Psychology service for children and young people with sickle cell disease and thalassaemia
This specialist psychology service provides psychological support for children and young people aged 0 to 18 with sickle cell disease and thalassaemia and their families.
We understand that living with sickle cell disease and thalassaemia can have an impact on the overall quality of life, including school, academic progress and peer relationships. This can also affect emotional wellbeing, which may lead to feelings of worry, sadness or anger. Psychological support can enable children, young people and their families to find effective ways to manage these difficulties.
Contact us
If you would like more information about our service, please contact Dr Joanna Adebayo, Clinical Psychologist.
Email: lg.sicklethalpsychology@nhs.net
Who we can help
We are available to children and young people under the care of the sickle cell and thalassemia teams at University Hospital Lewisham and Queen Elizabeth Hospital. We also work with their parents or guardians, as well as other family members.
How we can help
We provide a specialist support service specifically for the range of common difficulties related to living with sickle cell disease and thalassaemia.
These include:
- Understanding, coping and living with sickle cell disease and thalassaemia
- Improving adherence to medication
- Pica (eating non-food items)
- Managing and coping with pain
- Managing difficult feelings related to living with sickle cell disease or thalassaemia, such as worry, sadness or anger
- Neuropsychological assessments to identify and support with difficulties relating to educational attainment and progress.