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<resolution public-private="public" resolution-stage="Agreed-to-Senate" resolution-type="senate-resolution" star-print="no-star-print">
	<form>
		<distribution-code display="yes">III</distribution-code>
		<congress display="yes">112th CONGRESS</congress>
		<session display="yes">2d Session</session>
		<legis-num>S. RES. 286</legis-num>
		<current-chamber>IN THE SENATE OF THE UNITED STATES</current-chamber>
		<action display="yes">
			<action-date date="20111005">October 5, 2011</action-date>
			<action-desc><sponsor name-id="S051">Mr. Inouye</sponsor> (for himself
			 and <cosponsor name-id="S290">Mr. Chambliss</cosponsor>) submitted the
			 following resolution; which was referred to the
			 <committee-name committee-id="SSJU00">Committee on the
			 Judiciary</committee-name></action-desc>
		</action>
		<action>
			<action-date>January 31, 2012</action-date>
			<action-desc>Committee discharged; considered, amended, and agreed
			 to</action-desc>
		</action>
		<legis-type>RESOLUTION</legis-type>
		<official-title display="yes">Recognizing May 16, 2012, as Hereditary
		  Angioedema Awareness Day and expressing the sense of the Senate that more
		  research and treatments are needed for Hereditary Angioedema. </official-title>
	</form>
	<preamble>
		<whereas><text>Whereas Hereditary Angioedema (HAE) is a rare and
			 potentially life-threatening genetic disease, affecting between 1 in 10,000 and
			 1 in 50,000 people, leading to patients being undiagnosed or misdiagnosed for
			 many years;</text>
		</whereas><whereas><text>Whereas HAE is characterized by symptoms including
			 episodes of edema or swelling in various body parts including the hands, feet,
			 gastrointestinal tract, face, and airway;</text>
		</whereas><whereas><text>Whereas patients often experience swelling in the
			 intestinal wall, causing bouts of excruciating abdominal pain, nausea, and
			 vomiting, and swelling of the airway, which can lead to death by
			 asphyxiation;</text>
		</whereas><whereas><text>Whereas a defect in the gene that controls the
			 C1-inhibitor blood protein causes production of either inadequate or
			 non-functioning C1-inhibitor protein, leading to an inability to regulate
			 complex biochemical interactions of blood-based systems involved in disease
			 fighting, inflammatory response, and coagulation;</text>
		</whereas><whereas><text>Whereas HAE is an autosomal dominant disease, and 50
			 percent of patients with the disease inherited the defective gene from a
			 parent, while the other 50 percent developed a spontaneous mutation of the
			 C1-inhibitor gene at conception;</text>
		</whereas><whereas><text>Whereas HAE patients often experience their first HAE
			 attack during childhood or adolescence, and continue to suffer from subsequent
			 attacks for the duration of their lives;</text>
		</whereas><whereas><text>Whereas HAE attacks can be triggered by infections, minor
			 injuries or dental procedures, emotional or mental stress, and certain hormonal
			 or blood medications;</text>
		</whereas><whereas><text>Whereas the onset or duration of an HAE attack can
			 negatively affect a person’s physical, emotional, economic, educational, and
			 social well-being due to activity limitations;</text>
		</whereas><whereas><text>Whereas the annual cost for treatment per patient can
			 exceed $500,000, causing a substantial economic burden;</text>
		</whereas><whereas><text>Whereas there is a significant need for increased and
			 normalized medical professional education regarding HAE; and</text>
		</whereas><whereas><text>Whereas there is also a significant need for further
			 research on HAE to improve diagnosis and treatment options for patients; Now,
			 therefore, be it</text>
		</whereas></preamble>
	<resolution-body>
		<section display-inline="yes-display-inline" id="S1" section-type="undesignated-section"><enum></enum><text>That—</text>
			<paragraph id="IDbf6c9169fc0f449eb721af6581fb3eb4"><enum>(1)</enum><text>the
			 Senate—</text>
				<subparagraph id="id2879A385070046BE99114E164E06233B"><enum>(A)</enum><text>recognizes and
			 celebrates May 16, 2012, as Hereditary Angioedema Awareness Day; and</text>
				</subparagraph><subparagraph id="id663E89CE6B3848A0B72CA1B26DD4AF17"><enum>(B)</enum><text>supports
			 increased awareness of Hereditary Angioedema (HAE) by physicians and the
			 public.</text>
				</subparagraph></paragraph></section></resolution-body>
</resolution>
