{"id":5432,"date":"2010-04-19T11:07:40","date_gmt":"2010-04-19T16:07:40","guid":{"rendered":"http:\/\/pmedicine.org\/epatients\/?p=5432"},"modified":"2010-04-20T11:22:24","modified_gmt":"2010-04-20T16:22:24","slug":"health-2-0-europe-a-moveable-feast","status":"publish","type":"post","link":"https:\/\/participatorymedicine.org\/epatients\/2010\/04\/health-2-0-europe-a-moveable-feast.html","title":{"rendered":"Health 2.0 Europe: A Moveable Feast"},"content":{"rendered":"

Ernest Hemingway wrote that Paris is a moveable feast<\/a>, not fixed in time or place. I think that describes great gatherings of any kind, including great conferences, which begin before the first speaker takes the stage and don’t end simply because the participants have left the building.<\/p>\n

Health 2.0 Europe began, for me, in February, when I started thinking about some of the topics that the Patients and Online Communities panel would discuss. My post, “Privacy can kill, openness can heal,”<\/a> kicked off a discussion about health data rights, the role of health professionals, security\/confidentiality\/privacy, patient-driven research, and why relatively few patients have joined formal patient communities while naturally-occurring communities on Twitter\/MySpace\/Facebook have blossomed.<\/p>\n

The feast of ideas continued as I talked with Indu Subaiya<\/a>, the moderator, and Gilles Frydman<\/a>, Jamie Heywood<\/a>, and Alexander Schachinger<\/a>, three of my six co-panelists. I did as much research as I could on the other three panelists, but was a bit hampered by my inability to read German <\/a>or Italian<\/a>! I needn’t have worried — their presentations were fantastic (and in beautiful English).<\/p>\n

I decided to use my opening remarks to dispel a couple of myths (the internet does not replace doctors<\/a>, for example) and to hopefully spark a conversation (even if it was only in the audience members’ heads) about how it is time for Health 2.0 to evolve. Why? <\/strong><\/p>\n

Because nobody in that room needed to hear about the basics of patient networks. <\/strong><\/p>\n

Instead, it is time to talk about the power of health conversations informed by data<\/a>, the self-experimentation<\/a> that people engage in using information often found online, the impact of real-world experience on drug safety<\/a>, and of course, participatory medicine<\/a>.<\/p>\n

Here’s what I said:<\/p>\n

For those of you who don\u2019t know me, I work for the Pew Research Center\u2019s Internet & American Life Project<\/a>, which studies the social impact of the internet. The best way to explain it is to say I am an internet geologist.\u00a0 I measure patterns in the internet landscape. Here\u2019s a very important distinction:\u00a0 A geologist does not judge the rocks. She studies them. I don\u2019t say one technology is better than the other. I don\u2019t say one outcome is better than the other. I provide data to help you make those judgments.<\/p>\n

Fox health2eu slides<\/a><\/strong><\/object><\/p>\n
View more presentations from Pew Research Center’s Internet & American Life Project<\/a>.<\/div>\n<\/div>\n

All of my reports and data sets are available for free on the Pew Internet Project\u2019s website and you can argue (or agree) with me about our findings on Twitter <\/a>or on e-patients.net<\/a>.<\/p>\n

Today I\u2019m going to give you just a few data points to think about as we discuss patient networks and participation in health care.<\/p>\n

Pew Internet surveys show that about 8 in 10 American adults have access <\/a>to the internet, but access varies according to someone\u2019s age, education, income level, and health status.<\/p>\n

Only about two-thirds of people living with chronic conditions<\/a> go online, including people living with diabetes, heart conditions, high blood pressure, lung conditions, or cancer.<\/strong><\/p>\n

E-patients are listening to each other<\/a>, consulting hospital reviews and doctor reviews, and posting which treatments work for them. Internet users living with chronic disease are more likely than others to look online for information about prescription or over the counter drugs<\/a> \u2013 about half do so.<\/p>\n

However, the internet does not replace doctors, nurses, and other health professionals.\u00a0 93% of people living with chronic disease<\/a> turn to a health professional for medical advice. The internet is a supplement. The internet is changing people\u2019s relationship to information<\/strong>, which affects their relationship with health professionals, but we need to move past this notion that doctors should fear the internet\u2019s influence any more than we need to fear the telephone.\u00a0 This is evolution.<\/p>\n

Part of the evolution is recognizing that patients and the people who love them are not just your target audience, but your colleagues<\/a>. They are a resource for innovation and knowledge.<\/p>\n

Instead of marketing to your audience, ask them to participate. Our data shows they are ready.
\n<\/strong><\/p>\n

I think Health 2.0 is at a critical moment in its evolution.\u00a0 Ask yourself how you are evolving. Are you adapting to the shift to mobile? Are you adapting to the rise of participatory medicine?\u00a0 What is your goal and which technologies, policies, and practices best fit that goal?\u00a0 As we crawl out of the primordial soup of the first decade of Health 2.0, think about whether you want to be a creature that walks on land, flies in the air, or swims in the sea.<\/p>\n

I would argue that we have two archetypes on stage:\u00a0 ACOR <\/a>is a community of cancer patients who communicate via email: in text, in narrative.\u00a0 PatientsLikeMe <\/a>is a community of people with life-changing diagnoses who also communicate in text, in forums, but also share and compare data.\u00a0 Cancer may lend itself better to the ACOR approach, whereas ALS may lend itself better to the PatientsLikeMe approach. Both are founded on a principle of openness. But before we go farther, let\u2019s make sure we\u00a0 are aware that by choosing narrative, by choosing data, by choosing open sharing or by choosing closed systems, we are evolving in certain directions.<\/p>\n

Pew Internet data shows that the deck is stacked against people living with chronic disease.\u00a0 They are likely to be older, less educated, living in lower-income households. But if they can get online, they have a trump card, a secret weapon: each other<\/strong>.\u00a0 If they can get access to the internet, they adapt to the opportunity.\u00a0 Chronic disease actually makes it more likely that someone will participate in the online conversation, to consume user-generated content, to seek and share peer advice. If they can adapt, why can\u2019t you?<\/strong><\/p>\n

—<\/p>\n

What followed was, in my opinion, a stellar discussion and series of presentations (and you know I’m honest about failed panels<\/a>). I can’t wait for the video to be posted (as long as they leave off any frighteningly close shots of my face – yikes those cameramen liked the zoom) but in the meantime the feast continues:<\/p>\n

On Twitter:<\/strong><\/p>\n

Archive of Health 2.0 Europe tweets (PDF<\/a>)<\/p>\n

Follow related conversations: #health2eu<\/a> #hcsm<\/a> #hcsmeu<\/a> #WhyPM<\/a><\/p>\n

On blogs:<\/strong><\/p>\n

Matthew Holt: Health 2.0 Europe–My Take<\/a> (tying lots of threads together)<\/p>\n

Denise Silber: Health 2.0 Europe (quite a few posts<\/a>)<\/p>\n

David Doherty: Health 2.0 Europe\u00a0Review<\/a> (unvarnished, even stinging, so his praise is especially appreciated)<\/p>\n

Colleen Young: Health 2.0<\/a>: Why SharingStrength will be in Paris this spring (wins my award for Most Valuable Tweeter<\/a> and <\/em>she seemed to soak up more knowledge than anyone else I met at the event)<\/p>\n

Please join me at the table. What’s next for patient networks? What are you building today that is different from what was available 5 or 10 years ago?\u00a0 What should be preserved as we go forward?
\n<\/strong><\/p>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

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