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Charlie’s Parents End the Fight for his Life

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Charlie Gard case: Parents withdraw application to bring sick baby to US

FNC: With tears streaming down their faces, the parents of terminally ill baby Charlie Gard on Monday withdrew their application seeking to take the child to the United States for an experimental medical treatment, with the couple’s lawyer announcing “the window of opportunity has been lost.”

Attorney Grant Armstrong said at London’s High Court it was too late for the 11-month-old child to receive treatment. Recent medical tests revealed Charlie has irreversible muscular damage.

“It’s too late for Charlie,” Armstrong said. “The damage has been done.”

Charlie’s parents, Chris Gard and Connie Yates, cried in the courtroom as the lawyer announced the news — their last bid to seek permission to take their child to the U.S. for treatment.

“As Charlie’s devoted and loving parents we have decided that it’s no longer in Charlie’s best interests to pursue treatment and we will let our son go and be with the angels,” Yates said in court.

The couple was expected to present new evidence in court on Monday, but they arrived in court to say the dragged out case has wasted “time. A whole lot of wasted time.”

“Had Charlie been given the treatment sooner he would have had the potential to be a normal, healthy little boy,” Yates said, referencing the recent medical test that ultimately led to the couple’s decision to withdraw.

“I only wanted to give him a chance at life,” Yates said. “We will always know in our hearts that we did the very best for Charlie and I hope that he is proud of us for fighting in his corner.”

Charlie, who was born on Aug. 4, 2016, suffers from a rare genetic condition, Mitochondrial DNA depletion syndrome. He has brain damage and is unable to breathe on his own. Doctors at Great Ormond Street Hospital, where Charlie has been treated since last October, have been locked in a prolong court battle, claiming more treatment would only cause pain to the child. They have argued to switch off Charlie’s life support to allow him to die peacefully.

But Charlie’s parents dispute the claim and have argued that their child should receive every possible treatment until his death.

Posted in Citizens Duty, government fraud spending collusion, Health Disease, Obamacare, The Denise Simon Experience.

Denise Simon