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Proposed

Bill · 119th Congress · HR 8067

Candis King Hope for Sickle Cell Families Act

Refreshed 24 min ago

Introduced 2026-03-24Topic: public health · health care · labor

Summary

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This bill directs the federal Department of Health and Human Services, through the Centers for Disease Control and Prevention (CDC), to run a Sickle Cell Data Collection program. The program would give grants to states to collect data on how many people have sickle cell disease, who they are, and how they use health care, and to work with the CDC and other grantees to standardize tracking methods. The bill authorizes $10 million per year for fiscal years 2027 through 2031. It also requires the department to reinstate employees of the CDC's Division of Blood Disorders and Public Health Genomics who were removed on or after January 1, 2025, through actions that removed 3 percent or more of the division's staff within 60 days.

Full text and official record on Congress.gov

Sponsors

Action history

DateChamberActionStatus effect
2026-03-24HouseReferred to the House Committee on Energy and Commerce.refer
2026-03-24Introduced in Houseintroduce
2026-03-24Introduced in Houseintroduce
Source: GovInfo Bill Status (Library of Congress), fetched 2026-09-11. Provisions and opinion polling arrive in a later release.