H.Res. 536 · 111th Congress
Expressing support for the HHT Foundation International's designation of a "National Hereditary Hemorrhagic…
Full title
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.
Key: what the circles and colors mean
Each circle is a bill. The ring fills as it moves through Congress:
Under the number: the Yea · Nay count of its final (or latest) recorded vote. On a member's page, the small badge is how that member voted: Y Yea / Aye, N Nay / No, P Present, – Not voting.
Gold and violet are only for Yea and Nay; they never mean a party. A member's party is the letter on their photo.
Never voted on. It didn't reach a floor vote before the 111th Congress ended, so it expired. A bill has to be introduced again to be considered in a new Congress.
D
NealSponsor32 cosponsors · 20 D, 12 R
R
Wilson
GB
R
Brown-Waite
LC
D
Capps
EG
R
Gallegly
BG
D
Gordon
JG
R
Gerlach
BB
D
Braley
JP
R
Pitts
MT
D
Thompson
TL
R
Latham
CM
R
Miller
MC
D
Capuano
JC
D
Costa
SF
D
Farr
DK
D
Kildee
JO
D
Oberstar
TR
D
Ryan
CD
R
Dent
BF
D
Frank
CC
D
Carney
JH
D
Himes
SI
D
Israel
WA
R
Akin
TH
D
Holden
RB
D
Boucher
RD
D
DeLauro
AS
D
Schwartz
TM
R
McCotter
JC
R
Campbell
TB
D
Baldwin
KC
R
Calvert
JS
D
Sestak1 signed on when it was introduced; the rest joined later. Cosponsors who withdrew aren't shown.
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.
What it does: CRS summary · Introduced in House · Jun 11, 2009
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.
Written by the nonpartisan Congressional Research Service. All summary versions on Congress.gov
About this bill and sources
Official title: 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.
Latest action (Jun 12, 2009): Referred to the Subcommittee on Health.
Policy area: Health · Origin: House · Introduced: Jun 11, 2009
Official page on Congress.gov · Bill text (GovInfo) · Status record (XML)
No recorded floor vote found.