Charlie Gard: Life support to be turned off, parents say

  • 03 July 2017
  • From the section London
Image copyright PA
Image caption Charlie Gard’s rare disease has left him unable to cry

The parents of terminally-ill baby Charlie Gard have said his life support machine will be turned off later.

Chris Gard and Connie Yates have criticised doctors after their request to bring their son home to die was denied.

Great Ormond Street Hospital believe Charlie has no chance of survival and said it was a “distressing situation”.

On Tuesday, Charlie’s parents lost their final legal appeal to take him to the US for treatment.

Judges at the European Court of Human Rights concluded that further treatment would “continue to cause Charlie significant harm”, in line with advice from specialists at Great Ormond Street.

Ten-month-old Charlie is thought to be one of 16 children in the world to have mitochondrial depletion syndrome, a condition which causes progressive muscle weakness and brain damage.


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Media captionCharlie Gard’s parents say their wish to take their son home to die has been denied

Timeline

  • 3 March 2017: Mr Justice Francis starts to analyse the case at a hearing in the Family Division of the High Court in London
  • 11 April: He says doctors can stop providing life-support treatment
  • 3 May: Charlie’s parents ask Court of Appeal judges to consider the case
  • 23 May: Three Court of Appeal judges analyse the case
  • 25 May: Court of Appeal judges dismiss the couple’s appeal
  • 8 June: Charlie’s parents lose fight in the Supreme Court
  • 20 June: Judges in the European Court of Human Rights start to analyse the case after lawyers representing Charlie’s parents make written submissions
  • 27 June: Judges in the European Court of Human Rights refuse to intervene

Doctors have said he cannot see, hear, move, cry or swallow.

He has been receiving specialist treatment at Great Ormond Street Hospital since October last year.

In a video statement Ms Yates, from Bedfont, west London, said: “We’ve promised our little boy every single day that we would take him home, because that is a promise we thought we could keep.

“We were told he has to die in that hospital.”

Charlie’s parents say they have “begged” administrators to “give us this weekend” to allow his family to say goodbye.

“Some of our family can’t come until tomorrow so the last time they saw Charlie is the last time they will ever see him”, Mr Gard said.

A spokesperson for Great Ormond Street Hospital said: “As with all of our patients, we are not able to and nor will we discuss these specific details of care.

“This is a very distressing situation for Charlie’s parents and all the staff involved and our focus remains with them.”

Charlie’s parents raised £1.3m on a crowdfunding site to pay for the experimental treatment in the US.

Ms Yates had already indicated the money would go towards a charity for mitochondrial depletion syndromes if Charlie did “not get his chance”.

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