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Prenatally and Postnatally Diagnosed Conditions Awareness Act Introduced.

National Right to Life News

| August 01, 2007 | COPYRIGHT 2007 National Right to Life Committee, Inc. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

Senator Sam Brownback (R-Ks.) used a July 18 press conference to highlight the importance of the Prenatally and Postnatally Diagnosed Conditions Awareness Act which would assist parents of unborn and born children diagnosed with disabilities. The proposed legislation would require that families who receive a diagnosis of Down syndrome or any other condition, prenatally or up until a year after birth, be given up-to-date information about the nature of the condition and connection with support services and networks that could offer assistance. Sen. Edward Kennedy (D-Mass.) is a co-sponsor.

The press conference featured a baby with Down syndrome, disability rights advocates, and an adult with Down syndrome who outlined his achievements. David Egan of the National Down Syndrome Society delivered a speech that helped dispel the myth that persons with Downs cannot function independently or enjoy meaningful achievements as productive members of society.

Brian and Michelle Ray, parents of a baby with Down syndrome, explained the need for more information and support for parents who receive news of the diagnosis for their baby.

Sen. Brownback observed, "We as a society must offer as much protection as we can to 'the least of these.' When a mother receives the news that her unborn child may be born with a disability, she should be supplied with current and reliable information about the many options available for ...

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Source: HighBeam Research, Prenatally and Postnatally Diagnosed Conditions Awareness Act...

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