Helpful Hints and Practices- NHP MDT | National Haemoglobinopathy Panel | NHP Haemoglobinopathy England | Sickle Cell Thalassaemia | Rare Inherited Anaemia UK | NHP Haemoglobinopathy England | Sickle Cell Thalassaemia | Rare Inherited Anaemia UK

First published on 7th July 2026 this document was created to address a number of the most common areas of uncertainty and error that are associated with the NHP MDT process, timelines and data management. this is so for regular and new referrers alike but particularly the latter. The simple document touches on a number of issues from neuropsychometric and liver workup data requirements, to associated  GDPR matters. 

We are aware that there will be many more iterations due to additions and changes in various protocols and information. Get in touch if you feel there is something that should be included. We love to hear from our colleagues.

Click Here for the current version.