The National Institutes of Health recently gathered a group of consumers and people who study them. We met off-site at a hotel in Bethesda, which I thought was an apt metaphor for the day’s question: How can NIH better communicate with the public? First, I said, make it easier to access your research. Make your […]
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Safety Net Populations–Susannah Fox
I recently spoke at a workshop entitled Patient Online Access in the Safety Net. (Check out these related posts.) Click image to view full size original. The organizers, Ted Eytan and Veenu Aulakh, asked me to create a participatory presentation, which definitely pushed me out of my comfort zone since I had to be ready […]
Comarow on Quality–Susannah Fox
Avery Comarow’s blog on USNews.com is my personal find of the week. I once worked with Avery, so I know he tells it like it is, and he’s tackling an important topic. Check out his take on the CMS Hospital Compare page: Hospital Deaths Go Public.
Not Just a Pretty Picture–Susannah Fox
The Journal of the National Cancer Institute published health risk data in a way that only a researcher would love (Reason.com’s Hit & Run blog links to the subscription-only charts here in case you want to marvel at the ugliness). Luckily The New York Times took notice and painted a picture that everyone can appreciate. […]
Eyeballs AND Data, Please–Susannah Fox
Jeff Howe’s blog post, “Can We Crowdsource Medical Expertise?” elicited the following comment from Daniel Reda of CureTogether.com: “Personally, just like I have batting averages, crash test ratings and historical earnings, I’d like to see the data on whoever interprets my MRI and whoever makes my diagnosis, regardless of whether it’s an amateur in a […]
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