119-hres449

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Supports the designation of "ALS Awareness Month".

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Introduced:
May 29, 2025
Policy Area:
Health

Bill Statistics

3
Actions
3
Cosponsors
0
Summaries
1
Subjects
1
Text Versions
Yes
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Latest Action

May 29, 2025
Referred to the House Committee on Energy and Commerce.

Actions (3)

Referred to the House Committee on Energy and Commerce.
Type: IntroReferral | Source: House floor actions | Code: H11100
May 29, 2025
Submitted in House
Type: IntroReferral | Source: Library of Congress | Code: H11100
May 29, 2025
Submitted in House
Type: IntroReferral | Source: Library of Congress | Code: 1025
May 29, 2025

Subjects (1)

Health (Policy Area)

Cosponsors (3)

Text Versions (1)

Introduced in House

May 29, 2025

Full Bill Text

Length: 4,123 characters Version: Introduced in House Version Date: May 29, 2025 Last Updated: Nov 15, 2025 6:21 AM
[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[H. Res. 449 Introduced in House

(IH) ]

<DOC>

119th CONGRESS
1st Session
H. RES. 449

Supports the designation of ``ALS Awareness Month''.

_______________________________________________________________________

IN THE HOUSE OF REPRESENTATIVES

May 29, 2025

Mr. Crow (for himself, Mr. Calvert, Ms. Sewell, and Mr. Fitzpatrick)
submitted the following resolution; which was referred to the Committee
on Energy and Commerce

_______________________________________________________________________

RESOLUTION

Supports the designation of ``ALS Awareness Month''.

Whereas amyotrophic lateral sclerosis (referred to in this preamble as ``ALS'')
is a progressive neurodegenerative disease that affects nerve cells in
the brain and the spinal cord;
Whereas the life expectancy for an individual with ALS is between 2 and 5 years
after the date on which the individual receives an ALS diagnosis;
Whereas ALS occurs throughout the world with no racial, ethnic, gender, or
socioeconomic boundaries;
Whereas ALS may affect any individual in any location;
Whereas the cause of ALS is unknown in up to 90 percent of cases;
Whereas approximately 10 percent of cases have a strong known genetic driver;
Whereas, on average, the period between the date on which an individual first
experiences symptoms of ALS and the date on which the individual is
diagnosed with ALS is more than 1 year;
Whereas the onset of ALS often involves muscle weakness or stiffness, and the
progression of ALS results in the further weakening, wasting, and
paralysis of--

(1) the muscles of the limbs and trunk; and

(2) the muscles that control vital functions, such as speech,
swallowing, and breathing;

Whereas ALS can strike individuals of any age but predominantly strikes adults;
Whereas it is estimated that tens of thousands of individuals in the United
States have ALS at any given time;
Whereas, based on studies of the population of the United States, more than
5,000 individuals in the United States are diagnosed with ALS each year,
and 15 individuals in the United States are diagnosed with ALS each day;
Whereas every 90 minutes an individual is diagnosed with ALS, and an individual
dies from ALS;
Whereas the majority of individuals with ALS die of respiratory failure;
Whereas military veterans are more likely to be diagnosed with ALS than those
with no history of military service;
Whereas, as of the date of introduction of this resolution, there is no cure for
ALS;
Whereas the spouses, children, and family members of individuals living with ALS
provide support to those individuals with love, day-to-day care, and
more; and
Whereas an individual with ALS, and the caregivers of such an individual, can be
required to bear significant costs for medical care, equipment, and home
care services for the individual as the disease progresses: Now,
therefore, be it
Resolved, That the House of Representatives--

(1) supports the designation of ``ALS Awareness Month'';

(2) affirms the dedication of the House of Representatives
to ensuring people with ALS have access to effective treatments
as soon as possible and identifying risk factors and causes of
ALS to prevent new cases;

(3) affirms the dedication of the House of Representatives
to empowering people with ALS to engage with the world in the
way they want;

(4) affirms the dedication of the House of Representatives
to reducing physical, emotional, and financial burdens of
living with ALS;

(5) affirms the dedication of the House of Representatives
to ensuring all people with ALS and their caregivers receive
high-quality services and supports that benefit them; and

(6) commends the dedication of the family members, friends,
organizations, volunteers, researchers, and caregivers across
the United States that are working to improve the quality and
length of life of ALS patients and the development of
treatments and cures that reach patients as soon as possible.
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