A resolution designating May 2025 as "ALS Awareness Month".

[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[S. Res. 266 Agreed to Senate (ATS)]

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119th CONGRESS
  1st Session
S. RES. 266

            Designating May 2025 as ``ALS Awareness Month''.


_______________________________________________________________________


                   IN THE SENATE OF THE UNITED STATES

                              June 5, 2025

Ms. Murkowski (for herself, Mr. Whitehouse, Mr. Cotton, and Mr. Coons) 
 submitted the following resolution; which was considered and agreed to

_______________________________________________________________________

                               RESOLUTION


 
            Designating May 2025 as ``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 ALS cases have a 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 it 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, in the United States, every 90 minutes someone dies from ALS, and every 
        90 minutes someone is diagnosed with ALS;
Whereas the majority of individuals with ALS die of respiratory failure;
Whereas, in the United States, military veterans are more likely to be diagnosed 
        with ALS than individuals 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, may 
        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 Senate--
            (1) designates May 2025 as ``ALS Awareness Month'';
            (2) affirms the dedication of the Senate to--
                    (A) ensuring individuals with amyotrophic lateral 
                sclerosis (referred to in this resolution as ``ALS'') 
                have access to effective treatments and high-quality 
                services and supports as early as possible after 
                diagnosis;
                    (B) identifying risk factors and causes of ALS to 
                prevent new cases;
                    (C) empowering individuals with ALS to maintain 
                their personal independence to the maximum extent 
                possible; and
                    (D) reducing the physical and emotional burdens of 
                living with ALS; and
            (3) commends the dedication of the family members, friends, 
        organizations, volunteers, researchers, and caregivers across 
        the United States who are working to improve the quality and 
        length of life of ALS patients and develop treatments and cures 
        that reach patients as soon as possible.
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