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Over the past several years there has been a virtual explosion in the presence and popularity of review websites that offer a platform for patrons and patients...
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The 2012 Connected Health Symposium showcased a myriad of engagement tools that promote innovation and improve patient compliance.
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How can we quantify the agony of facing an untreatable disease? Can we measure the harms we inflict because we can't bear to tell patients they have no options? Can we assign a numerical value to hope? For those aspects of disease that elude our measurement, we will forever depend on the insights and passions of our patients
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Increasing patient cost sharing was associated with declines in medication adherence, which in turn was associated with poorer health outcomes Via Richard Meyer
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Featured Guest Blogger: Janice M. Prochaska, Ph.D The passage of the Affordable Care Act and emergence of Patient Centered Medical Homes and Accountable Care Organizations has highlighted the nee...
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The HSJ100 is our annual list of the most influential people in the NHS and English health policy.
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Patients want to be more involved in their care but feel GPs are currently not delivering good communication or shared decision making, according to a snapshot of opinion published by The Patients Association today.
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Physicians often hesitate to give this kind of access to patients because they are afraid it will be abused but that is short-sighted. Just like with the telephone, I have complete control over whether I answer or my medical assistant does. Via Dean Berg, Pharmacomptoir / Corinne Thuderoz
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Vital Options presents Advocacy in Action (AIA), in partnership with the ESMO Cancer Patient Working Group and in collaboration with the ECCO Patient Advisor...
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Patients are the driving force and inspiration behind oncology related events, ESMO’s educational programs, and the reason why oncologists are constantly pushing the edge of science to revise existing therapies and find new treatment options. |
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A hospitalist physician shares insights and practices designed to promote leadership, provider and caregiver engagement in the patient experience.
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Most of the time, my patients are very willing to share their stories. From my perspective, there are practical reasons to understand social contexts and relationships.
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I follow patients to understand, to avoid complacency, to maintain compassion. And that is not something that can be learned from a textbook.
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In the past half century spending on healthcare across virtually all countries—regardless of how they are funded and organised—has increased substantially. At approaching £1 in £10 of its economic wealth, in 2010 the UK devoted more than twice the share of its gross domestic product (GDP) to public plus private healthcare spending as it did in 1960.
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Ann Connealy lived her first 50 years without ever being a patient in a hospital. Her run of good luck ended with a diagnosis of cancer of the appendix in 20...
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According to a new study published in the Journal of Medical Internet Research, wikis would be an effective participatory tool for patients in the development of a clinical practice guideline.
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The goal of the PCORI workshop was to “help PCORI build a patient-centered research community” through five specific discussion topics listed in my previous post. Patient-centered research and PCORI itself is still new enough that there are many questions about what “patient-centered” will look like
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We are dedicated to helping you become a powerful patient, a powerful caregiver, or a powerful friend to achieve better health.
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Measurement of the patient’s experience of the care received is essential for the delivery of high quality care throughout the patient’s journey from diagnosis. In October 2011 the NHS ...
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"This animated infographic shows the main outcome of the European Health Literacy Survey (HLS-EU), which formed part of the European Health Literacy Project from 2009-2012." Via Usalbiomedica, Camilo Erazo
Zjelco Felder's comment October 30, 2012 9:20 AM
Visit this link for more information: www.hls-eu.info
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I am a nurse. I am a patient. Until about a year ago I felt very clear about how each of these played a role in my life. I was sure about which one made me strong and which one made me weak. Which was helpful to others and which was a burden. The one that would aid me in my work and the one that would hold me back. Then an email arrived in my inbox that would turn all those beliefs upside down. But this certainly didn’t happen right away, because above all else, I am stubborn.
The email came from a friend and colleague. He said he had some ideas that he wanted to discuss with me but first, he asked if I would watch a video and give him some feedback on it. The video was a TEDTalk featuring e-patient Dave deBronkart. In the video Dave told a story about how he used the internet to connect to information and other patients to learn about treatment options his own doctor had not mentioned. He claimed that what he found saved his life.
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More than 15 advocates and survivors across all cancer types from around the globe came together to discuss international perspectives on patient advocacy. |