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Bills/119th Congress · House

H.R. 8067

Introduced

Candis King Hope for Sickle Cell Families Act

Sponsor
DEugene Simon Vindman· Virginia
Introduced
March 24, 2026
Policy area
Health
Latest action
Referred to the House Committee on Energy and Commerce.March 24, 2026
[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[H.R. 8067 Introduced in House (IH)]

<DOC>

119th CONGRESS
2d Session
H. R. 8067

To direct the Secretary of Health and Human Services to carry out a 
program under which the Secretary will collect data with respect to 
sickle cell disease in the United States, and for other purposes.

_______________________________________________________________________

IN THE HOUSE OF REPRESENTATIVES

March 24, 2026

Mr. Vindman introduced the following bill; which was referred to the 
Committee on Energy and Commerce

_______________________________________________________________________

A BILL

To direct the Secretary of Health and Human Services to carry out a 
program under which the Secretary will collect data with respect to 
sickle cell disease in the United States, and for other purposes.

Be it enacted by the Senate and House of Representatives of the 
United States of America in Congress assembled,

SECTION 1. SHORT TITLE.

This Act may be cited as the ``Candis King Hope for Sickle Cell 
Families Act''.

SEC. 2. SICKLE CELL DATA COLLECTION PROGRAM.

(a) In General.--The Secretary of Health and Human Services, acting 
through the Director of the Centers for Disease Control and Prevention 
(in this Act referred to as the ``Secretary''), shall carry out a 
program under which the Secretary will collect data on the incidence 
and prevalence of sickle cell disease in the United States, to be known 
as the Sickle Cell Data Collection program, through awarding grants to 
States for the following purposes:
(1) To collect and maintain data on sickle cell disease to 
gain a better understanding of the incidence and prevalence of 
sickle cell disease in the United States, the demographics of 
individuals in the United States living with sickle cell 
disease, and the healthcare utilization patterns of individuals 
in the United States living with sickle cell disease.
(2) To collaborate with other entities who received grants 
under the Sickle Cell Data Collection program of the Centers 
for Disease Control and Prevention (as in effect on the day 
before the date of the enactment of this Act) and the Centers 
for Disease Control and Prevention for purposes of increasing 
the standardization of methods for sickle cell disease 
surveillance.
(b) Authorization of Appropriations.--There are authorized to be 
appropriated to carry out the program referred to in subsection (a), 
$10,000,000 for each of fiscal years 2027 through 2031.

SEC. 3. DIVISION OF BLOOD DISORDERS AND PUBLIC HEALTH GENOMICS.

(a) In General.--The Secretary of Health and Human Services shall 
reinstate any covered employee of the Division of Blood Disorders and 
Public Health Genomics of the Centers for Disease Control and 
Prevention.
(b) Covered Employee Defined.--In this section, the term ``covered 
employee'' means an employee of the Division of Blood Disorders and 
Public Health Genomics of the Centers for Disease Control and 
Prevention who was removed on or after January 1, 2025, under any 
agency action (including any reduction in force conducted pursuant to 
subchapter I of chapter 35 of title 5, United States Code or any agency 
reorganization) that provides for the removal of 3 percent or more of 
the total number of employees at such Division within a 60-day period.
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