing someone.”8 Without disinterested witnesses, the patient’s control over the “time, place and manner” of his death, is not guaranteed.

If one of your clients is considering a “Death with Dignity” decision, it is prudent to be sure that they are aware of the Act’s gaps.

What to Tell Clients

1. Signing the form will lead to a loss of control

By signing the form, the client is taking an official position that if he dies suddenly, no questions should be asked. The client will be unprotected against others in the event he changes his mind after the lethal prescription is filled and decides that he wants to live. This would seem especially important for clients with money. There is, regardless, a loss of control.

2. Reality check

The Act applies to adults determined by an “attending physician” and a “consulting physician” to have a disease expected to produce death within six months.9 But what if the doctors are wrong? This is the point of a recent article in The Seattle Weekly: Even patients with cancer can live years beyond expectations10. The article states:

Since the day [the patient] was given two to four months to live, [she] has gone with her children on a series of vacations . . . .

“We almost lost her because she was having too much fun, not from cancer,” [her son chuckles].11

Conclusion

As lawyers, we often advise our clients of worst-case scenarios. This is our obligation regardless of whether it is politically correct to do so. The Death with Dignity Act is not necessarily about dignity or choice. It also can enable people to pressure others to an early death or even cause it. The Act also may encourage patients with years to live to give up hope. We should advise our clients accordingly.

Margaret Dore is a Seattle attorney admitted to practice in 1986. She is the immediate past chair of the Elder Law Committee of the ABA Family Law Section. She is a former chair of what is now the King County Bar Association Guardianship and Elder Law Section. For more information, visit her website at www.margaretdore.com.

1 The Act was passed by the voters in November as Initiative 1000 and has now been codified as RCW chapter 70.245.

2 I-1000 color pamphlet, “Paid for by Yes! on 1000.”

3 RCW §§ 70.245.030 and .220 state that one of two required witnesses to the lethal-dose request form cannot be the patient’s heir or other person who will benefit from the patient’s death; the other may be.

4 id.

5 RCW § 70.245.010(3) allows someone else to talk for the patient during the lethal-dose request process; for example, there is no prohibition against this person being the patient’s heir or other person who will benefit from the patient’s death. The only requirement is that the person doing the talking be “familiar with the patient’s manner of communicating.”

6 RCW § 11.88.160(2).

7 RCW § 70.245.010(12).

8 People v. Stuart, 67 Cal. Rptr. 3rd 129, 143 (2007).

9 RCW § 70.245.010(11) & (13).

10 Nina Shapiro, “Terminal Uncertainty,” Washington’s new “Death with Dignity” law allows doctors to help people commit suicide – once they’ve determined that the patient has only six months to live. But what if they’re wrong? The Seattle Weekly, January 14, 2009. http://www.seattleweekly.com/2009-01-14/news/terminal-uncertainty.

11 id.

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Patients’ Rights Bill Stalled in Texas – Bill Backed by Disability Advocates, Right to Life and ACLU

This blog has visited the topic of futile care policies more than once. These policies allow hospitals to overrule advanced directives and/or the wishes of family members in removing/refusing life-sustaining treatment to someone unable to express his or her wishes.

Of all the states, Texas has given hospitals the most power in these situations. And the hospitals, safely protected by statute, have been aggressive in implementing their power to overrule families in “futile care” cases.

There have been repeated efforts to try to provide more protections to patients and families in Texas. Right now, it looks like the protection is allocated solely to the medical providers (or, I guess, “non-providers” might be more accurate).

Here’s the latest from the Dallas Morning News:

AUSTIN, Texas – Those who want to extend the time some hospital patients may live before their life support is cut off are worried that their proposal is running into a wall at the Capitol.

Legislation by state Rep. Bryan Hughes, R-Mineola, would require life-sustaining treatment to continue for patients whose condition is deemed futile by doctors until a transfer to another medical facility can be arranged, if their family requests it.

Currently, hospitals can stop life support after 10 days in certain cases if the patient is terminally or irreversibly ill and cannot express treatment wishes.

“No other state in the country has a law that Draconian,” Hughes said. “The balance of power is completely shifted against the patients and the families.”

Hughes’ bill is being pushed by Texas Right to Life, a group best known for its anti-abortion views. Groups for the disabled, including the Coalition of Texans With Disabilities and Not Dead Yet of Texas, also back Hughes’ proposal, as does the American Civil Liberties Union.

Got that? NDY, the Coalition of Texans with Disabilities, Texas Right to Life and the American Civil Liberties Union all back this bill.

That’s a broad base of support if I’ve ever see one. But the bill isn’t going anywhere.

That’s because the Texas Medical Association and the Texas Hospital Association, among others, oppose the bill.

I doubt those organizations could claim to represent as many constituents as the combined supporters of RTL, the disability coalition, NDY and the ACLU – I will bet that the TMA and THA give lots of money to political candidates in Texas. That’s the simplest, if cynical explanation for the current standstill.

And it doesn’t bode well for the future in Texas. –Stephen Drake

More bloggers on Vicious Attacks on Ari Ne’eman

Yesterday, I wrote about the vicious attack on Ari Ne’eman, president of the Autistic Self Advocacy Network (ASAN), by John Best – Best is a guy that seems to spend whatever free time he has spewing vile comments and barely veiled threats at people who don’t “hate autism” – that includes any supporter of neurodiversity. But he saves his most hateful stuff for the people who are autistic and have the audacity to say they’re happy with the way they are.

I already shared a link to Turning Trolls into Stone, a post with some good constructive suggestions about responding. It’s on the blog Whose Planet Is It Anyway?

Here are some other bloggers alerting others to the attack (apologies ahead of time to anyone I missed):

lastcrazyhorn at Odd One Out writes as someone who is already way too familiar with John Best in her post Death Threats on Ari Ne’eman.

Ms. Cripchick has written a letter to Newsweek on cripchick’s webblog.

At Wood’s Rules, Virginia Wood expresses sympathy for John Best’s situation but cuts him no slack when it comes to his behavior.

Kassiane at The Rettdevil’s Rants writes about the “Latest Mercury Malicia Target.” (This is my first encounter with the word “malicia” – I love it.)

That’s it for now. Good reading. –Stephen Drake

President of ASAN Under Attack – Including Death Threats

Before I write more about this, I feel compelled to share a couple of things in the interest of full disclosure.

First, I am a survivor of childhood hydrocephalus and have a neurological profile that fits what is called nonverbal learning disabilities (NLD). There’s enough overlap between NLD and Asperger’s that many workshops and groups lump them together as “spectrum disorders.”

Second, I am a fan and supporter of the Autistic Self Advocacy Network (ASAN). I consider Ari Ne’eman, president of ASAN, a friend.

Over the past few years, ASAN has risen in prominence in the disability rights community – and in terms of the media. This is due, IMO, to the group’s political savvy, clear message, and a message of realistic hope to individuals with autism and their families.

In brief, ASAN and its supporters in the neurodiversity movement advocate an alternative to the “cure or stomp every trace of difference out of the individual approach.” (Note: these are my words, not those of ASAN’s) They believe that every person with autism or other neurological condition can have a good life, with the right supports – and that the world can become a less hostile place for those who are different.

If you think the topic is a little out of the way for NDY, think again. Three-year-old Katie McCarron was killed by her mother in 2006. Katie had autism and court testimony revealed that Karen – Katie’s mother – wasn’t happy with any progress her daughter made. In fact, nothing short of Katie somehow being “normal” would satisfy her. Obviously, the vast majority of parents of kids with autism don’t kill their kids, but some who do are in that unrealistic and dismal place that Karen McCarron was.

The current storm was triggered by the news that Ari Ne’eman and the neurodiversity movement is to be featured in this week’s Newsweek.

On the popular “cure autism” site, Age of Autism, a response was made by a college student with Aspergers who disagrees with the neurodiversity movement in the form of an “open letter,” and contains some familiar moves:

  • He complains about the lack of a dissenting voice, ignoring the immense ammount of unchallenged coverage that the “autism is a curse that must be cured” has received;
  • He mischaracterizes positions promoted by the neurodiversity movement;
  • He relies on his individual voice serving to nullify the collective voice of a growing movement.

All that is mild, though, compared to the posts on “Hating Autism” (and everyone who has it, apparently). The blog is written by John Best, who writes by the name “foresam.”

His reaction to the news about the Newsweek article was to write a blog post titled: Ask Newsweek to Kill Ari Ne’eman. To be fair, the post itself refers to “killing” the article:

I hear that Newsweek is going to run another article allowing the sadist, Ari Ne’eman, to lie to the world about autism. Before that comes out, I think it’s useful for sane people to ask Newsweek to kill this article, or, at least allow us equal space to tell the truth about the horror of autism.

But John Best doesn’t end there. The really disturbing, creepy, scary and violent part comes in a comment he submitted later on:

I believe that everyone associated with Neurodiversity should be put to death for the propaganda they perpetrate against curing horribly disabled children. They are part of the lies told by vaccine makers and politicians who continue to cause autism intentionally.

I believe that autism is the greatest crime in the history of the planet and that anyone who has been involved with it in any way deserves to die, preferably slowly and with great pain. So, while I don’t suggest that anyone should shoot Ari Ne’eman in the head, I do think he deserves a trial for his role in this atrocity. I hope the outcome of that trial would be death.

You know, if I ever wrote anything remotely this incendiary about pro-euthanasia people – or even the Final Exit Networkspecial forces,” I’d be vilified by foes and allies would find various ways to distance themselves from me – fast. My guess is that this won’t hurt John Best at all and may even increase his support. Hate, like misery, loves company.

For more outrage, and a constructive way to retaliate, please check out Turning Trolls Into Stone at Whose Planet Is It Anyway?

Later today, you can check out my personal blog for some more discussion of the “cure” issue and my personal take on it. –Stephen Drake

HUMOR: Seniors apprehensive about graduation, possible euthanasia (LSU)

For the past couple of days, I’ve had to prepare for presentation (more about that later) by pouring over the press reports from the months following the murder of Katie McCarron. Unlike most of my work, there’s little in the way of emotional distance – even now – as I read over the events of 2006. It makes me sad and angry at the same time. It’s not a good combination.

So, today, for my benefit, I’m turning to something a little lighter. Hot off the press from the Tiger Weekly, the student newspaper of Louisiana State University, is a fun little piece that made me smile today. OK, I even giggled at one point.

With students all over the country graduating this month, the U.S. is eager to observe the effects of a new law which eliminates 30 percent of the graduating student population.

President Obama’s 2009 Job Market Fairness Act serves to create a less stressful environment for new graduates who would otherwise struggle in the current recession.

This year, the bottom 15 percent and top 15 percent of all graduating classes will be removed from the job market via lethal injection, giving mediocre college graduates a better chance at employment on their own merits.

Studies show that the top 15 percent of college graduates are not as immediately beneficial to the economy as the middle 70 percent, who will spend more money rather than save it. Conversely, the bottom 15 percent are nine times more likely to borrow more money than they can afford. Eliminating both extremes will allow the economy to stabilize within the next year, supporters said.

However, while an online poll indicates the new law has an 80 percent approval rating, many students are outraged by the initiative.

Read the rest of the article here. –Stephen Drake