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Discovering a world of hope

November 10th, 2007

From the [Toronto] Star:

Renate Lindeman, president of the Nova Scotia Down Syndrome Society, is the mother of two daughters with Down syndrome. She chose not to have an amniocentesis for her first pregnancy, but did so for the second even though she and her husband had decided to carry the pregnancy to term regardless of the test findings.

The result, she writes, was that the remainder of her second pregnancy was unpleasant and stressful, as she dealt with the reactions of those around her. An excerpt:

On top of the usual hormonal mood swings, I was now dealing with feelings of guilt. Society doesn’t always embrace people with special needs. Was it fair to bring my baby into this society with the challenges associated with Down syndrome?

With a kicking baby growing inside of me, I was asked: “Did you consider abortion?” … “Are you sure you know what you’re doing?”

Prospective parents who dream of having a perfect child suddenly face agonizing psychological, social and ethical dilemmas for which there seems to be no “right choice.” With only a physician’s view of a prenatal diagnosed condition as guidance, is it surprising that more than 90 per cent of parents choose termination?

The only advice I can give parents is that there is light at the end of the tunnel. Whatever you decide, make sure you know the true facts about your baby’s diagnosed condition so you can make a well-informed decision.

Know there is a world of hope, resources and support out there. We – families with special needs – might seem invisible to the general public, but we are many and we are a resilient, supportive and joyful bunch.

One Response to “Discovering a world of hope”

  1. William L. Freeman Says:

    Renate Lindeman wrote that society asked, “Was it fair to bring my baby (with Down Syndrome) into this society with the challenges associated with Down Syndrome? With a kicking baby growing inside of me, I was asked: ‘Did you consider abortion?’”

    Why is it considered OK to ask or raise those questions to women with a baby with Down Syndrome, both while pregnant (Renate Lindeman, and many others) or after the baby is in this world (Pat Bauer, and many others)? Is it appropriate to judge or question a woman’s decision about her pregnancy, when we others do not “walk in her moccasins”?

    Those questions were not asked to African American women just after slavery in societies with state-sponsored terrorism (that is, lynchings to preserve the stratus quo). They are not asked to women who are African American, American Indian or Alaska Native, immigrants from Mexico, Arab or Muslim American, in severe poverty, or in a lesbian relationship — whose children likely will experience the challenges of discrimination.

    Should we deal with the challenges of Down Syndrome, or of discrimination or worse, by always ending the pregnancy? I prefer to try to reduce unnecessary challenges.

    Thank you, Renate, Pat, and so many in this website, for helping to reduce such challenges.

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More than 50 million people in the United States have disabilities, a number that is growing rapidly as the population ages. Experts say disability will soon affect the lives of most Americans. This website attempts to aggregate news and commentary about disability, and to document the efforts of people who are seeking new ways to address familiar challenges.

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