[Congressional Record Volume 158, Number 15 (Tuesday, January 31, 2012)]
[Senate]
[Page S222]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]
HEREDITARY ANGIOEDEMA AWARENESS DAY
Mr. UDALL of Colorado. Mr. President, I ask unanimous consent the
Judiciary Committee be discharged from further consideration of S. Res.
286 and the Senate proceed to its immediate consideration.
The PRESIDING OFFICER. Without objection, it is so ordered.
The clerk will report the resolution by title.
The assistant legislative clerk read as follows:
A resolution (S. Res. 286) 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.
There being no objection, the Senate proceeded to consider the
resolution.
Mr. UDALL of Colorado. Mr. President, I ask unanimous consent that
the Inouye amendment which is at the desk be agreed to, the resolution,
as amended, be agreed to, the preamble be agreed to, the motion to
reconsider be laid upon the table with no intervening action or debate,
and any related statements be printed in the Record.
The PRESIDING OFFICER. Without objection, it is so ordered.
The amendment (No. 1495) was agreed to, as follows:
(Purpose: To strike provisions relating to increased research)
Beginning on page 3, strike line 8 and all that follows
through line 18 on page 4 and insert the following: ``the
public.''.
The resolution (S. Res. 286), as amended, was agreed to.
The preamble was agreed to.
The resolution, as amended, with its preamble, reads as follows:
S. Res. 286
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;
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;
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;
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;
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;
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;
Whereas HAE attacks can be triggered by infections, minor
injuries or dental procedures, emotional or mental stress,
and certain hormonal or blood medications;
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;
Whereas the annual cost for treatment per patient can
exceed $500,000, causing a substantial economic burden;
Whereas there is a significant need for increased and
normalized medical professional education regarding HAE; and
Whereas there is also a significant need for further
research on HAE to improve diagnosis and treatment options
for patients; Now, therefore, be it
Resolved, That--
(1) the Senate--
(A) recognizes and celebrates May 16, 2012, as Hereditary
Angioedema Awareness Day; and
(B) supports increased awareness of Hereditary Angioedema
(HAE) by physicians and the public.
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