Hear, hear. We don’t mince words, and we’re not at a loss for them either.

Blog posts

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  • Health Care Equity and Alternative Payment Models (APMs) - Sinsi Hernández-Cancio on the "Spotlight on Action" podcast

    Vice President of Health Justice Sinsi Hernández-Cancio was a guest on Health Care Payment Learning & Action Network's Spotlight on Action podcast to talk about moving the health care system towards one that effectively cares for every single person in this country – with dignity, excellence and respect.

  • Survey Says: We’re Missing an Opportunity to Engage Women in Their Health Care

    The 2017 NCI Health Information National Trends Survey (HINTS) survey included questions on consumer use of health IT. We look at what it says about how women access and use health information via digital health tools. 

  • The Power of Data Sharing to Improve Health

    When it comes to improving patient care and health outcomes, it is clear that place matters: where people live, work, worship and play affects both individual and population health in powerful ways. 

  • New York State of Mind

    GetMyHealthData is partnering with practices in New York to improve patient access to and use of health information.

  • Megan O'Boyle
    A Mother's Journey

    Megan is the mother of a child with a rare genetic syndrome. Here, she shares her story of overcoming many obstacles – from high fees to puzzling policies and procedures – to get copies of her daughter’s medical records so she can better coordinate her care.

  • Troubleshooting Tracers’ Stories

    We continue our Tracer Series this week by sharing common roadblocks Tracers have faced when they tried to get and use their health data.

  • A Tale of Two Tracers

    This week, we’re kicking off our series of Tracer stories by sharing stories from two patients who requested their health data and reported back to us about their experiences.

  • Get Your Health Data in 2016: Become a Tracer

    2016. This is it: the year I get my cholesterol under control. It’s not an easy New Year’s resolution, but it’s one I’m confident I can keep track of, in part because I have 24/7 access to my health records.

  • A Long Time Coming: Health Technology in the Hands of Patients

    Did you know that you may already be able to access your digital health records from home? Harnessing the power of technology to improve health and care doesn’t have to be complicated; you don’t need the latest Fitbit, Apple Watch or GoogleGlass for technology to make an impact on your life.

  • No Meaningful Use (MU) Without Me: The Power of Consumer Voices

    As you know, at the National Partnership for Women & Families, we strongly believe health IT is a real game-changer for patients, helping them take charge of their health and become true partners in improving our health care system.

  • MaryAnne Sterling
    Building Better Health IT Tools for Family Caregivers

    As we become immersed in the sights and sounds of the holiday season, there is a largely invisible group of people struggling to balance their daily responsibilities with the added stress of the holidays – family caregivers.

  • Your Health Information: Get It, Check It, Use It.

    It’s ushering in a new era in health care, with major benefits for women, caregivers, consumers and families.

  • How Do I Get to Healthy?

    What if, instead of plugging in your destination address, you could ask for directions to get to healthy?

  • Realizing the Value of Health IT: Jumpstarting Efforts to Reduce Health Disparities

    Health disparities and health information technology (IT). Those two issues aren’t linked very often, but they should be, and National Health IT Week presents a great opportunity to talk about why. Health information technology is a valuable tool we can use to reduce disparities for millions of Americans and improve the quality of health care.  

  • "Meaningful Use" of Health IT: What the FACA?!

    What happens when you put a couple of dozen doctors, technology vendors, consumer advocates, researchers, public health officials, state legislators and others in a room and ask them to agree on exactly what it means to ‘meaningfully use’ electronic health records? Not as many fights as you’d think. And thanks to the Federal Advisory Committees Act [1] – which created the FACAs responsible for creating the first draft of Meaningful Use criteria – we know!

  • An Opportunity to Reduce Health Disparities that We Cannot Afford to Waste

    One of America’s greatest assets is its incredible diversity. Today, one in five people in this country age five and older speak a language other than English at home. The U.S. Hispanic population has reached 50.5 million, accounting for more than half of the population increase since 2000.

  • Moving Forward on Health IT

    Delay access to health information you need now?  Pause efforts to ensure that an emergency room can get your medical data from your doctor immediately, if the need arises?  Patients and consumers say no.

  • Why Health IT is Truly the Cat's Meow

    Those of us who work in the health IT world spend our days analyzing policies, creating advocacy strategies, and talking about meaningful use criteria, quality improvement, and care coordination till we're blue in the face. But how does that play out when we leave the office? More often than not, we bring our work home.

  • Meaningful Use March Madness: SO/GI or Bust!

    Welcome to the final installment of Meaningful Use March Madness, a series of blog posts refuting frequently-heard arguments about the criteria proposed for the Electronic Health Record “Meaningful Use” Incentive Program.

  • Meaningful Use March Madness: Keep Up the Pace

    Welcome to Meaningful Use March Madness, a series of blog posts refuting frequently-heard arguments about the criteria proposed for the Electronic Health Record “Meaningful Use” Incentive Program.

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