The Red Cell Network is running Patient Reported Experience Measures (PREMs) surveys for adult and paediatric patients, and parents of paediatric patients, living with sickle cell disorder and thalassaemia. These surveys will close on 14th March 2026

Your answers help us understand the quality of care for people living with thalassaemia and sickle cell disorder, what is working well, and what needs improvement. The survey is anonymous and will not affect your care in any way.

For thalassaemia, there are 3 surveys: for adults with thalassaemia, for children and young people with thalassaemia, and for parents of children and young people with thalassaemia.

For sickle cell disorder, there are 3 surveys for each Trust within our network. Please find your Trust in the below list and complete the appropriate survey.  

 

Bedfordshire Hospitals NHS Foundation Trust

Adults

Parents

Childrens

Cambridge University Hospitals NHS Foundation Trust

Adults

Parents

Childrens

East and North Hertfordshire NHS Trust

Adults

Parents

Childrens

East Suffolk and North Essex NHS Foundation Trust

Adults

Parents

Childrens

James Paget University Hospitals NHS Foundation Trust

Adults

Parents

Childrens

Norfolk and Norwich University Hospitals NHS Foundation Trust

Adults

Parents

Childrens

North Middlesex University Hospital

Adults

Parents

Childrens

North West Anglia NHS Foundation Trust

Adults

Parents

Childrens

Princess Alexandra Hospital NHS Trust

Adults

Parents

Childrens

Queen Elizabeth Hospital King’s Lynn NHS Foundation Trust

Adults

Parents

Childrens

University College London Hospitals NHS Foundation Trust

Adults

Parents

Childrens

West Suffolk NHS Foundation Trust

Adults

Parents

Childrens

Whittington Health NHS Trust

Adults

Childrens

Parents