Since 2014, we've invited stakeholders from across the rare disease community to this informal networking event. Young people speak about their experiences of living with a rare disease, and patient advocates, researchers and health professionals talk about working in the field. Read on for highligh...
This free online course is designed for the early years workforce and healthcare professionals. It aims to improve your knowledge, skills and understanding of the benefits of effectively sharing information in a professional context.
This event was a great opportunity to network and learn more about how data is being used to monitor and improve neonatal care in the National Neonatal Audit Programme (NNAP). Take a look at the videos from the day's presentations.