HRES 536
111th Congress
House
Health
Blood and blood diseases
Cardiovascular and respiratory health
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Health promotion and preventive care
Hereditary and development disorders
Medical research
Expressing support for the HHT Foundation International's designation of a "National Hereditary Hemorrhagic Telangiectasia (HHT) Month" and supporting efforts to educate the public about HHT.
Introduced: June 11, 2009
Introduced by:
Neal, Richard E.
Democratic
· Massachusetts
See on congress.gov
Everywhere this bill has been
4 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Jun 12, 2009
Referred to the Subcommittee on Health.
Jun 11, 2009
Referred to the House Committee on Energy and Commerce.
Jun 11, 2009
Sponsor introductory remarks on measure. (CR E1380)
Jun 11, 2009
Introduced in House
Plain-English summary
Expresses support for: (1) the HHT Foundation International's designation of a National Hereditary Hemorrhagic Telangiectasia Month; and (2) the Foundation's work to find a cure while saving lives and improving the well-being of those affected by Hereditary Hemorrhagic Telangiectasia (HHT) through research, outreach, education, and support.
Recognizes the need to pursue research into better treatments and a cure for HHT.
What's happening now
Referred to the Subcommittee on Health.
Committees of jurisdiction
2