David Kibbe’s THCB post, Confessions of a Physician EMR Champion, has stirred debate in the comments section including some key insights from our own Gilles Frydman, who points out the need to add “patients” to the list of stakeholders, and Christine Gray, who writes about cultural differences among male and female doctors in adapting to […]
Happy Dogs in a Pile of Sticks (Spreading Improvement in Chronic Disease Care)
The California HealthCare Foundation’s Chronic Disease Care conference was so packed with great panels that I needed help choosing my targets. Here is the first in a series of posts about this event. Spreading Improvement: After the Innovators/Early Adopters
Patient Involvement Makes People Smile–Susannah Fox
Ted Eytan’s Photo Friday features a crowd of chronic disease care providers listening to patients tell their stories — and smiling as they see the impact of what they do. As I wrote in the comments, I’ll post here soon with more notes, but this photo is a good start toward understanding the impact of […]
Crowdsourcing a Survey: Reassured? Overwhelmed? Eager? Confused?–Susannah Fox
The Pew Internet Project is finalizing our fall health survey and we are now in the painful cut phase. Here’s a question I’m hoping to save in a shorter form: At any point in your last search for health information online did you feel any of the following things? At any point, did you feel…?
Participatory Medicine: Text of my speech at the Connected Health symposium–Susannah Fox
I should have posted this when I posted my slides, but better late than never.
Help Me Choose: Sessions at the Chronic Disease Care Conference–Susannah Fox
I will be heading to San Francisco this week to attend the Chronic Disease Care conference sponsored by the California HealthCare Foundation. Registration is closed but I promise to take notes on as many panels as possible. Please help me choose from the smorgasbord of topics and I’ll make you a plate.
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