In this FAQ section you will find answers to some of your questions.
Sickle cell anaemia is a genetic blood disorder that affects haemoglobin. The red blood cells take on an abnormal shape (sickle-shaped), which can block blood circulation and cause pain, infections and chronic anaemia.
It mainly affects people from Africa, the Caribbean, the Middle East, India and certain regions of South America. It is inherited from both parents who carry the gene.
A simple blood test can detect the presence of the sickle cell gene. This test is recommended before pregnancy or in families at risk.
Common symptoms include:
Painful seizures (known as vaso-occlusive seizures)
Anemia
Fatigue
Frequent infections
Growth retardation in children
There is no cure for all patients, but the disease can be managed by :
Medications (such as hydroxyurea)
Blood transfusions
A bone marrow transplant in certain cases
Regular medical check-ups
Our NGO works for :
Raising awareness of sickle cell disease
Supporting patients and their families
Promoting early detection
Training healthcare professionals
Funding research and healthcare access projects
There are several ways you can help us:
Make a donation
Become a volunteer
Take part in our awareness campaigns
Relaying our messages on social networks
We operate mainly in areas with a high prevalence of sickle cell disease: sub-Saharan Africa, the West Indies, Europe (particularly France), and certain regions of Asia and the Middle East.
If you are ill or the parent of an affected child, you can :
Fill in our online support form
Contact us directly by phone, email or social networks
Take part in our information workshops and support groups
Yes, we regularly organise free or reduced-price campaigns in schools, health centres and rural areas. Keep up to date via our website or our social pages.
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