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Supporting the designation of May 2020 as "ALS Awareness Month".
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IV
116TH CONGRESS
2D SESSION
H. RES. 970
Supporting the designation of May 2020 as ‘‘ALS Awareness Month’’.
IN THE HOUSE OF REPRESENTATIVES
MAY 15, 2020
Mr. CROW (for himself, Mr. FITZPATRICK, Ms. SEWELL of Alabama, Mr. CAL-
VERT, Mr. DEUTCH, Mr. LARSON of Connecticut, Mr. KING of Iowa, Mr.
CLAY, Mr. NEGUSE, Mr. HOLDING, Mr. O’HALLERAN, Mr. ROUDA, Mr.
VAN DREW, Mr. RASKIN, Mr. HURD of Texas, Mr. QUIGLEY, Mrs. AXNE,
Mr. MOULTON, Mr. CASTEN of Illinois, Mr. COLE, Mr. SCHIFF, Ms. CAS-
TOR of Florida, Mr. RODNEY DAVIS of Illinois, Mr. FORTENBERRY, Mr.
HUFFMAN, Mrs. RODGERS of Washington, Mr. GALLAGHER, Mr. CASE,
Ms. BLUNT ROCHESTER, Mr. SUOZZI, Mr. CONNOLLY, Mr. LAMBORN,
Mrs. DAVIS of California, Mr. PANETTA, Mr. ROSE of New York, Mr.
MCGOVERN, Mr. JOHNSON of Georgia, Mr. THOMPSON of Mississippi,
Mr. KING of New York, Mr. BOST, Mr. MARSHALL, Mr. WESTERMAN,
Mr. PRICE of North Carolina, Mr. BILIRAKIS, Ms. VELA´ZQUEZ, Ms.
FINKENAUER, Mr. BIGGS, Mr. TRONE, Mr. BUTTERFIELD, Mrs. BEATTY,
Mr. DEFAZIO, Ms. MATSUI, Mr. COHEN, Mr. JOYCE of Ohio, Mr.
THOMPSON of Pennsylvania, Mr. WELCH, Mr. MAST, Mr. VARGAS, Mr.
LAMB, Mr. TONKO, Mr. RUPPERSBERGER, Mr. ESPAILLAT, Mr. BISHOP
of Georgia, Mr. ENGEL, Ms. BONAMICI, Ms. ADAMS, Mr. LYNCH, Ms.
MCCOLLUM, Ms. CRAIG, Mr. TIMMONS, Ms. LEE of California, Mr.
CLEAVER, Mr. CURTIS, and Mrs. CAROLYN B. MALONEY of New York)
submitted the following resolution; which was referred to the Committee
on Energy and Commerce
RESOLUTION
Supporting the designation of May 2020 as ‘‘ALS Awareness
Month’’.
Whereas amyotrophic lateral sclerosis (referred to in this pre-
amble as ‘‘ALS’’) is a progressive neurodegenerative dis-
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•HRES 970 IH
ease that affects nerve cells in the brain and the spinal
cord;
Whereas the life expectancy for an individual with ALS is be-
tween 2 and 5 years after the date on which the indi-
vidual receives an ALS diagnosis;
Whereas ALS occurs throughout the world with no racial,
ethnic, gender, or socioeconomic boundaries;
Whereas the 2 different types of ALS are sporadic ALS and
familial ALS;
Whereas sporadic ALS—
(1) is the most common form of motor neuron dis-
ease in the United States;
(2) accounts for between 90 and 95 percent of all
cases of ALS in the United States; and
(3) may affect any individual in any location;
Whereas familial ALS (commonly known as ‘‘FALS’’)—
(1) is inherited; and
(2) accounts for between 5 and 10 percent of all
cases of ALS in the United States;
Whereas there is a 50 percent chance that each offspring of
an individual with familial ALS will inherit the gene mu-
tation for familial ALS and develop the disease;
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
about 1 year;
Whereas the onset of ALS often involves muscle weakness or
stiffness, and the progression of ALS results in the fur-
ther weakening, wasting, and paralysis of—
(1) the muscles of the limbs and trunk; and
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(2) the muscles that control vital functions, such as
speech, swallowing, and breathing;
Whereas ALS can strike individuals of any age but predomi-
nantly 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, slightly more than 5,600 individuals in the United
States are diagnosed with ALS each year, and 15 individ-
uals in the United States are diagnosed with ALS each
day;
Whereas, between 2015 and 2040, the number of ALS cases
around the world is expected to increase nearly 70 per-
cent;
Whereas the majority of individuals with ALS die of res-
piratory failure;
Whereas military veterans are approximately twice as likely
to be diagnosed with ALS as the general public in the
United States;
Whereas, as of the date of introduction of this resolution,
there is no cure for ALS;
Whereas the spouses, children, and family members of indi-
viduals living with ALS provide support to those individ-
uals 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 health care services
for the individual as the disease progresses: Now, there-
fore, be it
Resolved, That the House of Representatives—
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(1) supports the designation of ‘‘ALS Aware-
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ness Month’’;
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(2) affirms the dedication of the House of Rep-
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resentatives to working toward securing cures and
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better treatments for amyotrophic lateral sclerosis
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(referred to in this resolution as ‘‘ALS’’) as soon as
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possible;
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(3) recognizes the challenges that individuals
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with medically determined ALS face on a daily
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basis; and
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(4) commends the dedication of the family
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members, friends, organizations, volunteers, re-
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searchers, and caregivers across the United States
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that are working to improve the quality and length
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of life of ALS patients.
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Æ
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