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.