Parents Give Child With Genetic Disorder A Special Birthday Every Day

Have a look at the touching tribute movie made to observe Eliot life. Make sure that you have some tissues nearby, you are going to need them! “How beautiful it was to see. How fast they have been gone, just like you,” explained Matt at a movie devoted to their son. “So now we celebrate. While we miss you over we can express, our time just separated from you us. See you soon, son. Mom and Dad.” The couple first welcomed their son Eliot after getting some unsettling news in their doctor. As they diagnosed him with Edwards disorder, or trisomy 18 they were originally told that their child would not make it. This genetic disease causes babies to die in the first couple of days or at the womb after arrival, leaving Ginny and Matt hanging on to a shred of hope. The website of a hundred balloons in the sky may not mean much to a passerby, but for Ginny and Matt Mooney of Arkansas, it’s the show of love to their late son. They decided to celebrate one year of his birthday for every day that he was with them when he lived for years, to celebrate Eliot’s lifetime. Daily at 4:59pm — the time that Eliot was born — Matt and Ginny will snap a photograph of Eliot using a cake or poster announcing him a second year older. Sadly, Eliot’s journey came to an end on his 99th day of life. At his burial, his parents had everybody release balloons so that there were 99 floating away at precisely the exact same moment. When Eliot was born, he had lungs and also a hole in his heart, but his parents were ecstatic just to be in a position to hold him. When they shot him Matt and Ginny had to present round the clock care for their son. Regardless of the care, the couple were glad to have the ability to spend any time with their son they could, as they knew that his days were numbered.

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