Archive for the ‘national health reform’ Category

Insurance-palooza – the NAIC National Meeting in Seattle

Monday, August 23rd, 2010

The Summer 2010 Meeting of the National Association of Insurance Commissioners (NAIC) in Seattle Washington wrapped up last week. For those of us not lucky enough to spend a long summer weekend with a group of insurance commissioners, some friends of Community Catalyst provided the inside scoop on the meeting.

Victory on Medical Loss Ratios. The Executive Committee of the NAIC approved the medical loss ratio recommendation made by the subcommittee on this issue. In spite of receiving a lot of pressure from insurers, brokers and other industries, the Commissioners stayed the course and remained respectful of NAIC process by voting yes on the recommendation, with very few changes.  Thanks to the consumer representatives on the NAIC, who have worked for months to ensure the MLR definition is based on actual medical costs and evidence-based quality improvement efforts. And, thanks to advocates to who called their Insurance Commissioners about this issue. This is good news – and we expect HHS to accept the NAIC’s recommendation.  What this means for advocates: This is a procedural win that is gets us closer to a tool to fight unwarranted premium increases and get consumers better value for their insurance dollars. It also demonstrates that we need to monitor these decisions and make our voices heard as necessary to ensure consumers are protected.

Brokers feel the love. In a bizarre turn of events, the NAIC spent their summer weekend drafting an “ode to brokers.” The resolution, sponsored by a number of Insurance Commissioners, expressed support for the work that brokers do for the insurance market.  A clause in this resolution suggests that brokers should be favored as Navigators, the entities that will help to explain and enroll people in coverage and plans through the Exchange starting in 2014. This is inconsistent with the intent of the ACA, which clearly lists potential Navigators as “trade, industry, and professional associations, commercial fishing industry organizations, ranching and farming organizations, community and consumer-focused non-profit groups, chambers of commerce, unions, small business development centers, other licensed insurance agents and brokers, and other entities.” (Section 1311(i)). It is unclear what weight this NAIC resolution holds.  But one thing is certain: brokers were flexing their muscles in Seattle, and many Commissioners were impressed. What this means for advocates: We need to educate Insurance Commissioners and others in state government about the importance of community-based groups in providing public education, health plan information, and enrollment assistance, other critical roles of Navigators.

Everyone’s thinking about Exchanges. NAIC created a tentative workplan for the subgroup charged with working on Exchanges. They are dividing into 14 smaller workgroups (leads should be posted on the NAIC website soon).  But we hear that one of the subgroups will work on a “skeleton” model law for states, which will basically track the statutory requirements and no more. Other subgroups are likely to respond to HHS’s request for recommendations on (1) network adequacy, (2) marketing standards and (3) quality measures.  Another group will tackle “principles and priorities” on a number of other big exchange topics such as governance and operations. (TBD). Another high-level liaison group will work with state Medicaid heads on plans for collaboration. What this means for advocates: The NAIC may have helpful resources as states begin to design Exchanges.  More to come.

– Lastly, though not specific to NAIC, rate review grant announcements were also made last week. A number of Insurance Commissioners talked about using the funds to increase consumer involvement in the process and get more information out to public. What this means for advocates: If your state applied for and received a grant to increase rate review, now is the time to work with your Commissioner on a plan to increase consumer involvement in the premium oversight process.

– Christine Barber, Senior Policy Analyst

Senate proposal would gut funding to make Americans healthier and reduce health disparities

Thursday, August 19th, 2010

Update: Due to response to this blog post, we would like to share additional information with those who are interested in signing-on to the letter. If you would like to sign-on, please contact Trust for America’s Health by e-mailing rhamburg@TFAH.org.

A short-sighted proposal from U.S. Senator Mike Johanns, a Nebraska Republican, would gut the brand-new $15 billion Prevention and Public Health Fund, created as part of the health reform law, to pay for a change in business tax-reporting rules. The Prevention Fund was established to support national, state and local programs to make Americans healthier and reduce racial and ethnic health disparities. President Obama has already allocated $500 million from the fund.

Johanns’ amendment is slated for a vote on Sept. 14, the day after Congress returns from August recess, and has some strong business backing. Learn more about this strike at a key component of health reform on a 1 p.m. call tomorrow hosted by Community Catalyst and three partner organizations.

The Prevention Fund is key to our long-term health, to controlling soaring health costs, and to advancing health equity. Among the programs Johanns’ proposed amendment would wipe out are the innovative Community Transformation Grants. These grants are designed to help local communities address health disparities and reduce chronic diseases by promoting healthy living and tackling the social and economic causes of poor health. They are also the main avenue in the health reform law for addressing the root causes of health disparities, such as poor availability of healthy food and exposure to environmental hazards.

The Johanns amendment could also threaten initiatives to increase vaccination against disease, as well as millions of dollars a year in state grants to reduce obesity and tackle other public health problems. Congress envisioned all of these being supported by the Prevention Fund, which dedicates $15 billion over 10 years to beef up the tiny portion of health spending now devoted to preventing illness.

Johanns proposed the amendment to a bill (H.R. 5292, the Small Business Jobs and Credit Act) that would create a loan fund and tax breaks for small businesses.  His amendment would overturn a portion of the health reform law that requires business to provide more detailed reporting to the Internal Revenue Service about services and materials they buy. Small businesses, in particular, are concerned that the new reporting would be a burden, and passage of the amendment is a real possibility.

To offset the loss of tax revenue created by his proposal, Johanns would tap $11 billion from the Prevention Fund – all of the money allocated for the fund from 2010 through 2017. He would also weaken another critical component of health reform – the requirement that everyone who can afford health insurance must obtain it, or pay a penalty. Our partners at the Center on Budget and Policy Priorities have written a detailed analysis of the proposal.

Community Catalyst is signing onto a letter to Congress opposing the gutting of the Prevention Fund, and we urge other organizations to do the same. We also recommend contacting Senators directly to let them know that the Prevention Fund should not be up for grabs. Two small business organizations, Small Business Majority and Main Street Alliance, are also speaking out against the attack on the Prevention Fund, with Main Street saying it would “seriously undermine the improved access and cost containment goals of health reform.”

Ironically, Johanns’ attempt to wipe out the Prevention Fund comes just as Congress is considering separate measures to allocate hundreds of millions of dollars from the fund to the Community Transformation Grants for fiscal year 2011. Rules for the competitive grant program are still being developed, but the health reform law says the grants should go to state and local governments and community-based organizations for changes in policies, programs, environment and infrastructure including increasing access to nutritious foods, creating parks, and creating healthier school environments.

Senator Bill Nelson, a Florida Democrat, is offering an alternative that helps small businesses without harming the Prevention Fund. It scales back, rather than eliminates, the new tax reporting requirement, and funds the change by ending a tax break for the nation’s five large oil companies.  Nelson’s amendment is also slated for a vote on Sept. 14. Both this and Johanns’ amendment need 60 votes to pass, and the votes could be close.

It’s crucial to the success of health reform to beat back the Johanns amendment and send a message to others who would try to hijack the Prevention Fund for other purposes.

– Alice Dembner, policy manager

The Insider: The Cost of Compromise

Tuesday, August 10th, 2010

FMAP: Victory at a Price

SNAP Offset Graphic FinalThe Senate voted on Thursday to provide additional federal assistance to state Medicaid programs (and additional support for teachers to avoid layoffs) and the House followed suit today, but the price was high. After several attempts to pass an FMAP extension on an emergency basis (meaning no tax increase or spending cut to offset the new spending) were blocked by a united Republican Senate caucus, the leadership decided to pay for the financial assistance to states by rolling back a temporary increase in food stamps (SNAP). The SNAP increase, part of the American Reinvestment and Recovery Acct (ARRA), was originally projected to phase out in 2014, however, the slow growth in food prices would have extended the increase until 2018. The FMAP legislation means that the increase will indeed end in 2014, creating a cliff that at that time will cause a drop in SNAP benefits.

Senate leaders (supported by the administration) faced with the specter of failure on the fiscal relief legislation and the resulting layoffs of teachers and other state workers plus the scaling back of Medicaid benefits, decided that avoiding the harm now was the lesser of two evils. With luck there will be a chance to restore the SNAP benefit before the cut actually goes into effect in 2014.

The really sorry thing is what the FMAP/ SNAP trade says about the balance of power in the US Senate today. As much as we decry the use of SNAP as one of the funding sources, it is a sad fact that a more progressive source would have been unable to clear the Senate. Unfortunately, things are only likely to get worse in the short run. Republicans, aided by conservative Democrats, will continue to block important legislation (such as FMAP, or an extension of unemployment benefits or the energy bill) and then benefit from it electorally because the problem isn’t solved and people vent their bad mood on the party in power (see example here). With the electoral winds at their back – projections are for gains in the House, Senate and governorships – what’s the incentive for Republicans to change? The prototype for this behavior was health reform under Clinton which the Republicans were able to sabotage and then ride to victory in 1994. Running the same play in 2010 is likely to create new obstacles to ACA implementation in 2011. With a more closely divided Senate ahead, we can expect more replays of the FMAP dynamic until at least 2013.

What does the MO vote really mean? Not much, but VA decision more troubling

While ACA opponents are trumpeting the passage of Proposition C in Missouri, there really isn’t much ‘there’. The voter turnout was heavily weighted to GOP voters, making it more of a straw poll of Republican sentiment than a true test of public opinion. For example, in the Senate primary race 578,582 voted in the Republican primary while only 316,107 or 35 percent of the total voted in the Democratic primary – not too different from the 70-30 split on Prop C.

Further complicating the interpretation of Proposition C was the confusing wording of the multi-part question which addressed the mandate, the right to pay for health services and the ability to make changes to the rules for liquidating certain insurance companies. As a result, Proposition C is a much less accurate barometer of public opinion than the polling which is showing that public support for the ACA is growing (albeit slowly), opposition is declining and the “intensity gap is almost inside the margin of error.” However, the Missouri vote is likely to encourage continued ACA nullification efforts, which got something of a bigger boost from the Virginia court decision last week.

Essentially, the judge hearing the case ruled that, notwithstanding the supremacy clause of the Constitution, a state can pass a law that conflicts with federal statute and then sue to enforce it. To be sure, this is just a procedural decision and a number of legal experts believe the judge has erred and that the case will ultimately be resolved in favor of the ACA, but reading the judge’s reasoning can’t give supporters of the ACA great comfort; nor does the possibility of sending a case all the way to the current Supreme Court.

Be careful what you wish for

If ACA saboteurs really got their way, what would it mean?  Two new reports shed light on that question. A new analysis from economist Jonathan Gruber estimates that implementing the ACA without the Individual Mandate would increase premiums by 27 percent while Medicare Trustees say that total repeal would shift the Medicare trust fund into a deficit a dozen years earlier than current predictions (2017 vs. 2029). But then again, if your goal is to destroy Medicare and you don’t care about expanding coverage, maybe that doesn’t matter.

Is Howard Dean right about the Individual Mandate?

Criticism of the Individual Mandate does not only come from the right. Howard Dean recently was quoted as saying not only that the mandate would be repealed but that it wasn’t necessary. As evidence he cites his own state’s experience with providing near-universal coverage to children without a mandate. Actually Vermont, while offering good coverage for kids, is not unique. The state ranks 14 in the country with respect to the rate of children’s coverage according to Kaiser State Health facts, but even the state that ranks best – Massachusetts – lacks a mandate on kids coverage. The Massachusetts mandate applies only to adults. Does this prove Dean right? Not really.

Hypothetically a similar coverage result could be achieved without the Individual Mandate if Congress could be persuaded to make insurance subsidies sufficiently robust and accept a large migration of moderate-income workers from private to public coverage. However, the outcome of the Congressional debate over the ACA, when there were 60 Democratic Senators and a large majority in the House does not auger well for a large increase in publicly financed health insurance subsidies in the near future. Gruber’s analysis shows that only about 7 million people would gain coverage at current ACA subsidy rates without the Individual Mandate, as opposed to 32 million with the mandate.

The other alternative to the Individual Mandate often mentioned – late enrollment penalties – could work from the insurance industry’s point of view. Late enrollment penalties would protect against adverse selection by charging higher premiums to people who did not obtain coverage when it was available. It’s the method used to guard against adverse selection in Medicare Part D, but it is more likely to create insurmountable barriers to coverage for low-wage workers than it is to produce something approaching universal coverage.

– Michael Miller, policy director

Three Cheers for Dependent Coverage Expansion!

Wednesday, August 4th, 2010

While there are many provisions in the Affordable Care Act (ACA) that will benefit children and families, the expansion of dependent coverage to children up to age 26 is among the most important – especially in the short-term. In 2011 alone, as many as 1.64 million previously uninsured young adults are estimated to gain coverage under their parents’ health plans. The provision takes effect after September 23, 2010.

Recently, the federal government issued regulations further explaining how this provision will work. Here at the New England Alliance for Children’s Health, an initiative of Community Catalyst, we support these regulations because they clarify several important points that will benefit young adults and apply the law with their interests at heart:

-Young adults are eligible for coverage under their parents’ plan regardless of what state they live in and whether they are tax dependent, financially independent, or a student, employed, or married.
-Premiums or benefits cannot vary based on the age of a young adult who qualifies as a dependent.
-The provision applies to all health plans and only grandfathered health plans (those in existence prior to March 23, 2010) can exclude young adults with access to an employer-sponsored plan until 2014. After 2014, this exception no longer applies.
-Insurance companies must provide prominent notice to enrollees about the special enrollment period for dependents.
-States have the option to extend dependent coverage beyond age 26.

All of these clarifications and others included in the regulations will ensure that dependent children and their families can take full advantage of this important opportunity to secure the health coverage they need.

While we are enthusiastic about the regulations, we’ve also been working collaboratively with a group of our partners to offer some suggestions to the federal government on how to improve them in a few key areas:

-Clarify that stepchildren and adopted children are included in the definition of a dependent child.
-Further explain the situations where grandfathered plans can remove young adults who are eligible for employer-sponsored insurance to ensure that this does not unduly burden young adults.
-Require that prominent notice be clear and conspicuous—ideally in the form of a stand-alone document highlighting the availability of the new coverage option and how to enroll.

It’s our hope that the regulations will be revised soon to reflect these suggestions, but in the meantime you can find out more about the dependent coverage expansion here. This provision is one of the many examples of the very real opportunities that ACA provides to extend coverage to those who otherwise would go without.

– Patrick Tigue, Children’s Health Care Coordinator, New England Alliance for Children’s Health

Cross Post: Consumer Assistance: A Guided Tour to Your New Health Care Choices

Thursday, July 29th, 2010

Everyone has heard about some aspect of the Affordable Care Act (ACA), however many people are still confused about the new law. At Community Catalyst, we think Consumer Assistance Programs (CAPs) are vital to ensuring people understand what the changing health care system means for them, and will help people get clear, accurate information about their health care. The ACA set aside $30 million in 2010 to provide grants for state CAPs and ombudsman programs, and last week the Department of Health and Human Services Office of Consumer Information and Insurance Oversight (OCIIO) released the grant guidelines. Today on Say Ahhh! A Children’s Health Policy Blog, one of our senior policy analysts, Christine Barber, explains some of the provisions of the guidelines:

-The grant criteria take steps to ensure that the selected programs are independent. In particular, we are happy to see that the guidelines clearly welcome states to contract with non-profit organizations to provide consumer assistance.

-CAPs must assist people with all types of coverage and provide assistance that is culturally appropriate. In addition, programs must collect data about any problems and questions, which we hope will provide real-time, on-the-ground information about what’s working and what’s not. Regular feedback to state and local policymakers can help improve health reform implementation.

-Each state is eligible for one grant award. Therefore, it is important that states know about this grant program, so consumers can get help, no matter their zip code.

We applaud the guidelines, and have created a summary with the Community Service Society to further explain the grant criteria. Check out the rest of Barber’s post here, or read the full grant guidelines. Applications are due September 10.

– Christine Lindberg, Communications Associate

Are we speaking the same language? The problem with medical jargon

Wednesday, July 28th, 2010

Today, many families are struggling not only with the cost of and access to health care, but also with the quality of care they receive. A recent article in the Wall Street Journal, “Taking Medical Jargon Out of Doctor Visits”, articulates an incredibly important issue that sometimes gets swept under the rug in the talk about cost and quality of care: patient health literacy.

According to the Centers for Disease Control and Prevention, about nine out of 10 adults find it hard to follow routine medical advice, mostly because they don’t understand what their care providers are saying. The complex instructions and jargon that doctors use make patients more likely to skip necessary medical tests or not take their medication as prescribed. This confusion leads to poorer health outcomes and increased health care costs currently estimated at $238 billion a year.

There is a common assumption that lack of health literacy is limited to racial and ethnic minority populations. While these populations are disproportionately affected by low health literacy, according to a report from the National Patient Safety Foundation, Low Health Literacy: Implications for National Health Policy, the majority of people with low health literacy skills are white. Older people, recent immigrants and those with chronic conditions are likely to have low health literacy, as well.

Of particular note from the WSJ article is the federal strategy around health literacy entitled the National Action Plan to Improve Health Literacy. The plan seeks to engage organizations, professionals, policymakers, communities, individuals, and families in a linked, multi-sector effort to improve health literacy

We are headed in the right direction. However, there is still a fundamental need for greater change in the health care system – particularly in the areas of how care is delivered and paid for – if we are truly to achieve better access to quality, affordable care.

As our population grows older and larger, the impact on the health outcomes of patients and the costs to the health care system will only increase. These problems are compounded by the lack of care coordination for those with multiple chronic illnesses. People with multiple chronic diseases have increased interaction with the health care system, leading to more opportunities for confusion surrounding their medical care – which is in turn influenced by the number of doctors they see and what they hear from their doctors.

An older person with five or more chronic conditions (e.g. diabetes, hypertension, heart disease, arthritis, obesity), has an average of 37 doctor visits, 14 different doctors, and 50 separate prescriptions each year. How incredibly confusing would it be for that person to manage his or her own health? Older adults and their caregivers should be full partners in their care, and they should be provided with the information and support to manage their conditions so they can make informed health care decisions.

With the advent of the Patient Protection and Affordable Care Act (PPACA), the Campaign for Better Care, led by the National Partnership for Women and Families, Community Catalyst and the National Health Law Program, is working to ensure the needs of older adults and their families are highlighted and addressed.

Helping patients and providers communicate effectively with each other will be a crucial component to the quality of care that patients receive. The Campaign’s national consumer coalition has developed a “Yardstick” for Better Care, which identifies key elements of patient-centered practice for inclusion in new models of care

The Campaign for Better Care hosted a public event today in Washington, D.C. – the “Building Better Care” forum – and the forum webcast will be available online Friday. Special guests included Senator Sheldon Whitehouse, award-winning author Gail Sheehy, UCLA Geriatrics Division Chief David Reuben, journalist and activist Jonathan Rauch, HHS Director of Delivery System Reform Peter Lee, and more.

To learn more about these issues and how the Campaign is tackling them please visit www.campaingforbettercare.org.

– Jenelle Holder Williams, Field Director, Integrated Care Advocacy Project

Cross Post: A deeper look at health reform’s individual responsibility requirement

Thursday, July 15th, 2010

Community Catalyst recently worked with our partner, Georgetown University’s Center for Children and Families, to create a document answering prevalent questions about how the new mandate for insurance coverage will affect families. Here’s an excerpt from the Center for Children and Families’ blog post on the resource:

“With all of the controversy and rhetoric surrounding the requirement, it seemed a good time to take an objective, detailed look at how it will actually work.

“Plus, even though it doesn’t go into effect until 2014, we wanted to write about the individual responsibility requirement because it is the foundation on which much of health reform rests.  It allows the country to move forward with popular insurance reforms, such as the ban on excluding people from coverage if they are sick, and plays a major role in expanding coverage.”

Read the rest of the post that cites some of the themes that arose while working on the Q&A at “Say Ahhh! A Children’s Health Policy Blog,” or read the resource on our website.

– Katherine Howitt, policy analyst

Consumer Assistance: What makes health reform go

Monday, July 12th, 2010

It’s no secret that the passage of the Affordable Care Act means lots of new opportunities for health care coverage and access – and that most Americans are confused about what the law actually means for them.  Here at Community Catalyst, we have seen health reform as an opportunity to improve consumers’ ability to get clear information in lay terms from trusted sources to help them understand their health care options.  And consumer assistance programs (CAPs) are a critical way to make this happen.

The Affordable Care Act included $30 million in 2010 to fund state ombudsman offices and CAPs (Section 1002).  The grant guidelines for those funds are slated to come out in the next few weeks, and the grants will likely go to states, who will decide how to best use the funds.

While we’re not quite sure how the guidelines will read or play out in implementation, we have  some core criteria we think are necessary to providing consumers accurate, understandable information and helping them navigate the new world of health care.

1.     Be truly independent.  Consumers should be able to trust that the information and enrollment assistance they get is unbiased – not informed by state budget problems or politics.  Especially as 20 states’ attorneys general actively oppose health reform, consumer assistance programs should ensure there’s a wall between state and political issues and helping consumers.
2.    States need to do more than they already do.  Many states are currently overwhelmed and understaffed because of budget woes.  Consumer assistance programs need to be separate and robust from current activities in state Administrations – and actually have the capacity to provide necessary help, navigation and information.
3.    Meet the needs of the community.  Consumer assistance needs to be culturally and linguistically competent, and provided by people who understand working with vulnerable populations.  A well-trained staff should be trusted by members of the community, including people at different levels of income and insurance options (from Medicaid to private insurance).
4.    Allow for feedback to policymakers.  A critical reason for consumer assistance is the ability to get real-time, on-the-ground information about what’s working and what’s not.  Regular feedback to state and local policymakers can help improve health reform implementation
5.    Ensure every state has a consumer assistance program.  Even if a state does not set up a program, the federal government should be able to contract directly with an organization to carry out these important duties.

Based on these elements, we think that the best option for CAPs in most states is often non-profit community advocacy organizations.  Examples like Health Care for All Massachusetts’s Helpline, New York’s Community Health Advocates, and Health Assist Tennessee have shown us that strong consumer assistance programs can mean the difference between a failed attempt and successful reforms. The Helpline in Massachusetts saw their call volume increase from 500 to 4000 per month after the passage of that state’s health reforms in 2006.  People call with questions from enrollment assistance to help with paperwork to navigating the health system.
We hope that the grant guidelines will explicitly permit states to contract or partner with community organizations to provide consumer assistance.  We have seen these models work, and know that they are trusted sources of health care information for communities and families looking for help in understanding a system that’s about to get bigger and more complex.

– Christine Barber, senior policy analyst

Websites like wine: healthcare.gov good now, getting better

Friday, July 2nd, 2010

HealthCare.gov: Take health care into your own hands  Learn MoreThe web portal Healthcare.gov (@healthcaregov for all you twitterheads out there) went live, launching ahead of its July 1 deadline by hours Wednesday night. HHS deserves props for this site: not only was it delivered ahead of schedule, but it’s spiffy-looking, easy to use, and full of important info to help people get covered.

The website is what it says – a door through which consumers can check out what private insurance plans are available to them, depending on their age, state, current coverage, and health conditions.  There’s also information about public programs, like Medicaid, and how reforms in the new law affect people soon – such as the small business tax credit, high-risk pools for people with pre-existing conditions, and the ability of young people to join or stay on their parents’ plan till age 26.

If you haven’t checked it out yet, you should. We did a walk-through ourselves yesterday and were impressed by the clear, appealing design, the plain-language navigation to help consumers find out what their options are and, oh yeah, all that information.

In October, a more in-depth version will launch, and will include rates, coverage exclusions and other pricing information—a level of detail we think is critical for consumers looking for insurance options. To our mind, the more information, the better. And we’d like to see the portal move toward standard benefit descriptions that help people make “apples-to-apples” comparisons.

Other things we’d like to see on Healthcare.gov?  We think the website should include all private insurance products, such Medicare Advantage and Medigap plans. Right now, it doesn’t.

And it would be great instead of just describing and giving contact info or redirects to public programs, like state Medicaid agencies, if someone visiting the website could determine whether they were eligible and if so, enroll online.  Downloading an application, printing it out, finding out where to submit it, and getting there is often too many steps in a process that could be moved online. A report by the Urban Institute in January showed that there are 9.8 million uninsured individuals who are eligible for but not enrolled in Medicaid, and a one-stop online enrollment platform on the portal makes a lot of sense to help those people get health care coverage.

We’re glad to see that patient protections in the new law – what the administration’s calling the “patient bill of rights” – are prominent and spelled out clearly on the site.  In the future, we’d like healthcare.gov to point to consumer assistance programs, too, especially non-profit ones, which have a great track record of helping people navigate the system, determine eligibility, and enroll.

And for consumers with medical bills, we also want to make sure that the portal makes hospital financial assistance policies available, prominent, and easily searchable on healthcare.gov. We’re encouraged that there seems to be placeholder language about free and reduced care where more specific policy information will go in the future

Certainly there is room to refine and build. But this is day two. And improvements are already underway. In fact, a banner stretched across the top of every page says “Health care is getting better. So is HealthCare.gov. Help us improve by adding your comments”—this thing is a work in progress. But it’s also a work of progress, one we’ve proudly bookmarked.

–Kate Petersen, Health Policy Hub

“Show me” gender equity!

Wednesday, June 30th, 2010

Missouri is trying to remain true to its slogan, the “Show Me State,” by helping lead the charge in anti-health reform legislation prohibiting abortion services for health insurance obtained through the exchange – (the term used for the health care insurance marketplace instituted by national health reform).  Yet it certainly leaves one wondering…show me what?

Now sitting on Governor’s desk is a bill that strips the state exchange of offering any kind of abortion coverage to consumers– even through an optional rider.  Similar to the flurry of anti-reform constitutional amendments being adopted across many states, this legislation is based on a model developed by the Americans United for Life (AUL), a non-profit law and policy group.  The model, entitled “The Federal Abortion-Mandate Opt-Out Act,” is in the pipeline in almost 30 states, according to AUL.  Thus far, Mississippi, Arizona, Tennessee and Louisiana have passed the prohibition measure – the measure was vetoed in Oklahoma and Florida.

Claiming to be founded upon a pro-family platform, AUL aspires to stall the progress of health care reform by barring consumers from some patient services.  Yet eliminating family planning services from exchanges does not promote a family friendly policy environment – but supporting gender equity does.  According to the National Law Center for Women, 17 percent of Missouri women forgo needed care due to their higher cost of health care – these include a broad range of services.  Women in Missouri are, on average, poorer than men and tend to work for small businesses that do not offer health coverage.  This is not only a strain on women and their health but also their families.

Advocates can challenge these flawed attempts to dismantle health reform and propose a broader pro-family agenda by driving home the message of gender equity.   A pro-family message is one that encompasses supporting all women at all times in their lives – daughters, sisters, wives, mothers, and grandmothers alike.  Other states have stepped up to rid their health care systems of inequitable gender rating that charge women as much as 4-48 percent more than men for the same health care policy.

However, these positive steps are not without their critics.  Before Colorado passed its ban on gender rating in the individual market this past spring (in the week following health reform passage), an insurance underwriter commented to the legislature that perhaps “we should ‘blame God’ because men’s parts were on the outside and women’s parts were on the inside.”  State Senator Morgan Carroll responded to his comment by suggesting “perhaps his brain is on the outside.”  Further, Rep. Jim Kerr suggested that women enjoyed shopping and perhaps they should do a better job shopping for health insurance.

The absurdity of the discussion makes you laugh and grimace simultaneously – but the issue remains in play in many states.  Women are often the center of their families, before and after they procreate – a real pro-family policy would be for all to acknowledge their right to a healthy and long life.  So, show me gender equity!

–Eva Marie Stahl, policy consultant