Sickle Cell, Thalassaemia and Red Cell Disorder Service

We are a specialist centre for the diagnosis and management of adults with inherited haemoglobin disorders including sickle cell disease, thalassaemia.

Who we see

We see patients with different types of sickle cell disease, (including HbSS, HbSC and HbS thalassaemia), thalassaemia, and other types of red cell blood problems such as hereditary spherocytosis and G6PD deficiency.

We do not usually see patients with sickle cell or thalassaemia traits, and people who are affected by this can contact the community sickle cell and thalassaemia team for support and advice.