Federal
A resolution supporting the goals of International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Awareness Day.
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III
116TH CONGRESS
2D SESSION
S. RES. 633
Supporting the goals of International Myalgic Encephalomyelitis/Chronic
Fatigue Syndrome Awareness Day.
IN THE SENATE OF THE UNITED STATES
JUNE 22, 2020
Mr. MARKEY (for himself, Ms. COLLINS, Mr. VAN HOLLEN, Ms. STABENOW,
Mr. BOOKER, Mrs. FEINSTEIN, Ms. HARRIS, Ms. WARREN, Ms. SINEMA,
and Mr. CRAMER) submitted the following resolution; which was referred
to the Committee on Health, Education, Labor, and Pensions
RESOLUTION
Supporting the goals of International Myalgic Encephalomy-
elitis/Chronic Fatigue Syndrome Awareness Day.
Whereas the National Academy of Medicine (referred to in
this preamble as ‘‘NAM’’), formerly known as the Insti-
tute of Medicine, has found that Myalgic Encephalomyeli-
tis/Chronic Fatigue Syndrome (referred to in this pre-
amble as ‘‘ME/CFS’’) is ‘‘a serious, chronic, complex,
and systemic disease that frequently and dramatically
limits the activities of affected patients’’;
Whereas, in the past, outbreaks of viruses, including out-
breaks of coronaviruses, have triggered an increase in
ME/CFS-like symptoms in individuals infected by those
viruses;
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Whereas—
(1) between 836,000 and 2,500,000 individuals of
all ages, races, and sexes in the United States are be-
lieved to be afflicted with ME/CFS, and millions of addi-
tional individuals are afflicted by ME/CFS worldwide;
and
(2) the vast majority of individuals with ME/CFS
are undiagnosed or misdiagnosed;
Whereas ME/CFS is approximately 4 times more prevalent in
women than in men;
Whereas ME/CFS is a chronic disease with no known cure
and leaves 1⁄4 of individuals with ME/CFS housebound or
bedbound for extended periods of time;
Whereas between 50 and 75 percent of individuals with ME/
CFS cannot work or attend school;
Whereas, in the United States, the economic toll of ME/CFS
is $51,000,000,000 per year, including as much as
$14,000,000,000 in medical costs and $37,000,000,000
in lost productivity;
Whereas the cause of ME/CFS is unknown, there is no diag-
nostic test for ME/CFS, and there is no treatment for
ME/CFS approved by the Food and Drug Administra-
tion;
Whereas NAM has noted a ‘‘paucity of research’’ on ME/
CFS and that ‘‘more research is essential’’;
Whereas individuals with ME/CFS struggle to find doctors to
care for them, and ME/CFS is included in less than 1⁄3
of medical school curricula;
Whereas, in recognition of the dearth of research on ME/CFS
and the profound impact that the disease has on individ-
uals with ME/CFS and their loved ones and caretakers,
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the National Institutes of Health is ‘‘committed to unrav-
eling the underlying biologic cause(s) of ME/CFS as
swiftly as possible, and promoting research that will in-
form the development of effective strategies for treatment
and prevention of this devastating condition’’; and
Whereas, in 2020, May 12 is recognized as International ME/
CFS Awareness Day: Now, therefore, be it
Resolved, That the Senate—
1
(1) supports the goals of International Myalgic
2
Encephalomyelitis/Chronic
Fatigue
Syndrome
3
Awareness Day;
4
(2) recognizes and affirms the commitment of
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the United States to—
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(A) supporting research and medical edu-
7
cation for Myalgic Encephalomyelitis/Chronic
8
Fatigue Syndrome; and
9
(B) promoting awareness among health
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professionals and the public about Myalgic En-
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cephalomyelitis/Chronic Fatigue Syndrome; and
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(3) recognizes the continued importance of—
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(A) health care professionals and medical
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researchers who care for individuals with
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Myalgic
Encephalomyelitis/Chronic
Fatigue
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Syndrome; and
17
(B) individuals who work to discover the
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cause of, and develop and improve the diagnosis
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of, treatments for, and a cure for, Myalgic En-
1
cephalomyelitis/Chronic Fatigue Syndrome.
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Æ
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