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Amy Julia Becker

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Explaining Down Syndrome, To My Daughter, And Myself

Posted: 10/25/2011 5:27 pm

This post is part of Parentlode. Read Lisa Belkin's introduction here.

A few months back, I mentioned to our daughter Penny that she would be meeting another little boy who had Down syndrome, just like her. She didn't say anything in response, but later on that day, when Penny was at school and William was getting ready for a nap, he said, "Mom, what down syn mean?"

"Down syndrome, sweetie. Not down syn."

"I know drum," he replied. "What down syn mean?"

I nodded slowly, realizing that he was envisioning making music, and grateful that he didn't have a concept of "sin" on hand. So I said, "Well, it's all one word, and it doesn't have anything to do with an instrument." I searched a mental map for words to explain a chromosomal anomaly to a two-year old. I began, "It means Penny has an extra part in her body," but I realized that sounded as though she might grow a third arm. Then I said, "It's something that makes Penny special."
He stuck out his lower lip. "I want to be special."

I hugged him tight.

I haven't used that explanation since. But I've thought a lot about William's question. And I've realized that as much as I understand what Down syndrome is, biologically, I don't know what it means in any broader sense. I know Down syndrome is the presence of an extra chromosome 21 in every cell of Penny's body. I know it can cause heart defects and learning delays and hearing loss and vision problems. I know people within our culture tend to glorify or vilify it with stereotypes ranging from pronouncements about how people with Down syndrome are all sweetness and light to those that imply people with Down syndrome shouldn't exist.

On Monday of this past week, Sequenom, a biotechnology company in San Diego, released a new prenatal test designed to detect Down syndrome in the tenth week of pregnancy. In contrast to other screening tests, this one is 98% effective at identifying Trisomy 21. And in contrast to chorionic villa sampling and amniocentesis, this test is non-invasive, posing no risk to the health of mother or child. It's hailed as a great advancement in prenatal testing because it is both accurate and non-invasive. But as much as this test might be able to tell parents that their developing baby has an extra chromosome, I'm not convinced that this piece of information tells them much of anything at all.

I've seen Penny's karyotype, the graphic representation of her chromosomal makeup, including those three stubby lines clustered together like three old men squatting side by side. I've visited the doctors--the developmental pediatrician, the gastroenterologist, the cardiologist, the endocrinologist, the otolaryngologist, the ophthalmologist, the neurologist, the geneticist, even, for one harrowing season of unnecessary concern, the oncologist. I know that it is probably because of Down syndrome that Penny wears glasses, although three generations of typically developing women in my family have worn glasses at an early age, so maybe it's just heredity. It is probably because of Down syndrome that she is short, and yet I was always the smallest person in my class at school and still only top five feet in heels. I know that there are days when she is the loveliest child I've ever met--when she runs to my side and says, "Hug!", when she asks, "How was your day, Mom?", when she sings to her little sister and brings her toys, when she asks to pray for someone who is sick. But I also know that she is no more sweet or loving than her brother, and that she tests my limits and disobeys and deceives me about her intentions in equal measure too.

George Estreich, author of The Shape of the Eye: Down Syndrome, Family, and the Stories We Inherit explores the etymology of the term Down syndrome, and his explanation gives voice to my own confusion:

A syndrome means, at root, a 'running together.' When you have a child, it all runs together: the heart defect, the eyes, the way her voice sounds, the name of the speech therapist, the worries over the future, the joys of discovery, the sliding sense--slow, quiet, enormous, an avalanche in the skull--that different is not as different as you thought. The genes produce the child, who lives a story, whose story is bound up with yours. So reducing a child to a heap of medical fragments is, for a parent, a complicated and dissonant act. It is a necessary fiction, a story one tells only in order to move on.

Maybe we've moved on.

William hasn't asked again, but if he does, I still won't have a definition to give him. Instead I have a story, a story that includes trips to the doctor and an Individualized Education Plan, a story that includes Penny's first loose tooth and skinned knees and birthday parties, a story that includes William erupting into tears if his big sister forgets to give him a hug before she heads to school.

When Penny was first born, Down syndrome meant fear and sadness and worry. Now, it's just two words used to describe a biological reality that could never adequately define her as a person. Down syndrome doesn't mean much to me these days, but Penny--impulsive, adorable, a big sister who loves to pump on the swing and read books and sing songs--Penny means the world.

 
 
 
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This post is part of Parentlode. Read Lisa Belkin's introduction here. A few months back, I mentioned to our daughter Penny that she would be meeting another little boy who had Down syndrome, just...
This post is part of Parentlode. Read Lisa Belkin's introduction here. A few months back, I mentioned to our daughter Penny that she would be meeting another little boy who had Down syndrome, just...
 
 
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algegra
"Calmer than you are Dude"
09:41 PM on 10/28/2011
While in college I worked in a home for developmentally delayed children. We had 48 beds and about half of the residents had down syndrome. I also have a cousin who has down syndrome. He is a generally happy, meticulously dressed 48 year old now. His parents and step mom have all passed and he lives with his sister and has a great life. The young people I cared for were mostly sad frustrated children who had been abused - some horrifically. The majority never had a family member visit, received no gifts on birthdays or Christmas and did not have a sense of belonging. The family that any child is born into in large part determines their future but the challenges that a family can face with a special needs child can overwhelm them.

"A study from the National Center on Child Abuse and Neglect (NCCAN) found that children with special needs are maltreated at 1.7 times the rate of other children. Parents of children with disabilities come from every social class and value system, however, these parents may feel very much on their own may be stressed by ongoing health care needs, difficulties in finding suitable child care, financial burdens and social isolation, along with related difficulties such as depression and marital discord. Several research studies indicate that caregivers of children with special needs who perceive themselves as severely stressed are more likely to commit abuse. ." http://kcsos.kern.org/SpecialEd/stories/storyReader$428
08:52 PM on 10/27/2011
36 years ago, my family welcomed my brother David, who was born with Down Syndrome, into our family. This fall, my 12th novel, How David Met Sarah, was published. I wrote this story for my brother, who reads at the 3rd grade level, but doesnt like third grade level stories, because he's not a child. How David Met Sarah is both content and reading level appropriate for someone like my brother with lower level reading skills. Average readers find the book offers insights into the world of the developmentally disabled. Read more about our story at http://HowDavidMetSarah.blogspot.com.
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peegan
Silence like a cancer grows...S/G.
09:12 PM on 10/27/2011
What an excellent idea.
09:26 AM on 10/28/2011
When Penny was still an infant, my husband pointed out to me that there is a difference between intelligence and maturity. One of the problems that occurs when we try to describe adults with cognitive disabilities in terms of age or grade level is that it doesn't describe them in full. It sounds as though you've addressed this problem--your brother has a certain level of reading ability, but a different degree of life experience and maturity than a child with that same ability. Thanks so much for recognizing the difference and working to bridge the gap.
09:37 PM on 10/28/2011
Thanks for your kind words, Amy...i would be pleased to send you a copy of the ebook if you give me your email address...i can be reached at anniekelleher at aol dot com.
08:25 PM on 10/27/2011
I don't like what the mother said about her daughter being special to the question her little two year asked, and when he said, he wanted to be special, all she did was hug him. I think she should have effeminized that he was special too. She could have told him he was special in a different way than his sister. Example, as he was a special brother to his older sister... I know children and adults with downs and they are loving people. They take pride in their work. The kid that worked at McDonalds...the counters and tables were never so clean cause he took pride in his job. Just a little praise can go a long way .
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beth2216
07:42 PM on 10/27/2011
I know the fear that people have when it comes to thinking about having a children with a disability whatever it may be. Let me tell you from experience, even through all the hospital visits, Dr's appointments, tests, etc, that child will bring you more happiness, humbleness, thankfulness, and blessing than a child that is considered "normal". Now, don't get me wrong children who do not have a disability are still a blessing, but it's something about children with disabilities that may you look at each day as a blessing instead of taking things for granted. My youngest son has Congenital Heart Disease. He's already had one open heart surgery, one heart cath, many many tests, x-rays, etc. He will be having another heart cath to put a balloon in his aortic arch. Plus, he has other issues. He has helped me to appreciate each day that I have with him (since during his recovery he hit a rough patch and I thought I was going to lose him). Don't get me wrong I love my oldest son. The one thing I will always tell him when he gets older is that he was the only person who was able to cheer me up while my youngest was in the hospital. Both of my children bring a blessing, but it's my youngest that makes me thankful for each day that I have with my children.
07:42 PM on 10/27/2011
Your story is truly wonderful to me. My little sister has Down Syndrome and she is my world. I could not imagine a world where she and other people like her don't exist. Down Syndrome children are special and our very dear to our Heavenly Father and our gifts sent to families. Thank you for sharing your story Penny. My little sister is my families world.
05:56 PM on 10/27/2011
Why do all down syndrom children look the same ??? Do they share an identical gene ???
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Lisa Belkin
Life/Work/Family/Coffee
10:53 PM on 10/27/2011
Yes, in effect they do. The distinct facial structure is caused by the third copy of the 21st chromosome.
09:31 AM on 10/28/2011
I can still see the similarities in facial structure among people with Down syndrome, but because I now have a daughter with Down syndrome and know many other people with Down syndrome, they look as different from one another as any other kids. I think it's similar to visiting a foreign country--I suspect that if I were to visit Japan, at first everyone would look the same to me. If I started to live there and build relationships with people, I would start to see them as individuals who have some common features but essentially look quite different from one another.
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VA Jill
I'm not perfect and neither are you
06:52 PM on 10/27/2011
I hope this is more reliable than the AFP. My daughter has been pregnant 3 times, and every time her AFP has been abnormal. Her only daughter, prematurely stillborn, had spina bifida. Her sons are completely normal, but that was a LOT of worry. She well understands life with a special needs child as her brother is autistic.
06:49 PM on 10/27/2011
Children with Down Syndrome are wonderful, just like any other child, and if you don't feel you can take care of it, definently don't have an abortion. There are plenty of families that would love to have that child just as they are. They deserve life and no one should be givn the choice to terminate a life.
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Ken Overholt
06:39 PM on 10/27/2011
I am so very glad that these tests weren't around 27 years ago; otherwise I might not have my daughter. Back then Ashley wasn't diagnosed with DS until 2 months after her birth. When the chromosome tests came back positive my wife and I were devastated. We were also quite ignorant as to exactly what DS was and the vast range of possibilities for her life. We started with early intervention therapy and she was main streamed all thru school. Ashley is extremely high functioning to the point that she tested in the 80th percentile in English in high school and ultimately ended up taking and passing some college courses at Kent State University. Her biggest problem is social as she is so much higher functioning than the Downs boys we have met. She has worked at a local senior assisted living facility for the past 8 years and everyone there loves her, co-workers and residents alike. She has taught us so much about unconditional love and true happiness to the point that I couldn't imagine life without her. I would be a much more ignorant person and I would lack so much had she not ever entered my life.
06:15 PM on 10/27/2011
My daughter was injured at age 6 and is paralyzed from the neck down. Our younger children always knew their sister was different than others, but were NEVER told she was special. Being disabled for any reason doesn't make a child special, and being "normal" doesn't make a child NOT special. Our children (5 altogether) all know they are loved and they are each special in their own way, not because of what they are (the only boy, the red head, the eldest, the youngest, the smartest, the funniest, the quadriplegic), but because of WHO they are.
The writer needs to get that straight - all of her children are special, and yet none of them are. She has a daughter who happens to be born with Trisomy 21, not a "Down Syndrome child".
04:38 PM on 10/27/2011
When I was 27, I gave birth to a daughter with down syndrome & a congenital heart defect. I found out when I was 35 weeks pregnant after having 4 ultrasounds and a very good AFP blood test. I was the proud mom to Alyssa Madison for 8 months and 11 days. She had open heart surgery & caught a cold 5 weeks later and passed 2 months after her surgery in her sleep. No parent should have to bury their baby. That said, my husband & I wanted to take 1 year to grieve our loss, however, God had other plans as I found out I conceived 6 weeks after my angel passed and gave birth 1 year to the day from her open heart surgery. I was a nervous wreck my entire pregnancy & had every test imaginable including CVS. Luckily, all the tests came back good except that I had gestational diabetes, because I told my doctor that if anything happened to this baby, she might have to "commit" me. Although the saying goes, God doesn't give you more than you can handle, I don't think I could have handled losing or almost losing another child, as my son was injured at birth due to medical malpractice, he suffered a fractured skull, blood on the brain & seizures. Fortunatelty, we have the right to choose to have certain tests or not. I can't imagine our lives without our angel, however, I wouldn't wish what we went through
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beth2216
06:31 PM on 10/27/2011
I'm sorry that you lost your daughter. My youngest son was diagnosed with congenital heart disease (with that many different defects). It has been a hard journey for me as a mother. I pray every night for him as well as my oldest son. I am very nervous as another issue has presented itself on top of the previous issue. He did have open heart surgery at 3 days old plus many more procedures. We found out that he had CHD during an ultrasound, but I could not imagine my life without him. Both of my boys are my sunshine and my happiness. I'm glad the Lord has blessed you with another child.
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bmitche
03:30 PM on 10/27/2011
Penny is special, and she is lucky to have you as a mom.
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04:26 PM on 10/27/2011
I had a very special needs brother. He died when he was 14. We loved him VERY much. However, I would not bring a special needs child into the world. With the medical technology today, I would know if I was carrying a child that would be special needs and I would terminate the pregnancy before 12 weeks.
04:00 PM on 10/27/2011
Well that is why we live life, we all have different views and opinions on things, but my opinion with having kids is if you dont want to have a child becuase of the "risk" of it having a disability or problem then you should not try to have a child. We all take risks in life everyday: driving to work, walking in the park, playing your favorite sport, working out, drinking and eating things that "could" be contaminated with something that "might" make us sick, these are things we do daily and we do not worry about "what" might happen, just live life and enjoy it as much as you can.
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Bebe36
Grateful for every day.
05:52 PM on 10/27/2011
Except when there is a special needs child, the *mights* are certainties.
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Cliantha
04:36 PM on 10/27/2011
I understand why you would terminate. Raising a child with special needs is a blessing but it is also hard, and scary. If you can't deal with that then you shouldn't be judged poorly for knowing your limitations. That being said, not all special needs show up in a test or ultrasound. My son's condition was not something that could be tested for and we didn't see it on ultrasound until my partner was eighteen weeks into her pregnancy. Terminating at that point is easier said then actually done. Some special needs don't show up until after the child is born. Other children are fine until an accident. You take a risk when you become a parent and you have to be prepared for that. I take that back, nothing prepares you for it but you should be aware that there is always risk. The joy of parenting is the not knowing.
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05:53 PM on 10/27/2011
Thank you for being so passionate and understanding. You sound like a great parent. I would always love any child I had, not matter what happened. Sometimes it just seems that life is tough enough with the unknown that the known should be heeded. My Dad did tell me that he thought special children had special parents chosen by God especially for them. I always knew how special my parents were. I think you must be, too.
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sparkygirl91
Never apply lipstick while driving on gravel
03:21 PM on 10/27/2011
How can such a lovely, uplifting story, yield so many hateful comments? Unless you've walked an inch in this family's shoes, you've no real comment to make......other than of support.
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Bebe36
Grateful for every day.
05:53 PM on 10/27/2011
Works both ways, sparkygirl.
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sparkygirl91
Never apply lipstick while driving on gravel
06:39 PM on 10/27/2011
And your point is? Not making any mean-spirited comments on this story, and, admittedly, have NOT walked in their shoes so, again.........your point?
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petcraft
03:03 PM on 10/27/2011
Down syndrome children have their very own special talents & can bring lots & lots of love into parents' lives if they accept the job of raising them; although they may be demanding & require much supervision, they have lots to give to deserving & caring parents.