Join the association
JOIN RED
Joining RED means supporting a network committed to advancing care, research and training in sickle cell disease. Together, we can improve patient care and expand knowledge of the condition.
Would you like to contribute on a larger scale?
A separate form of support for major donors is available below.
Why join?
By joining RED, you are helping to develop a network committed to improving care for people with sickle cell disease through three core missions: care, research and training.
RED brings together healthcare professionals, researchers, partners and patient organisations to improve care for people with sickle cell disease.
Your membership helps to support, in particular:
- improvements to care pathways;
- the development of clinical and epidemiological research projects;
- the dissemination of knowledge and the training of healthcare professionals;
- initiatives to improve the quality of life of patients with sickle cell disease.
Each membership helps fund work for patients, families and the healthcare professionals who care for them.
Annual membership fee
Membership is valid for one year from the date of subscription.
Membership fee: 5 €
Membership fees contribute directly to funding the RED’s activities in the fields of care, research and training.
You can join online via HelloAsso.
Tax treatment
RED pursues a public-interest mission to improve care for people with sickle cell disease.
Under current regulations and subject to RED’s tax eligibility, donations and membership fees may qualify for tax relief. A tax receipt may be issued to eligible members and donors.
For further information, please contact 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.
