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Earlier Down Syndrome Test Proves Both Comforting And Challenging

Down Syndrome Test

By MALCOLM RITTER   06/12/11 12:02 AM ET   AP

NEW YORK -- The results of the blood test revealed only a risk, but when she saw them, she still threw up. Now she had to find out for sure.

So she lay on her back at a doctor's office, praying, comforted by her Christian faith and her mother at her side, while a needle was slipped into her belly.

Erin Witkowski of Port Jervis, N.Y., was going to find out if the baby she was carrying had Down syndrome.

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This is the first of a two-part series on prenatal testing and the ethical issues raised by it.

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For years, many women have gone through an experience like hers: a blood or ultrasound test that indicates a heightened risk of the syndrome, followed by a medical procedure to make a firm diagnosis by capturing DNA from the fetus.

Usually it's the needle procedure Witkowski had, called amniocentesis, done almost four months or more into the pregnancy. Sometimes it's an earlier test called CVS, or chorionic villus sampling, which collects a bit of tissue from the placenta. Both pose a tiny but real chance for miscarriage, and experts say highly skilled practitioners are not available everywhere.

But by this time next year there may be an alternative – one that offers accurate results as early as nine weeks into the pregnancy.

Companies are racing to market a more accurate blood test than those available now that could spare many women the need for an amnio or CVS. It would retrieve fetal DNA from the mother's bloodstream. And the answer could come before the pregnancy is obvious to others. For some women, that might mean abortion is a more tenable choice. For others it could be a mixed blessing.

Down syndrome slows mental and physical development, and people with it usually show mild to moderate disability in intellect and skills for everyday living. Physically, they often have a flat face with a short neck and smaller hands and feet. They're at risk for complications like heart defects and hearing problems. Life expectancy is about 60 years.

Most cases are diagnosed after birth now, but if the blood test is widely adopted it could become chiefly a prenatal event.

A diagnosis before birth can pose a difficult challenge for couples as they decide whether to continue the pregnancy. It's not only about child-rearing, but also about what happens as the child grows into an older adult and may need care that the aging parents struggle to provide, says Dr. Mary Norton, a Stanford University professor of obstetrics and gynecology.

Dr. Brian Skotko, a Down syndrome specialist at Children's Hospital Boston who has written a research paper for doctors on how to deliver a diagnosis, said "the vast majority of people with Down syndrome and families affirm that their contributions to their communities are significant, and their lives are very valuable."

Current prenatal screening has already cut into the number of babies born with the syndrome, which now stands at about 6,000 each year in the United States, or about 1 in every 691 babies, says Skotko, who serves on the board of the National Down Syndrome Society. He cites one study that concludes the number of Down syndrome births in the nation dropped 11 percent between 1989 and 2006, a time when it would otherwise be expected to rise 42 percent.

Initially, doctors are expected to use the new blood test with women at risk for a Down syndrome pregnancy, such as those older than 35. A negative result would indicate a woman could skip the amnio or CVS; a positive result would suggest she get one done to be sure.

Eventually it might replace the routine screening tests offered to all pregnant women. Since the test sounds fewer false alarms than current tests, fewer women would be told they need the invasive follow-up procedures, experts say. And some suggest that with further fine-tuning, it could largely replace amnio and CVS. With no miscarriage risk, more women might be willing to take it, and so more women would find out they have a Down syndrome pregnancy.

Two California companies, Sequenom Inc. and Verinata Health Inc., hope to offer the test to doctors in the United States by next April. They say it could be done in the first trimester, with Sequenom aiming as early as 10 weeks, and Verinata as early as eight weeks. Results would be available 7 to 10 days later. In addition, LifeCodexx AG of Germany says it wants to start offering its test in Europe by the end of this year, to be performed at 12 to 14 weeks initially. None of the companies would discuss its cost.

"I would have definitely taken a noninvasive test over the struggle for deciding whether to do an amnio or not," says Nancy McCrea Iannone of Sewell, N.J., who gave birth six years ago to a daughter with Down syndrome. She'd been alerted by screening results, but hesitated to get amniocentesis because of the risk of a miscarriage and the prospect of "a needle in my belly," she recalls. Ultimately, she did have one.

Iannone now counsels women who plan to deliver babies with Down syndrome. Her charitable group, Down Syndrome Pregnancy Inc., lists several reasons for getting a diagnosis before birth, such as more time to adjust, grieve and learn about the condition, preparing friends and family, and checking on available medical care and insurance.

But detecting the condition earlier in a pregnancy through the new blood test would be a mixed blessing, Iannone said.

The time between diagnosis and birth is "an unnatural state," she said, and "the longer that time period is, the harder it is."

"All you know is that they have Down syndrome. You're coping with that diagnosis in a vacuum, without a baby... It's fear of the unknown, you haven't met your baby yet. You spend a lot of time worrying."

That might weigh heavily on women who haven't decided whether to continue the pregnancy or not, she said.

Since the new blood test could deliver an answer so early – before a pregnancy is showing or the baby is kicking – it might make getting an abortion easier, several observers said. Women haven't bonded so much, and "they wouldn't have to explain to as many people," said Christie Brooks, who moderates an online support group for women who've gotten abortions for medical reasons.

"No one needs to know you're pregnant," said Skotko. "Maybe you haven't even told your husband."

Skotko said he respects that a woman's right to continue or terminate a pregnancy is a personal one for couples. But he's concerned that in the case of Down syndrome, many women may be getting bad information about what having the baby would mean. And if the new test became routine it would only exacerbate that problem, he said.

Studies show medical students are poorly trained about people with disabilities and that some doctors who make a prenatal diagnosis emphasize negative information about the condition, he said.

"We have a fleet of physicians who are saying they're untrained, unprepared and sometimes knowingly inserting their own personal bias," he said. "How are women today able to make a truly informed decision?"

Others say the blood test could thrust some women into a choice they didn't ask to make.

Hank Greely, a Stanford University law professor, said women sign forms for plenty of blood tests during prenatal care and often don't focus on them. Many California women are surprised to learn they'd authorized the screening test for Down syndrome, he said.

If these tests are someday replaced by the new blood test, many women may be told out of the blue not simply that they're at risk, but that in fact their baby almost surely has Down syndrome, Greely says.

"They're going to jump directly to the final answer, which is not necessarily something they wanted to get," Greely said. So the new test poses a challenge to the medical establishment about how to assure that women get adequate counseling to make an informed choice, he said.

Witkowski, who prayed as that needle was slipped into her swollen belly in 2009, got her answer: It was Down syndrome. As her doctor gave her the news, her baby kicked her and "I could see my belly move," she recalled.

Her doctor started talking immediately about abortion, a step Witkowski rejected. She changed doctors and gave birth to Grady in February 2010.

"When they first gave him to me," Witkowski said, "I saw tiny little hands, and he had the most beautiful eyes... He didn't have `Down syndrome' stamped on his forehead. He cried and he peed and he pooped. He was a baby."

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NEW YORK -- The results of the blood test revealed only a risk, but when she saw them, she still threw up. Now she had to find out for sure. So she lay on her back at a doctor's office, praying, comf...
NEW YORK -- The results of the blood test revealed only a risk, but when she saw them, she still threw up. Now she had to find out for sure. So she lay on her back at a doctor's office, praying, comf...
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05:54 PM on 06/14/2011
I had the CVS test with my first and second pregnancy as well as an amnio. Both test came back indicating that my children had DS. I now have a 13 year old son and a 9 year old daughter. Neither has DS. My 13 year old son has an IQ of 121. I had a consultation with a genetic specialist who, on both occassions, suggested that I abort the pregnancies due to the difficulties, time and financial, of raising a child with DS. I was 27 and 31 years old at the time of the pregnances, and I had been trying to have a child for 7 years, I was not willing to give up. I didn't even listen to them when the second test came back positive.

I have met many mothers of special needs children and their lives seem stressed and rough. Doctor's appointments, schools, just keeping up with these children can be tiring, but some normal children can be just as difficult. ADHD, autisim, just plain being a "smart-ass", will they some day make tests for these problems and let us decide if we want to keep these kids or abort them? Sometimes you have to play the hand your dealt. Cancer genes, blue versus brown eyes, short, bald, fat, these are the things that make us unique and some may kill us some day. Obesity kills more people than cancer. Take life as it is. That's the best that anyone can do.
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nonibright
06:39 PM on 06/13/2011
My 34 year old Down Syndrome daughter is the light of my life! I have learned so much from her and because of her. I was 33 when she was born, none of the tests available then were suggested to me as an option. When we brought her home, my older daughter said after being told that she would not be as 'normal' as everyone else, "I'm going to love her any way she is!". A wise declaration from a five year old.

In CA, we have some state legislation, the Lanterman Act, that helps provide many services for the DD population. My daughter started an infant stimulation program at the age of 5 mos. and continues to attend an activity program for adults. She is active in community activities, volunteer programs as well as leisure activities - they've even done musical productions. We chose this for her rather than have her just sit and sort nut and bolts in a workshop.

There are some things I have to compromise in my life to accommodate hers, in the end, the joy she brings me is sometimes overwhelming. She and I live together, she loves to go to Vegas, (she is very lucky too!), and she loves to attend the musical theater productions in Hollywood.

If I had to make the choice, I'm sure I would NOT miss the opportunity of being a part of her life!!
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MISTERUNCONVENTIONAL
The only attitude I've ever had is a bad one.
03:36 PM on 06/13/2011
I'm the brother of a special needs kid.

I could never bring myself to having children because of the sheer hell I saw my parents endure.

Seeing him being picked on, bullied, tormented, with me younger, and smaller, unable to stand up for him. Not just in school, he once got beat up in Sunday school.

That one cost my mother whatever faith she ever had in a loving God.

This was in the days BEFORE special education, when all the school system wanted to do was get rid of him.

My mother grew old fast trying to care for him, and create a half way decent life Working the medical system, battling the insurance companies over his care.

Now that my father is 87, my turn to care for my brother is coming soon.

My brother is a kind, intelligent, funny guy --- with no common sense whatsoever. I would never say I wish he hadn't been born, but....the children I might have had never will be because of what I saw him go through, and the possibility I too might have a special needs child.

A lot of pregnancies result in miscarriage. God, if He exists, simply doesn't plan for every embryo to be born.

Judge not! the bible says, over and over. The decision to bring a DS child into this world is the parents, and the parents alone.
03:15 PM on 06/13/2011
As a single Mom of a son with Down Syndrome, I certainly understand the need/desire for more accurate and earlier testing. However, that said, and having had an amniocentesis myself -- for both accuracy and to ensure that any health issues my son might have would be as anticipated and cared for directly after birth -- I would not have done anything different. Granted, it was one of the most difficult decisions of my entire life. However, now looking back when my son is 20 years old, I would not ever -- EVER -- trade what was given to me. My son has given me such a unique perspective on life. He will never be what the world terms as "normal," but that's how the world looks at him. To me, he's absolutely perfect in every way -- with a superb sense of humor, I might add! To any of you contemplating this in your life, it will not be without many wonderful rewards as parents, believe me!
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Arthur Spooner
Conservative govnmt is organized hypocrisy
01:52 PM on 06/13/2011
We are a working class one income family. I have a child with Down Syndrome. This falsehood that the government hands out checks to kids with disabilities has got to stop.You have to be damn near the poverty level to receive any aid. People need to understand, it's not the every day people who's robbing you of your tax paying dollars. It's the Rick Scott"s of the world who does.
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SF TKF
Cthulhu thinks you'd make a nice sandwich.
11:06 AM on 06/13/2011
Parents should be given the opportunity to decide if they’re ready to take on a developmentally disabled child as early as possible, and there should be no stigma assigned to whatever choice they make. I grew up around several developmentally disabled kids (DS, retardation, autism), and I can tell you right now that not every parent is able to handle it.
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MISTERUNCONVENTIONAL
The only attitude I've ever had is a bad one.
09:50 AM on 06/13/2011
I'd really like to call into question the Conservative "bootstrap" and Ayn Rand crowd here.

DS children will never pull themselves up by their bootstraps.

The simple fact is a DS child will require government help in their lives, from special education, to social security disability to Section 8 housing, to who knows what, unless the parents are, to be blunt, rich.

Any Conservative / Republican who would deny the DS child, and/or his family that help is in no position to comment on whether or not abortion should be safe and legal.

There are costs besides the financial ones. When the DS child starts getting picked on or bullied in school. It's a horror, because the parent/sibling can't be with them 24x7. When they grow old, and still need care.

This is what amazes me most about Sarah Palin, having a special needs child, and instead of giving him the care he needs, she's "out on the road" 24x7. Who is providing Trig his care? Nannies?

The rubber meets the road about loving others as we love ourselves when it comes to Special Needs kids, especially DS. And quit frankly, all I see from Conservatives / Republicans is a gigantic FAIL.
10:28 AM on 06/13/2011
Well said. Thank you!
10:50 AM on 06/13/2011
It's amazing the kind of cognitive dissonance involved in the mind of an ideologue.
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Devontate
PrObama
08:50 AM on 06/13/2011
If I was carrying a DS baby, I would be likely to abort because I would be concerned about providing the care my child needed throughout his/her life. If s/he is disabled and incapable of being a self-supporting adult, how can I guarantee that when I'm gone, s/he will be getting the care s/he needs? And how can anyone afford to have a child that will be financially dependent forever? I know making childbearing decisions based on finances is unpopular, but let's face it; without financial stability, it's a lot harder to provide ANY child, let alone a special needs child, with eeverything they want and need to be healthy and happy. I don't know how anyone affords children at all these days.
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08:48 AM on 06/13/2011
Some women choose to have a baby with DS, others choose not to. It is their choice to decide and neither group should be criticized for making this difficult choice,
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ray newman
Reality has a Liberal bias
09:55 AM on 06/13/2011
What about the women/woman who fakes a pregnancy and reveals a DS baby for evangelical political kudos ????
08:38 AM on 06/13/2011
My brother-in-law is learning disabled. He is blessed to have a family with members that are young enough, willing and able to take care of him when my mother-in-law is no longer capable. But it is a full time job for my mother-in-law who is now in her 70's. I have heard horror stories from her about women and men in their 80s, overwhelmed with trying to take care of their child. They can't do it physically or financially and both the caregiver and the child suffers. The mental anguish about what will happen to their child when they are no longer here, is all consuming. Having a handicapped child also affects marriages and the mental health of the other children in the family. It can eventually affect the other children's marriages and families. Many get caught in having to be the caregiver of a parent and a handicapped sibling. So if you want people to embrace having a handicapped child, put your money where your self-righteousness is and fund programs that will assist these families and the kids long term.
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fenderbender1
the stairway to heaven is missin a few steps
07:30 AM on 06/13/2011
Not all apples that fall from trees are good for making pie.Then again, not all apples that are not good for making pies are worthless. Some are made to study and be a force for information in hope of someday making apples better.
08:10 AM on 06/13/2011
Isn't it ALWAYS the 'apples' and 'oranges' conundrum?
02:05 AM on 06/13/2011
To be blunt, I take the comments of the posters with children or siblings who have DS with a huge grain of salt. Consider how awful the implications would be towards those they knew with DS if they were advocates for these tests and aborting babies with DS. Personally, I'm most interested in hearing what caretakers of people with DS would do if it they were pregnant.
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Peter Heffernan
clear-thinking compassion fan
02:35 AM on 06/13/2011
You're salting the wrong dish, Bluntington von Bluntstone. All my skepticism is reserved for those whose opinions are (very sturdily!) formed withOUT the benefit of knowing people with DS. Do yourself a favor this lifetime: get to know people who are very different from you. I especially recommend individuals with Down syndrome. Those of us who DO have DS in our families are not making political calculations based on the implications of our advocating one way or another. We're trying to get it through the rest of your skulls that these people we love are WORTH LOVING.
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gardengranny
Ever-hopeful for the best; preparing for the worst
09:45 AM on 06/13/2011
Of course they are worth loving. They are here and they are family.

However, to criticize someone who makes the decision NOT to bring a child with DS into the world seems judgmental at best.
02:37 AM on 06/13/2011
Yes, I think you should definitely disregard the comments of people who actually know people with Down Syndrome.
06:44 AM on 06/13/2011
A caretaker of people with DS doesn't actually know people with DS?
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Arthur Spooner
Conservative govnmt is organized hypocrisy
01:32 AM on 06/13/2011
As a parent with a child with Down Syndrome, it's astonishing to see how ignorant people really are. Googling Down Syndrome does not make one a laymen AND it's really not enough to make a informative opinion. You SHOULD NOT base your opinion on outdated material and old memories.
11:04 AM on 06/13/2011
This was my reaction as well to reading so many of these responses. (I'm also a parent of a young man with Down Syndrome).
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VanTroi
01:00 AM on 06/13/2011
I chose to have an amnio due to my age when I was pregnant with my son. I would not have an abortion no matter what the out come was. My Dr was aware of this as we had discussed it. I want to know to prepare myself. The amnio came back low risk, which allowed me to relax and enjoy my pregnancy. I think the earlier test may tempt women to have an abortion. An amnio is done way later than most would consider it.
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hoobit
GOP/TBs: The USA is Not a game!
04:46 AM on 06/13/2011
I'm glad your test came back "low risk," and you were able to "relax and enjoy [your] pregnancy." Shouldn't ALL women be able to relax and enjoy their pregnancy? Now what about those women whose tests come back as "high risk" -- shouldn't they, too, be afforded the option of having a pregnancy they, too, can enjoy and relax through? The words: sanctimonious and mean, come to mind. Just because abortion was not an option for you, personally, please do not assume a woman might be 'tempted' to have one if definitive tests are made available to her sooner; she will made the decision that is right for her in her specific situation. Besides which, it's no one else's business.
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VanTroi
11:17 PM on 06/13/2011
Yo chill out take a midol.
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gardengranny
Ever-hopeful for the best; preparing for the worst
10:25 AM on 06/13/2011
An amnio would have come back definitive for DS and other anomalies. It would not just assess "risk."

Maybe you are referring to a test like CVS, which is performed earlier in the pregnancy, and is not as specific.
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VanTroi
11:16 PM on 06/13/2011
I think I know what tests I had, I had a huge needle stuck in my abdomen. Yes risk of having a downs baby.
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funcrusherplus
twitter.com/edreese
12:22 AM on 06/13/2011
Anti-choice people, we don't really need your input here. We all know what you think, and it has nothing to do with whether or not the fetus has DS.
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TWeissMA
http://www.disabilitymessage.com
05:04 PM on 06/13/2011
The face-off between disability rights and abortion rights is certainly rough, isn't it? Many here would be quick to label me as an, 'anti-women's rights,' or, 'anti-abortion rights,' person when I am not. The dilemma I face is that disability rights will always take precedence over any other issue for me.

Does this somehow make me a, 'bad person?' I don't believe so. The issue is one of support for both parents and children with disabilities as far as I am concerned. Remember - this is my opinion, not something cast in stone or something. I have not committed a crime by having the opinion I hold.

Stating that I do not have a right to my opinion is something I find to be offensive, yet - that is indeed your opinion and I understand that. You of course, most likely find my opinion offensive, despite the fact that I support People with Disabilities, this nation's largest minority population.
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funcrusherplus
twitter.com/edreese
02:13 AM on 06/14/2011
Ok, take a deep breath, go back and read what I said, and try to imagine the spirit in which I was saying it.

"The face-off between disability rights and abortion rights is certainly rough, isn't it?"

Yes, it certainly is. Unless you are anti-abortion, in which case you are against it regardless, and therefore your opinion is redundant, understood, and the expression of it unnecessary.

The rest of what you said doesn't apply to anything I said. Disability rights are super important for you? Excellent. I am sure that those with disabilities can always use more advocates. Of course you haven't committed a crime. Of course you have a right to your opinion. I never said either of those things. Once again, the point of my statement was: "If you are against abortion under most or all conditions, then your opinion on this particular more nuanced issue does not need to be expressed. Because it will always be the same, whether the child has disabilities or not. It is more interesting, more important, for those of us who are pro-choice under most circumstances to have a dialogue about this, because some of us may find that "the face-off between disability rights and abortion rights" is rougher than we expected, and therefore more challenging to our previously held ideas.

Do you understand the point I was trying to make and how it differs from your response?