HouseH.Res. 1631119th Congress
Expressing support for the designation of the third week of October as "National Hunter Syndrome Awareness Week".
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[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[H. Res. 1631 Introduced in House (IH)]
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119th CONGRESS
2d Session
H. RES. 1631
Expressing support for the designation of the third week of October as
``National Hunter Syndrome Awareness Week''.
_______________________________________________________________________
IN THE HOUSE OF REPRESENTATIVES
October 19, 2026
Mrs. Foushee submitted the following resolution; which was referred to
the Committee on Energy and Commerce
_______________________________________________________________________
RESOLUTION
Expressing support for the designation of the third week of October as
``National Hunter Syndrome Awareness Week''.
Whereas Hunter syndrome, also known as Mucopolysaccharidosis Type II (MPS II),
is a rare genetic disorder affecting approximately 1 in 100,000 to
170,000 live male births worldwide;
Whereas Hunter syndrome is caused by a deficiency of the enzyme iduronate-2-
sulfatase, resulting in the harmful accumulation of complex sugars in
the body's cells and leading to progressive damage to organs and
systems, including the brain;
Whereas symptoms often appear in early childhood and may include developmental
delays, physical impairments, and a significantly shortened lifespan;
Whereas early diagnosis and intervention are critical to improving quality of
life and outcomes for individuals affected by Hunter syndrome;
Whereas increased public and medical awareness can lead to earlier diagnoses,
better treatment options, and expanded research efforts toward potential
therapies and a cure; and
Whereas families affected by Hunter syndrome face extraordinary emotional,
financial, and medical challenges, and deserve greater support,
understanding, and advocacy: Now, therefore, be it
Resolved, That the House of Representatives--
(1) supports the designation of ``National Hunter Syndrome
Awareness Week'';
(2) encourages Federal agencies, research institutions, and
advocacy organizations to expand efforts in education,
research, and the development of treatments for Hunter
syndrome; and
(3) urges continued congressional support for funding rare
disease research and initiatives that directly benefit
individuals and families in the Hunter syndrome community.
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