Federal
Expressing support for the designation of June 19, 2023, as "World Sickle Cell Awareness Day" in order to increase public alertness across the United States and global community about sickle cell disease, the continued need for empirical research, early detection screenings for sickle cell trait carriers, novel effective treatments leading to a cure, and preventative care programs with respect to complications from sickle cell anemia and conditions related to sickle cell disease.
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IV
118TH CONGRESS
1ST SESSION
H. RES. 514
Expressing support for the designation of June 19, 2023, as ‘‘World Sickle
Cell Awareness Day’’ in order to increase public alertness across the
United States and global community about sickle cell disease, the contin-
ued need for empirical research, early detection screenings for sickle
cell trait carriers, novel effective treatments leading to a cure, and
preventative care programs with respect to complications from sickle
cell anemia and conditions related to sickle cell disease.
IN THE HOUSE OF REPRESENTATIVES
JUNE 15, 2023
Mr. DAVIS of Illinois (for himself, Mr. BURGESS, Ms. LEE of California, and
Mr. BILIRAKIS) submitted the following resolution; which was referred to
the Committee on Energy and Commerce
RESOLUTION
Expressing support for the designation of June 19, 2023,
as ‘‘World Sickle Cell Awareness Day’’ in order to in-
crease public alertness across the United States and glob-
al community about sickle cell disease, the continued
need for empirical research, early detection screenings
for sickle cell trait carriers, novel effective treatments
leading to a cure, and preventative care programs with
respect to complications from sickle cell anemia and con-
ditions related to sickle cell disease.
Whereas sickle cell disease (referred to in this preamble as
‘‘SCD’’) is defined as a group of inherited red blood cell
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•HRES 514 IH
disorders that is a genetic condition present at birth and
is a major health problem in the United States and
worldwide;
Whereas the 2023 theme of World Sickle Cell Awareness
Day, ‘‘Shine the Light on Sickle Cell’’ is an immediate
call to action to improve the health and quality of life for
individuals living with SCD and their families;
Whereas, in 1972, Dr. Charles Whitten established the Sickle
Cell Disease Association of America to improve research,
education, and health care for sickle cell patients, which
is now headquartered in Hanover, Maryland;
Whereas, in 1972, Congress passed the National Sickle Cell
Disease Control Act which, for the first time, provided
authority to establish education, information, screening,
testing, counseling, research, and treatment programs for
sickle cell disease;
Whereas SCD is a gene mutation that causes a single mis-
spelling in the DNA instructions for hemoglobin, a pro-
tein that aids in carrying oxygen in the blood, results in
chronic complications related to anemia, stroke, infec-
tions, organ failure, tissue damage, intense periods of
pain referred to as vaso-occulsive crises, and even pre-
mature death in persons living with the disease;
Whereas sickle cell trait (SCT) occurs when a person inherits
one copy of the sickle cell gene from one of his or her
parents, and in the United States an estimated
3,000,000 individuals have SCT with many unaware of
their status; if both parents have SCT, there is a 25-per-
cent (or 1 in 4) chance that any child of theirs will have
SCD;
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•HRES 514 IH
Whereas the prevalence of SCD in the United States affects
approximately 100,000 individuals, 1 in every 365 Afri-
can-American births, and 1 in every 16,300 Hispanic-
American births, with roughly 1 in 13 African-American
babies born with sickle cell trait;
Whereas the global imprint of SCD affects millions of people
throughout the world; particularly among those persons
whose ancestors came from sub-Saharan Africa; Spanish-
speaking regions in the Western Hemisphere (South
America, the Caribbean, and Central America); Saudi
Arabia; India; and Mediterranean countries such as Tur-
key, Greece, and Italy;
Whereas the variance related to disease prevalence of sickle
cell trait ranges greatly by region, and there are levels re-
corded as high as 40 percent in certain areas of sub-Sa-
haran Africa, eastern Saudi Arabia, and central India;
Whereas in countries that are poor in resources, more than
90 percent of children with SCD do not live to see adult-
hood;
Whereas approximately 1,000 children in Africa are born
with SCD daily with more than half who will die before
their fifth birthday;
Whereas there is a high prevalence of SCD in India, most no-
tably within the central and western regions that results
in nearly 20 percent of babies diagnosed with SCD dying
by the age of two;
Whereas, 16 years ago, in 2006, the World Health Assembly
passed a resolution recognizing SCD as a public health
priority with a call to action that each country implement
measures to tackle the disease, and three years later, the
United Nations adopted this same resolution in 2009;
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•HRES 514 IH
Whereas newborn screening for SCD is a crucial first step for
families to obtain a timely diagnosis and the establish-
ment of comprehensive care, which in turn helps to de-
crease mortality and morbidity for higher survival rates
in children;
Whereas approved treatments for SCD remain few in number
with only four Food and Drug Administration-approved
therapies since 2017, and there is a robust SCD pipeline
with over 40 therapies in development;
Whereas considering the impact of this molecular disease that
results in the suffering of patients as well as their fami-
lies living with SCD, there is an immediate need for life-
saving therapeutics that can improve the duration and
quality of patients lives;
Whereas, in 2020, the National Academies of Science, Engi-
neering, and Medicine (NASEM) developed a comprehen-
sive Strategic Plan and Blueprint for Action to Address
Sickle Cell Disease, which cited the need for new innova-
tive therapies as well as to address barriers that may im-
pact delivery and access to approved treatments;
Whereas, in 2020, the Department of Health and Human
Services, in partnership with the American Society of He-
matology and SickleInAfrica, in collaboration with the
World Health Organization, hosted a webinar for a joint
effort to strengthen SCD efforts during the coronavirus
disease (COVID–19) pandemic and beyond;
Whereas American Society of Hematology member and re-
cently deceased Kwaku Ohene-Frempong, M.D., Pro-
fessor Emeritus of Pediatrics at the Perelman School of
Medicine at the University of Pennsylvania, who served
on the Global Coalition on SCD, has been a leader in ad-
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•HRES 514 IH
vancing the body of knowledge in SCD research, public
health, and medicine, and is recognized as immeasurably
benefitting thousands of children worldwide;
Whereas there are emerging genetic therapy technologies, in-
cluding gene editing, that can modify a patient’s own
hematopoietic stem cells with the goal of the patient
being able to generate healthy red blood cells to prevent
sickle cell crises;
Whereas while hematopoietic stem cell transplantation (com-
monly known as ‘‘HSCT’’) is currently the only cure for
SCD, and while advances in treating the associated com-
plications of SCD have occurred, more research is needed
to find widely available treatments and cures to help indi-
viduals with SCD; and
Whereas June 19, 2023, has been designated ‘‘World Sickle
Cell Awareness Day’’ to increase public alertness across
the United States and global community about sickle cell
disease, the continued need for empirical research, early
detection screenings for sickle cell disease trait carriers,
novel effective treatments leading to a cure, and prevent-
ative-care programs with respect to complications from
sickle cell anemia and conditions related to sickle cell dis-
ease: Now, therefore, be it
Resolved, That the House of Representatives—
1
(1) supports the goals and ideals of World Sick-
2
le Cell Awareness Day;
3
(2) commits to ensuring equitable access by
4
shining the light among economic, racial, and ethnic
5
groups to new treatments in order to improve health
6
outcomes for those living with sickle cell disease;
7
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•HRES 514 IH
(3) calls on the Department of Health and
1
Human Services to create global policy solutions
2
aimed at providing support for the global community
3
and at-home resources needed to provide access to
4
newborn screening programs, therapeutic interven-
5
tions, and support services in partnership with local
6
governments with the needed infrastructure for re-
7
search and treatment;
8
(4) supports eliminating barriers to equitable
9
access for innovative sickle cell disease therapies, in-
10
cluding cell, gene, and gene-editing therapies in the
11
Medicare and Medicaid systems for patients who
12
need them most;
13
(5) encourages the people of the United States
14
and globally to hold appropriate programs, events,
15
and activities on Sickle Cell Awareness Day to raise
16
public awareness of their sickle cell disease trait,
17
preventative-care programs, treatments, and other
18
patient services for those suffering from sickle cell
19
disease, complications from sickle cell disease, and
20
conditions related to sickle cell disease; and
21
(6) encourages the President of the United
22
States to form a Sickle Cell Disease Interagency
23
Cabinet, which would be convened by the White
24
House, bringing together departments and Federal
25
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•HRES 514 IH
agencies across Government to address sickle cell
1
disease on multiple fronts, which would include, but
2
are not limited to, the Department of Health and
3
Human Services, Department of Veterans Affairs,
4
National Institutes of Health, Food and Drug Ad-
5
ministration, and Centers for Medicare & Medicaid
6
Services to begin working toward policies that will
7
support equitable and appropriate access to innova-
8
tive SCD therapies, and in this regard, the House
9
of Representatives urges that the options to be con-
10
sidered not only address access to potential future
11
curative treatments, but also address the bias that
12
this population continues to face within both the
13
United States and global health care systems.
14
Æ
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