Once a year, I give a high-stakes presentation in front of a single audience member: my son’s teacher. I have 20 minutes to teach her how to save his life.
I need to explain the science of food allergy, list all of his many allergens, accurately describe the symptoms of anaphylactic shock, instill an appropriate sense of urgency and responsibility with one …
Stephen Wolfram’s essay, The Personal Analytics of My Life, begins, “One day I’m sure everyone will routinely collect all sorts of data about themselves.”
A Pew Internet survey suggests we have a long way to go: a September 2010 survey found that 27% of internet users age 18+ track their own health data online. There may be more self-tracking happening offline — please post any measures of that phenomenon in the …
This post is first and foremost a thank-you note.
Thank you to everyone who posted a comment, emailed me, or tweeted a suggestion in response to my request for input last July: Crowdsourcing a Survey. Six new topics came directly from those conversations. Thank you to Veenu Aulakh and the California HealthCare Foundation who provided funding for the survey. Thank you to Lee …
Recently, I dashed off this tweet:
PhD student just asked me which journals I read to stay up to date on health + tech. My answer: Twitter.
It was classic RT bait and indeed it was echoed dozens of times by fellow Twitter geeks — more than any other tweet I’ve written. But I would like to qualify it with a fuller explanation. I don’t just read Twitter and ignore journals. …
David C. Kibbe and Joseph C. Kvedar’s article, “Building a Research Agenda for Participatory Medicine” highlighted two of their “ready-to-go” research questions:
Recently, the Legacy Foundation’s Schroeder Institute focused …
Last year’s Mayo Transform 2010 symposium was a two-day excursion into the world of science, data, design, and the secret ingredient to health: love.
Patch Adams, MD, kicked things off in grand style. If you’ve never seen him speak, treat yourself to a hit of his energy:
In 1971, he and his compatriots opened a 24×7 hospital in a six-bedroom house to address every aspect of …
Ten years ago, I wrote the Pew Internet Project’s first report on the impact of the internet on health care, calling it “The Online Health Care Revolution.”
Back then, the idea that people were searching online for health information was revolutionary. All of a sudden, regular people had access to medical information that had always been locked up and out of reach.
Ten years later, I am ready to declare the access …
New concepts need gimmicks. Proven concepts do not.
The phenomenon of using the internet to gather and share health information is now mainstream. It’s time to change how we talk about it, revising and maybe even retiring certain terms.
Some history to build our case:
In 1998, only about one-third of American adults had access to the internet. Harris Interactive published pioneering research about how internet users gather health information online, dubbing these …
Speaking to the senior staff of the National Library of Medicine recently was like going before the best kind of murder board.
Picture it: 30 of the nation’s smartest health information mavens around a polished conference room table, asking me sharp questions, suggesting new lines of inquiry, and offering their own insights. In other words, heaven.
Our jumping-off point was the Pew Internet Project’s latest research on internet penetration, mobile use, and …
Someone going by the name “Darthmed” recently posted a comment that stopped me in my tracks:
… The remaining 95% of “patients” out there are not motivated to become informed, or invest the time/energy/money in using any of these tools. These are the folks that know that fast food isn’t healthy, but are just too tired to choose differently. Some (emphasis on some) will do a standard Google search when they …
In May, I spoke at the Chronic Care and Prevention Congress about my most recent report, “Chronic Disease and the Internet.”
I talked about the social life of health information and the internet’s power to connect people with information and with each other. Living with chronic disease is associated with being offline – no surprise. What’s amazing and new is our finding that if someone can get access to the internet, …
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