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Susannah Fox

I help people navigate health and technology.

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patient networks

Patient Communities… at Walgreens?

June 17, 2010 By Susannah Fox 30 Comments

Aisle of a Walgreens drug store

UPDATE: On Feb. 18, 2015, PatientsLikeMe and Walgreens announced a partnership: “Now, anyone researching a medication or filling a prescription on Walgreens.com can access a simple snapshot that shows how their prescribed medication has impacted other patients on the therapy, including medication side effects, as reported by PatientsLikeMe members.” One more step away from “crazy” and toward “obvious” […]

Filed Under: e-pts resources, patient networks Tagged With: American Well, CureTogether, Diabetic Connect, Diana Forsythe, E-Patient Dave, Google Health, Inspire, MedHelp, Microsoft HealthVault, patientslikeme, Rite Aid, Ted Eytan, Walgreens

Health 2.0 DC: Passion and Execution at Scale

June 8, 2010 By Susannah Fox 7 Comments

Exterior of the National Museum of American History in Washington, DC, with the Washington Monument in the background

I think conferences are deeply affected by the spirit of their host city.  San Francisco has its hackers and dreamers, Boston has its entrepreneurs and ivy, Paris has its pomp and worldliness. At Health 2.0 DC yesterday, my city showed that it has passion and execution — at scale. Leave it to others to point […]

Filed Under: patient networks, policy issues Tagged With: Chordoma, Data Transparency, David Hale, Gov 2.0, health 2.0, Indu Subaiya, Institute Of Medicine, John Mendelsohn, Josh Sommer, Ken Buetow, Patrick Soon-Shiong, pillbox, Tim O'Reilly, Todd Park

A New Conversation About Health Privacy: Who’s In?

May 21, 2010 By Susannah Fox 29 Comments

Light bulbs in the night sky - a photo by Ted Eytan

Facebook has sparked a new debate about privacy and I think it’s time to bring it to health care. What does it mean when millions of people flock to share/overshare information, even as Facebook’s default privacy settings have slowly become openness settings (but the company maintains radio silence)? Pew Internet research shows that a sizeable […]

Filed Under: health data, patient networks, policy issues Tagged With: Facebook, Hipaa, patientslikeme, Pew Internet, privacy

The Decision Tree: How Better Health Can Scale

May 1, 2010 By Susannah Fox 3 Comments

“The internet was created to connect people and groups. The first step is to share stories. The next step is to share quantitative observations.” “Health care has been locked up in regulatory amber. HIPAA was passed in 1996, almost perfectly timed to cut off health care from the internet. But there is a loophole: to […]

Filed Under: health data, patient networks, policy issues, positive patterns Tagged With: 23andme, chronic disease, CureTogether, Decision Tree, digital divide, Genetics, getupandmove, Health Data, Hipaa, patientslikeme, Pew Research Center, susannah fox, Thomas Goetz

Chronic Disease in Data and Narrative–Susannah Fox

March 24, 2010 By Susannah Fox 60 Comments

For the past 5 months I have been immersed in data and narrative about chronic disease. The result, “Chronic Disease and the Internet,” is a report sponsored by the Pew Internet Project and the California HealthCare Foundation. We find that living with a heart condition, lung condition, high blood pressure, diabetes, and/or cancer has an […]

Filed Under: patient networks, understanding statistics Tagged With: california healthcare foundation, chronic disease, Pew Internet, Pew Research Center

Privacy can kill, openness can heal–Susannah Fox

February 11, 2010 By Susannah Fox 34 Comments

If you follow Jeff Jarvis on Twitter or read his blog, you know (maybe more than you wanted to) about his fight against prostate cancer. I’ve mostly paid attention to what he’s written about technology and journalism, but check out this excerpt from his post, The German privacy paradox: I prefer to turn the question […]

Filed Under: patient networks Tagged With: ACOR, health 2.0, patientslikeme, privacy

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