Texas: David Coronado Breathing on His Own, Off Ventilator

About 3 weeks ago, this blog reported on the case of young David Coronado, a 6-month-old infant allegedly beaten severely by at least one of his parents. Initially, a court-appointed guardian planned to petition for removal of life-support. The scheduled hearing to hear the petition was cancelled due to unspecified “new information.” (We received detailed reports of developments thanks to attorney Jerri Ward, who agreed to represent the Texas NDY chapter in any hearings on this matter.)

There’s some good news today regarding David Coronado, at least enough to give rise to cautious optimism. David is now breathing on his own – which means that his condition has improved, lessening the threat of moves to end his life by his court-appointed guardian.

From the Dallas Morning News:

Just last month, attorneys were considering whether to withdraw life support from 7-month-old David Coronado Jr., whose parents are accused of inflicting scars too numerous to count.

Now the brain-damaged Dallas boy is breathing on his own, and authorities are looking into who might eventually get custody of David should he survive.

“He is off life support at this time, but the prognosis is still uncertain,” Michael Kotwal, an attorney representing Child Protective Services, told a judge Friday morning at a status hearing in Dallas County juvenile district court.

“We’re asking for about 90 days to see exactly what’s going to happen,” Kotwal said. “And possibly if there’s any – not that the child is ready to be moved or transferred to any kind of relative placement – but if the child’s condition does improve and that becomes an option, we need some time to explore the possibilities.”

The court-appointed guardian who originally petitioned for removal of life-support isn’t quoted in this article, but she’s mentioned:

On Jan. 12, the baby’s court-appointed attorney, Holly Schreier, filed a motion asking a judge to allow doctors to remove David from life support. While noting his parents had not consented, she said it would be in his best interest.

But the next week, Schreier withdrew the motion, citing a change in the baby’s condition. She did not return a call for comment Friday.

Who knows – perhaps Schreier still feels that dying would have been in David Coronado’s best interests. It would be nice to think there might be a day in the future when David himself might be able to venture an opinion on that.

Meanwhile, there’s another case sadly similar to David Coronado’s. An infant, severely abused, and there are deliberations going on regarding just who gets to make decisions regarding that infant’s life-support. We’ll see what, if any, lessons have been learned from David Coronado. –Stephen Drake

Reality Vs. Myths of Pet Euthanasia (Part 2)

Last week, there was a small burst of the “we’re kinder to animals than to humans” crap in the Australian press, courtesy of Peter Baume, a former Senator and an emeritus professor of Community Health at the University of New South Wales.

Baume was part of a panel discussion on euthanasia in Sydney, Australia. The panelists were covered and quoted in a way that revealed some pretty obvious bias on the part of the Sydney Morning Herald‘s Matt Buchanan. Here’s a relevant example of the less-than-objective wording describing Baume’s remarks:

Professor Peter Baume, speaking with quiet authority, said: “Dogs and horses have it better than us. We don’t let them suffer but we do let humans suffer.”

Just to make sure Baume’s points were driven home, the Herald also pubished an essay by him in the same edition, titled “We do not let dogs and horses suffer as we allow humans to suffer.” In the essay, he makes the same claim that we don’t “allow” dogs and horses to suffer, implying that euthanasia of pets is always an act of relieving the animal’s suffering – when in fact, many, if not most, killings of household pets have to do with the animal being old and harder to take care of, having a condition to expensive to treat, peeing indoors – or outside the litterbox, or maybe being more moody and prone to snapping once in awhile.

Baume wouldn’t have to ask me for evidence of this, he could have asked fellow panelist Philip Nitschke, affectionately known in Australia as “Dr. Death.” He’s been leading the public charge for legalization of euthanasia in Australia. As the most prominent pro-euthanasia activist in Australia, Nitschke has been personally involved with most of the figures in the movement – including Max Bell, who comes close to filling the role of a “martyr” for the movement there.

For a short time 1n 1996, voluntary active euthanasia was legalized in Australia’s Northern Territory. Max Bell, a taxi driver with stomach cancer, contacted Nitsche. Bell wanted to take advantage of the new law. Bell lived quite a distance from Nitsche and had to drive for 6 days to make the entire trip. Below, from an account by Nitschke, is a summary of Bell’s preparation for his travel to the Northern Territory:

So he put his house on the market, had his two dogs put down, organised himself to drive to Darwin and set out.

Given the current context – from Peter Baume, Gifford-Jones, and even Thaddeus Mason Pope – perhaps we should examine that throw-away line from Nitschke regarding Max Bell and his dogs.

How do we evaluate the “mercy killing,” “euthanasia,” “putting to sleep,” etc. of Max Bell’s dogs? Was Bell the victim of some ghastly cosmic coincidence so that not only he, but his two dogs were suffering from terminal illnesses?

Nitschke doesn’t tell us, but it doesn’t seem likely, does it?

Here are some alternative explanations:

  • Max Bell was too sick and pressed for time to find a home for his dogs;
  • Max Bell couldn’t find an alternative home for his dogs;
  • Max Bell didn’t try to find a home, believing that the dogs would be better of dead than having to live without him.

None of this means that Bell was cold or callous towards his dogs, but, like most people, had different beliefs about his commitments regarding animals than he might (presumably) have toward humans.

Personally, probably most of the people I’ve know have had their pets euthananized when they were neither terminally ill nor suffering. They often involved the increased expense and work that can accompany the chronic conditions aging animals develop. Cats that miss the litter box. Dogs that snap at owners when surprised. Expensive medical treatments. Failing hearing and eyesight. Animals, who live in the moment, don’t spend time dwelling on the “good old days” when they could run like the wind and mourn the loss. That’s a human characteristic – and something we like to project on our pets – so we can tell ourselves and our friends that we had them “put to sleep” because they suffered, avoiding the messier truth.

In the name of thoughtful debate and respect for critical thinking, can we put this issue to sleep? Because when individuals such as the ones addressed in this entry use this argument, only two explanations for the tactic come to mind:

  • They’re so entrenched into the myths surrounding pet euthanasia, they’ve set their critical thinking skills aside;
  • Their critical thinking skills are indeed intact, but use this argument to exploit the lack of critical thinking in others.

Surely they can do better. –Stephen Drake

Reality Vs. Myths of Pet Euthanasia (Part 1)

Over the years, I’ve gotten thoroughly sick and tired of the repeated use of the myths surrounding pet euthanasia as an argument in favor of providing the same “service” for humans. The latest of these is from a column by Dr. Gifford-Jones (I guess “Dr.” is his or her first name) published in the Edmonton Sun on February 7.

From the column:

Who was Debbie? If you missed her death notice, she was the world’s oldest polar bear at Winnipeg’s Assiniboine Park Zoo, who died at 41 years of age. Due to a number of strokes, zoo keepers decided Debbie had suffered enough and painlessly ended her life. But unlike the polar bear, a friend of mine recently experienced an agonizing death which has prompted this column.

I’ve often written that if I were allowed a committee to oversee my final hours, I’d want a veterinarian to be part of that group. I’m hoping they would treat me the same way as Debbie, or a loving pet. (emphasis added)

In the column, Gifford-Jones mentions being moved Sara McLachlan’s video to raise funds for the Society for the Prevention of Cruelty to Animals. Unfortunately, the SPCA spot really does help Gifford-Jones make a case, because in its emphasis on “rescue,” of abused animals, it avoids telling viewers the ultimate fate of the majority of the animals that end up in shelters. This open letter from a shelter manager paints a very different picture — one that McLachlan would be hard-pressed to provide vocal background for:

Odds are your pet won’t get adopted & how stressful do you think being in a shelter is? Well, let me tell you, your pet has 72 hours to find a new family from the moment you drop it off. Sometimes a little longer if the shelter isn’t full and your dog manages to stay completely healthy. If it sniffles, it dies.

Please note that the author is referring to pets that have been abandoned to the shelters by their owners. There’s every reason to believe that pets rescued from abuse have even lower chances of being adopted.

This is not a new phenomenon or limited to one particularly undestaffed and underfunded shelter. Last July, Dick Sobsey posted his own critique of the animal vs. human euthanasia argument in “Euthanasia, pets & people.” Here’s an excerpt, sharing some statistics on animal euthanasia:

  • They are abandoned and unwanted. (According to the American Humane Association, “56% of dogs and 71% of cats that enter animal shelters are euthanized,” that was 2.7 million animals in the 1000 shelters who responded to their survey. The total number is likely at least three times as high because another 2500 shelters provided no data.) [Editor’s 2023 note: Newer data is available HERE.]
  • They have a personality or behaviour problem. (According to the SPCA, this is the single most common reason for euthanizing dogs accounting for as much as 60% of cases, as many as 6,000,000 in a single year)
  • Their caregivers are no longer willing or no longer able able to continue caring for them.
  • They are considered to be unattractive.
  • They have a treatable health condition but euthanasia is a cheaper alternative.
  • They are getting old.
  • They have physical traits considered to be undesirable for their breed.
  • They have untreatable terminal diseases and are in pain.
  • In many cases, there is no single, clear reason.

Please notice that very few of the animals are abandoned or killed because they have painful terminal illnesses.

Note to Gifford-Jones – we kill our pets because we can – the law only requires that we do it humanely and doesn’t really care why we do it.

I can already hear objections from Gifford-Jones and people who have approached this argument in a similar fashion. Thaddeus Mason Pope, whose post on this column alerted me to it, might also object, since he agrees with Gifford-Jones.

After all, one might object, people who abandon their pets to shelters don’t even care enough about their pets to take them to a vet to have them “put to sleep.”

In order to answer those possible objections, I’ll discuss at least one case of a person who did go to a vet to have his pets put down – a story taken from the annals of the euthanasia movement itself.

Then let’s talk about what a great thing it is to treat humans in the same way we treat animals, even the ones we claim to love. –Stephen Drake

New Blog: “Water on the Brain – And Lots on My Mind”

Over the past month or so, I’ve been working on a launching a personal blog.

I suspect that I’ll still tinker with the settings and formatting, but other than that, it’s ready to roll out.

This blog will also be disability-oriented, but will cover (but not necessarily limited to) hydrocephalus, nonverbal learning disabilities, and neurodiversity.

This is something I’ve wanted to do for awhile now. For over 15 years, my life has intersected repeatedly with the neurodiversity community – even before the term “neurodiversity” was coined.

What to expect from the new blog:

  • personal experience of someone in the “nld” club, and views that depart from professional accounts of the label;
  • historical bits and pieces regarding hydrocephalus and other conditions – history regarding attempts to exterminate or to explain away unexpected competence in people with this and other conditions;
  • stories of adventures and encounters with both “neurotypicals” (that would be the average reader of this blog) and people who share unusual neurological wiring;
  • occasional rants when some advocacy group or other starts building its PR work by portraying some of us as “burdens,” “monsters,” or – in extreme but not rare cases – blaming us for our own murders;
  • items, topics, etc. that I can’t predict at the moment.

What not to expect:

  • Me being inspirational;
  • a lot of fussing about what a “correct diagnosis” means;
  • medicalization of my life and experiences.

OK, if you’ve read all that and you’re not sure just what the heck I’m going to be doing on this blog, then that probably makes two of us in all honesty. But I intend to have some fun doing it, and hopefully, some of you might find it fun or interesting as well.

Check out: Water on the Brain – And Lots on My Mind

I look forward to seeing some of you both here and there. –Stephen Drake

Pennsylvania: Important Guardianship Ruling — Strict, Narrow Limits for Refusing Life-Sustaining Treatment

Mark Murphy, Legal Director of the Disability Rights Network of Pennsylvania (DRN), emailed a summary of an important Superior Court decision that lays out a very stringent set of criteria that have to be met in order for a guardian to order refusal of treatment for an incapacitated person who isn’t at the end stage of a serious illness or permanently unconscious. The summary is available at this link, but is reproduced below, with permission.

Set forth below is a summary of an important new decision by the Pennsylvania Superior Court regarding whether, and under what circumstances, a guardian has the authority to refuse treatment for an incapacitated person who does not have an end-stage medical condition or is permanently unconscious. In brief, the court held as follows:

1. A court order that appoints a person as a plenary guardian does not authorize that person to refuse life-sustaining treatment for incapacitated persons who do not have end-stage medical conditions or who are not permanently unconscious. In other words, a guardianship order by itself does not authorize the guardian to make such a decision.

2. A guardian must secure a special court order to allow him to refuse life-sustaining treatment for an incapacitated person who does not have an end-stage medical condition or who is not permanently unconscious. The guardian has an “extraordinary burden” to prove by clear and convincing evidence that death would be in the incapacitated person’s best interests, i.e., that extending life would be inhumane under the circumstances. The guardian must present specific medical evidence about the incapacitated person’s diagnosis, prognosis, pain, etc. and, if at all possible, evidence concerning the incapacitated person’s wishes either prior to or during the treatment. The individual’s cognitive disability should generally not be considered.

In sum, this decision will make it extremely difficult, if not impossible, for a guardian to secure an order that would allow him to refuse life-sustaining treatment when an incapacitated person does not have an end-stage medical condition or is not permanently unconscious.

SUMMARY

D.L.H., an individual with mental retardation and a resident of Ebensburg Center, was admitted to the hospital with aspiration pneumonia. At the time, he did not have any terminal illness and was not in a permanent vegetative state. At the hospital, the doctors determined that he needed a ventilator to assist him to breathe. His parents, who had previously been appointed as his plenary guardians, objected and sought to decline treatment. The hospital refused to obey the guardians’ direction and placed D.L.H. on a ventilator. He used the ventilator for three weeks, at which time the pneumonia subsided to the point where it was no longer required and he could breathe on his own.

Prior to his recovery, the parents filed a petition that sought permission to refuse treatment, arguing that they should have the same powers to refuse treatment as a “health care agent” designated by a competent individual under an advance health care directive under Act 2006-169 (Act 169). DPW objected to the petition. The trial court refused the guardians’ petition, and they appealed to Superior Court.

On appeal, the Superior Court initially decided that, although the case was technically moot since D.L.H had improved enough that the ventilator was not necessary, it raised an issue that was capable of repetition yet evading review and presented important public policy questions. Accordingly, the court decided to address the merits.

Initially, the Court rejected the guardians’ assertion that their status as plenary guardians was itself sufficient to give them authority to refuse any treatment for D.L.H. The Court compared the guardianship statute to Act 169’s provisions regarding health care agents, noting that the former has nothing specific concerning when a guardian can make the type of decisions requested in this case while the latter expressly authorizes health care agents to refuse medical treatment if that is consistent with the instructions in a health care advance directive. The Court also distinguished guardians from agents under common law, finding that agents are subject to the power of the principal and are obligated to carry out the principal’s expressed wishes. In contrast, guardians act as officers of the court and are subject to the court’s control. Moreover, while guardians are charged with acting in the best interests of the individual, they are not required to honor their wards’ stated wishes. The Court further noted that guardianship creates an opportunity for abuse and that allowing guardians – merely based on their appointment as plenary guardians – to refuse life-sustaining treatment would be problematic because any judicial review would come too late. Accordingly, the Court held that the Legislature vested authority only in health care agents appointed under advance health care directives to object to life sustaining medical procedures when the principal does not have an end-stage medical condition or is not permanently unconscious and that the Legislature did not vest similar authority in guardians – even plenary guardians.

The Court also rejected the guardians’ alternative argument that, under the facts of the case, the trial court should have granted their petition to authorize them to refuse treatment on behalf of D.L.H. The Court assumed (without deciding) that a court could grant a guardian authority to decline medical treatment for someone who does not have an end-stage medical condition or is not permanently unconscious. However, the Court noted that such a decision would be even more compelling that sterilization, which also requires court approval before a guardian can authorize the procedure. Accordingly, the Court held that guardians who seek to decline life-sustaining treatment must petition the court and prove by clear and convincing evidence that refusing such treatment (i.e., causing the incapacitated person’s death) would be in the incapacitated person’s best interest.

The Court discussed at length the type of proof that would be required. The Court emphasized that the guardian in such a petition would have an “ extraordinary burden” to prove that death is in the best interest of the incapacitated person. In making the decision, a court must “consider only the best interest of the incompetent – not the interest or convenience of the parents, guardians or society in general.” “[A]t minimum,” the guardian “must provide reliable medical expert testimony documenting the incompetent’s severe, permanent medical condition (or severe, permanent medical condition with progressive features) and current state of physical/psychological deterioration and pain.” It would also be “wise (although not absolutely necessary depending on the severity of the medical condition) for a guardian to adduce additional evidence of the incompetent’s expressions, either through demeanor or conduct, which could reasonably be interpreted as evincing the incompetent’s wants, needs, and/or feelings during the course of medical treatment.”

In the absence of any evidence of an incompetent’s expressions during or prior to treatment, the quality of the medical evidence should be of such a character that a court is definitively convinced that the benefits of prolonging life, as a result of medical treatment, is markedly outweighed by the incurable nature of the incompetent’s medical condition and the consistent, recurring degree of pain. That is, based upon medical facts, diagnosis and prognosis of the particular case, a court should be able to conclude, without hesitation, that extending life would amount to an inhumane act that runs so contrary to basic notations of fundamental decency that death furthers the best interest of the incompetent. (citation omitted) Otherwise, in assessing the benefits of a prolonged life, a court should not place any emphasis on the fact that a life-long incompetent, prior to receiving medical treatment, suffers from a mental disability or other cognitive deficiency, because this is the incompetent’s natural state of being.
(citation omitted). A court may, however, consider the incompetent’s cognitive abilities as a starting point to analyze whether the current medical condition or proposed medical treatment has resulted, or would result, in a reduction in those abilities.

The Court, however, concluded that D.L.H.’s guardians failed to present any evidence that the refusal of mechanical ventilation would further D.L.H.’s best interests. They did not provide evidence that the aspiration pneumonia was a severe, permanent medical condition, that he suffered a remarkable amount of pain due to the ventilator, that he expressed any objection to the ventilator treatment, or that he ever expressed any intent to decline life preserving medical treatment through a written document or clear oral declaration.

Given that he recovered within three weeks, “the evidence was clearly inadequate” to show that refusing the treatment was in D.L.H.’s best interests.

mjm

Full court decision (in pdf format) can be found here.

Thanks for Judy Gran of the Public Interest Law Center of Philadelphia (PILCOP) for sharing this news with me and many others outside of Pennsylvania. –Stephen Drake