The Stars and Anzac Day

This week, we will mark Anzac Day in Australia and New Zealand. For the first time in over a century, there will be no attending official services. The pandemic changes how we mark historic events, just as it changes how we celebrate or grieve personal events. I’m aiming to be up at 6am next Saturday, to watch dawn from my front garden and to think about the enduring legacy of war, and how world events affect us here Down Under.

Just in time, there is a fabulous new review of my WWI Anzac story.

My heartfelt thanks to Baffled Bear Books for this brilliant, thoughtful review of The Stars in the Night.

The Stars in the Night is indeed a tale of enduring love. This review is well worth a read. I’m very grateful to find such wonderful readers!

https://baffledbearbooks.com/2020/04/18/stars-in-the-night-by-clare-rhoden-a-story-of-broken-lives-and-enduring-love/

Birthday memories

Today my dad would have turned 95, if he had survived this long.

Instead, the ghastly, grotesque illness called Motor Neurone Disease (that’s MND in Australia, and ALS or Lou Gehrig’s Disease in the US) diminished him to death at the age of 67, twenty-eight years ago. Even back then, in 1990, we were hoping for a cure ‘soon’. While some people live for a long (and extremely difficult) time with MND (notably the brilliant Professor Stephen Hawking), many die much sooner. For my dad, the progress of the disease from diagnosis to death was four short years.

While there has been some progress in the treatment and management of MND, we are all still waiting. This was brought home deeply by the recent Australian Story program, ‘The Enemy Within’, detailing the work and illness of the amazing Justin Yerbury.

I still miss my dad. And although I know that he would have completely supported my writing career, and that he always encouraged me, I really, really regret the fact that he doesn’t know about it, and that I haven’t been able to share this stage of my life with him.

Knuppels_1933

There are so many untold stories. I think one day they will appear. What I’m thinking about now is the last time I saw him, in the hospice, on the day he died. Dad explained that a male nurse, all in white, had visited his room in the night and said that it was time to leave. Dad said, ‘I told him I couldn’t walk, but he said it was time to go.’

I checked with the staff – no male nurse had been on duty the night before. Strange.

But a few hours later, after all his visitors had gone, my dad up and left.

Diagnosis blues

This week has been quite a difficult one. We discovered that our mother has a brain tumour. While this explains all of the bizarre and inconsistent and unreliable behaviour that we’ve been noticing recently, it’s a bit of a shock.

Did I tell you how Mum was acting more and more strangely and refusing help? Well, one day a couple of weeks ago she took herself off to the doctor in a taxi (at a time when she should have been home for the cleaner – resulting in multiple phone calls with the next step being the police! – because she didn’t tell anyone she was going – but that’s another story). Mum went to ask if she had dementia, so the doctor ordered a CT scan that afternoon. The first I knew about it was a call from Mum saying I had to take her to the hospital for a brain scan. All the way there, she criticised her children as being too managing, too interfering, too nosy, and for sending too many helpers, and making too many phone calls, and ordering the wrong food to be delivered. She was certain that the brain scan would show no dementia and that after the diagnosis we could all just leave her alone, thank us very much. Very Greta Garbo.

The upshot is, after a lengthy scan and a trip back to the GP, that she has a meningioma which is not malignant in itself, but steadily growing and impacting on her brain function. Off we went to the neurosurgeon next day, who ruled out surgery (her bad health and a long recovery time) and any other treatment (tumour too large for radio). And a palliative care team has been allocated to us.

So it’s been  an interesting time, negotiating all of us siblings and our diverse opinions. Mum, on the other hand, is very stoic and quite serene, and says she’s much happier now that she knows. She is calling everyone in her address book to tell them she has a brain tumour!

Greta Garbo ‘Wild Orchids’ film still from Wikimedia Commons at https://commons.wikimedia.org/wiki/File:Garbo_wild_orchids.jpg?uselang=en-gb

A creation fable

 

‘Are you sure?’ asked the god.

‘Yes. I can’t face another day of ordinary conversation. I want everyone to know how much I am suffering!’

‘I can’t reverse this process,’ he warned.

‘And I can’t turn back the clock. Just get on with it!’ Marta yelled.

A short while later, she left the god’s garden, looking much the same as usual. Her long hair, pulled back from her face, was the same dull, unwashed brown. Her comely mouth turned down at the corners in the usual way. There was something fierce in her dark eyes, but that was usual too.

Marta tested the god’s work. Deliberately, she walked into the village market place. Her gaze fell upon a young mother, squatting on the cobbles while she helped her toddler with his slice of apple.

Immediately, the god’s will kicked into action. Across every inch of Marta’s skin, multiple fonts burst into words. Blue as veins, stark as cemetery epitaphs, the moving letters came together. Across her forehead, I am crying inside. On one cheek, I will never see her again. On the other, I hate my life. On her neck, Let me die too. Over her shoulders, I hurt too much. Pulsing from her forearm, Don’t talk to me. Down one thigh, Don’t pretend everything will be fine. Down the other, My heart is broken. Across her feet, My tears will never end. From the ends of her hair, No-no-no-no-no…

The words kept rising to the surface, spilling from Marta’s skin onto the cobbles, into the drains, down to the creeks, the rivers, the seas, and up again through the mists and fogs into the weeping clouds.

Grief is what they called this new creation.