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An old man in a wheelchair sitting in the hallway of a nursing home
Image Credit: Mechastock - Adobe Stock
Humanize From Discovery Institute's Center on Human Exceptionalism
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Australian ALS Patient Denied Disability Support, Chooses Euthanasia

Originally published at National Review
Categories
Euthanasia

I really do try to write about other issues. But the awfulness keeps on coming.

Yesterday, I called attention to the Canadian bioethicist who claimed that lethal jabs are no different than hip replacements. Today, I came across an awful story out of Australia in which Tony Lewis, age 71 and experiencing Motor Neurone Disease — what we call ALS or Lou Gehrig’s disease — has asked for euthanasia because he was denied sufficient financial support for his disability. From the Hello Care report:

A Queensland man with Motor Neurone Disease has chosen to access voluntary assisted dying after being denied support through the National Disability Insurance Scheme because of his age, reigniting concerns about Australia’s two-tier approach to disability and aged care.

Tony Lewis is 71. Diagnosed with Motor Neurone Disease last year, he falls outside the eligibility criteria for the NDIS, which excludes people diagnosed after the age of 65. Instead, he must rely on the aged care system, where funding levels and response times are widely acknowledged as inadequate for fast progressing neurological conditions.

Lewis wants to go on living but believes his financial situation makes that impossible.

Mr Lewis currently receives funding that covers only a small number of basic services each week. The reality of his care needs far exceeds what is funded. Most of his daily support is provided by his wife, Gill, who has a nursing background and has taken on the role of primary carer…

Faced with the prospect of further decline without adequate support, Mr Lewis has chosen to begin the voluntary assisted dying process. He has been clear that the decision is not driven by a lack of will to live, but by the absence of appropriate care options that would allow him to remain at home with dignity.

Yeah, just like a hip replacement! This same kind of abandonment has happened in Canada, too. But euthanasia? Never a problem of access! Is it any wonder that disability rights activists oppose hastened death?

We keep hearing the magic word, “choice,” in this debate. Sometimes that word has as much meaning as it does for cattle being herded into slaughterhouse chutes.

Wesley J. Smith

Chair and Senior Fellow, Center on Human Exceptionalism
Wesley J. Smith is Chair and Senior Fellow at Discovery Institute’s Center on Human Exceptionalism. Wesley is a contributor to National Review and is the author of 14 books, in recent years focusing on human dignity, liberty, and equality. Wesley has been recognized as one of America’s premier public intellectuals on bioethics by National Journal and has been honored by the Human Life Foundation as a “Great Defender of Life” for his work against suicide and euthanasia. Wesley’s most recent book is Culture of Death: The Age of “Do Harm” Medicine, a warning about the dangers to patients of the modern bioethics movement.