S. 1810 (110th): Prenatally and Postnatally Diagnosed Conditions Awareness Act

Introduced:
Jul 18, 2007 (110th Congress, 2007–2009)
Status:
Signed by the President
Slip Law:
This bill became Pub.L. 110-374.
Sponsor
Samuel “Sam” Brownback
Senator from Kansas
Party
Republican
Text
Read Text »
Last Updated
Sep 26, 2008
Length
4 pages
Related Bills
H.R. 3112 (Related)
Prenatally Diagnosed Condition Awareness Act of 2007

Referred to Committee
Last Action: Jul 19, 2007

 
Status

This bill was enacted after being signed by the President on October 8, 2008.

Progress
Introduced Jul 18, 2007
Referred to Committee Jul 18, 2007
Reported by Committee Mar 13, 2008
Passed Senate Sep 23, 2008
Passed House Sep 25, 2008
Signed by the President Oct 08, 2008
 
Full Title

A bill to amend the Public Health Service Act to increase the provision of scientifically sound information and support services to patients receiving a positive test diagnosis for Down syndrome or other prenatally and postnatally diagnosed conditions.

Summary

No summaries available.

Cosponsors
6 cosponsors (3R, 2D, 1I) (show)
Committees

House Energy and Commerce

Senate Health, Education, Labor, and Pensions

The committee chair determines whether a bill will move past the committee stage.

 
Primary Source

THOMAS.gov (The Library of Congress)

GovTrack gets most information from THOMAS, which is updated generally one day after events occur. Activity since the last update may not be reflected here. Data comes via the congress project.

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Notes

S. stands for Senate bill.

A bill must be passed by both the House and Senate in identical form and then be signed by the president to become law.

GovTrack’s Bill Summary

We don’t have a summary available yet.

Library of Congress Summary

The summary below was written by the Congressional Research Service, which is a nonpartisan division of the Library of Congress.


10/8/2008--Public Law.
Prenatally and Postnatally Diagnosed Conditions Awareness Act -
Section 3 -
Amends the Public Health Service Act to require the Secretary of Health and Human Services, acting through either the Director of the National Institutes of Health (NIH), the Director of the Centers for Disease Control and Prevention (CDC), or the Administrator of the Health Resources and Services Administration (HRSA), to authorize and oversee certain activities relating to Down syndrome or other prenatally or postnatally diagnosed conditions.
Includes among such activities the awarding of grants, contracts or cooperative agreements to eligible entities to:
(1) collect, synthesize, and disseminate current evidence-based information relating to such conditions; and
(2) coordinate the provision of, and access to, new or existing supportive services for patients receiving a positive diagnosis for such conditions.
Includes within such supportive services:
(1) the establishment of a resource telephone hotline;
(2) the expansion of the National Dissemination Center for Children with Disabilities;
(3) the expansion of national and local peer-support programs;
(4) the establishment of a national registry, or network of local registries, of families willing to adopt newborns with such conditions; and
(5) the establishment of awareness and education programs for health care providers who provide, interpret, or inform parents of the results of prenatal tests for such conditions.
Requires the Secretary to place an emphasis on funding partnerships between health care professional groups and disability advocacy organizations in distributing funds.
Requires a grantee under this Act to make available to health care providers of parents who receive a prenatal or postnatal diagnosis:
(1) up-to-date, evidence-based, written information concerning the range of outcomes for individuals living with the diagnosed condition, including physical, developmental, educational, and psychosocial outcomes; and
(2) contact information regarding support services, including information hotlines, resource centers or clearinghouses, national and local peer support groups, and other educational and support programs.
Requires information provided to be culturally and linguistically appropriate and to be approved by the Secretary.
Requires the Government Accountability Office (GAO) to report to Congress concerning the effectiveness of current health care and family support programs serving as resources for the families of children with disabilities.

House Republican Conference Summary

The summary below was written by the House Republican Conference, which is the caucus of Republicans in the House of Representatives.


No summary available.

House Democratic Caucus Summary

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