The Neurological Alliance is seeking responses to its third patient experience survey from people receiving treatment for their neurological condition(s) in England.
The survey aims to collect vital information about the experiences of treatment and care, social care and welfare received by people affected by neurological conditions.
This is a great opportunity for us as an FND community to highlight FND and how it impacts us. the more surveys they receive the more leverage we have to impact change.
To complete the survey click here