Sickle Cell and Thalassaemia
Main Address
- Whittington Hospital
Department of Haematology
Level 5, Diagnostic Block - 020 7288 5437 / 5144
The Whittington has a long history of providing holistic care for people with thalassaemia and sickle cell. For more than 20 years we have embraced the principle of managing our patients within a multidisciplinary team comprising of hospital and community professionals.
We treat the largest number of people with thalassaemia in the country and already work with many hospitals. We can also help you to meet the national standards that exist already and those that are being developed to improve the care of
children and adults with thalassaemia or sickle cell.
We treat the largest number of people with thalassaemia in the country and already work with many hospitals. We can also help you to meet the national standards that exist already and those that are being developed to improve the care of
children and adults with thalassaemia or sickle cell.
Range of services
- Clinical Sickle cell disorders e.g. haemoglobin S/S; Haemoglobin S/C
- Alpha, beta Thalassaemia, including paediatric patients
The Red Cell Community Service is a new service that provide specialist nursing care and support for patients with sickle cell, thalassaemia, and rare inherited anaemias in their own homes with close links to primary, specialist, social and community care. You can find out about the Red Cell Community Service and team here
For out-of-hours emergencies the Switchboard has our oncall rota. A registrar may be first on-call but we recognise that you will be calling for consultant advice so please ask them to put you through to the covering consultant.
Locations See on a map
Department Card
Patient Leaflet
- Deferasirox treatment for iron overload
- Deferiprone treatment for iron overload
- Genetic Haemochromatosis
- Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency - Information for parents
- Glucose 6 Phosphate Dehydrogenase (G6PD) Deficiency - Information for patients
- Hereditary Spherocytosis
- Hydroxycarbamide Information for Teenagers
- Hydroxyurea (also known as hydroxycarbamide) - Information for patients
- Medications, vaccinations and travel with sickle cell - information for parents
- Medications, vaccinations and travel with thalassaemia - information for parents
- Medications, vaccinations and travel with thalassaemia - Information for patients
- Sexual health, contraception and preparing for pregnancy (for thalassaemia and sickle cell patients)
- Sickle Cell disease and pregnancy
- Sickle cell disease in adulthood
- Sickle cell home management action plan - Information for parents
- Thalassaemia syndromes and pregnancy
Last updated31 May 2024