By
AmyT on
September 6, 2012
We don’t talk about it all that much in the heart of the diabetes online community (DOC), but there’s actually an incredibly vibrant and growing larger community of online patient advocates out there who are banding together to do great things. No matter if you have prostate cancer, fibromyalgia, chronic migranes, or… diabetes.
I’m a member of a group called the Society for Participatory Medicine and on their email list, so I get to see…
Read more »
By
WilD on
March 15, 2012
Ever wonder who trains the trainers? We did, so we sent off our resident expert to take part in an official CDE (certified diabetes educator) training session. Here is his report, unfortunately with some unsightly results:
By D’Mine Columnist / Correspondent Wil Dubois
Thirty-three percent of people with diabetes (PWDs) have sufficient “clinical symptoms” for a diagnosis of depression. But in the chaos of a complicated disease, and with short office visits, depression is often…
Read more »
It might be hard to believe in this day and age of “participatory medicine” and empowered patients — or in any day and age, really — but the fact is that an Arizona-based nurse was fired from her job recently for simply providing a patient too much information on his treatment options.
The nurse’s name is Amanda Trujillo, a single mother living in Phoenix, and licensed nurse in Arizona since 2006. She specializes in cardiology,…
Read more »
By
AmyT on
October 21, 2009
Academic and medical journals — yawn, right? Not anymore. Today (at the Connected Health conference in Boston) marks the launch of a new kind of journal, which is marking a new kind of medicine, actually: the Journal of Participatory Medicine, an all-online pub that’s open and free-of-charge for all to read and enjoy.
The content, which will eventually include video clips and other multimedia stuff, is entirely dedicated to the ways in which patients are…
Read more »
