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.

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.