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April 28, 2010

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Barb

You got to meet and love your baby (supposed) defects and all. So many families do not get to share that love with their babies, their babies did not get to live this life. Either by "choice" or just an early death from their faulty genes. Thank you for sharing your message of hope, so many mothers only hear bad news. And they need this message of hope. People get to this earth in so many ways, and being unique is truly a blessing. I hope you guys keep on spreading the message about your experiences. It does make a difference!

Lynn

I appreciate hearing your thoughts on this! I am the parent of a 6-year-old with Down syndrome. I did not "know" before she was born. I opted out of pre-natal testing, because I did not want to "know," and because the testing was only to give me data to make a decision which I did not plan to make anyway.

But her birthday was a difficult day for me. I have often wondered what it would have been like, to know ahead of time. Would it have been easier on her birthday? Harder?

Your post just made me realize why her birthday was so difficult. I think the reason it was so hard, is because I was given a diagnosis before I actually held her, or even saw her. She was whisked away to the NICU, I was stuck in the hospital bed, recovering from a C-section. So the pediatrician came in my room and told me - he introduced the subject by saying "Well, I guess you didn't have an amnio..." Then he told me she had Down syndrome. So I had a label for her, before I held her, before I looked into her eyes and met her, before I had a chance to realize how much I loved her. If only I had been allowed to hold her first, and marvel at her many perfections, then it would have been so much easier to learn about the challenges that lay ahead.

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