The efforts that Charlie Gard's parents have made in hopes of finding a solution to save their baby's life or at least live those last moments in dignity are finally coming to fruition. Empathy to their cause has seeped across seas and beyond borders. Even though the child's survival is uncertain, the parents have proven they under no circumstances intend to give up.
There are still many legal hurdles to overcome before Charlie can start to get treatment in the United States. A transfer of legal responsibility and appropriate travel preparations need to be made, along with FDA approval of the experimental medicine that parents Chris Gard and Connie Yates hope will save baby Charlie's life.
Since the pope, President Trump, Cher, and others all publically stated their support for the parents right to seek medical help for their child, the British courts have given more thought to the matter, and reconsidered the parents' wish to seek medical help in the United States.
"The court sees itself as the final guardian, if you will, of Charlie and Charlie's best interests. And they have found that any effort to extend the treatment would only extend his suffering, the suffering of a baby that is going to die," he said.
Due to the severity of Charlie's condition, the doctor has not presented himself as 100 percent confident in being able to heal the child, but he has offered to try out drugs that he has used on less severe forms of mitochondrial depletion syndrome. He has informed the courts that at least it couldn't make the situation worse.
