The Patient-Centered Outcomes Research Institute (PCORI) will kick off their annual meeting on Tuesday, October 31. I will moderate the first panel, “Access to Results That Matter,” and, as I like to do, I’m starting the conversation early online. Here’s the session description: Traditional health research often does not provide the answers to patients’ questions […]
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How health systems are like newspapers
I’m honoring the contributions of my community colleagues over the years by pulling out some of their best comments and quotes. Dave Chase, in response to Recognizing the value of data (2014): As a confessed congenital optimist, I’ll give my optimistic view of how positive developments are little-noticed, as they were with epic shifts that […]
Access to data = access to power
Data about your health and that of your community can empower you to make — or demand — changes. When there are gaps in the record or the data don’t exist, participatory data collection empowers people to contribute to the public conversation. Access to data is access to power. On November 17-19, 2017, Data for […]
Under the right conditions, people will choose the path of information altruism
I’m honoring the contributions of my community colleagues over the years by pulling out some of their best comments and quotes. This comment was posted in 2011 and I’m featuring it now because it is an example of how we, as a health data community, have been — and need to continue — discussing a power […]
Regina Holliday brings beauty and wonder to health care
If you’re a regular reader of my blog, you may have noticed that the new design requires a big “featured image” at the top of every post. It’s an interesting creative challenge to illustrate some of the themes I bring out — peer health advice, medical errors, health data… Luckily, Regina Holliday generously posts gorgeous […]
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