HRES 536 · 111th Congress · Health

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 2009-06-11· Sponsored by Rep. Neal, Richard E. [D-MA-2]· House

Bill Progress

Introduced
2
Committee
3
House Vote
4
Senate
5
Enacted
Latest: Referred to the Subcommittee on Health.(2009-06-12)

Plain Language Summary

[AI summary unavailable — showing source text] 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.…

Summarized by Claude AI · Non-partisan · For informational purposes only

Cosponsors (20)

12 Democrats8 Republicans