British judge looks for new evidence in case of critically-ill baby Charlie Gard

LONDON, July 10 (Reuters) - The parents of a critically ill British baby have a few days to compile new evidence their son would benefit from experimental treatment in the United States, a judge said on Monday, adding that he would not be swayed by international interest.

Courts have previously denied Connie Yates and Chris Gard the right to send their 11-month-old son Charlie Gard to the United States on the grounds it would prolong his suffering without any realistic prospect of it helping.

SEE ALSO: Charlie Gard's mom says Trump, Pope intervention has 'saved his life so far'

Charlie Gard suffers from a form of mitochondrial disease, a rare genetic condition causing progressive muscle weakness and brain damage.

After a series of court battles, the family have been offered support by U.S. President Donald Trump and the Pope, the latter having sent a tweet offering to help.

"I have to decide this case not on the basis of tweets, not on the basis of what might be said in the press, or to the press," judge Nicholas Francis said on Monday.

The judge at London's High Court said the case will be held in full on Thursday. A lawyer representing the family had asked that the case be heard closer to the end of July. The judge said he might not make a decision immediately at that hearing. Francis who ruled on the original case in April said he would be delighted to change his mind but added "I want evidence of something that's different."

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Charlie Gard's parents
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Charlie Gard's parents
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
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
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
Chris Gard, who is battling to take his baby Charlie Gard to the US for treatment against advice from doctors that he should be taken off life support arrives at The High Court in London, Britain April 5, 2017. REUTERS/Eddie Keogh
Connie Yates, who is battling to take her baby Charlie Gard to the US for treatment against advice from doctors that he should be taken off life support arrives at The High Court in London, Britain April 5, 2017. REUTERS/Eddie Keogh
LONDON, ENGLAND - APRIL 07: Parents of Charlie Gard, Chris Gard and Connie Yates, walk through the grounds of the Royal Courts of Justice on April 7, 2017 in London, United Kingdom. Their crowdfunding campaign raising money for treatment in the US for their eight month old son, Charlie Gard, reached its target of �1.2million this past weekend. Charlie suffers from a form of mitochondrial disease and is the subject of a dispute over life-support between the Great Ormond Street specialists who are treating him and his parents. (Photo by Dan Kitwood/Getty Images)
LONDON, ENGLAND - APRIL 07: Parents of Charlie Gard, Chris Gard and Connie Yates, walk through the grounds of the Royal Courts of Justice on April 7, 2017 in London, United Kingdom. Their crowdfunding campaign raising money for treatment in the US for their eight month old son, Charlie Gard, reached its target of �1.2million this past weekend. Charlie suffers from a form of mitochondrial disease and is the subject of a dispute over life-support between the Great Ormond Street specialists who are treating him and his parents. (Photo by Dan Kitwood/Getty Images)
LONDON, ENGLAND - APRIL 07: Parents of Charlie Gard, Chris Gard and Connie Yates, walk through the grounds of the Royal Courts of Justice on April 7, 2017 in London, United Kingdom. Their crowdfunding campaign raising money for treatment in the US for their eight month old son, Charlie Gard, reached its target of �1.2million this past weekend. Charlie suffers from a form of mitochondrial disease and is the subject of a dispute over life-support between the Great Ormond Street specialists who are treating him and his parents. (Photo by Dan Kitwood/Getty Images)
LONDON, ENGLAND - APRIL 07: Parents of Charlie Gard, Chris Gard and Connie Yates, walk through the grounds of the Royal Courts of Justice on April 7, 2017 in London, United Kingdom. Their crowdfunding campaign raising money for treatment in the US for their eight month old son, Charlie Gard, reached its target of �1.2million this past weekend. Charlie suffers from a form of mitochondrial disease and is the subject of a dispute over life-support between the Great Ormond Street specialists who are treating him and his parents. (Photo by Dan Kitwood/Getty Images)
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LIFE SUPPORT

The family lost their legal battle at the end of last month when the European Court of Human Rights upheld the British court's decision that a trip to the United States would cause unnecessary suffering.

It ruled that that the children's hospital could turn off his life support.

On Friday, Great Ormond Street Hospital for Children, where Gard is being teated, said it wanted the court to hear new evidence relating to the case "in light of fresh evidence concerning potential treatment."

During the emotional hearing on Monday, Gard's parents shouted out several times. Yates said "this is really hard" as Great Ormond Street's lawyer Katie Gollop was speaking.

Yates said it was thanks to the high-profile support of Trump and the Pope that the case had got to this stage.

"It turned it into an international issue, a lot of people are outraged by what's going on. You know we've got new evidence now so I hope that the judge changes his mind," Yates told BBC radio. (Reporting by Sarah Mills; Editing by Alistair Smout and Ralph Boulton)

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