The Foundation for Sickle Cell Disease Research is a non-profit organization geared towards Sickle Cell Disease research. Our mission at FSCDR is to support innovative research in Sickle Cell Disease and establish a patient registry to collect data for scientific assessments of medical outcomes and to identify barriers to implementation of evidence-based research with the goal to maximize the quality of life and improved survival.

Get up to date information about our upcoming conferences and stay in touch with the latest directly on your iPhone. We will share the latest news, events, messages and information for physicians, patients and their families. You can also keep us informed on how we are doing and how we can serve the Sickle Cell Disease community better through the in app survey.