Grant Beaven
Let’s build a robot. A humanoid robot, one which might integrate. Where do we start? Two arms, two legs, can walk, can speak. It should have the values of an ordinary person. Integration is paramount – the robot’s ours, after all – so we’ll program it with care based on six human motivations:
- Integrity: the robot will always seek its output zenith;
- Discomfort/pain: a mechanism for guidance;
- Grace/graciousness: the study and application of empathy will be in front of its robot mind;
- Duty: the will of its owners will bind it, utterly;
- Shame/anxiety: to ensure all other system parameters function at full power;
- Hedonism – of course we want a happy-appearing robot!
And so, we have our creation. In fact, we have me. Asperger’s Syndrome has made a robot of me. I try so hard to be like you, I learn your systems, your ways, your technology slowly; I’m odd, I’ve gaps in ordinary knowledge, so I’m ever and remain slightly apart. The way a real robot would. But I’m nearly there. So close! Because I’m close, I’m hidden. And not by accident; I’ve hidden my lacks beneath layers of hubris. Integration’s my purpose. I don’t belong to myself, I belong to you. I mask. I camouflage my difficulties, and I reach the age of forty-two before someone officially confirms a neurological difference.


Did you know that among animals, especially rodents like mice and rats, the females decide when they are ready for some action? You know what I mean … wink, wink. That’s right, the female rodents decide when, and with which male, they want to mate to produce offspring. And this decision is made with the help of a particular type of neuron in the brain that is essential for maintaining fertility, called kisspeptin.


This digital world has a few tricks. It’s fast, lightning quick, bringing rewards with a few quick clicks. We skim and skip, casting for the tantalising bits. And if it ain’t got us hooked real quick, we give it the flick.
In the past ten months, my husband, his sister, and I have moved my husband’s parents – first one, and then the other – into different wings of the same managed aged-care facility. We then had to sell their Northland home, built by my in-laws and only reluctantly abandoned after fifty-five years of married life. When settlement finally eventuated, we had a few frantic days to travel to Northland and clear out the house. All this has occurred during the 2020 Covid-19 pandemic. My husband’s job at Auckland Airport dictated strictly no close contact with either his father or his sister (as she was helping their father move into the retirement village). Auckland’s second lock-down was announced three days into the final push, my husband was recalled to work, and the whole thing ended in a terrific rush.
Many people think of the hospice as a place where people with cancer go to die. Back in 2014, when I frequently walked past the Otago Community Hospice building in Dunedin’s North East Valley on my way home, that was my impression. What a sad place that must be to work, I thought. Although I practically lived on its doorstep, I had only ventured into this daunting place once. My partner had asked me to drop off a gift to a friend who was a hospice inpatient. I agreed, but only to leave it at reception. I didn’t want to go any further, in case I encountered dying people.