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Health Advisory Council Newsletter | 2018 Q3 | Member Q&A

Beth Battaglino, RN

CEO, HealthyWomen

Q. How would you describe your work at HealthyWomen and how it relates to HealthyWomen’s overarching mission?

A. As Chief Executive Officer for HealthyWomen, I am responsible for business development and strategic positioning for our organization. I pursue innovative partnerships with key health care professionals and consumer advocates to implement engaging and informative programs.

Our creative team and I work together to implement these programs to improve women’s health awareness. We continually examine how to grow and expand our programming to meet women’s needs and where and how women want to receive the information. We also understand that nothing is more important to women’s health than access to competent and affordable care, and we work to educate women about health policy issues.

Q. How long have you been at HealthyWomen, and what do you love most about your job?   

A. I’ve been with HealthyWomen in several positions for more than 25 years—long enough to witness so much important and exciting progress in women’s health care—and long enough to realize how much more there is to accomplish. One of the things I love most about my job is how different it is day-to-day. Creating new partnerships and engaging with long-standing partners provides fresh and creative insight about how best to communicate health information to women ages 35+—our core audience. And, of course, I love hearing directly from women about the health challenges they face and the information that matters most to them. Our audience has a huge influence on how we develop and launch program initiatives. We understand that when it comes to how we share information, it cannot be a one-size-fits-all approach. With the ever-changing communications touchpoints available to consumers, our objective is always to ensure the information and resources we create are delivered through a multi-platform approach so that we can reach women in the way they want to receive health and wellness information today. Our audience is why HealthyWomen exists, and we are committed to evolving to meet her needs.

Q. What are the biggest challenges and opportunities facing HealthyWomen today?

A. One of our biggest challenges is staying on top of technology advances and consumer preferences for online engagement. Technology changes on a dime, and we are constantly reviewing and tracking consumer preferences for receiving health information and evolving to deliver it efficiently, but there is always more to learn and new ways to reach women. Encouraging women to prioritize their health is another challenge – and an opportunity for HealthyWomen. We know from our HealthiHer Movement that women need encouragement to put their health at the top of their lists – and not after everyone else’s needs. Another opportunity for HealthyWomen is supporting women as they navigate today’s complex health care system. It’s funny…when I first started at HealthyWomen, I regularly answered a toll-free number for the organization, and I described my job to friends and family as holding someone’s hand and guiding her to the answers and resources she needs. We are still doing that 25 years later!

Q. What HealthyWomen initiatives would you like to share with the Council?

A. We recently released findings from our WomenTalk® 2018 survey that highlighted many insurance-related obstacles women encounter when they try to access quality, affordable health care. With open enrollment just around the corner, we will be alerting women to be sure they understand their health insurance options and choose health insurance that best meets their needs—for preventive health services as well as for chronic health care needs.

HealthyWomen is also collaborating with the Legal Action Center to provide legislators with resources on opioid use disorder to help them confront the many complex issues—many of which are unique to women’s health—presented by the opioid epidemic. Our new online tool kit, “Resources for Strengthening Families and Communities by Improving Access to Treatment for Substance-Use Disorder,” is one example of this effort. We are working with Women In Government to reach as many legislators as possible. Of course, HealthyWomen works daily to engage women on a broad range of health topics.

Q. What does HealthyWomen value about membership in NCL’s Health Advisory Council?

A. I value NCL’s commitment to make the marketplace safer and healthier for consumers and workers, and the support the Health Advisory Council provides to NCL for consumer education and advocacy. It is important to HealthyWomen to collaborate with our partners—in industry, nonprofit organizations, health professional groups and government agencies—with similar interests. Collaboration broadens our outreach and strengthens our impact. I particularly value NCL’s Health Advisory Council’s effort to engage diverse perspectives on the many issues facing organizations like HealthyWomen as we work together to help women be informed about their health. I look forward to working together with all of NCL’s Health Advisory Council membership to improve women’s health.

Latest Press Releases

NCL urges FDA and consumers to take action as GLP-1 shortage ends, but “infodemic” continues

May 21, 2025/in Featured Home - Food & Nutrition, Featured Home - Your Health, Press release Press Releases, Statements /by Lisa McDonald

May 21, 2025: Washington, DC — Despite the end of the GLP-1 shortage and May 22 FDA-issued deadline for companies to stop mass compounding of the products, the National Consumers League (NCL) is concerned that the epidemic of GLP-1 misinformation will continue to confuse consumers with fake products that can put their health at risk. Both the U.S. Food and Drug Administration (FDA) and consumers have roles to play in responding to the “infodemic.”

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DOT’s abandonment of Southwest litigation will leave passengers worse off 

May 19, 2025/in Featured Home - Consumer Protection, Press release Press Releases, Statements /by Lisa McDonald

May 19, 2025: Washington, DC — Last week, the U.S. Department of Transportation (DOT) quietly dropped its historic lawsuit against Southwest Airlines, which had originally been filed over the carrier’s unrealistic scheduling. The litigation would have been the first time an airline attempted to defend its chronic delays in court.   

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NCL Denounces Illegal Attempt to Fire CPSC Commissioners

May 9, 2025/in Featured Home - Consumer Protection, Press release Press Releases, Statements /by allisonc

May 9, 2025: Washington, DC – Washington, DC – The National Consumers League calls on the Trump administration to rescind the illegal attempt to fire Democratic Commissioners on the Consumer Product Safety Commission (CPSC). “This unprecedented assault on our nation’s regulator of household product safety is in direct contravention of the spirit and letter of the law, runs afoul of decades of Supreme Court precedent, and threatens to cripple the CPSC’s ability to carry out its lifesaving mission,” said Daniel Greene, the Senior Director of Consumer Protection & Product Safety at the National Consumers League.

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158 Advocates Send Letter Opposing Plan to Eliminate the CPSC

May 8, 2025/in Featured Home - Consumer Protection, Press release Press Releases, Statements /by Lisa McDonald

May 8, 2025: Washington, DC – Today, the National Consumers League, Consumer Federation of America, Consumer Reports, and 156 other product safety advocates sent a letter to Russell Vought, the Director of the Office of Management and Budget, expressing their strong opposition to any attempt to eliminate, defund, or weaken the Consumer Product Safety Commission (CPSC).

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https://nclnet.org/wp-content/uploads/2025/05/Social-Media-Images-27.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-05-08 14:04:282025-05-13 18:08:49158 Advocates Send Letter Opposing Plan to Eliminate the CPSC

National Survey Shows a Vast Majority of Americans Want Comprehensive Reform of the 340B Drug Pricing Program

May 8, 2025/in Featured Home - Your Health, Press release Press Releases /by allisonc

May 8, 2025: Washington, DC – Today, the National Consumers League (NCL) released results from a new Morning Consult national poll of more than 10,000 American adults, revealing overwhelming concern about the burden of medical debt and strong public demand for comprehensive reforms of the 340B Drug Pricing Program. Nearly four in five surveyed adults (78%) support establishing requirements to ensure that qualifying patients directly benefit from 340B drug discounts through reduced out-of-pocket prescription drug costs. More than three in four surveyed adults (77%) believe hospitals should be required to pass 340B savings directly onto patients.

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https://nclnet.org/wp-content/uploads/2025/05/Social-Media-Images-70.png 788 940 allisonc https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png allisonc2025-05-08 13:36:592025-05-08 13:46:14National Survey Shows a Vast Majority of Americans Want Comprehensive Reform of the 340B Drug Pricing Program
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PBPA Commends HHS Funding to Support Maternal and Infant Health

The Preterm Birth Prevention Alliance (PBPA), a coalition of maternal and women’s health advocates dedicated to improving preterm birth outcomes in the United States and addressing its disproportionate impact on women of color, applauds the U.S. Department of Health and Human Services (HHS) for awarding nearly $350 million to states across the country to improve support for safe pregnancies and healthy babies.

“For far too long, U.S. maternal health care has lagged behind that of other developed countries, particularly for women of color,” noted Sally Greenberg, Executive Director of the National Consumers League. “This additional funding will enable local health departments and nonprofits to better address the health care needs of the most vulnerable mothers and their babies.”

The funding, awarded by HHS’ Health Resources and Services Administration (HRSA), will support home visiting services, increase access to doulas, address infant mortality and maternal illness, and improve data reporting on maternal mortality.

“Maternal health care in the U.S. has consistently failed women of color,” Greenberg continued.  “We applaud HHS for this additional funding that will help to improve the maternal health for all mothers and babies, especially women of color and those most at-risk.”

The funding announcement follows the release of a report by the U.S. Commission on Civil Rights which found that Native American women are more than two times more likely to die from pregnancy-related complications than white women in the U.S. This disparity was further exacerbated for Black women in the U.S., who are three to four times more likely to die from pregnancy-related complications than white women.

“In addition to expanding programs to support maternal health, we must increase representation from racially and ethnically diverse groups in research and clinical trials, particularly those studying treatment options to prevent maternal morbidity and mortality,” said Greenberg.  “The need for the additional HHS funding and the report from the Commission on Civil Rights clearly illustrate how critical representative research and real world evidence are to ensuring all mothers and their babies have the same opportunity for the best possible health outcomes.”

Diverse research for a diverse America: The value of equitable, real-world research

August 12, 2021/in Blog, Health, Prevention Blog Post

By Sally Greenberg, NCL Executive Director

While the COVID-19 pandemic has led to hardship for all Americans, it is clear that people of color have been disproportionately burdened. Across the health care continuum, addressing this disparity has become part of the broader conversation about the history of systemic racism and the underlying social determinants of health that negatively affect the mental, physical, and economic health of individuals and entire communities.

The pandemic has underscored persistent health disparities, and there is growing recognition that representation in research and clinical trials can have a profound impact on health outcomes. A lack of representation from racially and ethnically diverse groups in research and clinical trials have typically led to gaps in data, missing the opportunity to assess the full impact of various treatments and drugs across a range of populations. The collection and use of real-world research and data to inform the potential use, risks, and benefits of medical products and treatments can ultimately lead to better health outcomes, particularly for those who have been underrepresented in the past.

Existing efforts to improve inclusion

Efforts to expand diversity and representation in medical research are underway in Congress. Policymakers are encouraging the incorporation of Real World Evidence (RWE) in drug development through the recent Cures 2.0 draft legislation released by Reps. Diana Degette (D-CO-1) and Fred Upton (D-MI-6). While the status quo limits us from effectively reaching underserved populations, the proposed legislation would allow studies that include RWE for some drugs after they have been approved. At the heart of this issue is a growing appreciation that the same therapy can affect different populations in different ways, which is why Cures 2.0 supports collecting data that more accurately reflects the unique experiences and needs of patients across diverse populations.

Recognizing the potential for RWE in maternal health

The lack of representative research in the field of maternal health is undeniable, and its implications are staggering. The dismal state of maternal care in the United States reflects how our health care system has failed women of color, including by not adequately studying treatment options to prevent maternal morbidity and mortality. The need for RWE is clear when you consider the persistent disparities in health outcomes that plague minority communities.

Preterm birth and its disproportionate impact on women of color is a stark illustration of the need to make progress on representative research in maternal health. Preterm birth is the second-largest contributor to infant death in America today. Despite the tremendous physical, emotional, and financial toll that preterm birth continues to take on our country — disproportionately so on women and families of color — not enough therapeutic tools currently exist to prevent it.

Today, “17P,” the only FDA-approved treatment to help reduce the likelihood of spontaneous, recurrent preterm birth in the United States is at-risk of being withdrawn from the market in all its forms, including the branded product and five generic versions. Unfortunately there is conflicting evidence from two different clinical trials, one representative of a diverse U.S. population and another studied in a largely white population in Europe. It’s not a straightforward comparison. If 17P is withdrawn, the women most affected by preterm birth, predominantly women of color, would be left without an FDA-approved treatment option.

The FDA is considering the path forward, including additional data collection through leveraging RWE from past patient use. The success of the first (approval) trial for 17P in the impacted communities signals the importance of RWE. Continued access to 17P is, at its core, a matter of health equity. Black women must not yet again be left vulnerable to a system that historically has overlooked them.

PRETERM BIRTH PREVENTION ALLIANCE APPLAUDS FDA’S GRANTING OF HEARING FOR THE ONLY FDA-APPROVED THERAPIES TO REDUCE RECURRENT PRETERM BIRTH

WASHINGTON, DC, August 26, 2021 –

Preterm Birth Prevention Alliance a coalition of maternal and women’s health advocates dedicated to improving preterm birth outcomes in the United States and addressing its disproportionate impact on women of color, commends the U.S. Food and Drug Administration (FDA) for granting a public hearing to discuss 17P, the only FDA-approved class of branded and generic treatments to reduce preterm birth in indicated patients.

We appreciate the FDA’s willingness to hear directly from individuals facing prematurity and the providers who treat them about their experiences with 17P,” said National Consumer League’s Executive Director Sally Greenberg. “It is an important step towards better understanding variations in efficacy across diverse populations and ensuring all women have an equal chance at the best possible outcomes.”

Last week, the FDA agreed to grant Covis Pharma, the manufacturer of the branded 17P product Makena its request for a public hearing to discuss 17P. Hydroxyprogesterone caproate—or “17P”—has been approved since 2011 and is the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth in the United States. In 2020, the FDA proposed withdrawing 17P in all its forms, including the branded product and its five generic versions, based on conflicting efficacy data from two studies composed of vastly different populations, one predominantly inclusive of women in the U.S. most vulnerable to preterm birth and one not.

“Mothers and birthing people deserve access to the best possible treatments to prevent preterm birth. We cannot achieve birth equity if we study pregnant women as a monolith,” said Blythe Thomas, Initiative Director of 1,000 Days. “It is only by systematically researching the real-world, post-market impact of 17P on individuals from a variety of racial and ethnic backgrounds, while maintaining access for all affected, that we can reduce disparities in maternal and infant health.”

While the hearing date has not yet been set, the Alliance looks forward to sharing the perspectives of affected individuals and their physicians with the agency once the hearing is scheduled and will continue to advocate for at-risk moms and babies of all races and ethnicities.

###

ABOUT THE PRETERM BIRTH PREVENTION ALLIANCE

The Preterm Birth Prevention Alliance (PBPA) is a coalition of maternal and women’s health advocates who share a common concern about the state of preterm birth in the United States and the proposed market withdrawal of 17P, the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth. Formed in 2021 by the National Consumers League, the 15 partners in the PBPA seek to improve preterm birth outcomes in the United States by maintaining access to safe, FDA-approved treatment options and advocating for more diverse medical research that adequately represents the experiences of women and newborns of color. Women of color need a seat at the table. To learn more, visit www.pretermbirthalliance.org

LEADING PATIENT ADVOCATES LAUNCH PRETERM BIRTH PREVENTION ALLIANCE TO PROTECT CRITICAL ACCESS TO THE SOLE FDA-APPROVED CLASS OF THERAPIES TO REDUCE RECURRENT PRETERM BIRTH

WASHINGTON, DC, April 20, 2021 – Today, the National Consumers League (NCL), along with a coalition of patient advocacy organizations dedicated to advancing the health of mothers and infants, announced the launch of the >Preterm Birth Prevention Alliance.

Members of the Alliance are joining forces in an effort to preserve patient access to the only Food & Drug Administration-approved class of treatments for pregnant women who have previously had an unexpected, or spontaneous, preterm birth. Together, Alliance members seek to ensure that the Food & Drug Administration (FDA) hears concerns from the full range of stakeholders about the potential risks and impact of withdrawal for at-risk pregnant women and their providers.

For the fifth year in a row, the U.S. preterm birth rate has increased (to 10.2 percent of births), and preterm birth and its complications were the second largest contributor to infant death across the country. Preterm birth also represents a significant racial health disparity, with Black women in America experiencing premature delivery at a rate 50 percent higher than other racial groups throughout the country.

However, in 2020, the FDA >proposed withdrawing hydroxyprogesterone caproate, commonly called “17P” or “17-OHPC”, the only FDA-approved class of branded and generic treatments to help prevent the risk of preterm birth in women with a history of spontaneous preterm birth. The FDA is currently determining whether to hold a hearing on the status of 17P, based on conflicting efficacy data from two studies composed of vastly different patient populations, one inclusive of women in the U.S. most vulnerable to preterm birth and one not.

“We’re fighting for a more inclusive healthcare system that gives everyone an equal chance to have the best outcomes possible,” said Sally Greenberg, executive director of the National Consumers League. “We don’t believe that removing 17P from the market without gaining a better understanding of who could benefit the most from its use is in the best interests of patients, nor their healthcare providers, particularly as there are no other approved treatment options available.”

To date, 14 organizations have joined NCL to advocate for the health interests of at-risk pregnant women and infants, including: 1,000 Days; 2020 Mom; American Association of Birth Centers; Black Mamas Matter Alliance; Black Women’s Health Imperative; Expecting Health; Healthy Mothers, Healthy Babies Montana; HealthyWomen; Miracle Babies; National Birth Equity Collaborative; National Black Midwives Alliance; National Partnership for Women & Families; Sidelines High-Risk National Support Network; and SisterReach.

“As a trained obstetrician and gynecologist, I know firsthand the impact of preterm birth on Black women and birthing people. I also know that racism – not race – is the driving factor leading the disproportionate impact of preterm birth on Black women and birthing people thereby exacerbating systemic inequities in maternal and infant health. To achieve birth equity, which is the assurance of the conditions of optimal births for all people with a willingness to address racial and social inequities in a sustained effort, we must work to protect and uphold a standard of care for spontaneous, recurrent preterm births and ensure it remains accessible and affordable for all who stand in need,” added Dr. Joia Crear Perry, founder and president of the National Birth Equity Collaborative.

The Preterm Birth Prevention Alliance is calling for the FDA to grant a public hearing to fully consider all of the data, additional research methods, and stakeholder perspectives before deciding whether to withdraw approval of this critical class of therapies. The health of America’s moms and babies warrants the utmost care and consideration.

###

ABOUT THE PRETERM BIRTH PREVENTION ALLIANCE

The Preterm Birth Prevention Alliance is a coalition of maternal and women’s health advocates who share a common concern about the state of preterm birth in the United States and the proposed market withdrawal of 17P, the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth. Formed in 2021 by the National Consumers League, we seek to improve preterm birth outcomes in the United States by maintaining access to safe, FDA-approved treatment options and advocating for more diverse medical research that adequately represents the experiences of women and newborns of color. Women of color need a seat at the table. To learn more, visit www.pretermbirthalliance.org.

Initial support for the Preterm Birth Prevention Alliance is provided by Covis Pharma.

MEDIA CONTACT:

Carol McKay, carolm@nclnet.org

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