Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
The Sickle Cell Data Collection (SCDC) program collects health information about people with sickle cell disease (SCD) to study long-term trends in diagnosis, treatment, and healthcare access for people with SCD in the United States. The program will help inform policy and healthcare standards that improve and extend the lives of people with SCD.
Early screening, diagnosis, and treatment have allowed people with SCD to live much longer, making now a more important time than ever to study SCD health across the life course.
The SCDC program strives to improve health outcomes for people with SCD. By documenting health information of patients with SCD in the United States over time, the program can identify critical gaps in diagnosis, treatment, and healthcare access for people with SCD.
+myBinderRelated Content
-
Implementation of an Educational Intervention to Optimize Self-Management and Transition Readiness in Young Adults W...Background: The transition from the ped...
-
Shine the Light on Sickle Cell – Webinarhttps://www.youtube.com/watch?v=IIG0UUO5...
-
Africa Sickle Cell Alliance (ASA)Africa Sickle Cell Alliance was founded ...
-
Michael MatthewsHailing from Pittsburg, PA, Michael L. M...
-
2021 Sickle Cell Houston Amazing Race & 5K/1K – VirtualThe 2021 Sickle Cell Houston Amazing Rac...
-
Attorney Terri Booker talks about life with Sickle Cell on World Sickle Cell Awareness Dayhttps://www.fox29.com/video/576000...
-
College Scholarships Dealing With Sickle Cell AnemiaCollege Scholarships.org is a site creat...
