The liberation that several near death experiences in quick succession gives you is, well, liberating. And on that note fellas, just how are your testicles today?

As if Jacqueline needed another reminder of what's important. Picture: Bronwyn Kidd

I ask this because I am quite convinced that few people realise that the ‘boys’ begin their existence as ovaries (a foetus starts out with ovaries, which early in the pregnancy descend to the groin to emerge as gonads, producing a male child, or stay in their originating location and produce a female baby) – yup – those mysterious, and little discussed bits within women that dictate an enormous amount of the female physiology, health and reproductive capabilities are just as necessary to a woman, as testes are to a man. Ovaries are a woman’s battery packs.  Are you getting my drift here?

Let me have another sip from my glass of neat Vodka – slice of lemon and a chunk of ice (I will no longer pretend to drink champagne as I detest the stuff and find it such a clichéd, girly drink – there’s that liberation again) as I paint a picture for you.

I have just survived a number of pulmonary embolisms – blood clots to my lungs, a deep vein thrombosis (DVT) in my pelvis, five ovarian tumours, life threatening surgery, oh, and the summer school holidays and a home renovation.

Hence, my absence for some time from pages of The Punch. It all began early last year, I began to feel absolutely knackered – no pun intended, which I initially put down to having spent weeks driving truck convoys and distributing humanitarian aid during the Victorian Bushfire emergency, my eldest daughter wed at the end of March and I was still juggling my work with Operation Angel up at Kinglake and Marysville, so my candle was not only burning at both ends, it was a puddle of wax.

My weight began to increase enormously and let me tell you, fifteen extra kilograms on my little frame (164cm) is a lot to haul around, and I was waking up exhausted, literally calculating the hours from when I opened my eyes until I could crawl back into bed and close them again.

So off I trotted to my GP with my list of symptoms – I was fobbed off seven times by pats on the head and mutterings about my age, my possible closet eating and perhaps the need for more exercise.  I pointed out I was going to the gym and walking the dog for an hour each day, but that I was still gaining weight even though I was truly eating very little.

I asked if I could have a blood test to check if I was menopausal and the results came back indicating that I was ten years off the change of life.  At my last consultation with my local doctor, I told him that I was finding it difficult to climb the stairs at home and that I was inexplicably breathless, exhausted and bone weary.  My medico replied that I should exercise more, eat less and really just admit that I was depressed as he handed me a prescription chit for anti-depressants.

Now, I was not depressed at all – I know depression and I simply didn’t have it.  I had absolutely nothing to be depressed about, if not for the tiredness and the huge ass I had developed, I was deliriously happy.

My marriage was in great shape, my eldest children were well and truly home after fourteen years of a torturous abduction that had headlined the media for years and was played out over international borders, my youngest children were now in primary school and thriving, and I had just been picked up as a columnist for The Punch in Australia and the Sunday Times Magazine in the UK.

I’d even come out of retirement to direct a short documentary and my books had hit the best seller’s list in Russia!  Following the abyss of despair I had teetered on when my kids, Iddin and Shahirah had been kidnapped in 1992 – I knew what depression was, and I knew that I didn’t have it.

Two days later, I awoke with chest pains so severe, I downed a couple of soluble aspirins and called an ambulance thinking I was having a heart attack.  Those aspirin saved my life – allowing what was later found to be a large blood clot to pass through to my lungs without killing me. But where had the clot originated and why, was the question on my lips.

After being put through the rigours of so much nuclear based medical imaging that I probably glowed in the dark, the verdict came back – five large tumours had taken up residence on my ovaries and fallopian tubes.

Bottom line I was told -  they would almost certainly be malignant.  These masses had caused so much pressure in my pelvis that a significant DVT had developed which threatened to throw off another clot that could travel to either my heart or my lungs and kill me.

“Would a stiff drink be out of order at this point?” I joked to the Haematologist.

“Not again!” was the other really coherent thought that screamed through my brain – I was a mother of four children, two fully grown, and the other two only 6 and 8 years old; ironically, almost the same ages as their older siblings were when they were abducted to Malaysia all those years ago.

Was this to be yet another case of not being able to raise my own children?  The irony was not lost on me, nor was the need for haste more urgent than an Exocet missile.  So I took charge of my own health, I learned that all the symptoms I’d been experiencing for over nine months were classic hallmarks of Ovarian Cancer – even my rapid weight gain.  I also knew that to have a chance at raising my children, I had to put myself in the hands of Professor Michael Quinn of Melbourne’s Royal Women’s Hospital.

I was given a few days to get my affairs in order prior to surgery – prepare a Medical Power of Attorney so my husband could switch me off if brain dead, my Will, organ donor forms, instructions to my girlfriends on how to finish off my kids bedrooms mid renovation, long and secret sobbing sessions in my ensuite at dawn when my husband lay in bed pretending to sleep, he himself, wracked with terror at our uncertain future.

I turned my mind to organising food drops for my family, injecting blood thinners into my stomach twice daily, and making sure my big kids and little kids knew I loved them to the depths of my soul, all this whilst I remained confined to bed.

The night before the surgery, Professor Quinn and Professor Orla McNally briefed me in front of the whole surgical team.  “Ovarian cancer” they said, “spreads like a dusting of icing sugar – that’s how other organs become affected”.

The DVT might shift during the operation and kill me and I was to be prepared for a radical hysterectomy which would result in immediate menopause, I might have to have my bowel re-sectioned, lose part of my liver, also my gall bladder as I had a cyst on that, and I agreed on the embedment of a chemotherapy port in my abdomen so I could undergo the most aggressive and experimental type of treatment they could muster.

All this so I could grasp at a couple more years with my children – I was aware of the odds, one woman in Australia dies every eleven hours from this disease. There is no test for this illness, so most cases are detected too late, it is rare to make it to the five year mark after diagnosis and treatment – it’s the single most insidious killer of women we have.

I said goodbye the night before, holding my kids tight and cracking jokes, I rang all my closest friends with last minute instructions about how to take care of my family, and I talked long into the night with my husband about the what ifs and the things he needed to know about the kids and all those intimate matters that needed to be voiced about our love for each other.

My entire body was wracked with chills and teeth chattering as the wheeled me into the operating theatre, not with fear of dying, but fear of leaving my family and what it would do to them.  No matter what anyone assured me about looking after my two youngest, I knew from bitter experience that it wasn’t alright for them to lose their Mum, they needed me and if I was going out, it would be with fingernails gouging at the floorboards as I was dragged off to meet my maker.

And then, forty eight hours later I was labelled a statistical anomaly as my morphine hazed mind attempted to grasp the amazing news – the five tumours had been removed along with a lot of semi-superflous women’s plumbing and I was left with a tiny portion of an ovary to keep my batteries going and to stave off a premature menopause.

Ten days later, pathology showed that I was cancer free. The skill of Professor Quinn and his team was remarkable – I knew then that my future was going to be about finding a cure and a reliable way of detecting this disease in its early stages.

So have you rung your Mum, your wife, your sister, your Grandma, your daughter today and how are your bits hanging today. How are your energy levels, feeling fit, batteries fully charged … how are your testicles today?

It’s not the women in your life, it’s the life in your women.

NB:  Of the five women (aged in their 20’s, 30’s & 70’s) with whom I made friends during my time in the Oncology only one is still living. I am now Fundraising Chairperson of the Women’s Cancer Foundation in Australia.

We Can Walk It Out – our annual Fun Run takes place in Melbourne this Sunday, 28th February at 10am around “The Tan”

Womens Cancer Foundation Website

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70 comments

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    • Julia says:

      05:30am | 24/02/10

      You’re a tough one, Jacqueline. I think I might have crumbled at the first hurdle all those years ago when the kids were taken from you.

    • Sonia K says:

      06:15am | 24/02/10

      Phew! Food for thought and a very raw article. Thanks for the info, its what every women should know. Thankyou Jacqui

    • Robbie says:

      06:40am | 24/02/10

      Very brave letting it all hang out Jacqueline. I agree with Julia, your a tough bird. Thanks for the facts and 4 sharing

    • Charles says:

      06:48am | 24/02/10

      Good to read your words and we are all blessed that you are here to write them.  One husband, two kids & a dog - a great formula for a support team.  Hang in there, you are a fighter (as if we didn’t know that already).

    • Jacqueline Pascarl says:

      07:52am | 24/02/10

      Thanks Charles for the comments - most appreciated, but please do me a favour and get some other fellas to read this and keep their women healthy. Cheers, Jacqueline Pascarl

    • Fred Flintsone says:

      07:50am | 24/02/10

      Insightful reading, who knew gonads = ovaries. I’ll be making sure my wife is taking care of herself more after this article

    • Ellen Jones says:

      07:56am | 24/02/10

      Bloody hell. You made me cry at work. I wish you all the best.

    • shane says:

      08:27am | 24/02/10

      wow.  great article.  I remember the late Sen Ferris writing that she had been brushed off by doctors until she literally rocked up at the hospital and refuse to leave until someone had told her what was wrong with her.  Our bodies tell us when something is wrong.

    • Sarah Robbins says:

      08:27am | 24/02/10

      Tears for me too Ellen. One bloody strong woman. Hope they get a lot of walkers

    • Phillip Sanderson says:

      08:29am | 24/02/10

      Hum, testicles so early in the morning but then again it explains a lot to us mere males. Good on you for getting it out there

    • Eleanor says:

      08:31am | 24/02/10

      Holy. Shit. You are an absolute legend Jacqueline.

    • Richard J says:

      08:32am | 24/02/10

      Easy to understand but you still didn’t expalin why we put up with PMS every month from our ladies. Stay healthy Jackie! Best wishes

    • Samantha Flint says:

      08:34am | 24/02/10

      Would there be more money for research from the Fed Govt if it was gonads instead of ovaries? Something to ask the pollies. Take care and stay well Jacqueline

    • MarK says:

      11:07am | 24/02/10

      Despite the oncorrect labelling Gonads as male, Well if we ingore, that if it was testes instead of ovaries, i am sure the funding would dissapear/be diverted to breats cancer quicker than you could tie a pink ribbon

    • Simon says:

      08:47am | 24/02/10

      Tears and I’m a bloke - lost my Mum and my sister to this disease. A bit more attention to our women guys. All the best Jacqueline

    • Samuel R says:

      08:49am | 24/02/10

      Very informative and honest article. Hard to read about these things by well done jacqueline keep healthy.

    • Bee says:

      09:03am | 24/02/10

      I have to agree with your experiences here. I went to my doctor complaining of chest pain which she insisted was a chest infection and prescribed me 8 nurofen plus a day for over 6 months. Ended up in hospital with a stomach ulcer so bad it had eaten a hole in the main stomach artery, causing massive internal bleeds and nearly costing me my life - I had to have about 13 blood transfusions, a massive operation during which I nearly bled out,  and spent over a month in hospital. I knew something was wrong - I was always really exhausted, falling asleep at my desk at times - but I listened to my doctor who insisted it was a chest infection, stress, and that I was probably depressed and didn’t realise it (well, I was depressed because I could barely make it out of bed in the morning because I was bleeding internally and was extremely anaemic). Big mistake - my surgeon is currently reporting her to the AMA for malpractice - I went in the day before the artery burst, told her I was dizzy as hell and she didn’t even offer to take my blood pressure - which had dropped so low three hours later I collapsed in my bathroom and my husband had to get an ambulance because I couldn’t walk five steps to get out of the house.

      So I agree whole heartedly with Jacqueline - we have to listen to our bodies, we can’t just blindly listen to doctors - if they fob you off with simple prescriptions or don’t offer to give you any tests - go find one that will. I went to a new doctor after my surgery and he, in one consultation, sent me for a test that proved that I also had an ovarian tumour (fortunately benign) - but how scary that it had been there for what looked like years, and I had been to my original doctor complaining about the pain and she again fobbed me off with the advice to take ‘nurofen plus’  (I’m guessing she had shares in the company or something!) It is a lesson learnt - I try to look at the positives now - I’m now healthier than I’ve ever been, forced myself to do more regular exercise now that I have the energy to do it (estimates were that I had been slowly internally bleeding for a good couple of months), know I have a wonderful husband who will do absolutely anything for me - taking months off work to be there for me 24/7, and appreciate what I have. But it is frustrating to think that I had 4 months of my life basically taken away because of the negligence of a medical professional (and that’s just the recovery time for the surgery - for months and months before I had just been ill constantly).

    • julia says:

      10:42am | 24/02/10

      I’ve had some shocking doctors in my time. I remember when I had some issues and I demanded a referral to a gynaecologist (even told her which one I wanted to go to) and she thought i was being silly and even used a tone of voice designed to put me off.

      My new GP is brilliant. Super responsive and refers me on whenever she thinks its beyond her. She sends me for ultrasounds regularly and makes me have a pap smear regularly.

      We pay a lot of money to doctors for their advice, they should be brave enough to admit when they don’t know everything and refer us on or do tests to rule serious issues out.

    • Sarah Allen says:

      09:51am | 24/02/10

      A brilliant piece of writing from a very brave woman with a strong message.

      Let’s tell this story again and again.

      Thanks Jacqueline. You’re a lover, a fighter and survivor, no matter which way I look at it.

    • SD says:

      09:58am | 24/02/10

      Great to hear you are cancer free.

      I must admit that I don’t understand the testicles reference.
      I’m sure you are making a clever point there - but it is lost on me.
      Anyone care to explain it?

      Else - besides a heart warming story detailing one person’s cancer ordeal and subsequent survival, I think this article can also be intrepreted as a warning of the less than great treatment methodology of many GPs.

    • sam kinsella says:

      10:16am | 24/02/10

      Here is an amazing treatment being ignored in Australia even though its available in Hospitals all over the world. If we had this here and people realised the ease in which many cancers can be treated with no side effects and no loss of quality of life, I feel more would be a tad more proactive in cancer checks. This group is having a huge impact on getting the treatment to Australia as well as helping people realise the options available.
      http://www.facebook.com/group.php?gid=43255564285&ref=mf

    • Shane says:

      10:36am | 24/02/10

      I’m a guy, but really enjoyed that article. Jacqueline, did you go public or have private health cover?

    • Jacqueline Pascarl says:

      03:40pm | 24/02/10

      Dear Shane, I started off in a private hospital for the Pulmonary embolism and had very little luck for 5 days as they didn’t want to give me a scan. Took myself off to the excellent Royal Women’s Hospital in Melbourne and Professor Michael Quinn and Professor Orla McNally - along with their amazing team on the Oncology ward cared for me. Professor Quin and his people fundraised so that his ‘ladies’ have private rooms in the public system. He runs sponsored marathons to fund it!  Regards,

      Jacqueline

    • Eric says:

      10:43am | 24/02/10

      Samantha Flint - in fact the government spends much more money on women’s health problems than on men’s health. Just look at all the breast cancer awareness programs for one example.

      This disparity is probably partly responsible for the fact that men die seven years earlier than women on average. Our society and government care much more for women’s welfare than that of men.

    • AFR says:

      11:28am | 24/02/10

      Eric, I pity you more and more every day. Perhaps us men should get off our bums more and campaign for more money. Are you with me?

    • Kim says:

      11:46am | 24/02/10

      Hey Eric,  Not sure if you know but a large proportion of the breast cancer money is raised from public donations.  Only about 50% of the money utilised for the breast cancer awareness actually comes from the government.

      Loved the article Jacqui.  All the best to you and your family.

    • Eric says:

      11:48am | 24/02/10

      AFR, the first step in campaigning is raising awareness. Which is precisely what I am doing here.

    • formersnag says:

      12:38pm | 24/02/10

      Spot on Eric, but, the money women suck out of the pool available for all medical research has not been coming at the expense of men alone. There is less money available for paediatric research as well. That’s children’s, diseases & medical problems girlie’s. Also geriatric medicine, that’s, old people of both sexes.

      Everything the fauxmanistas do, leads to child abuse in some form or another. All money, for all, medical research should go into a central “university medical research fund” and then be distributed according to good old fashioned medical principals, like “triage” & “evidence based medicine”. Which medical problems are killing, disabling the most people? In what percentage of the whole population?

      Are the feman-nazis suggesting that a board of medical professionals, from all specialities & both genders, in equal numbers, would be incapable of deciding these matters fairly?

    • Mistress D says:

      06:07am | 25/02/10

      Eric- You’re not really campaigning for awareness….you’re moaning about the disproportionate funding. You’re right, there is more care for women probably because women are taking an active role in looking after themselves. On average most men don’t look after their own health, don’t go to the doctor and figure if no one tells them something is wrong then it’s not.

      Yes, the government may well spend more money on awareness programs for womens but tell me why is it that women have to pay for a vaccine for the paploma virus? (probably didn’t spell that properly)  If it were testicular cancer, I’m sure it would be fully funded.

      Nevertheless, the shift is changing and men are being encouraged more and more to discuss their problems and what they need to look out for. But MEN need to do it, I doubt you’ll find a pink ribbon supporter who won’t also support your cause.

    • MarK says:

      11:21am | 24/02/10

      Congratz on surviving,
      No thanks for the uneccessary feminizing of men,
      Did you know (apparently not fromt he opening of your article) that we all being with Gonads, then they develop into either ovaries or testes. Gonads are not testes, testes are gonads, Ovaries ar also gonads
      Thanks for the advice if i put on 25kg (equivalent for my not so small frame, and chronic fatigue and struggle to make it up the stairs i will eb sure to go to the doctor

    • maybe says:

      01:06pm | 24/02/10

      I was going to point that out too.  Although ‘gonads’ or ‘nads’ refer to testicles in the vernacular, technically this is not the case, and everyone (provided they haven’t any developmental issues) is born with a set of gonads, and boys never have ovaries. It’s not hard to do a little bit of research to check your facts.

    • Sophie C says:

      01:09pm | 24/02/10

      gonads were obviously being used to prove a point in terms of common Aussie language - not necessarily medical. I bet guys understand the terms as testicals anyway MarK. But all that aside, fearless and selfless Miss Jacquie! Thanks for the adivce and the informatoin.  Pity more people aren’t brave enough to write it out like you. Funny to - stay well.

    • Helen says:

      02:15pm | 25/02/10

      Ooh, I’m glad we sorted that one out, because as we all know, to partake of an attribute that’s coded female makes one a lesser human being. or to put it more succinctly, “Erk! Girl cooties!”

      We are really a very woman-hating society (and some people say feminism isn’t necessary any more!)

    • Julie says:

      01:08pm | 24/02/10

      All very well to say listen to your body.  Perhaps we should try for doctors to listen to their patients.  I have had a chronic and debilitating cough as a residue from having pheunomia for over two years; more than a decade ago.  Was constantly then, as now, informed I was fine by numerous doctors and specialists.  Always treated as a hypochondriac although I have had no other issues in that time or previously.  Is an enormous source of concern for the family, as well as embarrassing for myself.  Swine flu last year was so much fun - my cough could clear a restaurant in minutes.  Have spent thousands with doctors and not one has ever followed up or shown any interest whatsoever.  I’m over them all.

    • Rose says:

      01:15pm | 24/02/10

      Balls, testes, gonads, boys, scrotums, penis. Good way to get men reading this article Jacqueline.  Very clever and brave and comedic. Maybe some men will now urge there signicficant others to be vigilant about their health. Well done and keep writing - we have missed your humour.

    • Judith Curran says:

      01:35pm | 24/02/10

      Well said my friend. And it seems you have started a healthy debate.

    • Tinman says:

      01:55pm | 24/02/10

      Hearing what your body tells you is one thing ! Getting the arrogant medical industry elite ( whom long ago ceased to be a profe$$ion ) to listen to you, telling them , what your body has told you, is another matter altogether !

    • June Rhodes says:

      02:14pm | 24/02/10

      Agree with this. had a friend with lung cancer (and emphysema) and was prescribed a chemo drug to cost $15,000. She enquired with the manufacturers about its appropriateness for her cancer and they warned her off as it weakens the heart (hers was already weakened by the emphysema) so this may have killed her. As for the $15,000, apparently it only actually costs $10,000. Who’s pocketing the difference? By the way she had Cyberknife treatment overseas (as mentioned earlier somewhere) and is now doing fine (except for the emphysema!!!)

    • vicki pavlos says:

      01:56pm | 24/02/10

      I’ve lost two friends to ovarian cancer. Each had long ordeals of pain, physical suffering and mental torment, and left behind a husband and children. I’m all for supporting your cause, Jacqueline. You are indeed luckier than many others. We do need to listen to our bodies and to persist when doctors fob us off with incorrect diagnosis, or dismiss us with an opinioon of hypochondria. We are the best guardians of our own health.

    • 6clegs says:

      02:04pm | 24/02/10

      As someone that has also experienced complex medical problems I well understand what you went through, before getting your shocking diagnoses.

      Cheers to you, and *anyone else* that’s had to go up against the medical profession because they had slightly more than a bad cold. It is soooo waring, and one questions oneself daily as to ones sanity.

      Thank you for sharing your story - and without adding extra drama (like it wasn’t dramatic enough for you and family) - but isn’t that usually the way? it’s the real drama queens/kings that exaggerate the slightest headache and need attention from everyone.

      Best of luck for a healthy future for yourself & family. grin

    • Jacqueline Pascarl says:

      03:12pm | 24/02/10

      Thank you for the good wishes - we are so very lucky to be with each other after such a scare and every day is a gift indeed.  I tried to explain in the article that testicles are a man’s battery pack to a great degree, and ovaries are a woman’s.

    • Erica Gibbs says:

      03:16pm | 24/02/10

      A lesson for us all and a well written column - thanks Punch for giving it so much space. Brave lady! Everyone must look after their own health instincts and strange changes don’t get sent away with a prescription but not a real answer. I hope that lots of woman do read this I have passed it on to several girlfriends.

    • Rodney Jones says:

      03:19pm | 24/02/10

      Jacqueline, how many more things are you going to go through I hope for your sake that everythig will just go swimmingly for you. Good that this story is out there and in such easy to follow way. Best of luck for the future.

    • Alan Yip says:

      03:24pm | 24/02/10

      Is this disease more often found in White Anglo saxon females or is it wider? Courageous to speak about this stuff publicly. Good luck with the Marathon this weekend. Sincerely, Alan Yip

    • Amy says:

      09:58pm | 24/02/10

      Anglo saxon is “White”.

      Jacqueline, well done on a great article. I teared up by the end. Glad to hear you are okay.

    • Angela says:

      03:43pm | 24/02/10

      Your courage is amazing and an inspiration. You are right, more people need to listen to their body but also give GPs the information they need to make a correct diagnosis. They are not God, they merely have the tools and resources to get us the help we need after a diagnosis has been found. If you are not happy with their opinion get another, and keep going until you get answers. We are responsible for our health and looking after ourselves, please don’t rely on someone else (GP) to do it for you, you life may depend on it.

    • Carolyn Blackburn says:

      05:11pm | 24/02/10

      I too had the run around when at age 28 I had a growing stomach and weird “pains”. My GP told me it was just my ovaries starting to work again after giving birth to my second child. - Funny how it hadn’t happened after the birth of my first child.
      Several doctors later I was sent for an ultrasound and a large mass was discovered in my abdomen. Like you Jacqueline, I was told to pack my bag and prepare for the worst in hospital. An 11cm tumour encasing my right ovary was removed and I was lucky enough to be also declared “cancer free”. Eight years and another baby later my specialist told me that new research had showed that the type of ovarian cancer they had found in my right ovary is usually present in both - so I underwent a radical hysterectomy and they did find cancer in my left ovary and once again they had caught it in time. Someone upstairs was looking after me!
      An early menopause was controlled with hormones and I was relieved to be finally rid of the fear of the cancer returning or invading my womb.
      My story also shows that follow-up is vitally important with this silent killer.
      I’m now 48 and enjoying watching my 3 children grow up. I hope the continuing research enables more women to have positive outcomes.

    • Isabelle Stephenson says:

      06:38pm | 24/02/10

      god, what would have happened if you hadn’t made them find the tumours? Can only imagine that they could have burst as a friend pointed out that even if malignant, ovarian growths can explode like an appendicitis. Thank you for the timely warnings and thanks to the editors of the Punch for bringing it to us. Continue to be strong as an example for us all Jaqueline and please enjoy your family but keep writing - we missed you

    • Ron & Beverly Carter says:

      06:42pm | 24/02/10

      What a terrific inspiration you are Jacqueline and a great writer. I have read both your books & all your columns here online. Even in despair you have a sense of humour. Keep safe and healthy and thanks for the frank writing.  Best to your husband and family

    • J McGlone says:

      06:50pm | 24/02/10

      Jacqueline, Glad to hear you are fighting back. Take care, with affection. I often think of you

    • Melinda says:

      06:51pm | 24/02/10

      The irony of your situation is not lost on us Jac. Have you read ‘The Feminine Mystique’ by Betty Friedan? I bet LOTS of women are ‘diagnosed’ with depression who simply don’t have it . . . . there are still so many myths to change. Good to have you back - The Punch article is great.

    • Alison says:

      07:18pm | 24/02/10

      Wow Jacqueline, what an amazing story. I have been ‘‘chronically unwell’’ for some years now, always fobbed off with antibiotics and pain killers. It has been a very frustrating and depressing time. But, not more! You have inspired me to take charge of my health! Thank you so much for telling us your story. I have shared it on facebook and I hope that many more friends will pass it on to their friends to spread the word around.  All the best for a happy and healthy future.

    • Kate Leslie says:

      08:00pm | 24/02/10

      Thankyou for sharing your story Jacqueline. What a brutal confrontation with your mortality. Its disturbing that your doctors failed to recognise the classic sympoms of your ovarian cancer. I wholeheartedly agree with your recommendation that we learn to listen to our bodies and take responsibility for our health.
      I was diagnosed with a brain tumour nearly 3 years ago and it’s been such a journey. Cancer is not well understood in our society. I’ve come to understand its a multi-factorial, chronic, degenerative disease. To stay cancer free, even become ‘weller than well’, can I suggest Ian Gawler’s book ‘You Can Conquer Cancer’? Happy healing….

    • Julie says:

      08:37pm | 24/02/10

      You are a remarkable woman…I have followed your story from when your children were taken…read your books, cried with you, laughed with you & shared in your joy when your eldest children came home…I believe they were sent back by a higher power to help give you strength to fight this new battle…your a fighter, survivor & the most beautiful woman who will continue to inspire me & women around the world.

    • Jules says:

      10:47pm | 24/02/10

      Great article Jacqueline, keep the good writing coming.

      On another note; doctors should be reminded that they are providing a service to us, not us meek, mild paying abeyance to a God.
      The arrogance we encountered when my mother was diagnosed with a blood disorder was designed to intimidate, I have now decided when I encounter that arrogance again it really speaks of incompetence.

    • Rosina Alberti says:

      11:29pm | 24/02/10

      I want to say thank you as well for sharing your story. I feel like I already know you after reading a lot of what you have written like your books and other things. I have shared a link on my Facebook to this Punch website so my friends can read about the symptoms and get in volved in their own health from a point of knowledge. Will you be writing articles here from now on? I heard about this story on Twitter and like to keep up with things. I really liked the article on botox and also male menopause cars it really made me laugh. You are a good writer and a even better human being. Get better soon. Sincerely Rosina Alberti

    • Louisa Amberly says:

      11:36pm | 24/02/10

      How come some male readers completely missed the metaphor about batteries and the similarity and importantce of testicles and ovaries. Jacqueline so obviously meant it as a trigger for intellectual empathy or to put the importance of ovaries and reproductive health in women into language and values that blokes can comprehend. Yes breasts to get all the whoha and all the money because boobs are visible but they don’t keep a person going in terms of energy. Seems to me that after reading this column ovaries are vital to a community’s wellbeing as sick women mean life just comes to a standstill for those around them. Keep up the good work Jacqueline and thankyou Punch for publishing.

    • Leonie B says:

      11:41pm | 24/02/10

      I agree with Jacquline, life is too short to pretend about liking things when you don’t. I’m taking a leaf from her book and am speaking my truth. Have another Vodka on me and stay well, happy and writing stuff like this Jackie. Thanks a lot!!!

    • Sandra says:

      11:48pm | 24/02/10

      OMG how can this woman still find a laugh in all of the pain and terror. hats off to you Jackie. I cried as I read of your journey. thank you for sharing it.

    • Barbara says:

      11:56pm | 24/02/10

      Maybe Jacqueine was spared so she could write this magazine article and help others maybe even save them? My mother has been complaining about the same issues. I am insisting I take her to see a Gynacologist tomorrow. Thank you for your bravery and for putting your experiences out there with wit.

    • Di says:

      12:57am | 25/02/10

      One wonders what Dr’s do learn? - it used to be have a Bex and a lie down; I had a rare disorder that took more than 10yrs to diagnose, I was labeled a hypocondraic etc, at diagnosis i had less than 12 months to live; having researched my disorder I can’t believe how Dr’s missed it for so long - You are right - listen to your body! and Dr’s listen to your patients - and look at your patients, anemia is easy to spot - especially chronic anemia; I have become an expert in my particular illness - and more than once I have had a stand up argument with GP’s re insisting on evidence based practice. You are one special lady
      I am sending this article to my Daughter.

    • Sarah Emily V says:

      07:11am | 25/02/10

      “Hey Jack, that’s an awesome article! And it’s really good to see lots of women AND men commenting on it. So glad your healthy again! Your a strong lady. Well done for spreading the word.

    • Cat Moseley says:

      07:35am | 25/02/10

      Dear Jacki
      Your story is so similar to my own which started in Nov 2008 - going to my doctor numerous times and even turning up at a hospital emergency centre with abdominal bloating and significant pain and so much fatigue only to be told I had irritable bowel and was approaching menopause.  Finally i said to the doctor i was seeing “could my symptoms be masking another condition like ovarian cancer” and she said ‘no’.  It took another visit a week later before she sent me for an ultrasound when the radiologist nearly fell over the chair at the sight of a 20cm tumor hanging off my ovaries and uterus.  Emergency surgery on Christmas Eve 2008 followed by chemo and then a trial drug avastin which i have only just finish and yes I am now cancer free..

      Like you i owe my life to Professor Penny Bloomfield and my oncologist Rob Mcintosh here in Tasmania. But we have to work so hard to raise the awareness of our general practice doctors that when women go to see them they should be alert to what these symptoms can be hiding and not send us away with pats on the head and tell us it is our age or that we are depressed.  It costs so little and takes such a short amount of time to have an ultrasound done and as you would know the survival rate of women when their ovarian cancer is diagnosed early is far greater than if this insidious disease has spread.

      I wish you well on your journey and we need women like you to continue to raise the awareness of this horrible disease.

    • Tony Ascott says:

      08:29am | 25/02/10

      Sometimes its best not to know whats wrong with you. This story was in our local paper of a man who tried everything within his power to save his wifes life and now she has passed he is left a single dad of 2 with the financial burden of trying to beat cancer. he is helping others win as he now raises awareness where as he had no support when looking for options for his wife. Harsh experience but at least he’s doing something positive, like you. Well done
      http://www.northernstar.com.au/story/2010/02/22/family-struggles-with-medical-debt-in-sickness-and/

    • IMHO says:

      10:18am | 25/02/10

      I agree with all the comments about being an advocate for your own health. Your body does indeed give you signals about your own health that shouldn’t be ignored.

      Whilst this is a great human interest story, it is a medical anecdote. Be careful not to tar all doctors, indeed most doctors, with the same brush. There are some shockers out there but it is a highly regulated profession both internally and externally. True incompetence rarely goes unnoticed for long.

      The business of diagnosis is a tricky one. Many of ovarian cancer’s ‘classic symptoms’ are quite non-specific (ie occur in many other conditions). Historically it has been hard to diagnose, and patients often present very late in their disease. I agree by all means let’s get to the bottom of it, let’s research the crap out of it until we are able to diagnose it earlier, and get better outcomes.

      But let’s put it in perspective - there are many diseases that kill us, many more common than ovarian cancer, and research has to continue into those as well. And until Australia wins the lottery, there is only a finite amount of money for medical research.

      So it’s natural for everyone to want to push the barrow for their own causes but administrators and researchers have to work within clinical and budgetry restraints. I believe they’re doing the best they can in most cases.

    • Jacqueline Pascarl says:

      03:23pm | 25/02/10

      Dear IMHO, My GP’s made a mistake - they were overwrought at what had occurred and have apologised to me and my family.  As well, they have changed their practice ethos (encompassing 8 doctors in all) and are now very vigilant about these issues.  The promote my story in their rooms urging women to ask questions and locally, have called a meeting of all their counterparts in the area to make them aware of the symptoms of Ovarian Cancer.  I couldn’t ask for more and if you were to give me a choice - angry legal letters and castigation - of community education by a good collection of doctors who are now bitterly aware of the symptoms and the outcomes - well, I vote for the latter.  This por-active wake up call means that perhaps, another family will avoid the trauma, anxiety and panic that a diagnose of a life threatening disease brings - early detection is foremost key to beating these types of tumours.

    • IMHO says:

      11:05pm | 25/02/10

      Hi Jacqueline - my comments were broadly addressed to some of the commenteers who took the opportunity to have a bit of a general doctor-bash sesh. No doctor likes to miss a diagnosis of cancer, and I’m sure your GP is feeling terrible. Good to hear they are doing some education sessions.

      More importantly, you have had a terribly rough ride by the sounds of it and I wish you well for a full and speedy recovery.

    • Jacqueline Pascarl says:

      11:41am | 26/02/10

      Thanks IMHO - glad that you participate in this discussion.  I’m doing well and just glad to have a future.  I have worked very closely with the medical profession on various issues and think that doctor bashing is abhorrent - awareness and education is really the key.  If you are in Melbourne, feel free to join us for the “We Can Walk It Out” for the Women’s Cancer Foundation around the Botanic Gardens on Sunday, 28th Feb at 10am.

    • Nikki says:

      03:08pm | 25/02/10

      Very moving column - I lost my mother-in-law to Ovarian cancer 3.5 years ago.  still miss her.

    • Elizabeth L says:

      01:34pm | 26/02/10

      Maybe you have just saved a life my symptoms ar ejust like yours Jacqueline. I have book an appointment with my doctor and my gyacologist. Thank you for sharing your journey.

 

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