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

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Donald L., Palm Coast, FL

Health Care Blog

  • The Facts: The Affordable Care Act, the Constitution and the Courts

    Tomorrow, judges of the United States Court of Appeals for the 11th Circuit will hear arguments in a case challenging the constitutionality of the Affordable Care Act. Four weeks ago, judges in the 4th Circuit heard arguments in two similar cases. Last week, an additional case was argued in the 6th Circuit.

    In all of these cases, the plaintiffs may be different, but the arguments they bring to the courthouse are essentially the same. The challenges focus primarily on one provision of the law - people on both sides of the debate agree that the vast majority of the act is clearly constitutional.  And the arguments for overturning the Affordable Care Act are simply without merit.

    Opponents of reform claim that the law’s individual responsibility provision exceeds Congress’ power to regulate interstate commerce because it penalizes “inactivity.” They are wrong. Individuals who choose to go without health insurance are actively making an economic decision that affects all of us. When people without insurance obtain health care they cannot pay for, those with insurance and taxpayers are often left to pick up the tab.

    That’s why the Affordable Care Act requires everyone who can afford it to carry some form of health insurance. 83 percent of Americans already have insurance and only those who are able to afford health insurance will be responsible for obtaining it. And the Congressional Budget Office estimated that only 1 percent of all Americans would pay a penalty for not having health insurance in 2016.

    The individual responsibility provision also enables us to finally ban discrimination against individuals with pre-existing conditions. Without the individual responsibility provision, people could wait until they’re sick or injured to apply for coverage since insurance companies could no longer say no or charge more.  That would lead to double digit premiums increases – up to 20% – for everyone in the individual insurance market.

    We know that there will be a number of arguments and decisions in courts across the country in the weeks and months ahead and when the legal process ends, we are confident that the Affordable Care Act will be found constitutional.  

    Stephanie Cutter is Assistant to the President and Deputy Senior Advisor.

  • Continuing Steps to Implement the National HIV/AIDS Strategy as the Pandemic Turns 30

    As we reflect on the thirtieth year of the HIV pandemic, our work continues.  I wanted to share with you two developments at the White House as we mark this somber, but important milestone.

    HHS Announces New Steps to Implement the National HIV/AIDS Strategy

    Yesterday, I participated in a call with Health and Human Services Secretary Kathleen Sebelius and key leaders in her Department who announced new actions to support the implementation of the National HIV/AIDS Strategy.

    Mary Wakefield, PhD, RN, Administrator of the Health Resources and Services Administration (HRSA)discussed the Administration’s continued commitment to supporting States in responding to the challenge of state waiting lists in the AIDS Drug Assistance Program (ADAP).  Funding for ADAP has enjoyed broad bipartisan support.  Even in a tough budget climate and at a time when other critical health programs received cuts, the Administration fought for and achieved a $50 million increase in funding for ADAP in FY 2011 compared to the enacted level for FY 2010.  This year, the Federal government alone will invest $885 million in the ADAP program.  Administrator Wakefield announced that the increased funding will allow a temporary program established last summer with $25 million in emergency funds to continue and HRSA will allocate the remaining increase through both the ADAP formula program and through a targeted, competitive grant process to assist States with waiting lists or other cost containment measures that could impede access to critical medications.  While there are challenges in ensuring that individuals have access to life saving medications, HRSA is working closely with states and encouraging pharmaceutical companies to help bridge the gap in this program until state economic conditions improve and the Affordable Care Act alleviates some of the pressure on this program. 

    Ms. Cindy Mann, Deputy Administrator of the Centers for Medicare and Medicaid Services (CMS) and Director of the Center for Medicaid, CHIP, and Survey and Certificationdiscussed a State Medicaid Director (SMD) letter, issued yesterday, that informs States of various opportunities in Medicaid to improve care coordination and care delivery for people living with HIV, as well as opportunities to use Section 1115 HIV demonstration waivers to expand access to Medicaid for people living with HIV.  To facilitate States considering a Section 1115 demonstration waiver, CMS also issued a template and stated that they will work with States to develop streamlined and flexible approaches to meeting legal and policy requirements for these waivers.  The commitment to issue this waiver guidance was made in the Federal Implementation Plan for the National HIV/AIDS Strategy and in some states, could provide a mechanism for relieving pressure on ADAP while also providing more coordinated and high-quality care. 

    A blog post by CMS Administrator Don Berwick can be found HERE. The SMD issued by CMS can be found HERE.

    Dr. Tom Frieden, Director of the Centers for Disease Control and Prevention (CDC)described CDC’s vision for high-impact HIV prevention.  He announced that even in a very difficult budget environment, CDC was increasing its investment in HIV prevention services by $31 million in FY 2011.  He also described some of the targeted new prevention investments CDC is making as it realigns its entire HIV prevention portfolio to have a bigger impact.  He spoke of the need, articulated in the National HIV/AIDS Strategy, to focus on the geographic, demographic, and programmatic characteristics of the HIV epidemic.  In particular, he highlighted the need to better address gay and bisexual men of all races and ethnicities (but especially gay and bisexual men of color), because they reflect the majority of new infections and the only group in the US where infection rates are rising.  He discussed the Enhanced Comprehensive HIV Prevention Planning (ECHPP) initiative in the twelve cities and surrounding metropolitan areas that account for nearly half (44%) of the HIV cases in the United States.  He described this as a platform for making improvements in planning that will be applied across CDC’s HIV prevention programs.  He discussed CDC’s investments in helping state and local jurisdictions track and report CD4 and viral load measurements in order to track community viral load.  Research studies have demonstrated that when a community is able to lower the mean viral load across all people living with HIV in that community that this leads to a lowering in HIV incidence.  Therefore, tracking community viral load is an important tool for reducing the number of new infections.  CDC is doing important work to support states and localities in building their capacity to track community viral load. 

    Each of these agencies announced significant new initiatives yesterday that move us forward in implementing the National HIV/AIDS Strategy.  Their impact, however, is greatest when viewed together.   We have a stronger evidence base than ever before and a clearer vision of how to support individuals and communities in lowering their risk of becoming infected with HIV, helping individuals living with HIV to learn their status, and how to bolster the programs that support individuals with HIV in accessing the care and services they need (including access to antiretroviral therapy).  Our work continues, but we are making definite forward progress.

    Champions of Change

    Champions of Change is a weekly White House  initiative to highlight Americans who are making an impact in their communities and helping our country rise to meet the many challenges of the 21st century.  Last week, we invited a diverse group of people living with HIV to join me; Health and Human Services Assistant Secretary for Health, Dr. Howard Koh; Brian Bond, Deputy Director of Public Engagement and former ONAP staffer and Senior Scientist at CDC, Greg Millett - both people living with HIV; as well as Allison Nichol and David Knight of the Civil Rights Division at the Department of Justice and David Vos, Director of the Office of HIV/AIDS Housing at the Department of Housing and Urban Development for a round table to discuss their experiences as people living with HIV. 

    For more than two years we’ve been working in close partnership with many members of the HIV community and as we enter our fourth decade fighting HIV/AIDS, we believed it was important to again hear from the collective wisdom of people living with HIV in order to assess our progress and make plans for concerted efforts going forward.  Everyone has something to contribute toward ending this pandemic. That’s why we have been working with people living with HIV every step of the way.  We felt it was important to meet with HIV positive leaders and hear about the lived experiences of people who may be still facing stigma in their own communities.  Many who may still struggle to gain access to services, yet who are working everyday to support their communities as they respond to HIV.  The discussion was very powerful and it generated a lot of good ideas.  

    Check out this introductory post from Brian Bond HERE and learn about these incredible individuals HERE.  And check back, as this page will be updated throughout the week with posts by each of these individuals.

    Jeffrey S. Crowley is the Director of the Office of National AIDS Policy

     

  • Promoting the Dialogue on HIV/AIDS

    I am grateful to be here today with a wonderful group of committed individuals from across the country who have been so graciously asked to come to Washington, DC to talk to White House and federal officials about the 30th anniversary of the HIV/AIDS epidemic. Many people have begun to reflect on this somber anniversary. Many individuals who were living during the early years remember the period of losing many friends, family members and lovers who were dying of a relatively unknown disease within the gay community. I have also listened to these stories and I’m touched by personal loss and grief.  I could never imagine losing so many loved ones so quickly. As one friend told me, “I was going to a funeral about once a week. And after a while, you become emotionally exhausted and numb.” This is a tragic moment in our nation’s history that we should never forget.

    As a gay Latino man who is living with HIV/AIDS and who was diagnosed 4 years ago, I grew up in a world where HIV/AIDS has always existed. My generation grew up with discussions about the importance of using a condom. Such information became commonplace in sexual educational courses at school, but more importantly amongst friends and family about using protection. This became part of our lives, about being “safe and protected.” Growing up as a teenager in the 1990s in New York City, I recall going to the Gay Center in the West Village trying to understand and connect with people in the LGBT community. One of the things I vividly remember were the health-related/HIV prevention posters plastered around the walls of the Center. Specifically, these were posters of good-looking gay men posing in a photograph sometimes holding a condom or in a group setting with similar looking individuals. Often, the text would state “use protection,” “be safe,” “it’s better to know.” And for a while, these messages resonated or encouraged dialogue within the community. Perhaps with the discovery of Highly Active Antiretroviral Therapy (HAART) in the 1990s, our collective struggle to overcome HIV/AIDS shifted.

  • Champions of Change: HIV/AIDS – 30 Years of Activism on the Frontlines

    Ed. Note: Champions of Change is a weekly initiative to highlight Americans who are making an impact in their communities and helping our country rise to meet the many challenges of the 21st century.

    This month marks the 30th year of the HIV/AIDS pandemic, when the Center for Disease Control and Prevention reported the first case of which would become known as HIV/AIDS. More than 50,000 people in the United States are infected with HIV annually, and today, more than 33 million people around the world are living with HIV. Two million people across the globe die every year from AIDS. Over 600,000, fathers, mothers, daughters, sons, aunts and uncles in this country have died due to this pandemic. Like others marking this milestone, some of the people who have been lost over the past 30 years are individuals that I had the privilege of calling my friends.

    There have been many positive efforts in combating this devastating disease, but more work needs to be done. Last year, the President announced the first comprehensive National HIV/AIDS Strategy for the United States. This strategy focuses on combinations of evidence-based approaches to decrease new HIV infections in high risk communities, improve care for people living with HIV/AIDS, and reduce health disparities. Also, the Administration increased domestic HIV/AIDS funding to support the Ryan White HIV/AIDS Program and HIV prevention, and to invest in HIV/AIDS-related research.  

    But as the President has said, “government cannot take on this disease alone.” That is why, as part of the Champions of Change initiative, the White House invited nine inspiring HIV/AIDS advocates for a roundtable discussion to meet with Administration officials including Office of National AIDS Policy (ONAP) Director Jeffrey Crowley, the HHS Assistant Secretary for Health, Dr. Howard Koh, and key staff from HHS, DOJ and HUD. The roundtable was intended to provide an opportunity for people living with HIV to reflect on their own lives and personal experiences as the Nation reflects on what has been achieved over the last three decades. It is also an opportunity for us to continue shining a light on this pandemic.

  • U.S. Surgeon General Regina Benjamin Will Headline White House Faith-Based Conference in New Orleans

    The White House and the U.S. Department of Health and Human Services' Offices of Faith-Based and Neighborhood Partnerships will host a “Connecting Communities for the Common Good” event in New Orleans, LA on Monday, June 6.  Faith and community leaders from across the Gulf Coast region will join Gulf Coast native Dr. Regina M. Benjamin, U.S. Surgeon General and Joshua DuBois, Executive Director of the White House Office of Faith-based and Neighborhood Partnerships, for a conversation on how government can partner with nonprofit organizations to provide adequate health care services, prevent youth violence and promote healthy communities.

    What:  
    Obama Administration Community Event: “Connecting Communities for the Common Good”

    Event Featuring:   
    Dr. Regina M. Benjamin, Surgeon General of the United States Public Health ServiceJoshua DuBois, Special Assistant to the President and Executive Director of the White House Office of Faith-based and Neighborhood Partnerships

    When:
    Monday, June 6, 2011
    8:30 a.m. to 12:30 p.m.

    Where:
    Ernest N. Morial Convention Center, New Orleans (MCCNO)
    Hall B Entrance, Rooms 353-355
    900 Convention Center Blvd.
    New Orleans, LA 70130-2226

  • Engaging Immigrant Health Professionals

    Download Video: mp4 (9MB) | mp3 (1MB)

    As an immigrant, I was thrilled to receive the Champions of Change award last week. Along with the honor came the opportunity to join other honorees in a substantial conversation with several Administration officials, where we talked about successful immigrant integration strategies and the role the Administration can play in supporting these on-going, community based efforts.

    My area of interest and expertise is the cultural and linguistic diversification of the U.S. health workforce as a means of reducing racial and ethnic disparities in health. To that end, I started ten years ago the Welcome Back Initiative, a program designed to identify, guide, and support immigrant health professionals in their quest for relicensure or recertification in the U.S.