DemocratBill · S. 5488· Senate(119-S-5488)

Sickle Cell Disease Treatment Centers Act of 2026

Rep. Van Hollen
Age: 67 years
Maryland
Introduced
9/23/2026
Last activity
9/23/2026 — Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Sponsored by
Chris Van Hollen
Cosponsors
Democrat - 2Republican - 0
Health
  1. Introduced
  2. In Committee

What this bill would do

This bill establishes a grant program to create treatment centers for sickle cell disease and other heritable hemoglobinopathies using a hub-and-spoke framework. Eligible entities receiving these grants must include a medical hub, at least one medical spoke, and a community-based nonprofit organization working in partnership. The program aims to promote lifelong coordinated health care, improve health outcomes, and help patients transition from pediatric to adult care. Additionally, the legislation creates a National Sickle Cell Disease Coordinating Center and expands data collection through the Centers for Disease Control and Prevention. Finally, the bill requires regular reports to Congress on the impact of these treatment centers.

Yes· 3 of 21

  • Does this make health care easier to get in general?+8

    The bill establishes a hub-and-spoke grant program and coordinating center to drastically improve access to comprehensive, coordinated sickle cell disease care.

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

    Sickle cell disease disproportionately impacts Black Americans, and the legislation specifically funds centers and outreach to address this condition.

  • Would households on low incomes be better off under this?+6

    Grant funds assist low-income patients with health insurance premiums, cost-sharing, and addressing basic social determinants of health.

The opposite

No question was scored the opposite.