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Health

Health

Access to Quality Healthcare Is a Right, Not a Privilege

Rising medical costs, confusing insurance rules, and misleading information make it harder for consumers to get the care and medications they need. Millions of Americans face barriers to affordable prescriptions, safe treatments, and reliable health guidance, putting their well-being and financial security at risk.

How We Help

Our work advocates for policies that improve healthcare access, affordability, and safety. From pharmacy benefit manager reform to fighting medical misinformation, promoting vaccine awareness, and ensuring equitable treatment for obesity and chronic conditions, NCL provides consumers with the tools, resources, and support to make informed health decisions and live healthier lives.

Key Issues

  • Pharmacy Benefit Managers

  • 340B Drug Pricing Program

  • Medication Adherence

  • Medical Debt

  • Vaccinations

Featured Programs

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Script Your Future helps patients and caregivers understand the importance of taking medications as prescribed by providing tools, education, and support to improve adherence and communication with healthcare providers.

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Health Advisory Council brings together partner organizations to support health advocacy and education, share insights, identify common goals, and guide the National Consumers League’s efforts to improve health outcomes for consumers.

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The 340B Drug Pricing Program was created to help low-income and uninsured patients access life-saving medications, but some hospitals and middlemen exploit it. NCL pushes for reforms to ensure it serves the patients it was meant to help.

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Pharmacy Benefit Managers (PBMs) are middlemen who often drive up consumers’ costs for life-saving medications by keeping discounts and adding fees. NCL advocates for transparency and fairness so all consumers get a fair deal.

Featured Content

Obesity medicine specialists, health providers, insurers and employers urged to make obesity treatment a right of all Americans

October 13, 2023
With growing evidence that U.S. adults with obesity feel stigmatized and ignored by their health care providers, the National Consumers League (NCL) and National Council on Aging (NCOA) today urged health professionals, insurers and employers to join a national movement to define quality obesity care as a right for every American.
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https://nclnet.org/wp-content/uploads/2023/07/Social-Media-Images-22.png 788 940 Katie Brown https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Katie Brown2023-10-13 20:11:362025-05-20 20:36:49Obesity medicine specialists, health providers, insurers and employers urged to make obesity treatment a right of all Americans

Unveiling the flaws in the 340B Drug Pricing Program: Hospitals, medical debt, and consumer struggles

September 18, 2023
September 18, 2023: In 1992, Congress created the 340B Drug Pricing Program to help ensure vulnerable patients would be able to access medications they need but may not be able to afford. This program provides steeply discounted drugs to health care providers – mostly hospitals – serving low-income patients with the intent that the providers would pass those discounts along to patients. Unfortunately, that is not what is happening. The National Consumers League (NCL) is increasingly concerned about this program, especially as it relates to hospitals’ abusive and aggressive debt collection practices, and how those practices lead to consumer medical debt.
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https://nclnet.org/wp-content/uploads/2020/08/Sally2017_92px.jpg 968 968 Katie Brown https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Katie Brown2023-09-18 12:41:262025-05-20 20:40:43Unveiling the flaws in the 340B Drug Pricing Program: Hospitals, medical debt, and consumer struggles

NCL statement on PBMs and new GAO report

September 18, 2023
The National Consumers League (NCL) today released a statement following a recently released U.S. Government Accountability Office (“GAO”) report on Medicare Part D rebates.
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https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png 0 0 sepidehk https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png sepidehk2023-09-18 11:40:432025-06-16 23:14:46NCL statement on PBMs and new GAO report

NCL applauds FDA for its latest decision to approve an updated COVID-19 vaccine

September 11, 2023
The NCL applauds the FDA’s announcement approving the latest COVID vaccine, which will be available to many Americans immediately or very soon to patients who are eligible.
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https://nclnet.org/wp-content/uploads/2023/09/Social-Media-Images-20.png 788 940 sepidehk https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png sepidehk2023-09-11 19:30:592025-05-20 20:41:16NCL applauds FDA for its latest decision to approve an updated COVID-19 vaccine

New insurance schemes to carve out specialty drugs deserve skepticism and scrutiny

August 11, 2023
August 11, 2023: Employers seeking to cut healthcare costs should remember this simple rule of thumb: If an offer to save money seems too good to be true, it usually is. That seems to be the case with offers to try “Alternative Funding Programs” or AFPs.  This is a devious but growing cottage industry, which promises to cut employer costs for specialty medicines. 
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https://nclnet.org/wp-content/uploads/2020/08/Sally2017_92px.jpg 968 968 Katie Brown https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Katie Brown2023-08-11 08:00:592025-05-22 15:44:16New insurance schemes to carve out specialty drugs deserve skepticism and scrutiny

Safety in question: The alarming disparities between cannabis product health claims and research, and the magnified risks for women

July 27, 2023
July 27, 2023: When I started my National Consumers League (NCL) internship in May 2023, I quickly dove into NCL’s health policy work. NCL is leading on several efforts to protect consumers –one area of focus that stood out to me is their work in the cannabis policy space. NCL is a founding member of Cannabis Consumer Watch (CCW), which educates consumers on cannabinoids, their effects, the risks related to the unregulated marketplace, and the ways policymakers and regulators can help protect consumers.
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https://nclnet.org/wp-content/uploads/2023/07/Screen-Shot-2023-07-27-at-4.03.22-PM.png 1046 962 Katie Brown https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Katie Brown2023-07-27 20:06:122025-06-02 16:32:48Safety in question: The alarming disparities between cannabis product health claims and research, and the magnified risks for women

Financing the healthcare of tomorrow playlist: Tracks for consumers and policymakers

July 12, 2023
July 12, 2023: My husband has advanced Lewy Body Dementia and one of the few things we can still enjoy together is listening to music.  We used to curate playlists for all kinds of music. We even put together playlists to mark special occasions (like our daughter’s wedding).  Really, any topic became fair game for a playlist. I was invited to speak at the Patients Rising Disrupting Healthcare Summit summer conference in Washington DC.  My panel topic was Financing the Healthcare of Tomorrow.
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https://nclnet.org/wp-content/uploads/2023/01/Screen-Shot-2023-01-10-at-12.16.19-PM.png 387 491 Katie Brown https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Katie Brown2023-07-12 15:26:182025-06-16 23:15:04Financing the healthcare of tomorrow playlist: Tracks for consumers and policymakers

We must never forget the importance of vaccines

June 21, 2023
June 21, 2023: I have written before about being born into a family that experienced the agony of the polio epidemic. My uncle Roger Joseph’s battle with the disease—including his diagnosis in 1951 by my father, a practicing internist—devastated our entire family.
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https://nclnet.org/wp-content/uploads/2020/08/Sally2017_92px.jpg 968 968 Katie Brown https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Katie Brown2023-06-21 14:02:532023-06-21 14:10:26We must never forget the importance of vaccines

NCL and 36 leading patient organizations urge Congress to protect access to essential laboratory tests

June 7, 2023
The National Consumers League (NCL) today sent a letter signed by 37 leading advocacy organizations, including groups that represent patients with common and chronic conditions who depend on laboratory testing to manage their health, urging Senate and House leaders to protect access to clinical laboratory services by enacting the Saving Access to Laboratory Services Act (SALSA / H.R. 2377 / S. 1000) this year.
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https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png 0 0 sepidehk https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png sepidehk2023-06-07 21:05:252025-05-20 20:50:34NCL and 36 leading patient organizations urge Congress to protect access to essential laboratory tests

NCL statement on nomination of Dr. Monica Bertagnolli as the Director of the National Institutes of Health

May 15, 2023
The National Consumers League welcomes President Joe Biden nomination’s of Dr. Monica Bertagnolli as the Director of the National Institutes of Health (NIH).  
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https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png 0 0 Katie Brown https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Katie Brown2023-05-15 15:53:092025-05-20 20:51:06NCL statement on nomination of Dr. Monica Bertagnolli as the Director of the National Institutes of Health
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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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