About
Everything you need to know about RED
The mission of the Erythrocyte and Sickle Cell Disease Network (RED) is to improve care for people with sickle cell disease and other inherited red blood cell disorders. The association works to safeguard care pathways, promote research, training and innovation, encourage knowledge-sharing, and strengthen scientific and medical cooperation in France, ten African countries and Canada.
Our partners
Discover our partners and the initiatives they support.
RÊVE Consortium
REVolutionising Sickle Cell Disease and improving patients’ daily lives worldwide.
The Association
Founded in 2022, RED brings together an international community. Meet the members of its executive committees.
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.
