Media Watch

 

On the Web, Vol. 5, 2013

Neurofibromatosis Social Media Trends

According to a new survey, neurofibromatosis (NF) patients use NF-related social media for information gathering more than emotional support.

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Books & Literature, Vol. 5, 2013

Book Review: Far From the Tree

This book peeled back the personal, historical, cultural layers of caregiving in a manner that has forever shaken my perspective about best health.

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Books & Literature, Vol. 4, 2012

Book Review: Critical Decisions: How You and Your Doctor Can Make the Right Medical Choices Together

Better than any existing literature, this book highlights techniques and behaviors that clinicians must use to support the empowered patient, and suggests significant improvements to decision aids.

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Books & Literature, Vol. 4, 2012

Book Review: e-Patients Live Longer

This easily read Guide addresses the relationship and communication among the health care team (patients and their lay and professional caregivers), safety, information gathering, privacy, cost, and health care’s future.

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Conferences, Vol. 4, 2012

Health Camp KC: The Unconference

The overarching topic at this unorthodox conference weekend was “Patient Involvement, Engagement, and Empowerment.”

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On the Web, Vol. 4, 2012

IOM Calls for Enlisting Patients to Improve Care and Lower Costs

The new IOM consensus report, Best Care at Lower Cost: The Path to Continuously Learning Health Care in America, presents specific and very “participatory” recommendations for improving the efficiency and quality of the US health care system.

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Books & Literature, Vol. 4, 2012

Book Review: Depression: A Guide for the Newly Diagnosed

This book uses the author’s expertise as a clinical psychologist and that of other experts to pull together information about depression which many people want to know.

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Conferences, Vol. 4, 2012

Health Datapalooza 2012: Apps Are Making a Difference

Health Datapalooza III was a combination of upbeat speeches about the climate of innovation and public-private sector cooperation, and enthusiastic demonstrations by developers of new health care applications.

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Conferences, Vol. 4, 2012

HIMSS 2012 Highlights: What’s Hot

Central themes included Stage 1 and Stage 2 of meaningful use; ICD-10; mobile health; mHIMSS; business and clinical analytics; and patient-centered medical homes.

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Books & Literature, Vol. 3, 2011

Book Review: A Symphony in the Brain

This book offers a history and overview of neurofeedback, a type of biofeedback that aims to help patients control their brain activity.

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On the Web, Vol. 3, 2011

“Experience-Based Co-Design” Helps Providers Improve Care

The King’s Fund’s online toolkit for health care professionals promotes communication with patients to help design a better care experience.

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On the Web, Vol. 3, 2011

CMS Releases New Tools and Enhancements for Consumers and Providers

The Centers for Medicare & Medicaid Services (CMS) has released a new online tool and improved others to empower consumers to make informed choices about their health care, and to help improve the quality of care in American health care institutions.

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On the Web, Vol. 3, 2011

Recommended Website: “Team Up for Health”

This is a good example of an online tool that helps primary care providers support patients in the self-management of their chronic conditions.

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Books & Literature, Vol. 3, 2011

Book Review: “Out of Her Mind”

The selections in this book can help validate people struggling with mental illness, and they show how the mental health industry still needs to become more patient centered.

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Conferences, Vol. 3, 2011

Doctors 2.0 & You

This European conference is dedicated to understanding the physician’s perspective on use of new technologies and how physicians use these technologies to collaborate with colleagues, patients, payers, government, and industry.

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Conferences, Vol. 3, 2011

CHI 2011 Conference on Human Factors in Computing Systems

Health was a featured community at the CHI conference, and several papers in particular stood out as being relevant to participatory medicine.

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Conferences, Vol. 3, 2011

Mobile Health 2011: What Really Works: A Patient POV

The author offers a patient’s perspective on the Stanford 2011 Mobile Health Conference held in May 2011.

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Books & Literature, Vol. 3, 2011

A Handbook for Patients Who Want to Change Health Care

A new report provides inspiration and guidance for activists who want to advance their aim of health care that recognizes and welcomes the participation of all players.

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On the Web, Vol. 3, 2011

SPM Members Weigh in on “Quality”

To read more comments on Dave deBronkart’s recent JoPM article about quality, visit the Society for Participatory Medicine’s public listserv archives.

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On the Web, Vol. 3, 2011

Recommended Post: “Time to Tango”

JoPM’s Editor in Chief recommends his former co editor’s blog post reflecting on why doctor-patient partnerships are still not as common as we would hope.

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