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Eulogies

Some of the most moving and brilliant speeches ever made occur at funerals. Please upload the eulogy for your loved one using the form below.

For James Hoy: 'I still expect to see Dad walk through the front door again', by son Aidan Hoy - 2016

November 23, 2023

16 May 2016, Pinnaroo Valley Memorial Park, Perth, Western Australia

When a loved one passes away, it’s inevitable that you may never have had the opportunity to tell them some things. This must be particularly so, between father and son.

Over the past week, many people have told me about how proud my father was of me. But what Dad doesn’t know, is how proud I was of him.

I’m proud that Dad was Chinese in Australia during a time when Australia was not necessarily so welcoming. He was born in 1946, around the same time his parents received a letter from the government requesting that they depart. But Dad’s birth meant his parents could stay, and he would laugh and boast that he was the saviour of the family’s future in Australia.

These early years are mostly a mystery to me. However, as a child, Dad remembered sitting around warehouses watching his father and other Chinese men while they smoked opium. And up until a few years ago, a Northbridge history website had pictures from the late 1940s of young Jimmy, and his sister, outside of the Chinese furniture factory where their father worked.

But I’m also proud that Dad was staunchly Australian. His first car was an FJ Holden. Someone once said he was one of only a few Chinese playing football and cricket in Perth in the 1960s.

When I accompanied him to the East Perth Football Club rooms after a grand final victory in 2002, one-by-one several gentlemen, of similar vintage to Dad, came over to shake his hand and reminisce about East Perth’s good old days.

I asked him who these blokes were. He laughed and said, “I have no idea”. I can only conclude that the Chinese fellow that frequented the Inglewood and East Perth football scene in the 1960s was probably a novelty at the time.

Dad also cared about Australia in a more sophisticated sense. His grasp of politics was impressive. He read the newspaper every day from cover to cover and watched hours of TV news and current affairs every night. His vintage tight fit t-shirt celebrating Bob Hawke’s 1983 election victory would be the envy of many hip political advisors today. And I’m not sure many brickies bought a copy of former prime minister Paul Keating’s book on Australia’s international relations in the 1990s. But Dad did.

I’m proud that Dad was resilient. For decades he was up at 5am and off to the building site, and rarely did I see him visit a doctor. I once had to pick him up from work Christmas drinks at a bar. After Dad had bought all of his colleagues a round of shots, a young apprentice bricklayer turned to me and said: “I don’t know how your Dad has been doing this every day for 30 years; I’m already over it after 12 months”.

The ultimate test of his resilience was his battle with cancer. Yet he never let it affect his outlook on life, and he calmly shrugged off any concern from others. He was determined to not let his illness get in the way of so many things he wanted to do.

Never did I hear him complain about the medical treatment he received over the years.

Yet, for all of Dad’s strength, he wouldn’t have gotten through the final chapter without the love and support of Linda. And she helped to soften his tough exterior, just a little bit, for which I am very grateful.

I still expect to see Dad walk through the front door again at any moment.

 

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In SUBMITTED 4 Tags JAMES HOY, AIDAN HOY, 2010s, 2016, CHINA, IMMIGRATION, CHINESE AUSTRALIAN, FATHER, SON, AUSTRALIA, AUSTRALIAN, CANCER
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Three firends: Jessica, Linda and Divya

Three firends: Jessica, Linda and Divya

For Jessica Chan: 'Laugh as much as you breathe', by Divya Emanuel - 2015

May 12, 2020

15 January 2015, Our Lady of Lourdes Church, Singapore

Laugh as much as you breathe
Love as long as you live

These two lines sum up Jessica. She always had a smile on her face, laughed loudly and heartily. She spoke with passion and with such vehemence you wouldn't want to cross words with her. She loved food, friends and family. She was an impassioned Singaporean who showed us, her motley group of friends what true Singapore hospitality was.

She had a fiery temper, loved possessively and dearly and disliked with just as much fervor. She picked her friends carefully, but once inside her circle, it was a very special bond to be wrapped in.

Before I met Jess, our sons who were 6 months old were friends first. Jess used to bring Julian to the Bayshore clubhouse and my mum used to take my son there. While the boys played, Jess and my mum became friends. When my mum left for India, she asked me to go meet this lady Jess. One morning I went to the clubhouse, little knowing I was going to make a friend for life. So, thank you to 2 little boys here, for giving their mummies' such a beautiful journey to experience.

Life with Jessica was one big party. She organized endless events for the group. We participated in Christmas day lavish dinner, Chinese New Year open house, Julian’s birthday bash, Lantern festival, Halloween, all happening year after year. In between all that there were BBQs, trips to Pula Ubin and food trails to explore. She not only loved her friends dearly; she extended that love to our families every time they visited Singapore. If one thing shows in all of this, it was her energy and zest for life. She embraced it and made the best of her very short, young life.

When she was diagnosed with small cell lung cancer early last year in March 2014 at 46, Linda and I sat crying by her side ...she cried with us but by then had sorted this disease in her head. She told us her life had been full & complete and she had no regrets. She married the love of her life, travelled, had Julian her miracle child and lived in a landed house, a Singapore dream. She accepted her fate and felt blessed for the life she had enjoyed.

Jessica's threshold for pain was very low and her wish was to pass away quickly. Unfortunately, her suffering was long and painful. Watching her these last couple of months, was the hardest thing to do.

Her pain is finally over. She was robbed of a full life, and has gone too early from us but as she lays peaceful, I know she's always going to be present among us , dishing out her worldly wisdom because that's what ten glorious years with her has given us - beautiful memories to love, cherish and hold onto.
We will miss you forever Jess .


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In SUBMITTED 4 Tags DIVYA EMANUEL, FRIEND, MOTHER'S GROUP, CANCER, MOTHER, SINGAPORE, LAUGHTER, LOVE, TOO SOON
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For Connie Johnson: 'Cancer really does take the f*cking good ones', by Carrie Bickmore - 2017

February 5, 2020

22 September 2017, St Paul’s Cathedral, Melbourne, Australia

Cancer really does take the f*cking good ones. And breathe . . .

I first met Connie about four years ago, when Connie and Sam launched Love Your Sister and Sam had this crazy idea to unicycle around the country. I joined him for a ride on the Perth leg of his journey and surprise him with Connie who flew over at the time. I didn't know either of them really before that and what I discovered during that ride was a brother and sister bond like no other and a drive just like mine to rid the world of cancer.

I don't think Sam realised at the time that that ride was as beneficial for me as it was for you, I know what your mission was, but for me it was a chance to chat to someone who watched someone they loved dearly in a huge amount of pain, and that chat will stay with me for a long time. It felt like a private chat even though it was broadcast to the nation.

I continued to follow your journey over the years and watched as the village grows and your fundraising efforts soar. What you and Connie are achieving together is phenomenal and I say achieving together in the present tense because even though Connie has passed away her mission to rid this world of cancer is only just beginning. With Sam, and Emma, and your whole family all the team of villagers continuing Connie's legacy, Love Your Sister will continue to achieve incredible things and I don't think it's going to stop until no one dies from cancer again.

I have been reflecting a lot in the past few weeks about Connie and her journey and how Connie chose to fight her cancer battle publicly, not privately. She could have fought it privately, she had every right to fight it privately, but instead she let us all in on her journey and she taught us so much. She taught us to cherish being a mum, to make time to be silly with the kids and have fun. And I've certainly, in the last few weeks, had Connie at the forefront of my mind. Every time I played with my kids, I played a bit longer each time, think how lucky we are as mums to be able to play with our kids.

She's taught us what it's truly like to be a cancer patient, what it's really like. But most of all she's taught us how to be a bloody good human being. Cancer as we've spoken about tonight affects you not just physically but mentally, and also impacts every single person connected to the cancer patient, which makes being so open with the world incredibly hard and incredibly hard for those around you and your family as well. But that's why Connie touched so many hearts because we got to see the real journey, the highs, the lows, the small wins, the setbacks, the days where it seems impossible and it's ripping your family apart and then the days where everyone is unified and ready to battle. There are not many people that have the ability to rally a nation the way Connie has, all of you here know how personally she has touched your life, it will be different for every single one of us, but the size of her village shows just how wide her heart is and how long her arms are. No matter what type of cancer has affected your family we're all in this together — this country will continue Connie's mission.

To Mark and to the kids, we're also thinking of you and we know once the services stop and the casseroles stop being delivered and life goes back to normal, for most of us, it doesn't go back to normal for you, and I hope that you can transition into your new normal peacefully and privately knowing that we are all thinking of you.

The world is a smaller place without her big heart in it, but thank God we got the chance to know Connie Johnson, I will always be thankful for that.


Carrie Bickmore and Connie Johnson.png


Connie died on 8 September 2017. Donate now, or get your Connie Cottonsocks at https://loveyoursister.ecwid.com. Join The Village over at http://www.facebook.com/loveyoursister

Source: https://www.popsugar.com.au/celebrity/Carr...

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Tags CONNIE JOHNSON, CARRIE BICKMORE, SAMUEL JOHNSON, LOVEYOURSISTER, TRANSCRIPT, EULOGY, CANCER
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For Natasha Jones: ‘Such a beauty, such zest for life’, by Riley Jones - 2019

December 30, 2019

4 December 2019, Memo Music Hall, Melbourne, Australia

Some of you might think of me as a funny bugger, and may have even seen speak at Natasha’s Dad’s funeral back in 2015, where I managed to sneak in some Slovenian swear words and get some laughs. I’m not sure I can manage that today, though.

I’ve actually been dreading this for a long time. Basically, since the day that Natasha received her terribly cruel diagnosis, and if not that exact day then definitely that first week, I’ve lain awake at night, time and time again, wondering about what I might say at her funeral should she pass away. And now here we are, a little over 15 months later.

My thoughts ran the gamut from just angry ranting, to hysterical crying, to just focussing on the positives, to everything in between. I think today we’ll get a mix of all of those.

I should start by saying that we shouldn’t be here. She was only 43.

And apologies in advance to anyone who has survived cancer or who is even just over the age of 43, because I keep thinking: why do you get to live and she didn’t? And that includes me, I’m the sweet age of 46. Here’s an actual example of this thought process from yesterday: why is Moby alive? Nothing against him, by why him and not Natasha? I know Tash wouldn’t want me to feel like that, but she was much nicer and better than I. It’s just not fair. She should still be alive.

But her cancer was horrible, more horrible than I think we realised. In retrospect, I can now see that this was almost a certainty to happen, but we tried to keep hope alive, to try to ensure that she could be with us for as long as possible. And as it turned out, that was nowhere near as long as we expected. None of us, not her, I don’t think even her medical team, expected her to go last Tuesday. Only two days beforehand, on the Sunday, she’d told me that she wasn’t going to die this year.

But it looks like it WAS her time to go, and as I’ve noted in a pretty distressing post on the Tash Tribe on Facebook, she went relatively peacefully, probably unaware of my desperate attempts to revive her. And many people have reassured me that, if she had to choose a way to go, as opposed to the timing, it was almost perfect. She was in her bed, having just had her first shower in days, warm under a blanket in her dressing gown with the love of her life looking over her, caring for her. Her last words were in response to Declan saying “I love you”, and she whispered back “I love you, too”.

And then a few minutes later, she was gone, and all of a sudden, it was just me and the kids left. I must say that, if I didn’t have the kids, I don’t know what I’d do, because there’s a big Natasha-shaped hole in my life, that can never be filled. I’m so lost. I keep wanting to tell her stuff, or watch a TV show with her, and then remember that I can’t. I still can’t believe she’s gone and I bawl my eyes out every day. And it’s only been a week. How can I do this for the rest of my life?

A life that used to be pretty great – only a year and a half ago – and which is now just miserable.
But, there is some light, because Natasha gave me you three beautiful creatures. And even with that, it seems like she was planning ahead and looking after me – which is very Tash. Y’all may not know this, but Xander has been comforting me, quickly coming over and giving me a hug whenever he sees me tearing up, and Elektra and Declan have been wonderful as well. But it’s my job to look after you guys, and that’s what I’ll do. I just worry I’m not going to be as good at it as she was, or anything else she did for that matter. But there are a lot of people in this room who have offered to help me, too.

SO, apart from my kids, I struggle to find any positives in this, but here goes.

The main positive is – she’s no longer in pain. Ever since the chemotherapy started, she required pain medication, and the pain only got worse towards the end. She was willing to endure it to be with her family as long as possible, but now, thankfully, she’s no longer suffering.

Another weird positive is that, once she was diagnosed, I had to step up and do all of the things she used to do, which was an astounding amount. And taking the kids to their dermatologist one day led to discovering that I had a small skin cancer in my scalp – it was benign, but could have got a lot worse. If Tash hadn’t been diagnosed, I wouldn’t have gone to that appointment, and I wouldn’t have had that skin cancer cut out, and then who knows.

Also, thanks to her diagnosis and treatment, I got to spend pretty much every minute of every day for the last 15 months with her, and a lot of time with the kids, too. Much more intense time than we would have had otherwise. And I must thank my work colleagues for being so flexible with us and giving me that opportunity – I don’t know what I’d do without you guys.

And that brings me to another positive, not of her death, but her life - we all got to be with her at some point during her 43 years on this planet. And I think we can all agree that makes us very lucky, because she was amazing.

I guess that makes me even luckier than most, as I was with this incredible woman for 23 years – half of my life, and more than half of hers.

For those of you who don’t know the story, Natasha and I got together 23 years ago in around November 1996. We had passed each other on the stairs in the Union Building at Monash Uni, our eyes had met, and we knew straight away there was a connection. We later chatted at a Union Night, trying to work out if we’d met before, but there was nothing we could pin down, so it just must have been destiny.

And then Natasha introduced me to her friend, Jade, and Jade told us that she had actually had to pull us apart at the Chocolate Ball at the Palace, here in St Kilda, many months before. So it was either destiny, or a drunken pash that neither of us remembered, but it turned out that we had fortuitously each found our respective soul-mate.

She was my wife, lover, travel companion, fellow music aficionado, partner in all things and, most of all, my best friend. We did pretty much everything together and I can confidently say that pretty much every good thing I’ve ever done and every good memory I have – she was there.

I loved everything about her – the obvious stuff that you all loved – her kindness, her smile, her thoughtfulness and generosity. But I also loved weird stuff – I loved her taste and her smell. She used to complain sometimes that she hadn’t had a shower and thus would smell, and I honestly told her numerous times that she had never smelt, never had an unpleasant odour, EVER. I meant that very seriously. It’s a pity the feeling was not mutual… (Let’s just say that she didn’t think my natural, aluminium-free deodorant from Byron Bay was very effective.)

Another thing I loved: her voice. Not just her singing voice which some of you may have heard – she sang like an angel. But her regular voice – I told her that I loved listening to voicemail messages she left, because hearing her voice just gave me a little thrill.

And I loved her feet. Not in a fetish-y way. But her nerves were a bit damaged from the chemo, and something she really appreciated was her feet being rubbed. So I would volunteer every night to massage her feet, and she looked surprised every time, and then happily thrust her feet at me, nearly kicking me in the face, and I would massage her feet and calves for an hour while watching one of our many TV shows that we mutually loved. Because we didn’t have as much alone time together, it was something I looked forward to.

Also, she was super-hot, but we all know that.

Another thing we all know is that Natasha was the nicest person you could ever meet, and so thoughtful. Even when going through the worst things personally, she would think of others.

As a very weird example, she kept suggesting women I could be with after she died, who would be good for me and the kids, and maybe even put up with my comic book movies. Some of her suggestions are in this very room! But I had to beg her to stop thinking like that, and pimping me out to her friends – I was married to her, and I didn’t want that to end, or to even have to think about it. But she was still just trying to look after me.

In that respect, the timing of her passing also seems like she planned it. In particular, she completed her magnus opus – the renovation of our house. She had been driving that for almost two years – getting permits and dealing with heritage issues and so forth, so when she was first diagnosed she asked me, if she died, would I complete the renovation. And I said “no”, because I’m an idiot. But she just went “Right!”, and decided to get it done. And for most of the last year, while she was dealing with everything else, we’ve been living in our partially renovated home. But it was finally completed so that we were able to move back in in late in October. And she loved it, and got to enjoy it for her last month, referring to it as her legacy, while snidely remarking that my next wife had better appreciate it.

She also stuck around just long enough to teach me most of what she knew about running the house and raising our three beautiful kids.

The first day that I drove the kids to a school thing after last Tuesday, Xander said to me “Dad – it’s lucky we’re all so used to you doing this for us”.

So that’s small comfort, but more importantly, the kids also got to have the best Mum ever. She devoted herself utterly to them. She fought tooth and nail to get them into their school, to help them with any health or other issues, to encourage them and drive them to whatever activities they were interested in. She was so proud of you all, even though she might ask you to play outside, or clean up your pig-sty room, you were still her pride and joy. OUR pride and joy. You three are truly greater than the sum of your parts – you’re like Mum, you’re like me, and ultimately you’ll be better than both of us.

There are so many other things I’d like to talk about, if I could go all day. Her love of books and the fact that we were hoping to one day to open a book bar for her to run. Her love of photography – she was so talented. Her love of travel, of course – she’d famously been to 56 countries. Her connection to Slovenia and Australia’s Slovenia: Tasmania. I hope she would appreciate that her coffin is hand-crafted Tasmanian Blackwood. Her dog, Indy, who gave her so much joy. And, of course, her many, many friends. She has SO many friends, and many of them have written very touching tributes to her online and on Facebook. A common thread with all of them is that Natasha made everyone she spoke to, everyone she dealt with, feel special. Because she thought you were special.

So when it came to organising today, I honestly found it too hard to pick even a few friends to speak – it would just always leave someone out, some group out, which is why I basically just went with Myshell to talk about Natasha pre-Riley, and me to try to cover everything post-Riley. But know that she loved you all, individually, and cherished the time she spent with each and every one of you.

Everything about this has been hard, so I want to just quickly thank some people who have helped me and our family through this. (I then went into some personal thank-yous...)

And that brings me to possibly the hardest thing about this service: choosing photos for the upcoming Tribute. How could I fit her life into 80 photos? She’s in so many AND looks great in all them. In the end, I just had to pick a selection from the ones already on my computer, so I know it’s not representative of her whole life. There are numerous trips around the world that are completely missed. But fortunately the booklets you’ve received today include some of those photos plus many others.

Also, I deliberately chose not to have any photos from the last month and a half, when she really started deteriorating.

These photos remind us of Tash in her prime. Such a beauty, such zest for life. A shining star.
I also want to explain the two songs accompanying this Photo Tribute. They’re both by Biffy Clyro, a band Natasha and I saw many times and which we even managed to take the kids to, back in 2014. The first song is called Folding Stars, and it was written by the lead singer when his mother, Eleanor, lost her battle with cancer. It’s very on point and will likely make you cry. The second song is Mountains. This song is a bit more uplifting, but also has a special connection to me and Tash. She bought this picture here for my birthday a few years ago, with some of the beautiful lyrics from Mountains on it. “Nothing lasts forever, except you and me. You are my mountain, you are my sea. Love can last forever, between you and me. You are my mountain, you are my sea.”

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Source: https://rilestar.blogspot.com/2019/12/its-...

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In SUBMITTED 3 Tags EULOGY, FAMILY EULOGY, HUSBAND, WIFE, TRANSCRIPT, CANCER, LOVE
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for Jim Stynes: 'There's never been anyone like Jim Stynes and there never will be', by Garry Lyon - 2012

September 20, 2018

2 April 2012, St Patrick’s Cathedral, Melbourne, Australia

Big Jimmy would have loved this.

He thrived on a big crowd. If he was here, he'd have us all standing up, waving our hands above our heads, and singing, and turning to the person next to you giving them hugs and shoulder massages. It's the sort of weird stuff he did and it took us a long time to get our head around it.

He loved to take people outside their comfort zone, to get them to do things that they didn't think they were capable of, which is not surprising really when you strip it all back to the very start of his extraordinary journey.

How else is a young lad form Ireland arrive on the doorsteps of the Melbourne footy club, another world away in very sense of the word, if he wasn't prepared to step out of his own comfort zone?

It was to be a consistent theme throughout his time here. That he would struggle initially was inevitable. That he would eventually fail was likely. That he eventually debuted as a Melbourne Footy Club player in 1987 was admirable. That he was the best and most dominant Australian Rules footballer in the country four years later, was to begin to understand and appreciate the sort of athlete and person we were dealing with.

Consistency was a cornerstone of Jim's footy career. He was consistently our best preseason performer, defying logic as he powered up mountains, leaving us all in his wake. There's enough team mates of ours here to know that he was consistently our worst in season trainer, as he hobbled around the training track from Monday to Friday, attempting to overcome all manner of injuries from the previous game. He was a horrible trainer during the season.

And then he was consistently our best performer when it mattered most, as he wheeled himself from contest to contest, game after game, year after year. So I wanted Jim to be consistent today, and he would be disappointed if I didn't take the chance to have a laugh at his expense. It's what I enjoyed doing most with him. So here's some home truths.

If he wasn't tight with his money, he was very careful with it. You only had to look at the way he dressed to realise he didn't spend money on a wardrobe. I've never seen a man get more excited about a club issue of a pair of runners every year. Mainly to discard last year's and move into the new fashion.

Which is why recently he turned up at our blazer presentation night, only a ... You know where I'm going with this Sammy ... a week or two ago, and he was crook and his eyesight was failing him. And I realised how crook he was because the raffle tickets were being handed around. Jimmy wasn't a big raffle ticket buyer, he was a $5 man. And I saw him and Sam arguing, having a blue over the envelope, and there was 20s and 10s and 50s flying everywhere and I thought, "Shit, Jimmy's crook. He's going for a 50." And it wasn't until two days later I spoke with Sammy and she said no, even with his failing eyesight, she saw Sam put a 50 in, and he was diving in to try and get 45 out.

He wasn't opposed to stretching the boundaries in the pursuit of victory either, and at the risk of starting an international incident, and I know there's a strong Irish contingent here, I've got to get this story off my chest. Some of my favourite times with him were in the International Rules series where I was coaching and he was assistant. And they were tense times, and we were always in the back of my mind wondered whether he was a double agent or not. And we got to the game and Croke Park, 75-80,000 people there. Not sure who you were barracking for either Brian.

And I said to him, "Jim, get the walkie talkie sorted out. Make sure we've got two way down to the bench."

And he said, "Yeah okay, okay." So he's fiddling around with it, trying to get onto the right channel and all of a sudden he said, "Shut up, listen." And there was a cross reference and we logged into the Irish coach's box.

And I said, "Jim, you can't do that." And he said, "Shut up." So for the first five minutes, we listened to the coach of the Irish team make his moves, and we trumped them and we eventually went on and won the game, and I reckon the next day I heard or read somewhere they said the Australians were well prepared, they anticipated every move the Irish team made. Damn right they did, because Jimmy was listening to the coach all the way through.

So he was a bit deceptive. He didn't lose his temper much, but he did on that day. The game was really close and it got towards the end of the match, and we were a few points down and he was in charge of our whiteboard, with all the magnets and the men around it. And someone did something wrong and I smashed the table in frustration, stuff went flying everywhere but I kept watching the game. It was about 30 seconds to go and I said, "Jim, who's on number 20?" Nothing. So I was getting a bit agitated at this stage, so I said, "Jim, who's on number 20?" And there was still nothing. I said, "Jim, if you don't tell me-" and he cut me off and he said, "Well how to fook do I know? He's crawling round on the floor trying to pick the magnets up." They'd been flying everywhere. Fook's an Irish word for flaming, so we're okay with that.

That was about it. That was about it. It's all I got. The truth is finding fault in anything he did was a fruitless exercise. I sat down and wrote a list of words that best describe him as a footballer: consistent, reliable, dependable, trustworthy, honest, strong, durable, sincere, loyal, courageous, caring and resilient. They're wonderful qualities to possess in a footballer. They're even more significant qualities to possess as a man. And what I find most amazing of all, is that all the kids from around the world we could have attracted in the game when Melbourne took the audacious steps of looking beyond our shores in the albeit unlikely hope of unearthing a footballer, we found him. Jim Stynes. And as a result, we knew never to question the boundaries of what one man is capable of achieving on the playing field, but also to never question the ability of the same man to have an impact away from it. There's never been anyone like Jim Stynes and there never will be, which is why we loved him, and we miss him so much today.

Source: https://www.youtube.com/watch?v=8hFyw2Bsu7...

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In PUBLIC FIGURE C Tags GARRY LYON, JIM STYNES, STATE FUNERAL, FOOTBALL, FOOTY, MELBOURNE FC, TRANSCRIPT, EULOGY, CANCER
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For John Taylor: 'On 83, dad finally faced the inevitable, unplayable delivery', by Patrick Taylor (read by Jonathan Agnew) - 2018

August 21, 2018

I don’t know Patrick. But I’m thinking of him and his family this evening. Good job I read this ‘blind’. Wouldn’t have got through it otherwise pic.twitter.com/OBLucbKylE

— Jonathan Agnew (@Aggerscricket) August 20, 2018

20 AUgust 2018, Lord's, London, United Kingdom

My Dad, John Taylor, had – unlike the current England batting line-up – dug in and battled doggedly to reach 83.

He built gradually through his 50s as a true gentleman, a pharmacist, a sportsman and a father of two boys before unexpected cloud cover descended just as he was looking to break free from the shackles and play with the freedom that retirement would bring.

On an ever-increasingly sticky wicket, he faced up and defended against a beamer in the form of leukemia, the yorker of muscular dystrophy, the googly of Parkinson’s, the reverse swing of diabetes, and latterly, was struck down by the vicious bouncer of dementia.

But like fellow Yorkshireman Brian Close, he never winced, complained or succumbed to the temptation of amateur dramatics, he just accepted the cards he was dealt and squeezed every last drop out of life that he could on a single-by-single basis with his amazing care team acting as runners.

On 83, dad finally faced the inevitable, unplayable delivery and left the field of play.

I use this cricket analogy because Test Match Special has been and will continue to be an institution of great importance to generations of our family.

Dad was rushed to hospital on Thursday 9th August with another bad chest infection. On Friday, we were told that he had 24 to 48 hours to live and that he may in fact never regain consciousness.

On the Saturday I visited Dad in hospital with my wife, and after an hour she had the inspirational idea of getting Test Match Special on my mobile. After five minutes, he opened his eyes and was completely in the room and aware of us.

He was able to convey that he was comfortable and was at peace. I was able to tell him what a wonderful father he is and just how much I love him.

Not one comfortable with massive shows of emotion, after 15 minutes he requested that we listen to the cricket.

For three hours we listened to Chris Woakes crashing it about at Lord’s and making his maiden Test century. We got a digital radio into Dad’s hospital room and he listened to Test Match Special the next day.

I don’t think it’s any coincidence that he passed peacefully just after England had sealed victory.

Source: https://www.bbc.com/sport/cricket/45258754

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In SUBMITTED 3 Tags JOHN TAYLOR, PATRICK TAYLOR, JONATHAN AGNEW, TEST MATCH SPECIAL, BBC, CRICKET, LETTER, FAN, FATHER, SON, LEUKEMIA, CANCER, COMA, TRANSCRIPT
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Dan Kennedy 1.jpg

for Daniel Kennedy: 'He was a true hero to us all', by Sean Dooley - 2005

March 14, 2018

4 July 2005, Leongatha, Victoria, Australia

Daniel Kennedy was born in Barham NSW, second child to Pam and Peter, on the 18th of October 1983. 1983. The 80s weren’t that long ago— I’ve still got shirts from then. I think I’m wearing one now. Normally at a funeral the person you’ve come to farewell was usually born in the 1920s or 30s. There is a whole life that has been lived that we can celebrate. Dan’s life was only just beginning. This shouldn’t have been the whole story. It just seems so wrong.

Dan Kennedy was a remarkable person. Now I’m only a second cousin and probably most of you here knew him a hell of a lot better than I did. But even though I rarely saw Dan more than a couple of times a year there are few people that have made a bigger impression on me.

Over the past few days talking to those who loved him, it dawned on me that I wasn’t the only one to feel this way. And I am not the only one who feels so ripped off that Dan has gone. But this is not the sort of attitude that he lived his life by. I’m sure he had his moments of despair and self-pity like the rest of us but the Dan Kennedy that we all knew wouldn’t have dwelled on the negative stuff for too long; he would be out there trying to make the best of things, to make the most out of what we’ve got. Dan took whatever life threw at him head on; he didn’t have time for making a fuss. He didn’t want fanfares, he never asked for anyone’s pity. He just wanted to get on with living.

And he was always this way. As a baby Dan basically skipped walking. By the age of 9 months the family had moved to Tarra Valley and later, Toora, and Dan went from crawling straight to running. At first it was chasing after his big sister Melissa, and then later, running from his little sister Amanda. And he didn’t really stop running, as was evident by the number of accidents he had as kid: running into a fence and damaging his front teeth, running through another fence—barbed wire this time— and straight into a dam where he almost drowned himself. It was amazing he even made it to Toora Primary school at all.

But he didn’t stop running then. Pam would send Dan off with his lunch every morning and every afternoon it would come home in his bag untouched. Not that he didn’t like the sandwiches she made, just that he was so busy running around at lunchtime that he never had time to eat it. Pam soon learned not to make tuna sandwiches, or anything that would go off after sitting in a school bag all day.

For those of you who knew Dan only in the last few years when the leukemia and the complications of the treatment had ravaged his body, it may come as a surprise that Dan was an outstanding junior sportsman. Following the influence of Pam and Peter, Dan was into virtually every sport going. Little Athletics was his first competitive sport, but he also excelled at basketball, footy, cricket and word is he had the strongest throwing arm in the district. He won a number of athletic events at regional competitions and placed in a few at state level. Dan represented the Alberton Football League in the under 13 & 15 teams, made the representative sides for basketball and cricket and in 1998-99 won the “Dean Jones Alberton Junior Cricket Association Player of the Year.”

He not only played with the Toora Under 16s cricket team for seven years, but being a small town, often the adult teams were a few blokes short and Dan was more than willing to fill the breach. Pam remembers Dan filling in for the senior team when he was eleven. The ground was a cow paddock in the off season and the mongrels made him field down at fine leg amongst all the divots and everything else. Not the easiest surface to pick which way the ball would bounce. By the end of the days play Dan had more divots in him than the cow paddock. It was around this time that at a game played at Tarwin when they were again short of numbers. Dan trotted out onto the field to fill in and following was his six-year-old, three-foot-high sister, Amanda. It was a scorcher of a day and a number of the older boys were feeling the heat and had to leave the field. Not those two idiot Kennedy kids, they stayed out under the blazing sun the entire day.

In February 1999 the family moved to Leongatha as all the kids were attending Mary McKillop College. Dan joined the Leongatha Football Club and commenced playing on the U16 team.  During a match towards the end of June he kicked a goal as the half-time siren sounded. As the huddle formed it was realised that Daniel was nowhere to be found. He was still lying where he had kicked the goal, unable to move as he had torn his hamstring. Little did anyone know that this would be the last time Dan would play footy.

In August 1999 Dan didn’t seem himself.  A trip to the doctor ensued. Blood tests were taken and results came through at 10pm that night.  Midnight saw Dan at the Royal Children’s Hospital which was to become his second home for the next six years particularly Ward 6 East. Dan’s footy and cricket days were over. But he didn’t let that get him down, merely turning the same tenacity he showed on the sporting field to dealing with his disease. At times the treatment seemed worse than the cancer but Dan never allowed his spirit to remain unbowed for very long. The horror of what he went through never changed who he was. For instance, he hated using his mopep. A mopep is a small blower that he needed for clearing the gunk from his lungs. Dan didn’t think he needed to use it but the physios insisted. He usually managed to wangle his way out of it by distracting the physios—chatting with them, cracking as many jokes as he could so that by the end of the session he hadn’t got around to doing his exercises.

For six years Dan was in and out of hospital and it’s just impossible to imagine what he had to go through. And as strong and resolute as Dan was he wouldn’t have been able to fight as well as he did without the unbelievable support of his family. Pam, Peter, Melissa, Amanda, his grandparents Jan and Tarz and I’m sure many others that I don’t know about provided the most sensational support crew and were the strength Dan needed when he’d used up his own reserves. Amanda even went the extra step when in 2003 Dan relapsed and it became apparent that he needed a bone marrow transplant and she volunteered to be the donor. Some families would break under such strain, not this one. They not only continued to love and support each other but were able to help Dan live as normal and productive a life as possible in the times he was out of the hospital.

The leukemia didn’t totally spell the end of Dan’s sporting days. In remission he was well enough to take up lawn bowls and was soon playing pennant at Toora and actually skipped a Division 5 rink at Corinella soon after.  The highlight for him was making it into the final of the ‘100 up’, which he played against his father, Peter.  He was unsuccessful at his first attempt but turned the tables 3 yrs later at Leongatha when he got to beat Peter in the 100 up final. Now his old man might try and claim he was playing dead that day but I wouldn’t be believing it.

With treatment started in preparation for his bone marrow transplant, the bowls pennant finals were nearing and Dan was hoping he would be well enough on the day to play.  As it turned out he was too sick to compete but someone up there must have been in his corner because that day the rain and hail came down by the bucket load and with the green underwater the match was postponed to the next Saturday, by which time Dan was fit enough to play and they went on to have a memorable win.

Though he had an incredible struggle, and several times we all thought we’d lost him, Dan kept on fighting and making the most of the times when he was well. When he first started treatment he used to come down to our place at Patterson Lakes to go fishing with my Dad who was also undergoing cancer treatment. Though there was a fifty year age gap, Dan and Baz really bonded as they reeled in bream after bream after bream. Later when asked by the ‘Make a Wish’ Foundation what he would like to do for his wish he chose a trip to Cairns, deep sea fishing where he caught a nice 3-and-a-half foot shark and a couple of large Coral Trout.  He was still speaking of that trip the week before he died.

Another habit I think he might have picked up from my old man was a love of the races. Sick of running down to place his bets at the TAB, Pam soon set up a telephone account for Dan. He was so good at the caper that he soon had the nurses and doctors and even the hospital chaplain coming to him for tips. Even in the intensive care unit he had a form guide by his side. Once Dan turned 18 he gained a membership at Stony Creek Race Club and would attend as many meetings as possible with Rex, Coral & Mook, summoned to pick him up and deliver him home.

Dan was an avid Carlton fan. No one is exactly sure why Dan chose to barrack for Carlton— Peter is a Bulldogs supporter and his Mum goes for Melbourne. But typically, Dan chose his own path. It was as if he didn’t want to take sides and that too was typical of Dan. Always fair and considerate of others, the last thing he ever wanted to do was cause a fuss.

But last year we did get to make a fuss over Dan. The family had to twist his arm but for those of us lucky enough to attend Dan’s twenty-first, it was an incredible experience. It was a real celebration of life and I know that it meant the world to Dan and he felt it was the best thing he had ever done. Having his 21st allowed Dan to reconnect with some of his mates from school and for the past year he felt like he was back involved in real life, one that didn’t involve hospitals and needles and isolation units.

And then came the infection that led him to hospital for the last time. He was going to have some of his toes amputated but Dan dealt with it in typical fashion. I spoke to him just after he’d gone in and within minutes we were joking about how toes were over-rated anyway. He was like that right up to the end. Solid, unflappable, going about what he had to do with as little fuss as possible. But I reckon just like his twenty-first, he wouldn’t mind the fuss we are making today. It’s so good to see so many people here who like me feel blessed just for having the chance to know such a wonderful person as Dan Kennedy.

Sure, he wasn’t here for anywhere near long enough but the way he lived his life, rose to meet every adversity with grace and courage and acceptance, is an inspiration. In just twenty-one years he showed us all how to go about living. As Peter and Pam said to me, he was a true hero to us all. And you can’t argue with that.

Goodbye Dan.

 

 

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In SUBMITTED 3 Tags DANIEL KENNEDY, SEAN DOOLEY, FOOTY, LEUKEMIA, CANCER, TRANSCRIPT, LEONGATHA, COUNTRY VICTORIA, COUSIN
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Neil Dunlop 2.jpg

For Neill Dunlop: This is all too soon', by daughter Sally Brincat - 2015

August 15, 2017

21 August 2015, Melbourne, Australia

To my darling Dad, This is all too soon.

I know you didn't want fanfare or photos or fuss, and I hope you will forgive us for doing it anyway. Your life and your adventures deserve to be celebrated. You spent most of your life giving to others and today we give back to you the love and kindness you have shown to us over your life. You touched many people Dad, and today and for the days to come we will remember that.

We miss you terribly. You gave me courage and tenacity (or is that stubbornness?) and you did what great fathers do - you taught me that I could do anything.

I know you were as proud of me as I was to call you my Dad. You were a fantastic father-in-law and grandfather to Lucas and Eden and your little princess will grow up knowing you through our memories of you (and some pretty funny videos we have of the two of you being cheeky together). She's been talking to you on the phone the last few days and telling you about her adventures. I hope she keeps doing that Dad, because she adored you, just like we did. We'll keep making her Vegemite toast just like Grandpa used to.

The blossom trees have bloomed in the week you've been gone and they will forever remind me of you. We are in a million bits. Who will call me 'buttons' now? I love you to the moon and back.

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In SUBMITTED 2 Tags SALLY BRINCAT, EULOGY, TRANSCRIPT, FATHER, DAUGHTER, LOVE, CANCER, NEILL DUNLOP
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for Shelli Whitehurst: 'She bitch-slapped cancer so hard', by Wendy Hargreaves - 2017

July 30, 2017

28 July 2017, Elsternwick, Melbourne, Australia

My first glimpse of Shelli Whitehurst was through a crowd of freeloaders at a restaurant launch here in Melbourne. Shelli was holding court with a huddle of listeners.

Melbourne’s queen of social media was in the house.

I was with the old-school journos on the other side of the room. Back then, there was always a line in the sand… bloggers and journos never mixed.

But I was drawn to Shelli like a moth to a flame – like all of you.

There was this energy about her. It almost fizzed over. And if she allowed you into her orbit, you got a big fat dose of that energy, and then some.

Even on her darkest days, Shelli impacted the world. She was like a magic pill for any problem in her path.

Shelli’s amazing surgeon Chantel Thornton nailed it with this comment:

“Sometimes people enter our lives that will change the way we think. Michelle Whitehurst was one of those women – a woman of integrity, enormous courage and incredible tenacity for life. I have been privileged to be a part of your medical team.”

I have to agree. It really was a privilege to know Shelli… to be one of her people.
She loved introducing us to each other, and making magic happen.

Just ask Jenny and Chris… introduced by Shelli and now engaged to be married over in Shelli’s spiritual home, the U.S of A. Or Marty and Adam – not a romantic coupling, but brought together by Shelli to open the ridiculously successful South Press in Toorak Rd.

And let’s not forget Shelli’s other magic superpower - problem solving. I’ve lost count of the number of times Shelli pulled my head out of arse in times of strife and gave me a plan. And I know I’m not alone.

Shelli’s wonderful cousin Brendan and his partner Dean won’t mind me telling you that Shelli pushed and shoved them into following their hearts to start a new business (For My Petz in Yarraville… if you have fur babies, it’s fabbo).

Shelli had a gift for making lists and getting shit done. I’m sure many of you have been bossed around by Shelli. She’s given me so much hell for faffing about. There were never any excuses. World domination or don’t bother.

Ask Kimberlee Wells, a friend from Shelli’s advertising days. She said:

“We had big dreams of world domination. Kept the walls coloured with post-it notes. Had the private jet on order. Drank only in large format. And laughed and loved for more than 20 years. Shelli’s kindness and impact had no boundaries. And now, nor does her spirit.”

There were similar sentiments from Shelli’s biggest hero, New York advertising guru Cindy Gallup, who sent me a message saying Shelli would be kicking ass in heaven as much as she kicked ass here.

Shelli lived large and played hard, with a charisma that demanded attention.

Shelli was fierce, and nobody’s fool. And she knew how to enjoy life.

Like when she went for a foot massage with her mate Teela in Atlanta. Shelli enjoyed it so much that she ordered her masseur to start over again. And she wasn’t joking.

Others tell of Shelli’s antics in sparkly Minnie Mouse ears at SXSW, or hitting New York in her Tiffany & Co Nikes in the robin egg blue colour she loved so much.

Melissa remembers a 6pm dinner date with Shelli at Di Stasio, only drawing breath at midnight when the waiters turned the lights out. Those men in white jackets had been politely polishing glasses for at least an hour before hitting the lights.

That was how Shelli rolled. Deep communication was her jam.

When she was planning a visit to her dear friend Tom Miale in New York a few years ago, she got the ball rolling by demanding he cook a fancy meal. It became a running joke. She’d say stuff like… "Tom, I won't be happy unless there is a parade of shirtless men constantly pouring me bubbles.” When it came time to choose a meal, Shelli chose a much simpler affair - steak.

This is how Tom tells the story:

“Shelli arrived at home with bearing gifts for all - toys for my two children and about $200 worth of gourmet cheese for my wife and I. She said ‘I couldn't choose, so I bought all the cheese at the shop’. After a simple meal with some good wine, and loads of cheese, I asked her why she chose something as simple as steak for dinner. "She said, ‘I'm tired of the fancy stuff. Tonight, I need a meat-and-potato meal with a family’. To me, that interaction was who Shelli was. She appreciated the good stuff, she was always the life of the party, she loved to jet-set around the world, she never turned down an invitation to a fancy restaurant, but at her core she was most happy having simple, intimate interactions with friends and family. I can honestly say that I don't know anyone else that had as many close friends and family all over the world.”

If Shelli called you a friend, she’d give and give and give. Then she’d give some more. She even turned her cancer diagnosis into an act of giving, helping countless others with the extraordinary Kit for Cancer.

And she gives hope with her clever catch cries – like that amazing line broken crayons still colour. Shelli’s communication skills were legendary.

And she was always coming up with big ideas, more recently at 2 or 3 in the morning while talking to a dozen of her insomniac mates at once on Messenger.

Her notebooks bulged with them, and some were on the cheeky side, like the phone app called “Plus One” she plotted with a certain top restaurateur about town… a portal to hook up single professionals with hot and suitably sophisticated plus-ones so they never have to turn up anywhere alone (and no, it wasn’t an escort agency, but if things got saucy, the customers were all grown ups).

Shelli’s latest project, Because We Can, was all about generosity, sharing cool stuff and celebrating joyfulness with her connections around the world.

Wouldn’t it be a wonderful if Shelli’s global network continued disrupting shit on her behalf?
If you’re lucky enough to be one of Shelli’s people, it’s now your job to stay connected and dream big. And more importantly… don’t be scared to fail.

She gave this lesson to my teenage daughters Vivienne and Lauren, sneaking away for secret conversations on the importance of big dreams and open hearts. My girls loved her like an aunty, and have promised to make her proud.

On one of my many insomniac chats with Shelli on Messenger, she made me promise to make today’s send-off about her good bits – not dwelling on cancer.

Turns out, she asked the same of her friend Marty, who said:
“Shelli wanted me to make sure that we all didn’t remember her as a sick person, but as someone who was an entrepreneur, someone who was witty, someone who was successful and someone who was an incredible amount of fun. Shelli was every one of these before she was sick but more importantly she was all of these while she was sick.

"I don’t know of anyone else who would make their sickness into one of her projects, to ensure that no one would go through it like her.

"This in itself speaks of her courage and strength to always reach for the stars, knowing that when she got there it may benefit others more than her. This is why her legacy will live on.”

Beautiful words Marty.

Shelli will be all of those things and more, for those who knew her, and for a whole heap of people who didn’t.

To Betty and Don… I hope these words help you understand the sheer size of the huge tsunami of love out there for your beautiful daughter.

Finally, let me quote another one of Shelli’s US friends, Jeff Loya. I’ve followed Shelli’s wishes and avoided the dreaded C word for most of this eulogy, but I can’t resist this quote:

“She didn’t die from cancer. She bitch-slapped cancer so hard, it will think twice about entering another human”.

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In SUBMITTED 2 Tags SHELLI WHITEHURST, FRIEND, WENDY HARGREAVES, CANCER
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For Elizabeth Joan Buddle (Betty): 'I am in awe of the way Betty conducted her life', by husband Roger Buddle - 2016

August 8, 2016

6 June 2016, Mount Barker, South Australia

Betty was born Elizabeth Joan Collins on December 1st, 1942 at the Queen Victoria Maternity Hospital, Rose Park, South Australia.  Her parents were Gilbert Roland Collins and Elsie Vera Collins who lived at 68 First Avenue, Nailsworth. Betty was the youngest of seven children and her six siblings were Mervyn, Beryl, Alan, Hazel, Marjorie and Kevin.

She entered the world feet first by breech birth and, given the state of the world in December 1942, maybe she was reluctant to join it – or maybe she wanted to hit the ground running, which was the way she mostly led the next 73 years of her life.

Almost from the very start she was known as Betty and that name stuck, although in later life she much preferred her full name of Elizabeth on formal occasions. Betty’s mother was a chronic invalid and a large amount of her early upbringing was by her two closest sisters, Hazel and Marjorie.

Betty attended Nailsworth Primary School from 1947 to 1954 and Adelaide Girls High School from 1955 to 1958, when she matriculated with her Leaving Certificate. After leaving school she worked as a Drafting Assistant at the SA Lands Titles Office.

I started work as a Technician-in-Training with the then Post Master General’s Department in 1957. There I met another trainee, Kevin Collins – Betty’s brother. Sometimes I would visit Kevin at home when we were studying for exams and that is how I met Betty. At that time she was still at Adelaide High and she told me years later that if she saw my car parked in front of her house as she was coming up the street on her way home from school, she would run all the way home in case I left before she got there. That accounted for her always being breathless and bright-eyed as she hung around annoying Kevin and me while we tried to study. A couple of years later I plucked up the courage to ask her out and we started courting.

One thing led to another and on August 6th, 1960 we were married at the Broadview Methodist Church. Our honeymoon was spent at Encounter Bay.

At first we lived with Betty’s sister and brother-in-law, Hazel and Ian Lovett, at Enfield and then we rented a house at Evandale while our new home was being built at 4 Farm Drive, Redwood Park. Meanwhile Catherine had been born. We moved into our new home in January 1962. Things were very tough financially and, having sold our car to raise the deposit on the house, our transport was a motorbike and then we upgraded to a motorbike and sidecar.

In those days Redwood Park was on the outer fringes of the metropolitan area with very few services or shops. Betty used to trek the six kilometres return trip to the Tea Tree Gully post office, pushing the pram, to get the monthly child endowment allowance.

Our second child, Noelene, was born in January 1964 and then Steven in September 1966. The children attended the Kathleen Mellor kindergarten in Tea Tree Gully and Betty was involved in managing the kindergarten op shop. She was also active in the Ridgehaven Primary School parent’s activities while the children were there.

In 1969 I came home from work one day to the news that Betty had seen an advertisement in the paper for a canteen assistant at the Blacks Road drive-in at Gilles Plains and she had applied for and got the job. Getting to the interview for the job had involved catching the bus into Adelaide, joining a large queue of job applicants and dragging the pusher, with Steven in it, up a flight of stairs to the office. She worked at the drive-in from 1969 to 1971 and became expert in making hamburgers, nut sundaes and banana splits.

It wasn’t long before she saw another ad for interviewers for a sport and recreation survey for the proposed Monarto satellite city. She got that job, undertook the training and completed the survey work. That led to her being employed part time as a population survey interviewer with the Bureau of Census and Statistics. She worked in that position from 1973 to 1976.

Those jobs involved interviewing randomly chosen people in their homes to gather statistics on unemployment and other domestic matters. She soon realised that she had a natural ability to listen and relate to people as they opened up to her about things that had nothing whatsoever to do with the questions in the survey.

Anyone who has had a conversation with Betty will know what I mean.

So she undertook an aptitude test with a career advisor and was told that she was suited to being either a teacher or a social worker. Luckily she chose social worker and it wasn’t long before she saw yet another ad in the paper for a cadetship with the Department for Community Welfare to study full time for the Associate Diploma of Social Work at the South Australian Institute of Technology, which is now the University of South Australia. She commenced her study in 1976 and gained her Diploma at the end of 1977.

She then worked as a Community Welfare Worker at the Elizabeth office of the Department for Community Welfare, which she described as a baptism by fire. She worked there for three and a half years from 1978 to 1981 and during that time she discovered she had a talent for helping young girls and women who were victims of abuse, both physical and sexual.

This led to her applying for the position of Social Worker at the newly formed Sexual Assault Referral Centre at The Queen Elizabeth Hospital, Woodville. This was an initiative of Dr Aileen Connon and the centre initially had a staff of three – a doctor, a nurse and a social worker and liaison with the police sexual assault unit.

At first the Centre was located in the old child care building at the hospital, then later it moved to a floor in the nurses quarters and gained additional professional and support staff.

While working there Betty studied part time for her Bachelor of Social Work at the University of South Australia and graduated with her degree in 1988. She also undertook post graduate study, and in 1994 gained her Graduate Diploma of Education, Adult Training.

This all sounds very clinical when presented in a chronological fashion like this, but we need to realise that all this was achieved while Betty was holding a husband and three children together as a loving family. Driving through traffic from Redwood Park to Woodville every day, then listening to absolutely horrible and ghastly things that had happened to her clients and then driving home to cook dinner and nurture her family in the evening (which included helping with homework). In 1975 she even did it on her own while I was working in Sydney for three months.

As she gained experience in her profession she developed a model for helping victims of sexual assault through their trauma and pain. She wrote a paper on her method and called it Simple Things that Work.

In 1986 she was invited to present her paper to The First International Symposium on Rape in Jerusalem and she travelled there alone to speak at the symposium. It was the first time she had gone overseas.

Then, in 1987, she travelled to San Francisco to present her work to a conference on trauma recovery.

In 1989 her work was published in the International Journal of Medicine and Law.

After fifteen years of working in this field, listening to things every working day that nobody should have to hear, her body was starting to break down. Her health was suffering both physically and psychologically and she needed to get out. Finally she was granted retirement on grounds of ill health and she was able to start to regain her health and equilibrium.

On retirement Betty enjoyed her gardening, travel, our grandchildren - and then croquet took over. She became treasurer of the Victor Harbor Croquet Club and was responsible for gaining many thousands of dollars in grants for equipment and facility upgrades.

I am in awe of the way Betty conducted her life. She was constantly optimistic and cheerful. She could always find good in people, but by the same token she would not suffer fools lightly. She was the glue of our marriage and she tolerated my many faults and shortcomings with loving understanding. She loved our three children without reservation and absolutely adored our five grandchildren.

After she became ill with cancer she spent a lot of the last eighteen months educating me in subtle and not so subtle ways on how to survive when she was gone. She taught me to cook (well, she tried), she labelled everything, she made me recite where things are kept, she made lists and generally handed me the reins.

Betty was a unique and wonderful person. Her infectious laugh, her sparkling eyes. She was an amazing wife, companion, friend, mother and grandmother.

Coupled with this is the legacy that she has left of all the lives she has touched, and in some cases saved, of both women and men, through her work in sexual assault counselling. Going through her papers I came across many letters and cards from people who she helped regain control of their lives. A quote from just one:-

I wanted to tell you about all the good things that have come from our sessions together but I find that I am a bit lost for words when I try to thank you. To have met you has been a privilege. You are an amazing person! To think back to some of the things that you said makes me feel in awe of you… you have incredible depth and sensitivity. You are courageous: able to look Hell in the face and to venture into places that may not be safe.  

Lastly, Betty made me promise that when I wrote this I would leave you laughing so here goes…

Some time ago, before she became ill, Betty went to the chemist to get a prescription filled for my anti-reflux tablets. Unknowingly she had picked up my prescription for Viagra instead.

When she returned to the chemist later to pick up the prescription the assistant handed her the box of pills and said “That will be seventy six dollars.”

Betty said “What!, they’re not usually that dear!”

The assistant said “No, that’s the correct price.”

Betty, waving the box of Viagra above her head for all the other customers to see said “Oh well, I don’t care how much they cost as long as they do the job!”.

I loved her so much.

This is an excerpt from a poem by Leonard Cohen

A Thousand Kisses Deep

I’m good at love, I’m good at hate
It’s in between I freeze
Been working out but its too late
(Its been too late for years)
But you look good, you really do
They love you on the street
If you were here I’d kneel for you
A thousand kisses deep
The autumn moved across your skin
Got something in my eye
A light that doesn’t need to live
And doesn’t need to die
A riddle in the book of love
Obscure and obsolete
And witnessed here in time and blood
A thousand kisses deep

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In SUBMITTED 2 Tags ROGER BUDDLE, BETTY BUDDLE, ELIZABETH BUDDLE, HUSBAND, WIFE, CANCER, BIOGRAPHY
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For Steve Jobs: 'Steve always aspired to make beautiful later', by sister Mona Simpson - 2011

April 16, 2016

16 October 2011, Memorial Church of Stanford University, San Francisco, USA

There is no audio or video of this speech

I grew up as an only child, with a single mother. Because we were poor and because I knew my father had emigrated from Syria, I imagined he looked like Omar Sharif. I hoped he would be rich and kind and would come into our lives (and our not yet furnished apartment) and help us. Later, after I’d met my father, I tried to believe he’d changed his number and left no forwarding address because he was an idealistic revolutionary, plotting a new world for the Arab people.

Even as a feminist, my whole life I’d been waiting for a man to love, who could love me. For decades, I’d thought that man would be my father. When I was 25, I met that man and he was my brother.

By then, I lived in New York, where I was trying to write my first novel. I had a job at a small magazine in an office the size of a closet, with three other aspiring writers. When one day a lawyer called me – me, the middle-class girl from California who hassled the boss to buy us health insurance – and said his client was rich and famous and was my long-lost brother, the young editors went wild. This was 1985 and we worked at a cutting-edge literary magazine, but I’d fallen into the plot of a Dickens novel and really, we all loved those best. The lawyer refused to tell me my brother’s name and my colleagues started a betting pool. The leading candidate: John Travolta. I secretly hoped for a literary descendant of Henry James – someone more talented than I, someone brilliant without even trying.

When I met Steve, he was a guy my age in jeans, Arab- or Jewish-looking and handsomer than Omar Sharif.

We took a long walk – something, it happened, that we both liked to do. I don’t remember much of what we said that first day, only that he felt like someone I’d pick to be a friend. He explained that he worked in computers.

I didn’t know much about computers. I still worked on a manual Olivetti typewriter.
I told Steve I’d recently considered my first purchase of a computer: something called the Cromemco.

Steve told me it was a good thing I’d waited. He said he was making something that was going to be insanely beautiful.

I want to tell you a few things I learned from Steve, during three distinct periods, over the 27 years I knew him. They’re not periods of years, but of states of being. His full life. His illness. His dying.

Steve worked at what he loved. He worked really hard. Every day.

That’s incredibly simple, but true.

He was the opposite of absent-minded.

He was never embarrassed about working hard, even if the results were failures. If someone as smart as Steve wasn’t ashamed to admit trying, maybe I didn’t have to be.

When he got kicked out of Apple, things were painful. He told me about a dinner at which 500 Silicon Valley leaders met the then-sitting president. Steve hadn’t been invited.

He was hurt but he still went to work at Next. Every single day.

Novelty was not Steve’s highest value. Beauty was.

For an innovator, Steve was remarkably loyal. If he loved a shirt, he’d order 10 or 100 of them. In the Palo Alto house, there are probably enough black cotton turtlenecks for everyone in this church.

He didn’t favor trends or gimmicks. He liked people his own age.

His philosophy of aesthetics reminds me of a quote that went something like this: “Fashion is what seems beautiful now but looks ugly later; art can be ugly at first but it becomes beautiful later.”

Steve always aspired to make beautiful later.

He was willing to be misunderstood.

Uninvited to the ball, he drove the third or fourth iteration of his same black sports car to Next, where he and his team were quietly inventing the platform on which Tim Berners-Lee would write the program for the World Wide Web.

Steve was like a girl in the amount of time he spent talking about love. Love was his supreme virtue, his god of gods. He tracked and worried about the romantic lives of the people working with him.

Whenever he saw a man he thought a woman might find dashing, he called out, “Hey are you single? Do you wanna come to dinner with my sister?”

I remember when he phoned the day he met Laurene. “There’s this beautiful woman and she’s really smart and she has this dog and I’m going to marry her.”

When Reed was born, he began gushing and never stopped. He was a physical dad, with each of his children. He fretted over Lisa’s boyfriends and Erin’s travel and skirt lengths and Eve’s safety around the horses she adored.

None of us who attended Reed’s graduation party will ever forget the scene of Reed and Steve slow dancing.

His abiding love for Laurene sustained him. He believed that love happened all the time, everywhere. In that most important way, Steve was never ironic, never cynical, never pessimistic. I try to learn from that, still.

Steve had been successful at a young age, and he felt that had isolated him. Most of the choices he made from the time I knew him were designed to dissolve the walls around him. A middle-class boy from Los Altos, he fell in love with a middle-class girl from New Jersey. It was important to both of them to raise Lisa, Reed, Erin and Eve as grounded, normal children. Their house didn’t intimidate with art or polish; in fact, for many of the first years I knew Steve and Lo together, dinner was served on the grass, and sometimes consisted of just one vegetable. Lots of that one vegetable. But one. Broccoli. In season. Simply prepared. With just the right, recently snipped, herb.

Even as a young millionaire, Steve always picked me up at the airport. He’d be standing there in his jeans. When a family member called him at work, his secretary Linetta answered, “Your dad’s in a meeting. Would you like me to interrupt him?”

When Reed insisted on dressing up as a witch every Halloween, Steve, Laurene, Erin and Eve all went wiccan.

They once embarked on a kitchen remodel; it took years. They cooked on a hotplate in the garage. The Pixar building, under construction during the same period, finished in half the time. And that was it for the Palo Alto house. The bathrooms stayed old. But – and this was a crucial distinction – it had been a great house to start with; Steve saw to that.

This is not to say that he didn’t enjoy his success: he enjoyed his success a lot, just minus a few zeros. He told me how much he loved going to the Palo Alto bike store and gleefully realizing he could afford to buy the best bike there.

And he did.

Steve was humble. Steve liked to keep learning.

Once, he told me if he’d grown up differently, he might have become a mathematician. He spoke reverently about colleges and loved walking around the Stanford campus. In the last year of his life, he studied a book of paintings by Mark Rothko, an artist he hadn’t known about before, thinking of what could inspire people on the walls of a future Apple campus.

Steve cultivated whimsy. What other C.E.O. knows the history of English and Chinese tea roses and has a favorite David Austin rose?

He had surprises tucked in all his pockets. I’ll venture that Laurene will discover treats – songs he loved, a poem he cut out and put in a drawer – even after 20 years of an exceptionally close marriage. I spoke to him every other day or so, but when I opened The New York Times and saw a feature on the company’s patents, I was still surprised and delighted to see a sketch for a perfect staircase.

With his four children, with his wife, with all of us, Steve had a lot of fun.

He treasured happiness.

Then, Steve became ill and we watched his life compress into a smaller circle. Once, he’d loved walking through Paris. He’d discovered a small handmade soba shop in Kyoto. He downhill skied gracefully. He cross-country skied clumsily. No more.

Eventually, even ordinary pleasures, like a good peach, no longer appealed to him.

Yet, what amazed me, and what I learned from his illness, was how much was still left after so much had been taken away.

I remember my brother learning to walk again, with a chair. After his liver transplant, once a day he would get up on legs that seemed too thin to bear him, arms pitched to the chair back. He’d push that chair down the Memphis hospital corridor towards the nursing station and then he’d sit down on the chair, rest, turn around and walk back again. He counted his steps and, each day, pressed a little farther.

Laurene got down on her knees and looked into his eyes.

“You can do this, Steve,” she said. His eyes widened. His lips pressed into each other.
He tried. He always, always tried, and always with love at the core of that effort. He was an intensely emotional man.

I realized during that terrifying time that Steve was not enduring the pain for himself. He set destinations: his son Reed’s graduation from high school, his daughter Erin’s trip to Kyoto, the launching of a boat he was building on which he planned to take his family around the world and where he hoped he and Laurene would someday retire.

Even ill, his taste, his discrimination and his judgment held. He went through 67 nurses before finding kindred spirits and then he completely trusted the three who stayed with him to the end. Tracy. Arturo. Elham.

One time when Steve had contracted a tenacious pneumonia his doctor forbid everything – even ice. We were in a standard I.C.U. unit. Steve, who generally disliked cutting in line or dropping his own name, confessed that this once, he’d like to be treated a little specially.

I told him: Steve, this is special treatment.

He leaned over to me, and said: “I want it to be a little more special.”

Intubated, when he couldn’t talk, he asked for a notepad. He sketched devices to hold an iPad in a hospital bed. He designed new fluid monitors and x-ray equipment. He redrew that not-quite-special-enough hospital unit. And every time his wife walked into the room, I watched his smile remake itself on his face.
For the really big, big things, you have to trust me, he wrote on his sketchpad. He looked up. You have to.

By that, he meant that we should disobey the doctors and give him a piece of ice.

None of us knows for certain how long we’ll be here. On Steve’s better days, even in the last year, he embarked upon projects and elicited promises from his friends at Apple to finish them. Some boat builders in the Netherlands have a gorgeous stainless steel hull ready to be covered with the finishing wood. His three daughters remain unmarried, his two youngest still girls, and he’d wanted to walk them down the aisle as he’d walked me the day of my wedding.

We all – in the end – die in medias res. In the middle of a story. Of many stories.

I suppose it’s not quite accurate to call the death of someone who lived with cancer for years unexpected, but Steve’s death was unexpected for us.

What I learned from my brother’s death was that character is essential: What he was, was how he died. Tuesday morning, he called me to ask me to hurry up to Palo Alto. His tone was affectionate, dear, loving, but like someone whose luggage was already strapped onto the vehicle, who was already on the beginning of his journey, even as he was sorry, truly deeply sorry, to be leaving us.

He started his farewell and I stopped him. I said, “Wait. I’m coming. I’m in a taxi to the airport. I’ll be there.”

“I’m telling you now because I’m afraid you won’t make it on time, honey.”

When I arrived, he and his Laurene were joking together like partners who’d lived and worked together every day of their lives. He looked into his children’s eyes as if he couldn’t unlock his gaze.

Until about 2 in the afternoon, his wife could rouse him, to talk to his friends from Apple.

Then, after awhile, it was clear that he would no longer wake to us.

His breathing changed. It became severe, deliberate, purposeful. I could feel him counting his steps again, pushing farther than before.

This is what I learned: he was working at this, too. Death didn’t happen to Steve, he achieved it.

He told me, when he was saying goodbye and telling me he was sorry, so sorry we wouldn’t be able to be old together as we’d always planned, that he was going to a better place.

Dr. Fischer gave him a 50/50 chance of making it through the night.

He made it through the night, Laurene next to him on the bed sometimes jerked up when there was a longer pause between his breaths. She and I looked at each other, then he would heave a deep breath and begin again.

This had to be done. Even now, he had a stern, still handsome profile, the profile of an absolutist, a romantic. His breath indicated an arduous journey, some steep path, altitude.

He seemed to be climbing.

But with that will, that work ethic, that strength, there was also sweet Steve’s capacity for wonderment, the artist’s belief in the ideal, the still more beautiful later.

Steve’s final words, hours earlier, were monosyllables, repeated three times.

Before embarking, he’d looked at his sister Patty, then for a long time at his children, then at his life’s partner, Laurene, and then over their shoulders past them.

Steve’s final words were:
OH WOW. OH WOW. OH WOW.

Source: http://www.nytimes.com/2011/10/30/opinion/...

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In EDITORS CHOICE Tags STEVE JOBS, MONA SIMPSON, SISTER, APPLE, CANCER, LAST WORDS, TRANSCRIPT
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For Jim Stynes: 'I love you Jim', by Garry Lyon - 2012

September 2, 2015

22 March, 2012, Channel 9, Melbourne, Australia

Jimmy Stynes was a giant in every sense of the word right from the very first moment I laid eyes on him.

It would be wrong to suggest we were close from Day 1, he was a novelty and for a 16-year-old kid from country Victoria he fulfilled all of my pre-conceived notions of what an Irishman should be - pale, lean and with an accent that was perfect for telling Irish jokes.

Beyond that I didn’t give him too much thought, my mind was captivated by the real footballers at our club, most notably the legendary Melbourne footy club figure Robbie Flower. He was the man I aspire to be.

How did it come to pass then that 27 years down the track, with the greatest respect to Robbie, that the Irish curiosity that I first encountered in the carpark outside of the MCG was to become, and will remain, the person that I judge and measure myself by?

With time and age or some form and degree of maturity comes perspective and I realize that life is more than just football and I now see the irony in that I was to become the leader of the football club and help set a standard for others to follow, all the while it was Jim who was doing the real leading and setting the real standard.

I see that with such clarity now. I didn’t then and it led to doubts about Jimmy.

Why was he not fanatical and obsessed like I was? Why did it appear that football was just a game to him when it was much more to me? Why could he smile an hour after a losing game whereas it took me a whole weekend to get over it?

Why did he not embrace the so-called 'manly elements’ of our game as enthusiastically as the next bloke where drinking beer and attracting girls was a badge of honour, worn as proudly as anything achieved on the playing field? Why could he be as passionate about the welfare of others outside of the club when I was predominantly obsessed with what happened solely within?

Jimmy refused to let the game define who he was. It was just a part of him and it allowed us to marvel at his determination, unwavering self-belief, resilience, strength, skill, endurance and courage.

Why was he so prepared to buck the system and explore an alternative path when the rest of us were so aligned to the one that had trod so rigidly for decades? Why did he not shy away from displaying his emotions where I saw it as a weakness to do so?

Why was he so fervently proud of his Irish heritage when I had barely given mine a second thought? Why was he so sensitive to issues of racial and religious tolerance, ahead of his time, while I was ignorantly part of the problem?

I thought he had it all wrong. What I now know to be true is that those doubts were less about Jim and more about myself, and I say that not self-consciously but with some degree of pride because it means that I’ve truly come to appreciate the man that Jim Stynes was and if that paints me in a lesser light then I’m fine with that because there are few that can compare to him.

Quite simply Jimmy refused to let the game define who he was. It was just a part of him and it allowed us to marvel at his determination, unwavering self-belief, resilience, strength, skill, endurance and courage. But he never let the game compromise what else he had going on in his life.

He showed me that you could be committed but not obsessive, the need to separate the playing field from the field of life, that you can gain satisfaction out of the contest regardless of the result, that you could enjoy the environment and male bonding that footy provided but always maintain a sensitivity to what is right and wrong, that you never get so tunnel visioned that you don’t recognise the needs of others, that you can be both passionate and ruthless in the pursuit of excellence.

He was secure enough to know that displaying vulnerability can be a strength and not a weakness.

So now he’s left us and it doesn’t feel right or fair in any way. I was honoured to have been able to spend some intimate time with him in the past few months and I’ll never forget those moments. We laughed more than we cried which as I’ve written about was consistent throughout our relationship.

I took a photo on one of the last occasions I sat with him and had the chance to say goodbye. It was deeply personal and highly symbolic of our 27-year friendship and it will serve as a constant reminder of him, what he stood for and how profound an impact he had on me, of just how right he got his 45 years.

The photo will sit on my wall at home and every time I look at it, I will think of the man that he was and the one I can only ever hope to be.

I love you Jim.

Source: https://www.youtube.com/watch?v=WNAn1b4NN0...

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In PUBLIC FIGURE A Tags GARRY LYON, JIM STYNES, AFL, AUSTRALIA, CANCER, FRIEND, TEAMMATE, TELEVISION
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