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Charlie Gard: Parents end legal fight to take sick baby to US for experimental treatment | Charlie Gard: Parents end legal fight to take sick baby to US for experimental treatment |
(35 minutes later) | |
Charlie Gard’s parents are ending their legal fight to take their critically ill son to the US for treatment. | |
Connie Yates and Chris Gard wanted to take baby Charlie, who has a rare genetic disease, across the Atlantic to receive experimental nucleoside therapy. | |
But they have now decided that "it is no longer in Charlie's best interests to pursue this course of treatment," according to a statement. | |
Barrister Grant Armstrong told a High Court judge the parents were “extremely distressed” by the results of new medical tests on the 11-month-old. | |
He said "window of opportunity has been lost" to help Charlie, as it is best to act as early as possible to treat mitochondrial disease. | |
The decision concludes a bitter five-month legal fight from Ms Yates and Mr Gard, whose appeal to give their son treatment was previously rejected by the European Court of Human Rights. | |
Doctors at Great Ormond Street in London maintained that it was kinder for the Charlie's life support to be switched off. | |
The case caused an international furore, with Donald Trump and Pope Francis offering to help baby Charlie, and a fresh hearing was underway after the possibility of new evidence emerged. | |
Charlie, who was born on 4 August 2016, inherited the faulty RRM2B gene, which affects the cells responsible for energy production and respiration, leaving him unable to move or breath without a ventilator. | |
Ms Yates and Mr Gard said they were aware the case had caused controversy, but now wish to treasure their remaining time with Charlie and asked for all protests to stop. | |
The judge said no one could begin to understand the parents' agony but they now had to "face reality" that it is in their son's best interests to die. | |
Ms Yates said she wanted to address Mr Justice Francis at the end of the hearing. |