April 18, 2026: Orlando, FL – The Floyd County 4-H Team was crowned the 2026 Varsity LifeSmarts National Champions in Orlando, Florida. Coached by Phyllis Allee and Abbie Salmon, the winning team consisted of Joe Rutledge (12th grade), Abigail Moon (12th grade), Tabitha Smith (11th grade), Finley Smith (9th grade).
Washington, DC — The National Consumers League (NCL) today welcomed the Senate HELP Committee’s hearing on generics and biosimilars as an important bipartisan step toward lowering prescription drug costs through increased competition.
April 2, 2026: Washington, DC — As March Madness reaches the Final Four—with billions of dollars on the line and millions of Americans placing high-stakes wagers—the National Consumers League (NCL) is warning that sports betting apps are doing more than fueling the excitement—they may be quietly draining consumers’ savings and damaging their financial health.
March 27, 2026: Washington, DC – Today, the National Consumers League, two former chairs of the FCC, and five other public interest organizations filed an amicus brief at the U.S. Supreme Court in FCC v. AT&T. The case was brought after telecom carriers were found liable for privacy violations that harmed their customers. The companies responded by suing to nullify the Commission’s primary fining authority under the Communications Act of 1934.
March 27, 2026: Washington, DC – Yesterday, Senator Durbin reintroduced the Protect Your Points Act, legislation that would protect consumers’ airline rewards points. Key components include a prohibition on points devaluation without at least one year’s notice, a requirement for the non-expiration of accrued points, a ban on junk fees for the redemption of rewards, and greater transparency into the dollar value of rewards points.
March 26, 2026: Washington, DC – Today marks a significant milestone in the State’s Attorney General’s antitrust case against Live Nation Entertainment, the parent company of Ticketmaster, LLC, as more than 30 state plaintiffs conclude the presentation of their case to the jury.
March 19, 2026: At a time when Americans are increasingly concerned about the cost of healthcare, a troubling contradiction is emerging within the hospital system meant to care for our most vulnerable patients. A new analysis from the National Consumers League reveals that hospitals participating in the federal 340B Drug Pricing Program— including many hospitals that treat high volumes of cancer patients — are more likely than non-340B hospitals to permit aggressive medical debt collection practices such as lawsuits, wage garnishment, liens, and credit reporting.
March 11, 2026: “You’re no Jack Kennedy,” is the immortal remark made by Senator Lloyd Bentsen to VP hopeful Senator Dan Quayle during their 1988 debate. It wasn’t a compliment. Now, these words are appropriate for the proposed candidacy of Dr. Casey Means for the critically important role of Surgeon General of the United States.
March 10, 2026: Washington, DC – The National Consumers League (NCL) today sent a letter to the Senate Environment & Public Works Committee in advance of the hearing on S. 3135, the Cold Weather Diesel Reliability Act. The legislation would grant the Environmental Protection Agency the authority to permit vehicle manufacturers to suspend engine shutdown features on diesel vehicles in extreme cold.
March 9, 2026: Washington, DC – As an organization focused on the safety of GLP-1 weight-loss drugs, the National Consumers League welcomes the agreement between Novo Nordisk and the telehealth platform Hims & Hers as an important step that could turn the tide away from consumers opting for unapproved GLP-1 weight-loss products.
The work of the National Consumers League is making a difference in people’s lives across the country. Meet some of the consumers touched by our programs.
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Paige, 55, a Nashville wife and mother of two, answered an employment ad for secret shoppers. Before sending payment to the scammers, she reached out to NCL.
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A grease fire flared up in Decklan’s kitchen. As his family scrambled and panicked, fearing that the whole house might erupt in flames, Decklan remained calm. He hurried over to the pantry, grabbed some baking soda, and dumped it on the fire quickly extinguishing the blaze.
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Cincinnati resident Charles, 45, lost his computer business — and health insurance— during a time of economic downturn. A diabetic, Charles was now unable to afford his medication. He stopped taking it which made him seriously ill and put his life at risk.
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Jeremy is a fast-food worker who has been employed at a number of Chipotle restaurants in New York City. When he was just 20 years old, he took part in an NCL research project that revealed that management practices within the fast food chain were putting workers—and food safety for customers—at risk.
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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.
