The night that Nathan was born, the pediatrician came in the recovery room following my c-section to tell us she "suspected" that he had Down syndrome. She then went into a laundry list of reasons why she "suspected" it and the tests that were to follow. I wasn't getting a good feel from her whether it was a remote possibility or an absolute certainty, so I cut to the chase and asked her what her gut instinct was. Gratefully, she was honest and told us that she believed he did. When I saw him later, I knew instinctively that she was right. In the first several weeks after Nathan was born, however, I struggled to find the features in his face. It seemed that it was only in photos - rarely in holding and interacting with him - that I was able to spot the physical features common to people with an extra 21st chromosome. Now that he is a little bit older, I can spot it more easily, but it's hard to tell sometimes if other people see it, too.
Nathan is a happy and friendly baby. He smiles a lot and, in particular, flirts with the ladies (oh, my!) Because he has a seven year old sister, he gets dragged all over the place - swim meets, guitar lessons, Target, Chick-fil-A, church... Often, he will catch someone's attention and they will talk and smile and coo back at him, and tell me he's beautiful. He IS beautiful. He has the most brilliant blue eyes - the same color as Sarah Kate's - and it is easy to get lost in them.
Whenever we are out-and-about interacting with people, my mind inevitably questions "Can they see it?" While it doesn't make any difference to me what they do or don't see, the next thought I always have is "Should I mention it?" For people who are friends or casual acquaintances, I usually do say something to the effect of "You know that he has Down syndrome, right?" I do that mainly because it feels like I'm keeping it a secret if I don't tell them, and since they are going to learn of it, anyway, I'd rather them hear it from me with a smile on my face than from someone else with pity in their voice. Friends and acquaintances, I have learned, will take their cues from me. If I am fine with it, they are fine with it.
With strangers it's a little bit tougher. If they don't see it, I don't want people to feel uncomfortable that I brought it up, but if they do see it, I want them to see me as positive and happy, and Nathan as a person to be valued. I don't want to draw attention to the fact that he's non-typical - after all, he is much more like other children than he is different from them - but I also don't want it to appear that I'm hiding his non-typical-ness. What I usually do is watch their face to see if I spot some glimmer of comprehension, and then decide whether to speak or not to speak. I always wonder if I have done the right thing.
The bottom line is that I really shouldn't give a rip about whether a stranger is or isn't comfortable nor whether they do or do not see it. I should be reminding myself of that old saying "The people that mind don't matter, and the people that matter don't mind", but I feel like it's not as simple as that. I want the world to see that he is, indeed, a beautiful and delightful little boy who just happens to have "a little something extra" in his chromosomal makeup.
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Andi, April said, "Mom, I just don't get it. Nathan is awesome and a very sweet, loving baby and I do not see anything different about him." She is right on target! That baby has been in my heart even before he was born. You are so truly blessed.
ReplyDeleteI love you and your entire family!
Leigh Ann
hi! I'm the gal with hang-on-little-tomato. Thanks for stopping by my blog! I am really enjoying reading yours. I so relate to this post. Now that Max is 17 months old I forget at times about these thoughts that haunted me in the beginning ( do they notice - should I tell them kind of thoughts ) It's funny to watch how things shift as our baby gets older and our experience of him in the world shifts as well.
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