Lynn Jenner
This is Part Two of “The Suitcases.” Part One can be read here.
My mother’s name was Lesley Jenner. She brought me up to call her Lesley, because she said she was a person, not just a mother. From her late eighties Lesley had dementia. Not long before Lesley died, she drew a map and gave it to a caregiver. Lesley had put the words ‘Rest Home’ on the map, and somewhere above that and to the right, sitting all by itself in the sky, like Jerusalem on a mediaeval map, was the house where she grew up, neatly labelled ‘6 Highcliff Road.’ There was a loop to indicate the Ross’s Corner tram terminus and two sentences written in pencil. One said, ‘Can you help me find my mother?’ and the other said ‘My parents are not well off.’ The fact that Lesley had organised a pencil and paper, written this plea for help and given it to a staff member spoke of her desperation. The accuracy of the map was proof of the islands of memory and logic Lesley still had inside her.
When I visited her in the rest home, Lesley never wanted me to leave. She never said, “Don’t go.” She would just look at me like an animal in a trap, and I knew what she meant. When her tea-time approached, or when the sun was setting, or when I just couldn’t stand being there any longer, I would tell her I had to pick up my partner from the train and Lesley would nod, because a man needing his dinner trumps everything in the lives of women. Lesley would watch me as I walked out. In the car I would sanitise my hands and look at the sun setting over the sea. I would try to breathe normally, and I would drive to the railway station where I would sit in the car until my partner’s train arrived. Sometimes that was an hour.

My mother’s name was Lesley Jenner. She brought me up to call her Lesley, because she said she was a person, not just a mother. Lesley was brought up in Dunedin in a Jewish family and was a quiet and polite person who never asked for much. She had green fingers and loved to be outside in nature. Her habit of mind was scientific. Lesley died in the autumn of 2019, a week before Pesach. Immediately afterwards, and for several months, I was occupied with the administration of her death. This followed a period of several years when I had been much occupied with Lesley’s life.
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.
What do you do, with these limitations given to you?
On the afternoon of Lockdown Day 16, I woke up from my siesta feeling as though we were all in a kind of suspended animation, with brave grins on our faces. I went outside to trim the hedge, but realised after a few minutes that, inside my skull, something had been at work, and needed my attention. So I went back indoors, and in five minutes had written down the words for a poem (finding the title took me two days). I was glad to snare these words as they came to me, because poems often take me weeks to work out.