See also Liz Hall-Down’s introduction to the Queensland, Australia poetry scene, as well as her selection of Queensland poetry. See also her article on her performance poetry Fit of Passion with Kim Downs ________ For another chapbook on illness and healing, see Lisa Katz’s Breast Art ________ With this issue, Liz Hall-Downs joins The Drunken Boat as a Contributing Editor ________ Some of these poems were written during a month-long writers fellowship at the Booranga Riverina Writers’ Centre (Wagga Wagga, NSW) in 2001. ________ Liz’s website |
My Arthritic Heart: Notes on a work-in-progress
by
Liz Hall-Downs
The poetry manuscript, My Arthritic Heart, is an autobiographical illness narrative in poetry which deals with my experience of living with the chronic, auto-immune disease Rheumatoid Arthritis (RA.), with which I was diagnosed at 20. It has been submitted as part of an MA (Creative Writing) at the University of Queensland, but as yet does not have a publisher. I have been writing and publishing throughout the 20 years since my diagnosis, but I have rarely written about the illness. My aspirations as a writer predated my illness, and as a young writer it felt imperative that I didn’t allow myself to be dismissed as ‘the poor girl with the terrible disease’. People’s good intentions can be unwittingly disempowering. The opposite reaction to the young person with Rheumatoid Arthritis is to assume that it’s just a few ‘aches and pains’, a ‘bit of arthritis’. Yet RA is a chronic, serious auto-immune condition characterised by periods of flareup and remission. It is not considered terminal, though it’s been estimated to shorten lifespan by fifteen years. RA affects 1-2% of the population, and occurs in women three times as often as men. It “typically occurs between the ages of 25 and 50 … (but) … has been reported in people of all ages including infants and children.” (Joint Action, Aventis Pharma) The pain and disability RA causes has taken so much from me personally – quality of life, youthful exuberance, career, family and income. All of this affects lifestyle and the ability to be self-reliant. It is, as a fellow sufferer once ruefully said, ‘the disease that just keeps on taking’. I came to a decision that I was ready to speak out about it through my work, not only for myself, but as a gesture of support for all those RA patients who aren’t writers and therefore can’t express the experience in this way. It should be said that I subscribe to the theory that the disease is exacerbated, if not caused, by the effects of severe stress on the immune system, in my case physical and emotional abuse in adolescence. At present the prognosis for people in my position is this: The new “biological treatments” (Enbrel, Remicade) have been extremely effective in halting the progress of RA in 65% of cases test-trialed. The drugs have been released and publicly funded in both the USA, the UK and New Zealand. But in Australia they have been twice refused funding by the Government Pharmaceutical Benefits Scheme. (A third attempt is currently in progress.) The sole reason given by the PBS committee for rejecting the drugs is that it would not be cost effective for the government. The cost per patient for ongoing intravenous or subcutaneous injection of these drugs is estimated at $18,000 Australian ($9,000 US) per year. This should be compared, however, with the cost of maintaining an RA patient’s welfare dependency through disability pensions, carer’s pensions, and the plethora of traditional subsidized anti-inflammatory and steroid drugs that are necessary while the new drugs remain unattainable to all but the wealthy. Would anyone suggest that Cancer treatments (costing between 20,000-60,000 per annum) should not be made available as a matter of course to those who need it? Yet the cost of the new biological treatments for RA is “out of the range of most family budgets yet this treatment can enable someone to go back to work and fulfil their potential in their community … it therefore seems a matter of equity that those with arthritis and their families should have their voice heard in [government funding decisions].” (Kirkham, Arthritis Action 1:1:2002)
No doubt there will eventually be more poems in My Arthritic Heart than exist in the current draft. After twenty years of waiting and hoping for a cure, my own personal battle is still to be fought, subject to the outcome of the current political one. Here follows a selection of poems from the manuscript that might begin, just a little, to chip away at the community’s ignorance of this condition and its devastating effects on the livelihoods and lifestyle of so many young (and young-at-heart) people.
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becoming continually punished my sin was that of becoming her hitting and hitting and hitting me for not letting her dictate my self to the letter as if what resides within this brain as if this blood typed rare and strange belonged to her to shape or maim years on i still carry the thrum – her hand whipping through air to connect with skin – and am grateful that eyes, spidered with red capillaries and skin, blushing red with the force of her slaps healed fairly quickly, (physically). I learned to hold elbows in close to my belly head bowed and hands clawed like an eagle’s talons clawed in the way later illness would emulate leaving me, madam frankenstein to unlearn these things: pain’s language, politics of fear, and medical marvels that leave me lying drugged and helpless here. she ran II she ran but didn’t get far the damage was already done burdened by generational pain her body completely broke down it was her own fault. she hadn’t kept up her end of the bargain she’d never chosen. for she was the long-awaited girl got up in pretty dresses like a porcelain doll, wore shiny shoes that looked alright but were so tight, followed her mother into fitting rooms, initiated into that female world of shopping for pleasure – because that’s what women do – and the shoes, sliding their new leather stitching up and down against still-baby skin produced blisters, large and fluid-filled that made the mother whinge ’cause now the girl needed carrying. if only she’d known of this bargain this deal with the devil she could have held her tongue as she grew pretended to have no opinions. still, dutiful daughter tried to please, worked harder and harder, turned to jesus who commanded to ‘honour your father and mother’ however bad their behaviour so she did the ironing, scrubbed the dishes, polished the furniture and silver and went to school, and studied hard and hoped to emerge with a future that would not include those slaps and screams, the threats to be sent to the government home for ‘uncontrollable’ teens. she went to church and studied hard, and ‘honoured’ a mother who was trying to break her. (other kids took drugs, did break and enters yet still possessed that indefinable lustre that drew love unbidden from worried mothers who held their sweaty courtroom hands, and made promises to judges) stress was her killer so yes, she ran but by then it was too late fate had leered at her, and shut the gate sin of eve, they surmised at the church when she turned her back on the flock that had compelled her to stay, to endure more than was reasonable or possible. sin of eve, who would not be dutiful, who would not lie down to be crushed by the weight of the role they had made for her. she read outside the canon, took lilith as mentor, as teacher and ran into life, taking enormous bites of the fruit of youth, stuffing her mouth and spilling the juice, while the hands could still open and close, while the feet could still stamp and dance, knowing she was on a countdown, time running out, feeling the cold and the rust eroding her clockwork, her frail sense of self. diagnosis I at the point of diagnosis it’s all too much to take in, so you refuse its clammy entrance, and make plans – to hitchhike across the nullabor while you still can – to go out dancing every night, to emulate flight, to be high on life high on the vibration through the soles of your beating feet that take you where your brain commands, without fuss, no refusals you know that the blood will refuse soon enough, and may wage war on your innocent joints so you refuse its daily attacks – its morning conundrums, its cold night sweats – take raw life in, pure oxygen racing against time / to get it all done all the things you thought several decades would take reduced to a slim / volume of years reduced to diagnosis / tears II overnight, the tight spring that had just begun uncoiling snapped closed. gone in two words the dreams of years, the plans to set my world aright through hard work and endurance i did not need to consult the medical textbooks still, I looked, vapid hope that things would be better than my nurses’ memory had filed away – ‘rapid degeneration’, ‘out-of-control- auto-immune reaction’, a very sad song; prognosis: lifelong my own white cells, oh macrophages! turn against me, eat my substance, my joint capsules, choosing a specific site for each feasting, I go to bed and sweat and sweat, nurse my pain and swelling with beer and codeine take the pills, the specialist says, endure the savages of stomach lining the fuzzy nodules of fainting suppress this excess of self-preservation this immunological self-destruction and plaster on a braver face be ‘nice’ inside this iron maiden take my hopes, abandon them hospital stay I susan who shares this in the neighbouring bed keeps a grinning face, she was eight when she got it neck bones fused and knees replaced, her hands can’t lift a teaspoon she scares me, takes obediently the penacillamine, the steroids turns her head as they inject her joints the tea tray comes but no nurse i lift her up the bed rip open the plastic packets of biscuits II physio plunges my hands in hot wax the social worker and the doctor, tag team, lecture me wrestle my youthful ego say you must realise you can’t have a life III drag me to support group to talk about it everyone else in wheelchairs or on sticks how can i speak? i still have feet funny, he said i saw you around, thought you were staff poverty poverty knows the bar-propping stranger’s hand on my knee, only an arm’s length from hunger knows fifty-five brown rice recipes, winning ways with plain potatoes knows how to scam that extra tenner, how to fight for its rights with rich doctors poverty knows the food store at st vinnies, knows the well-meaning grin of home visitors who promise prayers and novenas smiles and says thanks for their icons their ridiculous pictures of jesus knows to not appear bitter to not be a feisty fighter to be grateful for handouts of warm winter clothes, to be quiet, to be nice, to be nicer poverty knows there are no guarantees that life sometimes throws you a curveball and as hard as you stretch it sings past and you fall knows the cold of winter when the power cuts out, choice of eating or paying the bill knows the paint-peeling dwelling the room with no view the carving knife under the mattress poverty knows generosity is not the province of the wealthy but comes from strange quarters – drug dealers, hookers, and toothless young men with stealthy grins who shout you bread money, or coffee knows about invisibility, how to be a nameless statistic knows there’s no social status, no respect when you’re sick – you’re a vagrant, a loser, no-hoper if pride is a sin call me sinner – this, or open my legs to the monster they run away took it personally at first then came to see – to be abandoned is part of the curse. underneath it all they see that you are the coalmine canary a reminder of the body’s mortality but why contemplate this? it makes for knowledge of futility – and how then to go on making babies, reputations, money? better to ignore the sick or beat them with the stick of good intentions lock them up young in the terminal ward – i have seen them there, the cerebral palsied, the iron-lunged, the undeserving poor dying their days in front of television soaps being fed milky tea and lunchtime trolley slops, shitting their beds – it is a power for the powerless, of sorts. my flatmates packed in seconds flat on learning the truth of chronicity helped me to the bathtub once but might as well have drowned me. the friends i have now understand me with their quadriplegia, MS, their diabetes, HIV. we comprise an exclusive club, society of illness. its motto? abandon hope, all ye who enter here. sometimes i’m (for Christine Ferrari) sometimes i’m these cockatoos flashing my sulphur crest and screaming sometimes these unripe olives bitter and small amongst silvered leaves sometimes i’m that raven, too much to say and saying too loudly, caw in the naked tree and sometimes i’m currawong, defiant song chasing everyone else away i’d rather be these rocks solid, serene, slow changing or that red-breasted wren, twitching my tail alert, but careful, delighting the new spring i’d rather be that shy wallaby self-protective, scratching my sleekness then bounding away to where green shoots grow alert and silently watching but mostly i’m that old hills hoist skewed and broken and rusting my lines all stretched and sagging useless for holding the washing and thankful for the friend who’ll call maintenance in to straighten me out again ![]() |
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