Sickle Cell Data Collection

Tennessee

Who We Are!

The Tennessee Sickle Cell data collection program is dedicated to improving the lives of all people living with sickle cell disease. By collaborating with healthcare providers, patients, and communities, we aspire to advance health outcomes, improve access to healthcare, and support the needs of people with sickle cell disease. Please scroll down to learn more about our history and the work we are doing to improve the lives of those living with sickle cell disease. 

Our Background

The Tennessee Sickle Cell Data Collection Program is part of a national initiative led by the Center for Disease Control and Prevention to improve the lives of individuals living with sickle cell disease.Click the arrows below and explore the slideshow to get a glimpse into our background, history, and goals, and to find out more information about sickle cell disease 

 Explore the Milestones that have shaped the CDC’s Sickle Cell Data Collection Programs and its journey to improving the lives of people living with sickle Cell Disease

 Uncover the key moments that have defined the Tennessee SCDC’s mission to enhance outcomes and access to care for those living with sickle cell disease

These critical statistics highlight the impact of sickle cell disease and help us improve our understanding

The Tennessee SCDC Strives to provide innovative information about sickle cell disease. Look here to see what we hope to accomplish through our efforts.