Former Origin star Gavin Allen in desperate need of a heart transplant

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Kaz

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FORMER Queensland State of Origin star Gavin Allen needs a heart transplant, and is currently being kept alive by an electric pump implanted in his chest.

When the Maroons gathered in camp this week for Origin I, familiar faces Cameron Smith, Johnathan Thurston, Matt Scott and Cooper Cronk were missing.

So, too, was long-time team manager Allen, who has spent most of the year in hospital, including three weeks in intensive care, after surgery to install an artificial heart known as a Ventricular Assistance Device to keep him alive.

Allen played in the Broncos’ 1992 premiership team as well as Queensland’s unforgettable 1995 Origin series clean-sweep.

Few played rugby league with more heart than Allen, now, ironically, it is his heart that has handed him his hardest battle.

Allen has familial cardiomyopathy, a hereditary condition where the heart increases in size, leading to abnormal heart function, progressive deterioration and ultimately failure.

He is now under the care of the Advanced Heart Failure and Cardiac Transplantation Service team led by Dr George Javorsky at Brisbane’s Prince Charles Hospital, while he awaits a donor heart.

His father Don, now 85, had the same condition and underwent a successful transplant 27 years ago.

Allen was diagnosed with cardiomyopathy about 18 months after playing his last season of league with the London Broncos in 1996, and has been on medication to maintain his heart ever since.

“I never thought it was something I would have. I actually thought I always had asthma,” Allen told The Sunday Mail.

“The biggest reason why I retired wasn’t because I stopped liking the game. It was just the training. I hated it, couldn’t stand it, because it just hurt all the time.”

As a professional footballer, Allen maintained a healthy lifestyle, but after his diagnosis he gave away alcohol to give his body the best chance of dealing with the condition.

But two years ago the effectiveness of the medication began to wear off and Allen, without even knowing it, was getting ready to die.

“I must have had a feeling, because I painted the house inside and out, fixed everything up around the place, restructured a few things at work, sold a few properties to tie up ends,” he said.

“This was all before I knew, so I must have just had this feeling. It was a weird thing.

“It wasn’t until November of last year where I was really struggling to even walk up the stairs.”

After a Christmas holiday in his home town of Cairns to try to rest, the 53-year-old was booked in for a “transplant work-up” on January 29 to begin testing to see if he could have a donor heart.

“I went home and a few weeks later, I just felt myself getting worse and worse,” he said. “I just got in the car and drove myself to the hospital and parked in the carpark. I had to stop four times to get to the front counter.

“George walked past and saw me, and said ‘don’t worry about reception, just come straight with me right now’. He was shocked looking at me. I told him I came in because I didn’t think I would last until the end of January.”

Complications, including bleeding from the operation to insert the VAD, a blood infection and a reaction to the antibiotics, have slowed Allen’s recovery as he gradually regains the strength and energy he will need for the transplant procedure.

“I spent three weeks in intensive care … I have never done anything that tough in all my life,” he said. “Kristina and the kids would come up to visit me, and they would be talking and I just couldn’t say a word out of my mouth.”

Allen is an intensely private person and was reluctant to go public with his health battle.

But former Queensland teammates Allan Langer and Trevor Gillmeister urged Allen to tell his story to The Sunday Mail to raise awareness of the importance of organ donation.

“The staff here at the Prince Charles Hospital have just been outstanding. I can’t speak highly enough of them,” he said. “Everything is so positive, and they could not be more supportive of everyone in here.

“The work they do is amazing, so I thought, if my story just gets people talking about organ donation and makes their jobs a bit easier, then it is worthwhile doing.

“Having seen Dad go through it makes it so much easier, because I know the difference it made to his life.

“There’s no stress from me at all. I feel so much better with the pump in now, much better than I did before, and I will feel better again when the transplant is done, whenever that may be.

“I am actually enjoying feeling not too bad, because I felt like crap for such a long time.”

MAKE TIME TO HAVE DONOR CONVERSATION

ONE of Queensland’s leading heart transplant specialists says the simple art of conversation is the key to increasing organ donation rates in Australia.

Last year 105 Queenslanders donated their organs after death, saving the life of nearly 300 Australians.

The average waiting time for a heart transplant is currently about six months.

Dr George Javorsky is director of the Advanced Heart Failure and Cardiac Transplantation Service at the Prince Charles Hospital, and says potential organ donors need to ensure their loved ones know about their decision to give the gift of life.

“The challenge in Australia is, because we have only 25 million people, we see about 80-100 hearts per year for the whole country,” Dr Javorsky said. “Compare that to the United States, where they have a population of about 350 million, they will see about 2500 hearts per year. In Australia we still have more patients needing transplants than we have donors and the waiting times for a suitable organ to become available are unpredictable.

“The No. 1 thing is for people who want to donate organs is have a conversation with their families. The next time people have a family get together, or a Sunday night dinner, they should just let everyone know what their intentions are.

“After that, they just have to go on to the website and register. But the conversation is so important because even if a person dies, the family can still say ‘we don’t want to do that’.

“When a family is in grief and in the intensive care unit of a hospital, they can say: ‘Yes, we have had the conversation, we understand that this is their wishes, and we are supportive of making sure their wishes are fulfilled’.”

The option to register organ donation on a person’s driver’s licence was abolished more than 12 years ago in favour of a national register that can be done online in two minutes.

To register, go to donatelife.gov.au

https://www.couriermail.com.au/spor...t/news-story/f0a784f4423f586d30f5ff45cf5455e0

I know it's 2 weeks late, but couldn't find a link as it's paywall.

If you haven't please register.

I registered years ago.

Don't know if my heart would be suitable, with 2 heart conditions, my other organs are.
 

Heckler

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FORMER Queensland State of Origin star Gavin Allen needs a heart transplant, and is currently being kept alive by an electric pump implanted in his chest.

When the Maroons gathered in camp this week for Origin I, familiar faces Cameron Smith, Johnathan Thurston, Matt Scott and Cooper Cronk were missing.

So, too, was long-time team manager Allen, who has spent most of the year in hospital, including three weeks in intensive care, after surgery to install an artificial heart known as a Ventricular Assistance Device to keep him alive.

Allen played in the Broncos’ 1992 premiership team as well as Queensland’s unforgettable 1995 Origin series clean-sweep.

Few played rugby league with more heart than Allen, now, ironically, it is his heart that has handed him his hardest battle.

Allen has familial cardiomyopathy, a hereditary condition where the heart increases in size, leading to abnormal heart function, progressive deterioration and ultimately failure.

He is now under the care of the Advanced Heart Failure and Cardiac Transplantation Service team led by Dr George Javorsky at Brisbane’s Prince Charles Hospital, while he awaits a donor heart.

His father Don, now 85, had the same condition and underwent a successful transplant 27 years ago.

Allen was diagnosed with cardiomyopathy about 18 months after playing his last season of league with the London Broncos in 1996, and has been on medication to maintain his heart ever since.

“I never thought it was something I would have. I actually thought I always had asthma,” Allen told The Sunday Mail.

“The biggest reason why I retired wasn’t because I stopped liking the game. It was just the training. I hated it, couldn’t stand it, because it just hurt all the time.”

As a professional footballer, Allen maintained a healthy lifestyle, but after his diagnosis he gave away alcohol to give his body the best chance of dealing with the condition.

But two years ago the effectiveness of the medication began to wear off and Allen, without even knowing it, was getting ready to die.

“I must have had a feeling, because I painted the house inside and out, fixed everything up around the place, restructured a few things at work, sold a few properties to tie up ends,” he said.

“This was all before I knew, so I must have just had this feeling. It was a weird thing.

“It wasn’t until November of last year where I was really struggling to even walk up the stairs.”

After a Christmas holiday in his home town of Cairns to try to rest, the 53-year-old was booked in for a “transplant work-up” on January 29 to begin testing to see if he could have a donor heart.

“I went home and a few weeks later, I just felt myself getting worse and worse,” he said. “I just got in the car and drove myself to the hospital and parked in the carpark. I had to stop four times to get to the front counter.

“George walked past and saw me, and said ‘don’t worry about reception, just come straight with me right now’. He was shocked looking at me. I told him I came in because I didn’t think I would last until the end of January.”

Complications, including bleeding from the operation to insert the VAD, a blood infection and a reaction to the antibiotics, have slowed Allen’s recovery as he gradually regains the strength and energy he will need for the transplant procedure.

“I spent three weeks in intensive care … I have never done anything that tough in all my life,” he said. “Kristina and the kids would come up to visit me, and they would be talking and I just couldn’t say a word out of my mouth.”

Allen is an intensely private person and was reluctant to go public with his health battle.

But former Queensland teammates Allan Langer and Trevor Gillmeister urged Allen to tell his story to The Sunday Mail to raise awareness of the importance of organ donation.

“The staff here at the Prince Charles Hospital have just been outstanding. I can’t speak highly enough of them,” he said. “Everything is so positive, and they could not be more supportive of everyone in here.

“The work they do is amazing, so I thought, if my story just gets people talking about organ donation and makes their jobs a bit easier, then it is worthwhile doing.

“Having seen Dad go through it makes it so much easier, because I know the difference it made to his life.

“There’s no stress from me at all. I feel so much better with the pump in now, much better than I did before, and I will feel better again when the transplant is done, whenever that may be.

“I am actually enjoying feeling not too bad, because I felt like crap for such a long time.”

MAKE TIME TO HAVE DONOR CONVERSATION

ONE of Queensland’s leading heart transplant specialists says the simple art of conversation is the key to increasing organ donation rates in Australia.

Last year 105 Queenslanders donated their organs after death, saving the life of nearly 300 Australians.

The average waiting time for a heart transplant is currently about six months.

Dr George Javorsky is director of the Advanced Heart Failure and Cardiac Transplantation Service at the Prince Charles Hospital, and says potential organ donors need to ensure their loved ones know about their decision to give the gift of life.

“The challenge in Australia is, because we have only 25 million people, we see about 80-100 hearts per year for the whole country,” Dr Javorsky said. “Compare that to the United States, where they have a population of about 350 million, they will see about 2500 hearts per year. In Australia we still have more patients needing transplants than we have donors and the waiting times for a suitable organ to become available are unpredictable.

“The No. 1 thing is for people who want to donate organs is have a conversation with their families. The next time people have a family get together, or a Sunday night dinner, they should just let everyone know what their intentions are.

“After that, they just have to go on to the website and register. But the conversation is so important because even if a person dies, the family can still say ‘we don’t want to do that’.

“When a family is in grief and in the intensive care unit of a hospital, they can say: ‘Yes, we have had the conversation, we understand that this is their wishes, and we are supportive of making sure their wishes are fulfilled’.”

The option to register organ donation on a person’s driver’s licence was abolished more than 12 years ago in favour of a national register that can be done online in two minutes.

To register, go to donatelife.gov.au

https://www.couriermail.com.au/spor...t/news-story/f0a784f4423f586d30f5ff45cf5455e0

I know it's 2 weeks late, but couldn't find a link as it's paywall.

If you haven't please register.

I registered years ago.

Don't know if my heart would be suitable, with 2 heart conditions, my other organs are.
Grest read. Good luck to him. I hope it works out well for him and his Family
 

CroydonDog

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Yeah, i'm registered. Agree on not knowing what of my organs would actually be suitable.

I think we should follow a lot of other countries in adopting an opt out system. Make organ donor-ship the "norm". In some places that have adopted this practice, waiting lists have plummeted.
 

Kaz

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Yeah, i'm registered. Agree on not knowing what of my organs would actually be suitable.

I think we should follow a lot of other countries in adopting an opt out system. Make organ donor-ship the "norm". In some places that have adopted this practice, waiting lists have plummeted.
And make it the family can't over-rule it, if you wanting to donate.
 

The DoggFather

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@TANK 2.0 Sounds like this bloke is in the same situation you've been in the past .. well ... how long again?
6 years 3 months for me now.

I had dilated cardiomyopathy. Basically the same symptoms. I really feel for him as I have felt like him for 5 years waiting for the heart (which is fucking up still). Your ejection fraction percentage for VAD (heart pump machine) has to be at 12%, I hit 13% and narrowly avoided it. What the article doesn't mention is if you get on the VAD, they take you off the list for 6 months, because you are "too healthy" for a transplant.

I know the previous attempt by legends from the kennel and 1EE were rejected for a donor round, maybe now one of their own will bring the round into being.

I have always been a registered donor and still am. They took 3 working valves from my shitty heart and saved 3 babies with them. Donation really matters.

Please donate organs, doesn't matter what you believe, we don't need them when we go.

https://register.donatelife.gov.au/
 
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The DoggFather

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Kaz I wish you the best and an ear if you need with your conditions.
 

Kaz

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I know the previous attempt by legends from the kennel and 1EE were rejected for a donor round, maybe now one of their own will bring the round into being.
FFS.

Yet they have shit rounds like indigenous round & retro round. (Big fucking deal)

I emailed the NRL years ago, asking for motor neurone disease round, still haven't heard back.

A few players have had it or a form of it, Scott Gale, Mike Gregory. Sam Burgess father died from MND.
 

The DoggFather

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Screenshot_20180615-221917_Gallery.jpg
Don't know the size of his heart but this is the result of cardiomyopathy. This was in my chest (30cm ruler in the pic) it took so much of my chest cavity that I had 3% use of the left lung and 7% use of the right.

I could only take a quarter of a breath at a time. I cried, along with my misses and my long time nurse as I took a full breath for the first time in 5 years.

PS the pic is for shock value, to get attention not for me, but for the cause.
 

The DoggFather

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FFS.

Yet they have shit rounds like indigenous round & retro round. (Big fucking deal)

I emailed the NRL years ago, asking for motor neurone disease round, still haven't heard back.

A few players have had it or a form of it, Scott Gale, Mike Gregory. Sam Burgess father died from MND.
Probably because they can't sell jerseys for those rounds.

We don't need a song and dance and we don't want money. Just give out forms or even mention the website to register.
 

Kaz

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Kaz I wish you the best and an ear if you need with your conditions.
I know I will die posting on this forum. (heart conditions are being controlled with medication.)

Drs say I don't need an op.

Me:

 

The DoggFather

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I know I will die posting on this forum. (heart conditions are being controlled with medication.)

Drs say I don't need an op.

Me:

Lol you're not going anywhere you bitch! Lol

What conditions do you have? You can pm if you wish.
 

Kaz

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View attachment 6214
Don't know the size of his heart but this is the result of cardiomyopathy. This was in my chest (30cm ruler in the pic) it took so much of my chest cavity that I had 3% use of the left lung and 7% use of the right.

I could only take a quarter of a breath at a time. I cried, along with my misses and my long time nurse as I took a full breath for the first time in 5 years.

PS the pic is for shock value, to get attention not for me, but for the cause.
FUCK.

I knew the heart enlarged with cardiomyopathy, didn't know it got the large.
 

The DoggFather

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FUCK.

I knew the heart enlarged with cardiomyopathy, didn't know it got the large.
Because it doesn't pump properly (opening and more importantly closing of valves and chambers) the heart overcompensates by pumping harder and faster. Like every muscle, the harder you work it, the larger it becomes. My resting heart rate was between 130-160bpm pre transplant.
 

Kaz

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Lol you're not going anywhere you bitch! Lol

What conditions do you have? You can pm if you wish.
mitral valve prolapse.

What is mitral valve prolapse (MVP)?

Mitral valve prolapse is a condition in which the two valve flaps of the mitral valve do not close smoothly or evenly, but instead bulge (prolapse) upward into the left atrium. Mitral valve prolapse is also known as click-murmur syndrome, Barlow's syndrome or floppy valve syndrome.

What happens during MVP?

When the heart pumps (contracts) part of one or both flaps collapse backward into the left atrium. In some cases, the prolapsed valve lets a small amount of blood leak backward through the valve, which may cause a heart murmur.

Is mitral valve prolapse dangerous?

In most cases, it’s harmless. Most people who have the condition are unaware of it and their health is not affected. However, in some cases treatment is required.

http://www.heart.org/HEARTORG/Condi...-Prolapse_UCM_450441_Article.jsp#.WyOxVdInbio

And

Arrhythmia (Palpitations.)

https://www.heartfoundation.org.au/your-heart/heart-conditions/arrhythmias

Sometimes when the heart beats really fast, I have to lie down.

Have had to lie down in the middle of the supermarket aisle. lol

People look at me like I am a drunk, I just say haven't had a drink today. haha
 

The DoggFather

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mitral valve prolapse.

What is mitral valve prolapse (MVP)?

Mitral valve prolapse is a condition in which the two valve flaps of the mitral valve do not close smoothly or evenly, but instead bulge (prolapse) upward into the left atrium. Mitral valve prolapse is also known as click-murmur syndrome, Barlow's syndrome or floppy valve syndrome.

What happens during MVP?

When the heart pumps (contracts) part of one or both flaps collapse backward into the left atrium. In some cases, the prolapsed valve lets a small amount of blood leak backward through the valve, which may cause a heart murmur.

Is mitral valve prolapse dangerous?

In most cases, it’s harmless. Most people who have the condition are unaware of it and their health is not affected. However, in some cases treatment is required.

http://www.heart.org/HEARTORG/Condi...-Prolapse_UCM_450441_Article.jsp#.WyOxVdInbio

And

Arrhythmia (Palpitations.)

https://www.heartfoundation.org.au/your-heart/heart-conditions/arrhythmias

Sometimes when the heart beats really fast, I have to lie down.

Have had to lie down in the middle of the supermarket aisle. lol

People look at me like I am a drunk, I just say haven't had a drink today. haha
With your palpitations, were they AF's or VT's? Did they tell you or just left it at "palpatations"?
 

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Wow Tank... so you can literally say you have / had a big heart :D...

@Kaz the reason you won't hear back from the NRL is because in order to put on a charity round, the NRL demand not only payment to promote that round, but also take a percentage of the gate takings for that round. Not all the money ends up going to the charity. Pretty disgraceful of them, but then again it is the NRL we are talking about.

Our two awesome forum members @dogluva and @Sir Col "THE MU know more about it, because they were heavily involved trying to push Organ Donation round the other year. They can fill in the blanks if they want.
 
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