Posted on September 21, 2011December 14, 2012 by Mighty Casey e-Patients in Philadelphia. Echoes ensue. I had the opportunity/privilege to participate in a conversation with other health activists and e-patients about a Digital Patient Bill of Rights recently. I’ve posted an overview of the conversation on the Cancer for Christmas blog. Give it a read, and tell me what you think. Really. Related Posts:Pay people for their data – yes, or no?Whither Cochrane, for e-patients and everyone else?Democratization of knowledge, healthcare editionPrimary + People/Patients = Winning?