When I was a newbie in Washington, DC in the 90s working for US Department of Health and Human Services (HHS) in the Office of Organ Transplantation (DOT), one of my jobs was organizing public hearings to finalize organ allocation policies —


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Several hundred patients gathered at the Hilton Union Station in San Francisco last week to give voice to what is being called the New Patient — the network patient.  From blogs, RSS feeds, Im’ing, and e-scrips, there appears to be an app for that to keep patients informed about their health and treatment choices.  


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