Our missions
What does RED do?
The Erythrocyte and Sickle Cell Disease Network works to safeguard patient pathways in mainland France and the French overseas departments and regions, in both the prevention and treatment of sickle cell disease and rare red blood cell disorders. It promotes research and teaching, encourages the pooling of resources, and strengthens cooperation between France and other countries.
Fighting sickle cell disease
RED focuses on three complementary missions: care, research and training.
Our projects
Discover the projects through which RED is transforming care for people with sickle cell disease.
Siclopédie
A comprehensive patient-care tool that also builds an anonymised database for research.
Research news
Follow the latest research and project updates from RED.
Support us to give them a better future
Every donation funds direct action on the ground: equipping a screening centre, training a doctor or developing information tools for patients. Sickle cell disease affects millions of people but remains severely underfunded. Your support changes lives.
Our projects
We run practical programmes to support earlier diagnosis, better care and wider access to information. Our projects cover research, prevention, therapeutic patient education and access to healthcare in the regions most affected by sickle cell disease.
Our partners
RED is supported by a strong network of institutional, scientific and community partners. Within the RÊVE consortium and beyond, we combine our strengths to accelerate research and improve care wherever sickle cell disease occurs.
