On Nov. 1-2, 2017, Hope for Henry convened a diverse group of parents, kids, clinicians, designers, educators, and entrepreneurs to reimagine care for hospitalized kids. I’ll disclose that I am an advisor to Hope for Henry and helped organize the event, but I hope you’ll believe me when I say that it was, objectively, a […]
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Medicine’s cultural “caution tape”
I’m honoring the contributions of my community colleagues over the years by pulling out some of their best comments and quotes. Jack Penner, in response to “His doctors were stumped. Then he took over” (2017): In terms of how can we empower patient to become active participants, one thing that comes to mind is lowering […]
Why people participate in clinical trials: altruism and access
I’m honoring the contributions of my community colleagues over the years by pulling out some of their best comments and quotes. Rahlyn Gossen, in response to Peer-to-peer healthcare: Crazy, crazy, crazy, obvious (2011): By far the biggest hurdle to clinical trials recruitment is awareness. The public is generally not aware and doctors are not informing […]
Access to results that matter
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 […]
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 […]
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