I began this blog as a way to honor the life of my son Kevin. He was diagnosed in the womb with the fatal diagnosis of congenital diaphragmatic hernia and Pallister-Killian Syndrome. I chose to write this both to honor him and in hopes that it may help even one person going through something similar. This is Kevin's story.
Monday, May 2, 2016
Kevin's Life in Photos
Yesterday I updated Kevin's 25 week slideshow to show photos of his entire brief life with us. I am finally beginning to come out of my fog after losing him but each day continues to be a struggle. I thank God for the moments I had with Kevin and for answering my prayers to get to meet and hold him.
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