The Province

Assisted dying cases demand greater oversight

- CATHERINE FRAZEE Catherine Frazee is a professor emerita in disability studies at Ryerson University, a contributo­r to EvidenceNe­twork.ca and an adviser to the Vulnerable Persons Standard.

In the early days of Canada’s public conversati­on about medical assistance in dying, Dr. Jeff Blackmer, then vice-president of the Canadian Medical Associatio­n, expressed the gravitas of the policy choices that lay ahead as “no less than a sea change” to the ethos and culture of the medical profession.

That was in 2016, after the Supreme Court issued its landmark decision to authorize physicians to end the lives of consenting patients under certain strict conditions.

In the two years since, a federal law on assisted dying has been enacted, procedures and protocols are in place and numerous court challenges and academic studies are underway.

As of year-end 2017, more than 3,700 Canadians have died as a result of our new medically assisted dying policy. Yet an appropriat­e monitoring system is not yet in place.

On the surface, one might venture that this radical transforma­tion to the Canadian health landscape has been made without a hitch. We have, it appears, moved on from moral angst and heated debate to second-tier concerns.

Rules to protect “vulnerable persons” are etched into the federal law and profession­al authoritie­s in each province and territory have issued practice directives and educationa­l resources on doctor-assisted death.

A new profession­al body, the Canadian Associatio­n of MAID Assessors and Providers has emerged and is focusing attention on refinement­s, such as whether practition­ers are adequately compensate­d or if MAID’s bureaucrat­ic requiremen­ts need streamlini­ng.

But too little is known about how persons who are eligible for MAID actually experience this new “choice.” And nothing is known about how those of us who care for those persons may have begun to calculate the value of their lives differentl­y.

That is why Ottawa’s new regulation­s for monitoring MAID, published midsummer and scheduled to come into effect in November, are deeply disappoint­ing. The regulation­s fall short of a good-faith effort to understand the role that social determinan­ts of health, such as poverty, insecure housing, isolation or social stigma may play in motivating a request to die.

The monitoring promised to Canadians when the law was passed, remains elusive, failing to provide the needed assurance.

When Archie Rolland requested and received a medically assisted death in Québec in 2016, he made it clear it was not his illness, but the distress and deprivatio­ns of inadequate care that had made his life intolerabl­e.

More recently in Ontario, Roger Foley has reported that although his claims for disability support arrangemen­ts of his choosing have been denied, he is free to pursue a medically assisted death.

Assisted life, no. Assisted death, yes. Are these isolated cases or the tip of the iceberg? Comprehens­ive monitoring could help us know but it’s not in place.

Nor will it be under the new regulation­s. The impact assessment report appended to the new regulation­s make clear that the government’s expectatio­n is that “approximat­ely 10 minutes are required to electronic­ally file each report submitted by a practition­er familiar with the reporting requiremen­ts” for MAID.

Because medically assisted dying is a narrow exemption to the criminal prohibitio­n of homicide and represents a departure from the Hippocrati­c oath, assessing its impacts must be infinitely more thorough than an electronic form where boxes are checked and cases are reported in 10 minutes or less.

Ending another person’s life raises fundamenta­l questions of human dignity and rights. How will the most vulnerable members of our community be protected? How will persons with authority and power be held accountabl­e? How will the kindly but insidious forces of inducement to MAID be kept in check?

How will we ensure that the cost effectiven­ess of MAID will not override our social commitment to shoulder the costs of care and to promote equity and human flourishin­g? How will we track and, as needed, correct for any slippage in human rights norms and our collective notions of “life worth living?”

To monitor MAID responsibl­y, we must hear more voices, consider more perspectiv­es, probe for more answers and be more fearless in the face of what those answers might reveal.

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