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.

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Related Legislation

• S.Res. 141A resolution recognizing June 2009 as the first National Hemorrhagic Telangiecstasia (HHT) month, established to increase awareness of HHT, which is a complex genetic blood vessel disorder that affects approximately 70,000 people in the United States.

  2009-05-11Referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S5332)

  Related
• S.Res. 161A resolution recognizing June 2009 as the first National Hereditary Hemorrhagic Telangiecstasia (HHT) month, established to increase awareness of HHT, which is a complex genetic blood vessel disorder that affects approximately 70,000 people in the United States.

  2009-05-21Submitted in the Senate, considered, and agreed to without amendment and with a preamble by Unanimous Consent. (consideration: CR S5885; text as passed Senate: CR S5885; text of measure as introduced: CR S5877)

  Related

Legislative Actions

1. 2009-06-11

   Introduced in House

2. 2009-06-11

   Introduced in House

3. 2009-06-11

   Sponsor introductory remarks on measure. (CR E1380)

4. 2009-06-11

   Referred to the House Committee on Energy and Commerce.

5. 2009-06-12

   Referred to the Subcommittee on Health.