I experienced it profoundly.
When I started working in the field of palliative care, I was working at Maison Michel-Sarrazin.
The Maison Michel-Sarrazin is one of the most renowned homes for quality care. When I started working there, the law on medical assistance in dying did not exist. After a few years, I realized that even with more extensive palliative care, whether in the form of drug therapy or other supportive therapies, we were not able to respond to suffering on a psychological level, such as existential suffering.
To really respond adequately to patients at the end of life who asked us for relief, I always thought that the range of palliative care available was not always sufficient, especially to respond to this well-known existential suffering.
That is why, after the Act respecting end-of-life care came into force in Quebec in 2015, the Collège des médecins du Québec defined medical assistance in dying as being part of the continuum of palliative care. In other words, it is palliative care along with other forms of care. It is intended to respond, at the patient's request, to situations that traditional palliative care does not address.
In my practice, I have never had to deal with a conflict opposing palliative care and medical assistance in dying.