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“Without the Affordable Care Act, I simply could not have retired at 62.”

Read more stories at WhiteHouse.gov/Get-Covered.
Donald L., Palm Coast, FL

Health Care Blog

  • A Health Care Story from Nebraska

    Emily Schlicting lives in Omaha, Nebraska and, like many other young adults across the country, she is already benefiting from new provisions of in the Affordable Care Act. 

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    At a young age, Emily was diagnosed with a rare, chronic auto-immune disease.  Her illness sometimes set her apart from her peers and she suddenly found herself facing the “adult problems” of how she would continue to get access to routine care and preventive treatment.  Thanks to the Affordable Care Act, Emily will be able to stay on her parent’s health care plan and has the freedom to make decisions about her life without worrying about whether or not she’ll have health insurance. 

    "I had very limited choices in terms of what I wanted to do with my life after graduation because of the health and insurance situation that I was put in by my disease.  And now, that’s no longer a problem.  I have flexibility and freedom with what I want to do with my life post-graduation."

    View the map to hear Emily’s full story and see how people across the country are benefitting from the Affordable Care Act.

  • What Health Reform Means for African Americans

    Health care is very personal for me.

    I was born with a heart murmur, my mother is a breast cancer survivor but lost her mom at the age of 3, an aunt who lost her life due to cancer, and my dad cleaned hospital rooms for 29 years.   But because of having access to health care, my family’s dreams were not deferred.  I am sure that I am not the only African-American who has received a second, third and fourth chance of realizing my dreams due to being healthy enough to realize them.

    But for too many African-Americans, lack of access and unaffordable health care meant that their dreams were not realized.

    Now, due to President Barack Obama, Health & Human Services Secretary Kathleen Sebelius and Democratic Members of Congress, health care is no longer an unmet promise for African-Americans and all Americans, it is now the law of the land.

    But, you ask – how does health care help me? How does it help my family? I am glad that you asked.

    Dr. Garth Graham from the Department of Health and Human Service’s Office of Minority Health has posted a new video on WhiteHouse.gov/HealthReform that discusses some of the many benefits of the Affordable Care Act for African Americans.  Before the Affordable Care Act was signed into law, the African American community struggled more than most as a result of our broken health care system.  As Dr. Graham points out, African Americans are nearly twice as likely to be uninsured than the rest of country and are consequently more likely to experience serious issues with medical bills and medical debt. 

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  • Putting an Old Rumor to Rest

    Today, the Internal Revenue Service issued a sample W-2 form for 2011. The form looks just like the W-2 you have received in years past, with one important new piece of information. Beginning in 2011, employers will have the option of including the value of the health care benefits that you have received on your W-2 so you can know more about your benefits and you are an empowered consumer. In 2012, all employers who provide insurance will be required to include this information on their workers’ W-2 forms.

    And because this has been the subject of rumors, let’s be clear: you will absolutely not pay taxes on these benefits. Here’s the text, straight from the new W-2 form:
     

    Cost of employer-sponsored health coverage (if provided by the employer). The reporting in Box 12, using Code DD, of the cost of employer-sponsored health coverage is for information only. The amount reported with Code DD is not taxable.

    For months, opponents of health reform have falsely claimed that the Affordable Care Act would lead to the taxation of health care benefits. The claim wasn’t true when the rumor first surfaced, it isn’t true today and it won’t be true tomorrow.

    What is true is that the Affordable Care Act will strengthen the health care system for all Americans, end the worst insurance company abuses and put patients and doctors – not insurance companies – in control of their own care. In the last month, we’ve implemented a new Patients’ Bill of Rights that will protect consumers. Under the new law:

    • All insurance plans will be prohibited from putting lifetime caps on the dollar amount that they will spend on benefits, like cancer treatment, or canceling, or rescinding your coverage because you get sick, or you made an unintentional mistake on your application.
    • Young adults will be allowed to remain on their parent’s plan until their 26th birthday, unless they are offered coverage at work.
    • Most insurance companies will have restrictions on their ability to place annual limits on care. 
    • New rules will prevent most insurance companies from denying coverage to children under the age of 19 due to a pre-existing condition. 
    • And if you purchase or join a new plan:
      • Insurance companies must cover recommended preventive services, including mammograms, colonoscopies, immunizations, pre-natal and new baby care without charging deductibles, co-payments or co-insurance.
      • Insurance companies will be prohibited from denying coverage for needed care without a chance to appeal to an independent third party. 
      • You will be guaranteed your choice of  primary care provider within your plan’s network of doctors, including OB-GYNs and pediatricians, without a referral, as well as out-of-network emergency care.
         

    You can learn more about these new benefits, the myths and facts about the Affordable Care Act and read personal stories from Americans across the country who are benefitting from the new law by visiting www.WhiteHouse.gov/HealthReform.

    Stephanie Cutter is Assistant to the President for Special Projects

  • Building the Bridge to 2014

    When President Obama signed the Affordable Care Act into law, he made it clear that his Administration would move quickly and responsibly to implement the new law between now and 2014 when all Americans would have more affordable private insurance options and the worst insurance industry abuses are ended.   Fixing a broken health care system won’t happen overnight.   It will take time to implement new reforms in a way that protects consumers because, as the President said when he signed the Affordable Care Act into law, “We need to get this right.”

    Part of getting it right is ensuring a smooth transition in the market place between now and 2014, when the law is fully implemented, so that consumers don’t become worse off along the way.  Last month, we implemented a new Patient’s Bill of Rights that helps put doctors and patients, not insurance companies, in control of their health care.  Thanks to the Affordable Care Act, insurance companies can no longer drop your coverage when you get sick.  If you join a new plan, you will get preventive services, like mammograms and colonoscopies, at no out-of-pocket costs.  Young adults can stay on their parents’ plan until they turn 26.  And it is illegal for insurance companies to place a lifetime limit on the dollar amount of care you can receive.

  • ‘Blue Button’ Provides Access to Downloadable Personal Health Data

    In August, President Obama announced the creation of a new “Blue Button”—a web-based feature through which patients may easily download their health information and share it with health care providers, caregivers, and others they trust. Since then, the Department of Veterans Affairs (VA) and the Centers for Medicare & Medicaid Services (CMS) in the Department of Health and Human Services (HHS) have beta-tested their respective systems—with great success.

    Today the Administration is announcing the formal launch of Blue Button for Veterans and Medicare beneficiaries, as well as announcing the winners of a groundbreaking challenge by two leading foundations for private-sector vendors to create applications that have the potential to provide secure, reliable, and portable personal health records while supporting the Administration’s goal of encouraging greater use of health information technology, including electronic health records.

    Veterans who log onto My HealtheVet at www.myhealth.va.gov and click the Blue Button can save or print information from their own health records. Using a similar Blue Button, Medicare beneficiaries who are registered users of www.mymedicare.gov   can log onto a secure site where they can save or print their Medicare claims and self-entered personal information. Data from of each site can be used to create portable medical histories that will facilitate dialog with Veterans’ and beneficiaries’ health care providers, caregivers, and other trusted individuals or entities.

    This new option will help Veterans and Medicare beneficiaries save their information on individual computers and portable storage devices or print that information in hard copy. Having ready access to personal health information from Medicare claims can help beneficiaries understand their medical history and partner more effectively with providers. With the advent of the Blue Button feature, Medicare beneficiaries will be able to view their claims and self-entered information—and be able to export that data onto their own computer. The information is downloaded as an “ASCII text file,” the easiest and simplest electronic text format. This file is also easy to read by the individual; it looks like an organized report.

    The My HealtheVet personal health record includes self-entered health metrics (including blood pressure, weight, and heart rate), emergency contact information, test results, family health history, military health history, and other health-related information. The ASCII text file that Veterans can download will include this information. As additional personal health information becomes available to VA patients through the My HealtheVet personal health record, this will also be added to the VA Blue Button download. The VA’s Blue Button system has generated an overwhelmingly positive response since its soft launch this summer; more than 60,000 Veterans have already used it to access their records.

    Registered users of MyMedicare.gov have long been able to view their Medicare claims information, and they have been able to add their personal and health information such as emergency contact information, names of pharmacies and providers, self-reported allergies, medical conditions, and prescription drugs. Now, with the Blue Button, CMS is making it convenient and safe for them to download and share this information in an easy-to-read and portable format. The CMS Blue Button has generated a positive response since its soft launch as well; more than 5,600 beneficiaries have already used it to download their data.

    An open-government initiative, Blue Button results from a collaboration between VA and HHS to develop an online feature that would enable Veterans and Medicare beneficiaries to easily read, use, and share their personal health information with providers and others they trust. The ASCII text file format was selected for its ease of use by individuals, while allowing computers to easily “read” the information.

    In developing this opportunity, VA and CMS both stress the importance to users of protecting the electronic information on their personal computers with appropriate security measures. Once individuals download their data, they will need to ensure its safety—for example, by encryption or password protection.

    As of today, Blue Button will be accessible to all My HealtheVet accounts—about one million Veterans in all—as well as 47 million Medicare enrollees. The VA and Medicare systems protect patient privacy by allowing access only to authenticated users. Also, reflecting the Obama Administration’s emphasis on fostering new innovation ecosystems, Blue Button is designed to encourage and accommodate improvements by third-party application developers.

    In fact, to make this information even more useful, the Markle and Robert Wood Johnson Foundations recently challenged developers to create applications that expand on the Blue Button’s promise by helping consumers use their data to stay healthy and manage their care. Eighteen companies competed for the $2,500 prize and the opportunity to have coffee with Clay Shirky, author of Here Comes Everybody and Cognitive Surplus. Submissions were judged on their usefulness, potential impact on health, ease of use, and accessibly from a variety of computing platforms.

    Today we are pleased to announce the winner of this challenge: Adobe’s Blue Button Health Assistant. This new “app” provides a comfortable and familiar user layout and eases the linkage of consumer information—including immunizations, allergies, medications, family health history, lab test results, and military service histories—among patients, providers, and caregivers using My HealtheVet, or claims data for those using the CMS Button.

    Soon, Blue Button users may be able to augment the downloaded information that is housed on their computers—or that they transferred to a commercial personal health record or other health application—through automated connections to, and downloads from, major pharmacies including Walgreens and CVS; lab systems such as Quest and LabCorp; and an increasing number of inpatient and outpatient electronic medical records systems.

    Adobe’s achievement, along with the recently announced Blue Button capability for Microsoft’s HeathVault, demonstrates the innovative power that advanced information technology can bring to healthcare. The Blue Button challenge has empowered tens of thousands of Americans and seeded a growth industry that should help lower healthcare costs and improve quality.

    Aneesh Chopra is the U.S. Chief Technology Officer and Associate Director for Technology in the White House Office of Science and Technology Policy

    Todd Park is Chief Technology Officer at the Department of Health and Human Services

    Peter L. Levin is Senior Advisor to the Secretary & Chief Technology Officer at the Department of Veterans Affairs

  • ONAP Commissions Institute of Medicine to Examine Data Gaps in Monitoring Access and Quality of HIV Care

    This time last year, the Office of National AIDS Policy (ONAP) announced a contract with the Institute of Medicine (IOM) to conduct a series of policy analyses to help inform the National HIV/AIDS Strategy.  The first of three reports from this project was released two weeks ago and presents important information for policymakers and members of the public working to expand HIV testing and screening in order to identify and link to care all people living with HIV (http://www.iom.edu/Reports/2010/HIV-Screening-and-Access-to-Care-Exploring-Barriers-and-Facilitators-to-Expanded-HIV-Testing.aspx ).  The second report on policy issues surrounding access to care is forthcoming, while the workshop for the final policy analysis on increasing the HIV provider workforce took place last week (http://www.iom.edu/Activities/PublicHealth/HIVScreeningCare/2010-SEP-29.aspx ).  Each of these analyses will provide critical information that will help support the implementation efforts for the strategy.

    ONAP has recently partnered with the IOM on a new initiative. The implementation of the Affordable Care Act (ACA) and the development of the National HIV/AIDS Strategy create a unique opportunity to dramatically improve access to insurance coverage and the quality of care and clinical outcomes achieved by people living with HIV.  Various entities (Federal, state, local, private) collect data on people living with HIV related to financial status, demographics, insurance coverage, and use of health services, but these activities are not well coordinated.  As a consequence, there are gaps in our understanding of successful approaches and also barriers to ensuring that all people living with HIV receive the highest quality care.  As we work toward full implementation of the ACA in 2014, it will be useful to establish baseline measures and consider monitoring strategies to ensure that people living with HIV are receiving high quality, clinically necessary services designed to achieve optimal clinical outcomes. 

    Over the next two years, IOM will convene a Study Committee to consider questions such as:

    • What are the best sources of data (and which core data elements should be standardized) across public and private HIV care databases that track continuous care (and related services such as housing) for people living with HIV?
    • How do claims data and clinical data found in medical records differ?  Do these differences encompass gaps in measures for HIV care? 
    • How can Federal agencies efficiently analyze data that are already being collected in order to improve HIV care quality?
    • What models or best practices in data system integration can be gleaned from Federal agencies or private industry to make existing data systems and core indicators interoperable?

    The Committee will provide recommendations based upon these questions via a published report toward the end of calendar year 2011.

    Another important and related activity that we are asking IOM to tackle is to investigate and provide suggestions on how to obtain meaningful national level estimates of access to care and services utilization by people living with HIV.  The Committee will examine issues such as:

    • How do we obtain national estimates that characterize the health status of people living HIV in public and private settings?
    • How can we obtain data from a nationally representative sample of HIV-positive individuals in the United States to establish a baseline for health insurance coverage and health care access status from which to measure improvements?  If this is not readily feasible, are there other alternatives to a nationally representative sample that can provide useful data for informing national policies?

    IOM will prepare a second report that will be released near the end of the second year of the project that provides recommendations of how to best obtain these national data. 

    We believe that this new project will significantly support our collective efforts to implement and effectively measure our progress toward achieving the established metrics in the National HIV/AIDS Strategy and will support broader efforts to integrate people living with HIV in the implementation of the ACA.

    Jeffrey S. Crowley is the Director of the Office of National AIDS Policy
    Gregorio Millett is the Senior Policy Advisor in the Office of National AIDS Policy