I agree with you, the nhs, these providers and actually anyone else who can improve diabetes care can have my health data.
I want them to use it and make it better for us all now and to prevent diabetes/ help with a cure / treatment etc in the future.
Recently my daughter took part in one of the university screening programs for type 1. They consent and personal data information provided was really great. Only minimal data was needed for the test to be completed / get the results back etc.
But the availability to share anonymous or other data with researchers to prevent and treat these conditions makes research what it is. She’s 13 so is capable of making these decisions on her own. And she said she would rather share it and help diabetics than not.
What can someone do with information about your glucose levels anyway?
I dont understand what harm you think this can put you under?
Each to their own but if you are using the internet in anyway, have a record with the nhs or another public body, bank etc your data has been leaked so many times and is already on the black web, it really doesn’t make much difference these days
All our data is out there if you know where to look.
Best you can do is change your passwords regularly and be vigilant. But not sharing data when it adds benefit to you or others doesn’t make sense in my opinion.
Also just use the reader not your phone