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.

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.

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3 official files

• Introduced in House (text)

  Introduced in House · EN · 11 June 2009

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• Introduced in House (PDF)

  Introduced in House · EN · 11 June 2009

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• Introduced in House

  summary · EN · 11 June 2009

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