In Maryland, Sickle cell disease (SCD) grips the lives of thousands of individuals and their families, casting a shadow over their daily existence. As 2026 unfolds, there remains an urgent need for tangible action and commitment from our leaders to address the challenges posed by this genetic disorder.

Statistics from the Centers for Disease Control and Prevention (CDC) highlight that SCD affects approximately 100,000 Americans, with an estimated 5,000 individuals living with the condition in Maryland. The disease can manifest in a range of complications, including chronic pain, infections, and strokes, and disproportionately impacts African American communities.

To address these urgent needs, we are advocating for the passage and funding of two critical pieces of legislation in Maryland.

  HB 178 – Public Health: Sickle Cell Disease – Specialized Clinics & Medical Resident Scholarships
This bill proposes $6 million in funding to expand specialized sickle cell clinics and support medical resident scholarships. These investments will train more healthcare providers and improve access to high-quality care for sickle cell patients statewide.

  HB 60/SB 421 – Sickle Cell Disease in Institutions of Higher Education: Policies, Procedures, and Educational Campaigns – Third Reading Passed (131-4)
This legislation proposes $1 million in funding to support colleges and universities in developing policies, procedures, and educational campaigns that assist students living with sickle cell disease in managing both health and academic responsibilities.

The Maryland Alliance for Advocacy for Sickle Cell (MAASC) calls upon Maryland Planning Committee Members, advocates, partners, and community supporters to champion this vital initiative. By supporting these legislative efforts and allocating necessary resources, we can strengthen support systems for SCD patients, expand access to care, and improve educational opportunities for those living with this condition.

Sign this petition to urge Maryland’s elected officials to pass and fully fund HB 178 and HB 60/SB 421. Together, we can advocate for meaningful change and build a stronger future for individuals living with SCD.