Members of the select committee will be reading and hearing a great deal about old, frail, disabled or incapacitated people who feel they are a burden to their families, caregivers and society. The fact is, they are a burden and they don't want to be. But nor do they want to die.
Fine, say euthanasia advocates. Nobody is saying they have to die. It's their choice. But just as we respect their choice, so we should respect the decision of those who want to die, or at least to have that choice.
It's not that simple. If it becomes legally possible to die by choice, those who are a burden to their families will wonder if they should. They will say it is their choice but how could we be sure. They might be just thinking of us, though we certainly do not want them to die.
It is disturbing to discover in the commission's paper that judicial thinking appears to have adopted euthanasia's claim that "dignity" for the suffering resides exclusively in a chosen death.
There is in fact dignity in living with pain and incapacity and we should not take it away. Euthanasia would remove the one shred of dignity left to those who need the most personal and intimate care, which is that they cannot help their condition.
If they are given a legal option to die, they would always wonder, do those caring for them respect their choice? Can others see any dignity in their life?
Human rights decisions are usually a balancing exercise, weighing one right against another. The right of those in care to live with dignity has to be balanced by consideration for those who want the right to decide to die if they find themselves suffering with a terminal illness. I think the balancing device can be a practical test. How much does each side need the law to enforce their rights.
Those preferring life in difficult and dependant circumstances need the prohibition on euthanasia for their dignity. Those choosing death do not need the law. Those pressing for a right to choose death need the law to change only so that a doctor can do it, or supply them with the means to do it medically.
But in practice, doctors can do this now under certain conditions. They can turn off life support, they can administer heavy doses of morphine to relieve pain near death knowing the dose is quite likely to be fatal. Matt Vickers, writing in the Herald this week about a 17-year-old assisted death in Belgium, acknowledged that "palliative sedation" (induced coma until death by starvation) is legal in New Zealand.
So what is he campaigning for exactly? His late wife, Lecretia Seales, could have received palliative sedation if her suffering had reached the degree of agony her lawyers postulated in her application to the High Court. So long as doctors act with the intention to relieve pain, not kill, they can accept the likelihood of death.
Intention is important in principle even if it makes no practical difference. It is purely the principle that motivates Vickers, Seymour and many like them. They believe there is an inherent human right to die on request and do not yet dare apply that principle beyond the terminally ill.
This week, though, Vickers wrote, "There is certainly a case for broader laws, making a choice available to people with chronic degenerative illnesses . . ."
Let's not run this orange. Let's stop while we can.