The current digital information ecosystem shows risks and opportunities for those who suffer from a disease. Can we recount our illnesses better online or face-to-face? Could we improve the reliability of information that ill people find on the net? Could we involve patients and citizens in a virtuous process that increases the available knowledge and ensures better governance of the health system? Could we use web 2.0 to improve the available evidence?
panel discussions
| in Italian (without translation)
Health care 2.0
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Photos
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Isabella Baroni
Italian Multiple Sclerosis Association
Paolo Eusebi
co-founder Polygree
Salvatore Iaconesi
Art is Open Source (via Skype)
Tom Jefferson
Center for Evidence-Based Medicine
Tiziana Moriconi
Galileo Servizi Editoriali
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