The Society for Participatory Medicine is a 501(c) 3 is a not-for-profit organization devoted to promoting the concept of participatory medicine, a movement in which networked patients shift from being mere passengers to responsible drivers of their health, and in which providers encourage and value them as full partners.
The Society seeks to bring together all of the stakeholders in healthcare (patients, caregivers, healthcare professionals, payers, and others) to encourage collaboration, communication and cooperation that will foster provider/patient engagement, patient empowerment and education.
This partnership of cooperation is enhanced with the Society’s Four Pillars:
Provide a participatory medicine forum for collaborative research exchange and evidence based practice project collaboration.
Provide resources, reference tools and best practice standards that support participatory medicine.
Ongoing work with government officials, policy-making bodies, patient advocacy organizations to foster the ideals of participatory medicine.
Encourage collaboration and networking among members and organizations who are ambassadors for the participatory medicine movement.
- Matthew Katz on 23andMe: “Return to Sender, Genome Unknown: Seven Reasons I Will Return My Personal Genome Kit”--@yogileana
- Monthly introduction to e-Patients.net--e-Patient Dave
- My Reasons for Thanksgiving: On The Ultimate Loss of Control, Unclear Diagnoses, and Being a Patient--Daniel Z. Sands, MD, MPH
- Thanks from the Philippines--@yogileana