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Legislative proposals for physician-assisted suicide degrade the trusting relationship patients have with their providers, provide an illusion of autonomy, and harm the most vulnerable among us. We need to advocate instead for equality of care — a health care principle that aspires to offer the same access to care and health services to all people regardless of their health condition.
Every person has the right to receive health care and control their illnesses. ("Bodily autonomy should apply at life's end, too," Opinion Exchange, Jan. 25).
As a professor of medical oncology and internal medicine for over 40 years, as well as the first Mayo Clinic physician board-certified in hospice and palliative care, I see physician-assisted suicide as a personal issue for me. I have a unique lens through which to address principled end-of-life care and what constitutes real patient autonomy, having been at the bedsides of more than 30,000 terminally ill patients.
One patient experience, in particular, has riveted my soul. As a consulting hospice and palliative care physician, I was asked to see a patient for a goals-of-care consultation. I carefully reviewed the patient's history to understand his primary symptom management issues. He was terminally ill with metastatic non-small-cell lung cancer, in pain, short of breath and could not sleep.
When I first visited him and introduced myself, he said, "I know what you do. You are here to put me down. To end my miserable existence. Right?"
I explained that my specialty focused on improving patient care, creating better pain and symptom management, and supporting his overall well-being — not acting with the primary intention of ending his life.