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Jenny Bockerstette | Wednesday, 21 March 2007

Disability must be valued

American doctors are being told to screen all pregnant women for Down syndrome. But aren't we all imperfect in some way?

Sujeet Desai giving a lectureOn March 21, the second annual World Down Syndrome Day is being celebrated in communities around the globe. The date signifies the uniqueness of Down syndrome in the triplication of the 21st chromosome. In my community, the Down Syndrome Association of Northeast Indiana (DSANI) is hosting its seventh annual meeting featuring Sujeet Desai, an accomplished 25-year-old from Rome, New York. Sujeet plays six instruments including violin, piano and alto sax. He has a second degree Black Belt in Tae Kwon Do and holds several Special Olympics medals in swimming, alpine skiing and cross-country running. Sujeet and his wife Carrie Bergeron-Desai were recently featured in articles appearing in the Wall Street Journal and the New York Times. They have also appeared on national television on "20/20," "Oprah" and "The View." Both Sujeet and Carrie have Down syndrome.

Sadly, recommendations released in January by the American College of Obstetricians and Gynecologists (ACOG) cast a dark cloud on this celebration. The College now recommends "that all pregnant women, regardless of their age, be offered screening for Down syndrome. Previously, women were automatically offered testing if they were 35 years old and older."

What the College fails to note in their press release, yet reported in the Wall Street Journal in 2005, is that studies have shown that early detection of Down syndrome in pregnancies has resulted in an 80 to 90 per cent termination rate. Another study estimates that the number of Down syndrome live births in the U.S. declined by 7.8 per cent from 1989 to 2001, which its authors suggest is likely the result of prenatal testing, leading to termination of pregnancies.

While some may see ACOG's recommendations as just another reflection of the pro-choice versus pro-life debate, a more informed understanding of these alarming trends reveals a different issue at hand. Recommending guidelines, which have led to the termination of 80 to 90 per cent of a specific population, is tantamount to advocating the practice of eugenics, ie, selection by judgment of genetic worthiness. Down syndrome is a natural human condition, not a disease suitable for extinction. The College’s guidelines -- that all pregnant women, regardless of age, be screened for Down syndrome -- are a subtle yet important step down a different but very disturbing path of a selection process which takes the lives of people with disabilities first.

The National Down Syndrome Congress, of which our local Down Syndrome Association is an affiliate, "condemns" the recent recommendations as conveying "tacit approval for terminating pregnancies where the fetus has Down syndrome". The medical doctors comprising the National Down Syndrome Congress’ Professional Advisory Committee cite the concern that "recent studies by Dr Brian Skotko, published in the American Journal of Obstetrics and Gynecology (2005) and Pediatrics (2005), note that many doctors are inadequately prepared to deliver a diagnosis of Down syndrome, and often use negative language or out-of-date information".

Individuals with Down syndrome, like my own daughter Amy, and others with disabilities, present challenges, yes, but challenges are inherent to parenting any child. People like Amy also offer love and affection, laughter and joy. They teach us compassion and acceptance. They test our character. They also show us that followers can sometimes be the greatest leaders. Individuals with Down syndrome, just like everyone else, form friendships, establish goals and realise dreams. And, like Sujeet Desai and his wife Carrie, they want to form relationships, contribute to society, sometimes marry, and lead happy and fulfilling lives.

Disability is a natural part of the human condition as each of us is less than perfect. Why attack those with Down syndrome as less worthy than others in this world? Simply because that hereditary condition is now easier to diagnose prenatally? Over the past 30 years the United States has enacted progressive human rights legislation for people with disabilities, including the Americans with Disabilities Act and the Individuals with Disabilities Education Act. How can we celebrate our social enlightenment while targeting that same human population for termination?

As we celebrate World Down Syndrome Day on March 21, let us call upon our obstetricians, gynaecologists and family doctors, as well as each other, to value individuals with Down syndrome and all people with disabilities. Let us embrace and respect our humanity. For who among us is not worthy of this right?

Jenny Bockerstette is the mother of an eight-year-old daughter with Down syndrome, a founding member of the Down Syndrome Association of Northeast Indiana, and the incoming president of the association.

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Disability Benifits said... United States | Mon, 1 Sep 2008 at 11:44 am

Great article. We all are imperfect in our way and it is better to build up on our strengths than contemplate on weaknesses.


Scooter said... United States | Sun, 11 May 2008 at 4:30 pm

People need to understand that a life is a life and we should all have the same right to live. Just because you are different doesn’t make you worth less.


Elmer Lapena said... Philippines | Wed, 27 Jun 2007 at 10:59 pm

I fully agree that we can learn so much from people with down syndrome.  Their unique qualities and experiences can be life-changing and have strong impacts on many, many others.  We have an 11 year old son and we can’t seem to run out of nice (and not so nice) experiences with him.  He is a sheer bundle of joy and I would venture to say that people who are closest to them know best.  I fully support the move to inform others and advocate the cause of people with down syndrome, as well as other disabilities.  We are not alone in this world and they are indeed a part of us.  It is a blessing in disguise that early detection is not commonly available in the Philippines, coupled with the anti-abortion law.  Regardless, it is equally important that the many children born with down syndrome are given a chance to live a more normal life.  The advocacy campaigns and awareness seminars to promote information are key programs toward this goal. 

As in many developing countries, such efforts need to be driven by voluntary organizations, and we are no exception.  We have over 2000 registered members and many, many more (over 5000) who have attended our seminars and activities throughout the years.  Our organization has been in existence for 15 years now, thankfully through kind and generous donations as well as very strong and dedicated volunteerism from the members. 

Any support and donations are welcome.

Sincerely,
Elmer Lapena
Chairman
Down Syndrome Association of the Philippines, Inc.
2nd Floor, 6372 Agrifina Building,
Camia corner Meleguas Streets,
Guadalupe Viejo
Makati City
Philippines

Tel: +63 2 895 9642 / +63 2 895 3606
email:


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