As a network we have many different patient experiences that we would love for you to be a part of. Please see the below activities and join us

We would like to invite you, as a Sickle Cell patient or care giver, to participate in a survey on your experiences of care in hospitals.

The survey is being undertaken by the West London HCC (Sickle Cell NHS network) to gain an understanding of Sickle Cell patient experiences across the West London region. The network would really appreciate it if you can take part in the survey that takes approximately 10 to 15 minutes to complete.

The networks Patient Public Voice Group and Steering Group will be monitoring the data from this survey, which will inform recommendations to be given to clinicians and managers across the HCC to improve services.

The survey responses will be collected and used for internal review within the Network in order to improve patient experience. Participant’s details will be kept confidential.

The link for the surveys are below





Other Activities

Patient & Public Voice Group

Personal Stories

To get involved contact Ralph or Eni by clicking the email below