National Alliance for Sickle Cell Centers
Working Together to Combat Sickle Cell Disease

Our mission is to support sickle cell disease centers in delivering high-quality comprehensive care by setting standards, promoting their adoption, identifying opportunities and resources to strengthen those centers, and advocating for access to comprehensive care to improve health outcomes, quality of life, and survival.

Thanks to our amazing sponsors for providing their support and helping NASCC provide the best treatments, techniques, and knowledge to centers around the nation.

Our Goals

We are committed to providing support, education, and other resources to sickle cell centers across America in order to enhance the quality of patient care and improve outcomes for patients and the centers alike.

Infrastructure
We are committed to creating an infrastructure for adult and pediatric sickle cell disease centers to define, enhance, and promote the adoption of standards of primary and specialized care.
Quality Improvement
Work to enable access to the Globin Research Network for Data and Discovery, a multi-site registry to optimize quality improviement and quality assurance through data analytics.
Collaboration
Work with the American Society of Hematology, the Sickle Cell Disease Association of America, and the CDC's Sickle Cell Data Collection program along with other organizations to collaborate on research, data collection, advocacy and other efforts.
Tools and Information
Develop tools and share information with sickle cell disease centers to use in implementing and operating a comprehensive care model within their organization.