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This weekend the Associated Press is publishing a story about CaringBridge and a similar site, CarePages. It relates the experience of several users, including my community and family during my cancer adventure last year (see my CaringBridge journal.).

Newcomers: if you’re looking for great resources for self-education on how to be an effective consumer in today’s healthcare system, here’s a post from my CaringBridge site a few weeks ago: …


RESOURCES FOR INTERNET PATIENTS

As regular readers know, during this past year I’ve become a strong advocate of all the ways patients can improve their outcomes and their experience, becoming active participants in their care, especially by using the Internet.

Here are some resources:

  • The E-Patients blog: E-patients are “empowered, engaged, equipped and enabled.” This blog covers a wide range of topics about the new world of participatory medicine. If you’re a patient or family in need, educate yourself by reading the wonderful “white paper” (manifesto) available on that site.
  • A community support site, like CaringBridge. It saves you an enormous amount of time corresponding, and lets your supporters check in anytime instead of keeping up with emails.
     To see how it works, you can get the whole year’s transcript (1/30/07 – 1/30/08) as a free download (one big file or single chapters), and read while you’re sitting in waiting rooms. :)
  • The New Life of e-Patient Dave is my blog about … well … my new life. Last year I was at the end of my mini-golf game, but I got a free replay. The New Life blog tells what I’m doing with that replay – mostly sharing what I learned during my adventure.

On the New Life blog I’m starting a beginner’s guide to participatory medicine. It’s my effort to share what I learned last year, with the intention that others can take a shortcut. In particular I recommend the chapter about “the five pillars of participatory medicine.”

Those sites have many links to other web sites. Do your own exploring – see where it takes you.

And by all means, get out there and PARTICIPATE. In the world of blogging, that means you click the Comments link (or Guestbook, on CaringBridge), and enter questions or comments.

Be an e-patient: Ask what you want to know; say what you think.

 

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