Dr. Morrison, maybe I'll try to word this in a way that respects your expertise in clinical ethics. To what extent should the quality of end-of-life care be considered as a factor when we're assessing this?
I take Dr. Widger's comments about wanting to make sure that specialized palliative care is available so that every child who may potentially find themselves in this situation has at least had the opportunity to make that informed choice and to experience the full range of care options. Does your practice or your expertise in this field inform anything that you can say on that?