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Supporting the goals and ideals of International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Awareness Day.
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IV
116TH CONGRESS
1ST SESSION
H. RES. 399
Supporting the goals and ideals of International Myalgic Encephalomyelitis/
Chronic Fatigue Syndrome Awareness Day.
IN THE HOUSE OF REPRESENTATIVES
MAY 22, 2019
Ms. LOFGREN (for herself, Mr. BERGMAN, Ms. WASSERMAN SCHULTZ, and
Mr. JOYCE of Ohio) submitted the following resolution; which was re-
ferred to the Committee on Energy and Commerce
RESOLUTION
Supporting the goals and ideals of International Myalgic
Encephalomyelitis/Chronic Fatigue Syndrome Awareness
Day.
Whereas the National Academy of Medicine (NAM), formerly
known as the Institute of Medicine, has found Myalgic
Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
to be ‘‘a serious, chronic, complex, and systemic disease
that frequently and dramatically limits the activities of
affected patients’’;
Whereas between 836,000 and 2,500,000 individuals of all
ages, races, and sexes in the United States are believed
to be afflicted with ME/CFS, with millions more afflicted
by ME/CFS worldwide, and the vast majority of individ-
uals with ME/CFS are undiagnosed or misdiagnosed;
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•HRES 399 IH
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 50 to 75 percent of individuals with ME/CFS can-
not work or attend school;
Whereas medical expenses and lost productivity related to
ME/CFS cost the economy of the United States an esti-
mated $17,000,000,000 to $24,000,000,000 annually;
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 that is approved by the Food and Drug Admin-
istration;
Whereas NAM has noted a ‘‘paucity of research’’ on ME/
CFS and that ‘‘more research is essential’’;
Whereas the Centers for Disease Control and Prevention
(CDC) has called ME/CFS ‘‘America’s Hidden Health
Crisis’’;
Whereas individuals with ME/CFS struggle to find doctors to
care for them, and ME/CFS is included in the curricula
of fewer than 1⁄3 of medical schools;
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,
the National Institutes of Health (NIH) is ‘‘committed to
unraveling the underlying biologic cause(s) of ME/CFS
as swiftly as possible, and promoting research that will
inform the development of effective strategies for treat-
ment and prevention of this devastating condition’’;
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•HRES 399 IH
Whereas, in 2017, 11 Institutes at the NIH and the Office
of the Director of the NIH contributed more than
$7,000,000 in grants to assist in establishing Collabo-
rative Research Centers and a Data Management Coordi-
nating Center to improve the coordination of ME/CFS
research and help accelerate understanding of ME/CFS;
and
Whereas, in 2019, May 12 is recognized as International ME/
CFS Awareness Day: Now, therefore, be it
Resolved, That the House of Representatives—
1
(1) supports the goals of International Myalgic
2
Encephalomyelitis/Chronic
Fatigue
Syndrome
3
Awareness Day;
4
(2) recognizes and affirms the commitment of
5
the United States to—
6
(A) supporting research and medical edu-
7
cation for ME/CFS; and
8
(B) promoting awareness among health
9
professionals and the public about ME/CFS;
10
and
11
(3) recognizes the continued importance of—
12
(A) health care professionals and medical
13
researchers who care for individuals with ME/
14
CFS; and
15
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(B) those who work to discover the cause
1
of, and develop and improve diagnosis of, treat-
2
ments for, and a cure for, ME/CFS.
3
Æ
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