DemocratBill · H.R. 8067· House(119-HR-8067)

Candis King Hope for Sickle Cell Families Act

Rep. Vindman
Age: 51 years
Virginia
Introduced
3/24/2026
Last activity
3/24/2026 — Referred to the House Committee on Energy and Commerce.
Sponsored by
Eugene Vindman
Cosponsors
None
Health
  1. Introduced
  2. In Committee

What this bill would do

The "Candis King Hope for Sickle Cell Families Act" directs the Secretary of Health and Human Services to run a program to collect data on sickle cell disease in the United States. This program will provide grants to States to track how common the disease is, the demographics of those affected, and how they use healthcare. It also aims to standardize surveillance methods. Additionally, the bill requires the reinstatement of certain employees from the Division of Blood Disorders and Public Health Genomics who were removed after January 1, 2025. Funding of $10 million per year is authorized from fiscal years 2027 through 2031.

Yes· 3 of 22

  • Would Black Americans be better off under this?+7

    Sickle cell disease disproportionately affects African Americans, making this targeted data collection highly beneficial.

  • Would people with disabilities be better off under this?+5

    Directly supports people with a lifelong genetic health condition.

  • Does this put more money into medical research?+5

    Allocates $10 million annually for data collection and surveillance of sickle cell disease.

The opposite

  • Does this reduce what the federal government owes?-1

    Authorizes $10 million in annual spending from 2027 through 2031.

  • Does this reduce what the federal government spends?-1

    Increases government spending via new grants and employee reinstatements.