In 2008, I asked for this community’s help in choosing which sessions to attend at the Chronic Disease Care conference sponsored by the California HealthCare Foundation. I loved the input I got and wrote 3 posts on what I learned about spreading improvement in care, how to include patient voices, and how to discuss emerging […]
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Mind the Gap: Peer-to-peer Healthcare–Susannah Fox
Update: My notes are now online: Mind the Gap: Peer-to-peer HealthCare. The newest material is in the section entitled, “Getting Past the Early-Adopter Stage” — roadblocks, opportunities, and beacons for change (patient leaders, clinician leaders, and technology leaders). Not surprisingly, the NIH audience members suggested adding “policy leaders” to that lineup. It was an extraordinarily […]
The e-Perspectives of e-Patient Dave–Susannah Fox
Our own e-Patient Dave is featured in an extensive interview with Kim Chandler McDonald, an Australian journalist who is passionate about what she calls the “meHealth movement.” Part one of their conversation is posted today to coincide with the TED conversation, “Let Patients Help.”
What I learned at Health Foo
Update on Feb. 7, 2019: There are so many broken links, I’m de-linking and crossing them out but not deleting them, for posterity. They once worked! Just in case anyone is curious: my notes from Health Foo, a meeting held last weekend in Cambridge, MA. It’s long, so skim for the 9 lessons if you […]
Are patients knights, knaves, or pawns?
Sachin Jain and John Rother’s JAMA commentary, “Are Patients Knights, Knaves, or Pawns?” is an article that begs to be shared. The first time I read it I had to stand up, I was so excited — how can I design a survey to capture these questions?! was my first thought. My second thought was […]
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