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.
- To guide patients and caregivers to be actively engaged in their health and health care experiences.
- To guide health professional practices where patient experience and contribution is an integral goal of excellence.
- To encourage mutual collaboration among patients, health professionals, caregivers and others allowing them to partner in determining care.
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.
- Add Your Voice: Meaningful Use Regulations Mustn’t Leave Patient Engagement in the Dust--David Harlow
- Announcement: SPM to advise ACP’s new Center for Patient Partnership in Healthcare--e-Patient Dave
- Patient Advocates Fight for Access to Medical Data: ‘It’s a Matter of Life and Death’ (KQED)--e-Patient Dave
- Guest post by Annette McKinnon: Power Equality: Why Is My Silo Two Miles Away?--Ileana Balcu