Leaning into the windy day

Apple blossom on my new tree

It’s a blizzard here today…despite it nearly being the end of spring! The completely bonkers weather reminds everyone that climate change is real, not a figment of our imagination. We have had rain, hail, gale force winds…and a little sunshine.

Today I have had to lean into what it brought me rather than my to-do list. I woke with a migraine and a crick neck and was running on half empty.

My husband has been away for the last week for work and arrived home after flight delays at 2am this morning. His work gave him the day off to rest and I took the chance to spend time with him and plan next week’s road trip.

From inside the house I could see the trees I purchased on the weekend being blown over yet couldn’t face the 60km gale force winds to plant them.

Finally the sun came out and the winds died down a little. Now, as part of my big changes to my garden to grow more food, my two apple trees and my pear tree are in the ground.

May the wind die off tomorrow and the sun shine.

And that’s a wrap

My 2017-2018 summer reading pile

This year is about to end and in some ways I feel like it has only just begun. So much has been packed into the year and time has slipped away. It’s really easy to only focus on the things that haven’t been completed and the things that went wrong, but I need to also remember all the things that went right.

Publishing highlights

This year I had some poetry and an essay published in Shaping the Fractured Self: poetry of chronic illness and pain. I bravely volunteered to read one of my poems at the launch at the DAX Centre in Melbourne. Up until the moment I read it out loud, I wondered how on earth I managed to have words of mine sit alongside such accomplished Australian poets. The feedback I received from the audience, and since from members of the public, was overwhelming. It has been absolutely heartwarming to hear people say that I was telling their story and that I had put their chronic pain into words. My own chronic pain (migraines and neck and shoulder pain) continue, but I refuse to let them take control of my life. Many of the other poems and essays within this anthology remind me that it is important to live life to the full, but to also know when to shut the door, and take some time for self-care. There is a wonderful review of this anthology by Kevin Brophy in The Conversation.

Shaping the Fractured Self

I have been fairly silent here for a little while as my migraines spiraled out of control with a long six month period of daily (nightly) migraines that robbed me of sleep (and sanity). Fortunately for me, a change of neurologist who made some subtle changes to my preventative treatment and some more drastic changes to my rescue treatment, my brain has now calmed down to a much more manageable level.

This Thursday, along with some other writers, I will be reading at the DAX Centre for the launch of Shaping the Fractured Self: Poetry of Chronic Illness and Pain. I am chuffed to have three poems and an essay included alongside some wonderful writers*.

My poems and essay in the book speak about my experience of over thirty years as a chronic migraine sufferer, but I am pretty sure anyone who has suffered from any long-term and chronic (and often invisible) pain will relate.

All of the writers have captured their experience of chronic illness and pain in their poetry. It is a great read. I’d love to see you at the launch and you can either grab at copy at the launch, or via the UWA Publishing website.

A massive thank you to Heather Taylor Johnson who came up with the concept, found us all, found a publisher and pulled it together.

*The other writers in the anthology are: Andy Jackson, Anne Carson, Beth Spencer, David Brooks, Fiona Wright, Gareth Roi Jones, Grant Cochrane, Gretta Jade Mitchell, Ian C. Smith, Ian Gibbins, India Poulton, Jessica Cohen, Kevin Gillam, Kristen Lang, Leah Kaminsky, Margaret Owen Ruckert, Peter Boyle, Quinn Eades, Rachael Guy, Rachael Mead, Rachel Robertson, Rob Walker, Sid Larwill, Sophie Finlay, Steve Evans, Stuart Barnes, Susan Hawthorne and Heather Taylor Johnson –also the editor of the anthology

On small wins and finding energy

…and self-doubt, ploughing on and remembering what I do.

You know the scenario. Life gets busy, real busy. You open your computer only to realise that there are over 300 unread emails, bills to pay, workshops to prepare for, short stories to edit, manuscripts to work on, manuscripts to edit. So you shut it. Then you worry that maybe you are not a writer after all, which stops you from opening the computer other than to deal with the basic administration for the family.

This year, on top of normal life, I have been juggling daily migraines and care of a child who has spent more time this year in hospital than out. It is easy for this to take away from my writing, and the writing I have done has been intermittent and angry. I am fortunate to have an excellent cheer squad who buoy me on and remind me that I am a writer.

Today I opened my computer and waded through the admin in the hope to find the headspace to write. While I was doing this, a new email arrived announcing the book launch of Shaping the Fractured Self: poetry of chronic illness and pain. It is brilliant to see the cover of the book that I have some poetry in. I am humbled to have an essay and my poems sitting alongside some of Australia’s finest poets.

The book launch is on 11 May, 6-8pm at The DAX Centre in Parkville, VIC and I would be stoked to see you there!

Of course not all great art has its genesis in pain, and not all pain – not even a fraction – leads to the partial consolations of art. But if lancing an abscess is the surest way to healing, can poetry offer that same cleansing of emotional wounds?

Shaping the Fractured Self showcases twenty-eight of Australia’s finest poets who happen to live with chronic illness and pain. The autobiographical short essays, in conjunction with the three poems from each of the poets, capture the body in trauma in its many and varied moods. Because those who live with chronic illness and pain experience shifts in their relationship to it on a yearly, monthly or daily basis, so do the words they use to describe it.

Shaping the Fractured Self gives voice to sufferers, carers, medical practitioners and researchers, building understanding in a community of caring.

Shaping the Fractured Self is available for preorder from UWA Publishing

Lessons from childhood

EchidnaLast Friday I set out for my second Going Solo hike. I headed back out to Werribee Gorge and took the track that I had planned to go on the first week.

It’s a hot day. The sun beats down on my head and as I put one foot in front of the other I’m reminded of hiking with my folks when I was young.

Mum and Dad took us out bushwalking often and sometimes, in fact most times, I would get about five minutes into the bushwalk and think, ‘I’ve had enough. It’s hot. I want to go back. I don’t like this. It’s hard work and I don’t think I can do it. My head’s starting to hurt, my legs are starting to hurt and the flies are annoying me.’

The hard slog 


Looking at this gorgeous tree it’s hard to believe editing your own manuscript could be hard.

I’m lying on our trampoline, just woken from a snooze and early spring sun is shining. My gum tree is full of birds feeding on blossom and bugs.

What could be so tough?

Truth is that I’m exhausted. Ten days into my ‘chapter a day’ and I’m tired.

Procrastinatory Disease

photoConditions are perfect – heater is ramped up to keep-me-toasty, oil burner is warming make-me-concentrate, stereo is blaring best-beats-for-study – yet I am distracted.

Is it that creepy little migraine that snuck in during the night that I can’t seem to beat away with a good stick of pain killer? Or is it the unwillingness to finish this assignment? Or the dark grey sky pelting out rain and hail making me wish I was under a doona with a fire burning, a warm cup of hot chocolate in one hand, a book in the other (and nodding off when I felt like it)?

Whatever it is, I have to push through. Due dates don’t move.

Do you suffer from a procrastinatory disease?