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CEO Thought Leadership Series from Trade Show

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AMANDA GREENE OF THE ALLIANCE FOR LUPUS RESEARCH AND TIFFANY PETERSON, LUPUS WARRIOR, DISCUSS HOW SOCIAL MEDIA HAS BROUGHT LUPUS PATIENTS FROM ACROSS THE GLOBE TOGETHER ONLINE.

To Link To post: http://www.vlogviews.com/amandagreenetiffanypeterson/

Robert Schwartz, Account Executive and Washington Correspondent of D S Simon Productions, spoke with Amanda Greene of the Alliance for Lupus Research, and Tiffany Peterson, Lupus Warrior, about how social media has helped open communication in the Lupus community at the State of Now/#140Conference in New York.

Amanda and Tiffany’s VlogViews:

“That’s what social media has done in the health world, it’s really inspired me to start Lupus chat and to really engage all of those patients with Lupus but not only the patients but the physicians and the organizations out there who are also on Twitter and we can kind of bring them in on Lupus chat and really connect, share information and increase our learning.

“The Society for Participatory Medicine is on Twitter and their all about sharing those doctor patient relationships and really getting them together online to engage in patient centered care.”