I have been pondering data sharing recently - Sharing information is essential for effective partnership working in health & care, especially in times like these. Data Protection, consent procedures & IG stuff are super important, but like the H&C system, can be pretty complex

How great would it be if people universally trusted the H&C system to use their data with integrity and respect? How great would it be to have trust WITHIN the system, helping information to be shared and used in a joined up way, to improve health and care for people.

But, it's hard to wholeheartedly trust something that you don't understand... Slow and clunky data sharing in H&C feels like a problem of our own creation, a product of the fragmentation of the system. How can we #MakeStuffBetter? Any thoughts would be much appreciated.