Congenital Diaphragmatic Hernia Research Act of 2012
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S 3396 — Congenital Diaphragmatic Hernia Research Act of 2012
Last action — Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
No card. One bill, free forever — alerts when it moves.
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✓Introduced
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✓In Committee
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Died in session
This bill died with 112th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
This bill is no longer active — its legislative session has ended, so there is no live prognosis. It would have to be reintroduced in the current session to move again.
Summary
Congenital Diaphragmatic Hernia Research Act of 2012 - Amends the Public Health Service Act to direct the Secretary of Health and Human Services (HHS) to carry out a national campaign to increase public awareness and knowledge of Congenital Diaphragmatic Hernia, including through: (1) the dissemination of information on the definition of Congenital Diaphragmatic Hernia and on good neonatal care of Congenital Diaphragmatic Hernia patients, (2) outreach to minority populations regarding Congenital Diaphragmatic Hernia, and (3) the promotion of good prenatal care and ultrasound to detect Congenital Diaphragmatic Hernia in utero. Requires the Director of the National Institutes of Health (NIH) to evaluate the amount of federal assistance provided for Congenital Diaphragmatic Hernia research at NIH to determine whether funding levels are adequate. Expresses the sense of the Senate that the Director should consider allocating funds and other resources for Congenital Diaphragmatic Hernia research.
Bill Text
We don't have the full text on file for this bill yet.
Read S 3396 on the official United States source →Action History
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Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
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Sponsor introductory remarks on measure. (CR S5135-5136)
Sponsors
- Jeff Sessions · Primary
Sponsorship breakdown
Export CSV (upgrade) →1 sponsors · 0 co-sponsors · 546 not signed on
Sponsors (1)
Co-sponsors (0)
None.
Not signed on (546)
546 members have not signed on to this bill.
Show all 546 →"Not signed on" means a member has not sponsored or co-sponsored this bill — it does not imply opposition. Members flagged Voted No have a recorded No vote on this bill.
Subjects
Frequently asked questions
- What does S 3396 do?
- Congenital Diaphragmatic Hernia Research Act of 2012 - Amends the Public Health Service Act to direct the Secretary of Health and Human Services (HHS) to carry out a national campaign to increase public awareness and knowledge of Congenital Diaphragmatic Hernia, including through: (1) the dissemination of information on the definition of Congenital Diaphragmatic Hernia and on good neonatal care of Congenital Diaphragmatic Hernia patients, (2) outreach to minority populations regarding Congenital Diaphragmatic Hernia, and (3) the promotion of good prenatal care and ultrasound to detect Congenital Diaphragmatic Hernia in utero. Requires the Director of the National Institutes of Health (NIH) to evaluate the amount of federal assistance provided for Congenital Diaphragmatic Hernia research at NIH to determine whether funding levels are adequate. Expresses the sense of the Senate that the Director should consider allocating funds and other resources for Congenital Diaphragmatic Hernia research.
- Who sponsors S 3396?
- S 3396 is sponsored by Jeff Sessions (R).
- What is the current status of S 3396?
- This bill died with 112th Congress. It reached “In Committee” and never advanced before the session ended, so it can no longer move — a new version would have to be reintroduced in the current session.
- Where can I track S 3396?
- Track S 3396 free on One Click Politics — get push/email alerts when it moves.
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