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“Will I walk again?”

December 2, 2019 3 Comments

Brian Bourke

In the summer of 2005 I was visiting my sisters in my home town. After Mass a woman approached, put her arms around me and said, “Brian you are still alive. You were such a lovely boy”. My wife was standing nearby with a puzzled look on her face. It was not every day that strange women put their arms around her husband. That woman was Monica. Monica had nursed me one-on-one when I was fourteen and they thought I was going to die from polio. It was 49 years since Monica had last stood beside me. In 1956, Monica was twenty, and in charge of the isolation ward of the Ashburton hospital. I only ever saw her in a long white gown, rubber gloves and a white mask. She had beautiful blue eyes and wore rimless glasses. Her quiet voice encouraged me to eat and she held on to me when I went to the toilet. I needed her help to get sitting to standing, and because I could not stand she held me during the entire operation.

She was patient with me as the paralysis took hold and was never cross with me when I fell out of bed. I felt the comfort of her arm around me when I cried, and I cried often. In the middle of the night she would shine her torch on me and ask if I was all right. Did I need a drink? Time and again I asked her, “Will I ever be able to run again?” She replied quietly, “We will see, Brian.” Even in the early stages of having polio, I knew that nothing would be the same again. Monica’s reply told me so.

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Filed Under: History, Infectious disease, Memoir, Polio

Circles

December 2, 2019 7 Comments

Millie O’Neill

As a child, you always see your parents as these invincible super-humans. After all, they did put up with my psychologically traumatic teenage hormones at their peak. Parents want to protect you, they put on a brave face, they try to shelter you from what is dark in life. But sometimes they can’t, and sometimes, it’s important for them not to. When someone you see as so incredibly strong is forcibly made weak by disease, it’s an adjustment, to say the least. Before he got cancer, I had only seen my father fighting for me, and in that battle he was undefeated.

The poem below is about the circular patterns and routines of life, and how something as incomprehensible as cancer can put it all into perspective. Suddenly so much that was so important seems trivial. I realise what I took for granted: the moments I should have savoured; the conversations I should have had in the car on the way to school instead of glaring at a screen. Suddenly it’s a struggle to go to do simple things, like open your book in class, or maintain a bubbly and bright aura in front of peers. Everything seems superficial and inauthentic to life’s true purpose. Everyone’s complaints about minor everyday problems enrage you. When events like this give us a broader perspective, sometimes our philosophy of life changes.

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Filed Under: Adolescent health, Cancer, Poetry

Dreaming with my body

December 2, 2019 Leave a Comment

Rata Gordon

“Dreaming with my body” follows on from a previous article by Rata Gordon, “Expressive Arts Therapy: Arts-based research and new motherhood”, which you can read here.

Motherhood is undervalued. And I feel like my culture’s view of what a mother should be is limited. I have a sense of somehow trying to claw back a self that is individuated from my child and active in the public sphere, because the question looms: is being just a mother enough? And what constitutes a good enough mother in the face of climate change, mass extinctions and a global mental health crisis? My child must live in this world.

I am trying to be intimate with the world around me, feeling the sharp edges with my toe and tasting the salt water with my tongue.

I wonder whether Attachment Theory’s usual version of a good enough mother, in terms of wiping your child’s nose, having ordinary devotion, cuts it. How can I nurture not only my own child, but the world that I am bringing her into, and all that I love?

I have found that there is no greater opportunity for being told how to think, act, breathe and scratch my nose than becoming a mother. A whole flurry of social and cultural institutions, norms and practices would like to dictate how I mother, and who I am now that I’m a mother. They land like fine silt, becoming denser and heavier with time if I don’t move beneath them.

I want to feel that the stories I tell are true, but I also want to show that there are other possible untold stories lingering underneath and in between.

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Filed Under: Art, Birth, Research, Women's Health

Menstruation, myth, and medicine

December 2, 2019 Leave a Comment

Sandy Thomson-Conklin

Otago Girls High School. Image courtesy McNab Collection.

I was twelve years old, munching away on some crackers in the back garden when I noticed an uncomfortable wetness in my knickers. I hopped to the loo and was surprised to discover that I had got my first period. I immediately grasped what had happened; my mother is a nurse and my family has a decidedly casual attitude towards the human body and its functions. I ran and proudly shared my news. Tearing up, Mum explained how I was now a young woman. Together we went over the practical accoutrements, and she presented me with a silver necklace adorned with hearts to mark the occasion (and satiate my rampant preteen consumerism). Though my experience of the bloody menses itself is not new or unique, I have learned that the openness and practical knowledge is. Roughly fifty percent of the world’s population is biologically female, and almost all females will menstruate for some 3,000 days in their lives. Most girls begin their monthly bleed between the ages of 11-16, and will continue to bleed for five (give or take) days each month for the next 30 years. Societally, menstrual blood is taboo. Historically, it has been taken as evidence of females being the ‘weaker sex.’ Keeping this shameful secret shrouded is a long-running custom. Time and time again inferiority has been upheld through religion, the medical profession, or internalised shame passed from mother to daughter.

In 1948, a young female medical student at the Otago School of Medicine, M. W. Wray, investigated menstruation as part of her fifth year Preventative Medicine dissertation. She found a serious lack of information about the average girl’s experience in New Zealand. Rather than accepting the status quo, Wray decided to collect some data. 120 permission slips were sent to parents of students at Otago Girls High School, requesting their daughters be interviewed about menstruation. A mere half of the permissions were returned signed, and fewer than sixty girls were interviewed.

[Read more…]

Filed Under: Adolescent health, History, Women's Health

Let there be light: macular degeneration and me

November 4, 2019 5 Comments

Renée

Let there be warriors…

There must be those among whom we can sit down and weep and still be regarded as warriors.” Adrienne Rich.

Renee

I was taught to read before I was five by my mother Rose. I read stories, then long books, then joined the library, changed both Rose’s and my books, read both, went out to work at the woollen mill when I was twelve and read my way around libraries wherever I worked. I worked at all sorts of jobs then, when I was forty, began studying for an extra mural BA degree. I began teaching in my forties and at fifty I began writing plays. Since then I have read and written (worked) every day. Now I am 90. I’ve just finished teaching a course on writing memoir, and The Cuba Press has just published my first crime novel, The Wild Card.

Two years ago I was told I had macular degeneration.

This is a desolate and unhappy place to be. Being labelled ‘vision impaired’ doesn’t go anywhere near describing the impact of it on my life. As a reader and a working writer it is the worst thing that has ever happened to me.

[Read more…]

Filed Under: Aging, Reading, Visual impairment, Writing

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Latest articles

  • “Will I walk again?” December 2, 2019
  • Circles December 2, 2019
  • Dreaming with my body December 2, 2019
  • Menstruation, myth, and medicine December 2, 2019
  • Let there be light: macular degeneration and me November 4, 2019
  • The Big Red Ride: a community bike programme November 4, 2019
  • Expressive Arts Therapy: Arts-based research and new motherhood November 4, 2019
  • Sir Cedric Stanton Hicks November 4, 2019
  • No Friend But The Mountains: seeking the human in asylum October 7, 2019
  • Crossing to surgery’s side October 7, 2019
  • “The Track”: word-walking through pain October 7, 2019
  • Emergency Accommodation October 7, 2019

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