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Candis King Hope for Sickle Cell Families Act

In committee: it can still change before the session ends.

US HR 8067 · House Bill · 119th Congress

Draft a letter
Stage
In committee
Started in
House
Sponsor
1
Latest action
Mar 24, 2026

What it does

The bill would direct the Secretary of Health and Human Services, through the CDC, to establish a Sickle Cell Data Collection program to gather and maintain data on the incidence, prevalence, demographics, and healthcare utilization of individuals with sickle cell disease in the United States, including by awarding grants to states and promoting standardized surveillance methods. It would also require the reinstatement of certain employees in the CDC’s Division of Blood Disorders and Public Health Genomics who were removed on or after January 1, 2025, under agency actions affecting 3% or more of the division’s workforce within a 60-day period. The bill authorizes $10 million annually for…

No official summary is available here. This one was written by AI from the bill’s text.

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Where it stands

  1. Introduced (Done)

    Mar 24, 2026

  2. Committee (Current step)

    In committee · Mar 24, 2026

  3. Floor (Not started)

  4. Law (Not started)

What moved

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Who is involved

Sponsors

The lawmakers who put their names on it, lead sponsors first.

Where it goes next

While a bill can still move, the questions are about people and money.

Work with this bill

Candis King Hope for Sickle Cell Families Act | 52