What I Wish I’d Known When Our Child Was Diagnosed with Down Syndrome

GET THE FREE DOWNLOADOn December 30, 2005, our firstborn daughter came into the world. It was an easy delivery—a little early, but not premature, no signs of distress or trouble, just a shock of black hair and a puffy face, and eyes the color of the sea on a cloudy day. But two hours after Penny was born, we learned that she had Down syndrome, the presence of a third copy of chromosome 21 in every cell of her body.  I was filled with worry, grief, confusion. Now my grief has turned to gratitude and worry to wonder. I want to share with you 5 things I wish I had known when we received the diagnosis. Because now, I look back on that young mother, and I want to be able to hold her hand and look into her frightened, angry, sorrowful eyes and tell her not just that it will all be okay. I want to tell her why it will be more than okay. I want to tell her how her daughter will change her life in ways she never could have expected. I want to take her worry and grief and confusion.  If I could, this is what I would say to her… Celebrating Down Syndrome Awareness month—it starts tomorrow!—with this gift for you:5 THINGS I WISH I’D KNOWN WHEN OUR DAUGHTER WAS DIAGNOSED WITH DOWN SYNDROME GET THE FREE DOWNLOAD

More with Amy Julia:

5 THINGS I WISH I’D KNOWN WHEN OUR DAUGHTER WAS DIAGNOSED WITH DOWN SYNDROMEBook: A Good and Perfect Gift: Faith, Expectations, and a Little Girl Named Penny Free Resource:  Missing Out on Beautiful: Growing Up With a Child With Down Syndrome

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