HEDA / The Health Data Program

[Tessa Richards @tessajlrichards]

Calling patients, policy makers and health professionals interested in progress, debate, and research on citizen access to EHRs. Join this network https://t.co/pYehU5ciZU

[Tessa Richards @tessajlrichards]

Uplifting to listen to impressive progress on patient access to EHR in Scandinavia. #Journalen10 on World Usability Day https://t.co/rjtAn5B4Wb

[Tessa Richards @tessajlrichards]

Unpaid carers struggle with many burdens. Not having access to the health information of those they care for is one of them. Improvements to proxy and shared access to EHRs needs to improve. Hearing about research to do that @Journalen10

[Anna Clareborn @clareborn]

Currently at #journalen10, mind-blowing numbers on unpaid healthcare labor in the US. @cmd418

[Anna Clareborn @clareborn]

Today is World Usability Day, and we’re acknowledging that by kicking off day 2 with a themed session at #journalen10! https://t.co/itZtGbv82E

[Anna Clareborn @clareborn]

Jumping straight into the final day 1 keynote at #journalen10! Catherine DesRoches, @cmd418, discusses how note sharing went from what was essentially a fringe practice, all the way to federal law in the US.

[HEDA / The Health Data Program @HEDAProgram]

You can join our growing network of researchers, patients, clinicians, and policymakers free of charge on our website:

https://t.co/eWbUgwc5Ua

[HEDA / The Health Data Program @HEDAProgram]

Today is the day we officially launch HEDA, the Health Data Program for researchers, patients, clinicians, and policymakers interested in all things involving health data.

#HEDA #healthdate #healthdataprogram