Charlie Gard parents given more time to say goodbye to terminally ill son

Charlie Gard's rare disease has left him unable to cry

Charlie Gard's parents have been told they will be able to spend more time with their terminally ill baby.

Chris Gard and Connie Yates had been expecting their 10-month-old's life support to be turned off on Friday.

Great Ormond Street Hospital has since disclosed it is putting plans in place for Charlie's care to allow his family to spend more time with him.

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

He has a rare genetic disease as well as brain damage and is believed to be one of 16 children in the world to have the condition; mitochondrial depletion syndrome.

Connie Yates and Chris Gard raised more than £1.3m for experimental treatment for Charlie

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

Charlie has been receiving specialist treatment at Great Ormond Street Hospital since October 2016.

'Massively let down'

His parents said they had been denied their final wish to be able to take their son home to die and felt "let down" following the lengthy legal battle.

Alongside a video posted on YouTube on Thursday, Charlie's parents wrote: "We are utterly heartbroken spending our last precious hours with our baby boy.

"We're not allowed to choose if our son lives and we're not allowed to choose when or where Charlie dies.

"We, and most importantly Charlie, have been massively let down throughout this whole process."

• Charlie Gard mum shares 'eyes open' photo

• Charlie Gard parents lose appeal for US treatment bid

• Watch: Charlie Gard parents 'inconsolable'

• Charlie Gard parents to keep fighting

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

A spokesperson for Great Ormond Street Hospital said earlier: "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 previously indicated the money would go towards a charity for mitochondrial depletion syndrome if Charlie did "not get his chance".