A resolution expressing support for the designation of June 19, 2026, as "World Sickle Cell Awareness Day" in order to increase public awareness across the United States and global community about sickle cell disease and the continued need for empirical research, early detection screenings, novel effective treatments leading to a cure, and preventative care programs with respect to complications from sickle cell anemia and conditions relating to sickle cell disease.

119th Congress Introduced by Cory Booker and 1 co-sponsor

Designate June 19, 2026 as World Sickle Cell Awareness Day and urge ongoing research, early screening, new treatments, cures, and preventive care to improve SCD outcomes.

Submitted in Senate

Summary of SRES 780 (Senate Resolution)

Purpose and intent

SRES 780 is a resolution expressing support for designating June 19, 2026, as “World Sickle Cell Awareness Day.”

The overarching goal is to raise public awareness in the United States and the global community about sickle cell disease (SCD) and to emphasize the ongoing need for empirical research, early detection screenings, novel and effective treatments, potential cures, and preventative care programs addressing complications associated with sickle cell anemia and related conditions.

Key provisions

Endorsement of a specific designation: The resolution urges recognition of June 19, 2026, as World Sickle Cell Awareness Day.

Emphasis on public awareness: Highlights the importance of informing the public about SCD, its health implications, and the burden of disease.

Calls for continued investment and efforts in research and healthcare:

Empirical research into SCD
Early detection and newborn/screening protocols
Development of new treatments and potential cures
Preventative care programs to manage complications and improve quality of life

Note: As a resolution, the bill primarily serves to express the sense of the Senate and does not, by itself, create new mandatory funding, establish programs, or alter existing law. It signals legislative support and may influence related policy discussions and advocacy efforts.

Affected parties and impact

Populations affected: Individuals with sickle cell disease and carriers, families, and communities affected by SCD globally and within the United States.

Broader impact: By designating World Sickle Cell Awareness Day and calling for continued research and care improvements, the resolution aims to:

Increase public and policymaker awareness
Encourage collaboration among researchers, healthcare providers, patient advocacy groups, and international partners
Support ongoing and future initiatives in screening, treatment development, and care programs

Procedural and timeline aspects

Referral: Referred to the Senate Committee on Foreign Relations on June 18, 2026.

Introduction date: Submitted in the Senate on June 18, 2026.

Co-sponsors: Chris Van Hollen and Cory Booker are listed as co-sponsors, signaling bipartisan endorsement within the Senate.

Additional context

As a resolution, it is primarily symbolic and informational, lacking the authority to impose new requirements or authorize new funding on its own.

The emphasis is on international awareness and continued advocacy for scientific and medical advances in SCD.

If you’d like, I can tailor this summary for a legislative brief, policy memo, or public-facing explainer, and add any available context about World Sickle Cell Awareness Day observances or related U.S. and global initiatives.