I think of myself as a public service researcher. The Pew Charitable Trusts and the California HealthCare Foundation provide the funds for the work I do and, in turn, I do everything I can to inject the findings into the public conversation: publish reports and data sets online, for free; talk to reporters and bloggers […]
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Ribbons, ribbons, everywhere
Peggy Orenstein‘s article, “Our Feel-Good War on Breast Cancer,” is worth one of your precious NYTimes.com chits (unless, of course, you’re a subscriber, in which case you have hopefully already devoured it). But don’t just take my word for it, read this post by Katherine O’Brien of the Metastatic Breast Cancer Network — the bloggers […]
A picture worth a thousand “What if health care..?” words
What if kids were given the support to participate in and understand their own health care? – @savingcase For more health care dreams, please see: What if health care…? (Storify) Or any of my other #whatifhc posts.
How I choose which conferences to attend
I wrote this as a comment last year in response to a question about why Medicine X was so magical. I’m elevating it to a post thanks to encouragement from E-patient Dave and because I’d love to hear from other people about how they choose events to attend. 5 criteria I consider when I receive […]
Must-read: Adding up diagnosis errors
Laura Landro’s column in the Wall Street Journal today is a must-read: Adding Up Diagnosis Errors. Why? Let me count the ways: She is one of the most thorough, informed health care reporters around. She is covering an important topic that should be of interest to everyone. The study is behind a paywall so media coverage […]
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