Mark W. Leach at Public Discourse argues that, at least in the case of the selective abortion of Down Syndrome children, being pro-life is simply not enough to stop abortion:
Therefore, while pro-life organizations advocate for social change in recognizing that fetuses also have a right to life, a different social change is needed to address expectant mothers’ concerns who are considering aborting their unborn children with Down syndrome. As the national advocacy organizations, NDSS and NDSC should be at the forefront in challenging public policy to effect this change. Instead of investing $16,000 of scarce public healthcare dollars to pay for aborting children with Down syndrome, why not invest those funds in early intervention therapies to enable them to be more self-sufficient? Instead of California investing millions since the 1980s in prenatal testing for Down syndrome, why was that money not used to provide better support resources for individuals with Down syndrome? And, instead of the federal government investing over $15 million in the development of new prenatal tests for Down syndrome and now requiring prenatal testing at no cost through the recent HHS regulations on preventive care services, why is there not a corresponding investment to fully fund the Prenatally and Postnatally Diagnosed Conditions Awareness Act to provide accurate information and support services to expectant parents?
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