To ask the Secretary of State for Health and Social Care, what data is collected on the prevalence of Complex Regional Pain Syndrome in England; and how this data is being used to understand the condition.
The National Congenital Anomaly and Rare Disease Registration Service (NCARDRS) is part of the National Disease Registration Service (NDRS) and NHS England. The NCARDRS aims to collect, curate, quality-assure, and analyse data from patients in England dia...
Complex Regional Pain Syndrome