A baby is condemned to death by socialized medicine
- Thread starter Tom B
- Start date
This is a travesty. This decision should be left to United Halthcare and Cigna.
Broken clock.
Parents of brain-damaged baby lose fight to keep him on life support
Published July 01, 2017
The mother and father of a brain-damaged 11-month-old baby on Friday were sitting bedside with the boy after losing a legal battle that would have kept the boy on life support.
The Wall Street Journal reported that doctors at the Great Ormond Street Hospital for Children in London, who are caring for Charlie Gard received permission from a court to discontinue life support.
The boy’s parents objected to the decision and wanted to take him to the U.S. for an unproven, experimental therapy.
Charlie suffers from a rare genetic condition and brain damage. He is unable to breathe unaided. Earlier in the day, parents Chris Gard and Connie Yates said they had expected the hospital to end life support for Charlie on Friday.
Related Image
Chris Gard and Connie Yates, who are battling to take their baby Charlie to the US for treatment against advice from doctors that he should be taken off life support arrive at The High Court in London, Britain April 5, 2017. REUTERS/Eddie Keogh - RTX347VA Expand / Collapse
Reuters (Chris Gard and Connie Yates)
But hours later, the hospital said in a statement that "together with Charlie's parents we are putting plans in place for his care and to give them more time together as a family."
Hospital officials also asked that the family and hospital staff be given "space and privacy at this distressing time."
It's not clear how long life support will be continued for Charlie.
On Tuesday, the parents lost a bid to take Charlie to the U.S. for trial therapy when the European Court of Human Rights sided with earlier rulings that continued treatment would cause "significant harm" and that life support should end. Specialists have said the proposed therapy wouldn't help Charlie.
Charlie was born in August. The Journal reported that he was diagnosed with infantile-onset encephalomyopathic mitochondrial DNA depletion syndrome.
“His brain, muscle and ability to breathe are all severely affected. In addition, he has congenital deafness and a severe epilepsy disorder,” a professor who specializes in mitochondrial diseases told the U.K. High Court that heard the case.
The appeal was the last legal option in the couple's four-month battle. After the final ruling, the hospital said there would be "no rush" to make any changes in Charlie's medical care.
His parents had complained that the hospital wouldn't allow Charlie to be brought home to die. The boy's parents have released a video saying "we're not allowed to choose if our son lives and we're not allowed to choose when or where Charlie dies."
Charlie's case has gained attention online, raising nearly $1.8 million on GoFundMe to send him to the U.S.
Yates has said previously that the funds will be used to support other children with similar genetic disorders should they lose their case.
“We are utterly heartbroken,” the parents wrote in a post on Facebook . “We and most importantly Charlie have been massively let down throughout this whole process.”
The Associated Press contributed to this report
http://www.foxnews.com/health/2017/...y-lose-fight-to-keep-him-on-life-support.html
Published July 01, 2017
The mother and father of a brain-damaged 11-month-old baby on Friday were sitting bedside with the boy after losing a legal battle that would have kept the boy on life support.
The Wall Street Journal reported that doctors at the Great Ormond Street Hospital for Children in London, who are caring for Charlie Gard received permission from a court to discontinue life support.
The boy’s parents objected to the decision and wanted to take him to the U.S. for an unproven, experimental therapy.
Charlie suffers from a rare genetic condition and brain damage. He is unable to breathe unaided. Earlier in the day, parents Chris Gard and Connie Yates said they had expected the hospital to end life support for Charlie on Friday.
Related Image
Chris Gard and Connie Yates, who are battling to take their baby Charlie to the US for treatment against advice from doctors that he should be taken off life support arrive at The High Court in London, Britain April 5, 2017. REUTERS/Eddie Keogh - RTX347VA Expand / Collapse
Reuters (Chris Gard and Connie Yates)
But hours later, the hospital said in a statement that "together with Charlie's parents we are putting plans in place for his care and to give them more time together as a family."
Hospital officials also asked that the family and hospital staff be given "space and privacy at this distressing time."
It's not clear how long life support will be continued for Charlie.
On Tuesday, the parents lost a bid to take Charlie to the U.S. for trial therapy when the European Court of Human Rights sided with earlier rulings that continued treatment would cause "significant harm" and that life support should end. Specialists have said the proposed therapy wouldn't help Charlie.
Charlie was born in August. The Journal reported that he was diagnosed with infantile-onset encephalomyopathic mitochondrial DNA depletion syndrome.
“His brain, muscle and ability to breathe are all severely affected. In addition, he has congenital deafness and a severe epilepsy disorder,” a professor who specializes in mitochondrial diseases told the U.K. High Court that heard the case.
The appeal was the last legal option in the couple's four-month battle. After the final ruling, the hospital said there would be "no rush" to make any changes in Charlie's medical care.
His parents had complained that the hospital wouldn't allow Charlie to be brought home to die. The boy's parents have released a video saying "we're not allowed to choose if our son lives and we're not allowed to choose when or where Charlie dies."
Charlie's case has gained attention online, raising nearly $1.8 million on GoFundMe to send him to the U.S.
Yates has said previously that the funds will be used to support other children with similar genetic disorders should they lose their case.
“We are utterly heartbroken,” the parents wrote in a post on Facebook . “We and most importantly Charlie have been massively let down throughout this whole process.”
The Associated Press contributed to this report
http://www.foxnews.com/health/2017/...y-lose-fight-to-keep-him-on-life-support.html
They mocked Sarah Palin when she pointed out that Obamacare would inevitably lead to death panels. Some faceless committee will have the power to determine if you or your loved ones receive life-saving treatment. The power they will wield is hard to imagine. Of course, that power will never be misused.
This happens now. Insurance companies in the US deny treatment like this everyday. It's so commonplace that it doesn't make the news.
And as sad as this story is, healthcare does have to be rationed. We (as a society) have to determine how that should be done. And that's the crux of the debate.
She lied, show me one instance of someone on Medicare being denied care.
you can't even speak with lefties they have become so dumb in their defense of everything big govt. then these same types who complain about discrimination make jokes about religion..
how you morons can support this... is beyond comprehension... this is 1984 govt making decision which offend freedom and liberty.
"On Tuesday, the parents lost a bid to take Charlie to the U.S. for trial therapy when the European Court of Human Rights sided with earlier rulings that continued treatment would cause "significant harm" and that life support should end. Specialists have said the proposed therapy wouldn't help Charlie."
His parents had complained that the hospital wouldn't allow Charlie to be brought home to die. The boy's parents have released a video saying "we're not allowed to choose if our son lives and we're not allowed to choose when or where Charlie dies."
how you morons can support this... is beyond comprehension... this is 1984 govt making decision which offend freedom and liberty.
"On Tuesday, the parents lost a bid to take Charlie to the U.S. for trial therapy when the European Court of Human Rights sided with earlier rulings that continued treatment would cause "significant harm" and that life support should end. Specialists have said the proposed therapy wouldn't help Charlie."
His parents had complained that the hospital wouldn't allow Charlie to be brought home to die. The boy's parents have released a video saying "we're not allowed to choose if our son lives and we're not allowed to choose when or where Charlie dies."
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LOL, look at right wingers pretending this is some unique situation of 'socialized medicine' when incidents like these happen everyday with the 'free market system'. The only reason you guys pretend to be upset about this baby dying is because some insurance shareholder is not able to make money off it.