Sweet

I'm making cupcakes with the kids. We have the big silver mixing bowl and the wooden spoons and the measuring cups spread out on the kitchen counter. Avery, my 4-year-old with Down syndrome, stands on a step stool; Bennett, Avery's fraternal twin, sits on a chair. And 8-year-old Carter stands at the end.
Let this be fun, I think as I try not to put my food-consciousness on them today. The cupcakes are from a boxed mix with candy sprinkles in it, and are so sweet just thinking about them makes my teeth hurt.
My husband's friend Scott tells a story about a little boy he knew growing-up. The boy's parents were so health-minded, so "crunchy" that not only did they bake their own bread, they even ground all the wheat. The little boy would come over to Scott's house and devour slice after slice of Wonderbread, as if he were eating manna from Heaven. He grew into a junk food addict--the result, I surmised, of all those years of what he felt was deprivation. I don't want the same thing to happen to my children, so even though we eat healthy foods most days, every now and then we make cupcakes from a box.
We crack the eggs, measure water and oil. Dump everything into the big silver bowl and while the boys take turns stirring, I wander over to the computer, which sits across from us on the kitchen counter. I check my emails; a friend has recommended a blog post about a father's first ultrasound with their second pregnancy. It's how it always happens--innocently enough. Things draw me in.
I find the post and begin reading. Reading and waiting, because I think there will be something about Down syndrome in the story--it's always about Down syndrome, these days. Waiting, reading. But nothing makes me cringe. It's simply a thoughtful, honest post about one family and their choices.
I read the comments, too, and there it is: A man writes, very matter-of-factly, that at this very moment, he and his wife are in the process of ending their pregnancy because tests confirmed a diagnosis of Down syndrome. I inhale quickly and touch my cheek. It feels as if I've been slapped.
How can he do this? How can he say they will go in tomorrow and it will all be over? A pregnancy that was wanted, and now he's typing this story in the comments on a blog as if he were speaking about taking his wife to get her cholesterol checked, or her teeth cleaned.
It's none of my business, I know. Why do I do this to myself? I know better. I stop reading and unsubscribe to the comments, as if clicking the blue link could make it all go away.
We are making cupcakes. Stirring around and around. Taking turns, one-two-three. My three sons, lined up against the kitchen counter. I pour the much-mixed batter into the tins, six giant ones and a dozen tiny ones. I don't want to make decisions for other people. I can't even make them for myself, some days. It's all so confusing. We are told we have choices, that all the prenatal screening is about freedom. But we're not told what to do with this information. Does your faith guide you? Your personal experiences? Your friends? Your heart?
I think about the shape of our family; what my last pregnancy meant to us, how it changed us, changed me. I'm not a black-and-white sort of person; not a person to choose sides. I'm more of a smoother-over, a finder-of-middle ground. But it's difficult for me to do, right now. It feels as if we've been judged, and that we come up lacking. Either a family with Down syndrome is acceptable, or it's not. And my answer is, and always will be, Yes.
The boys have sticky fingers and smudges of cake mix on their faces. They've licked the spoons and now they're sharing the bowl. From the back, they are just three boys. They have the same color hair, the same little-boy arms, the same skinny shoulder blades, budding like wings. Wings that will some day carry them away into the world, a place I can not protect them from, a place that is sometimes not-so-sweet.
I go to them and kiss each on the top of the head, one-two-three, and put the cupcakes in the oven to bake, because it's what I can do. Give them all the sweetness, and the love, that I can, and hope that it is enough.
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Reader Comments (Page 1 of 2)
Michelle Adams 10-10-2007 @ 11:13PM
Awwww, man.
I read that one too and deliberately didn't read the comments so I wouldn't get drug into it. Too much emotion there...
Great post, Jennifer!
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Melissa (Banana Migraine) 10-11-2007 @ 9:03AM
Those kinds of comments sting so much to me also.
Sometimes it is important to make goodies from a box - it's the process and togetherness that is so special.
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Jen (I Never Thought) 10-11-2007 @ 11:18AM
It's enough. It has to be; it's all we've got.
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Joy 10-11-2007 @ 11:19AM
When my son and his wife took the pre-natal tests, something came back that said down syndrome was a posibility. We all thought...we will deal with things that God hands us. She (our granddaughter) turned out not to have it. It was a false test but we would have loved her no matter what. I'm not sure if it's faith or just love. I just love your posts Jennifer.
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jennifergrafgroneberg 10-11-2007 @ 11:28AM
Michelle, good call on not reading the comments! I should have done that, too.
Melissa, thanks for not making me feel bad about the prepackaged mix!
And yes, Jen, it's all we've got! But too, it's no more than any parent has, and I do believe it's all we need.
Thank you, Joy. And I think you're right: it's love. Love is enough!
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courtney 10-11-2007 @ 12:06PM
I love reading these kinds of posts first thing in the morning... it sets the tone for the rest of the day. Leaves me thankful and full of love for my family :)
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courtney 10-11-2007 @ 12:06PM
I love reading these kinds of posts first thing in the morning... it sets the tone for the rest of the day. Leaves me thankful and full of love for my family :)
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courtney 10-11-2007 @ 12:06PM
I love reading these kinds of posts first thing in the morning... it sets the tone for the rest of the day. Leaves me thankful and full of love for my family :)
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Jennifer(Furore and Frenzy) 10-11-2007 @ 12:17PM
What a wonderful day it sounds like you had. I need to do those activities with my kids...sometimes it's easy to forget...
I'm sorry you had to read those comments and I'm sorry that that particular couple will never know the joy of their child.
We are close friends for many, many years with a family that has a daughter with downs syndrome. They have two other children that do not have downs. When we were expecting our children I never worried about test results, I had watched our friends for years and I had noticed the key. They were so careful to never treat their children differently. The same expectations were there for all. Sure there are a few things that become trying but they now have a beautiful daughter that is grown. She graduated from high school, she went on to college and earned an Associates Degree, she obtained a job, got her driver's license and just recently moved into her own apartment much to her joy :)
I guess my point is, don't ever let anyone tell you your little one isn't capable. He is, he just needs assistance to reach the same goals.
When our friend's daughter was born the dr asked if they would like to send her away to be institutionalized as was common at that time. They were horrified at the idea.
When she graduated from high school they sent that dr a graduation announcement :) He replied with a congratulatory note and a $100 check.
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cheryl 10-11-2007 @ 1:32PM
It took me having a child to understand what you are saying. I believed in tests before I knew who was being tested. I wish this issue was discussed more in real language by real people. Nice post.
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jennifergrafgroneberg 10-11-2007 @ 12:39PM
Thank you so much, courtney! It makes me happy, too!
And thank you for sharing your experiences, Jennifer! I love stories like yours; they help me when I feel foolish for having hope. Thank you, thank you.
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Melissa 10-11-2007 @ 1:28PM
"so even though we eat healthy foods most days, every now and then we make cupcakes from a box."
I've been reading your food posts for a while now, and I think this sentence sums up what I consider to be the "right" way for my family to eat. What's the point of living a long, healthy life if you can never have a cupcake?
The rest of your post - it touched me. I don't have enough experience with your situation to say "I understand," and I don't want to say anything trite, but it touched me.
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Jessica 10-11-2007 @ 2:38PM
Wonderful post! I always enjoy reading your posts!!
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jennifergrafgroneberg 10-11-2007 @ 2:10PM
Melissa, my husband has a phrase, "it will only FEEL like 100 years" by which he means the very same thing you're saying...what's the point, if you can't enjoy life, too?
And Cheryl, thank you. I think you're right...having a child changes you in so many ways. I too wish people could discuss these sorts of things in a calm and open manner. Thank you for supporting that wish!
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jennifergrafgroneberg 10-11-2007 @ 2:12PM
Thank you, Jessica. I always appreciate your comments and support!!!
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Niksmom 10-11-2007 @ 2:32PM
I feel sad for and angry at people like the couple you mentioned. They will never know the infinite capacity for loving and being loved that having a child with OR without special needs can bring.
Please kiss each ofyour boys for me, too! :-)
Mmmmm, cupcakes! Yum.
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Vicki Forman 10-11-2007 @ 4:47PM
Lovely. We can't know what makes others do and say what they do and say. But we can love each other, no matter our choices. I told Josie last night about the quote, "to err is human, to forgive divine." Thanks for writing this.
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randi 10-11-2007 @ 9:37PM
I am the mom of a child with Autism and a "typical" child. I really enjoy your posts. Thanks.
Randi
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Claudia 10-11-2007 @ 9:51PM
I believe absolutely that your book, Jennifer, is going to make a profound difference for many people making these decisions. I believe it because of the change it's made in me.
Thanks for putting so much that needs to be explained into such beautiful words, Jen.
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spritelyslp 10-12-2007 @ 10:23AM
What a timely post! I have a 4 y.o. daughter w/DS & a 7 y.o. who is typically developing, & we are expecting again! Today is my first prenatal dr appt, & I have been a wreck worrying about the attitudes I may encounter w/my new dr & how I will educate & spread awareness about DS. I just wish the first packet I received from my dr didn't include a plethora of info about genetic testing & risks, etc. Thank you for yet another lovely & intimate post!
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