PolicyBrief
H.R. 2497
119th CongressMar 31st 2025
Abortion Care Awareness Act of 2025
IN COMMITTEE

The Abortion Care Awareness Act of 2025 mandates a national public health campaign by HHS to educate the public on accessing abortion care, understanding related rights, and identifying misinformation.

Jasmine Crockett
D

Jasmine Crockett

Representative

TX-30

LEGISLATION

New Federal Campaign Mandates Medically Accurate Info on Abortion Access, Targets Disinformation

If you’ve ever tried to find clear, reliable information about reproductive healthcare online, you know the struggle is real. The Abortion Care Awareness Act of 2025 aims to cut through that noise by requiring the Department of Health and Human Services (HHS) to launch a coordinated, national public health campaign dedicated to educating people on how and where to access abortion and related health services. This isn’t just a website; it’s a mandate for the federal government to provide clear, medically accurate facts—including specifics on medication abortion (like mifepristone and misoprostol), whether through telehealth or in-person care, all while staying within existing state and federal laws (SEC. 2).

The Federal Fact-Checkers

This bill recognizes that getting accurate care often means navigating a minefield of misinformation. The campaign is specifically tasked with giving people the tools to identify the difference between legitimate healthcare providers and places often referred to as “anti-abortion centers” or “crisis pregnancy centers.” Think of it as a federal heads-up on potential scams and misleading claims about reproductive health. Furthermore, the campaign must teach people how to spot disinformation campaigns and protect their sensitive personal health information from misuse or spying, especially if they are seeking care online or across state lines (SEC. 2). For the average person, this means less time spent fact-checking and more confidence that the information they find is reliable.

Travel Rights and Targeted Outreach

One of the most practical aspects of this bill is its focus on clarifying the right to travel across state lines for care and providing information on organizations that can help support that travel. For someone living in a state with restrictive laws, this provision is massive—it’s the difference between knowing your options and feeling trapped. The campaign must also be designed to be culturally competent and accessible to underserved communities. This means the information won’t just be in English; it must actively reach people of color, low-income individuals, those in rural areas, non-English speakers, and LGBTQI individuals. For a single mom in a rural area, this means the information should be available in a format and language she can actually use, not hidden behind jargon or inaccessible websites (SEC. 2).

What the Feds Can’t Say

To ensure medical accuracy, the bill lays down some strict red lines for HHS. The campaign cannot promote misinformation about the safety of abortion services, nor can it promote the concept of “abortion reversal.” It’s also barred from promoting abstinence-only programs or any sexual education that isn’t comprehensive and medically accurate. Perhaps most importantly for digital natives, the Secretary is explicitly forbidden from collecting, keeping, using, or sharing any personal information from people who visit any website or resource related to this campaign. This privacy firewall means you can seek information without worrying that your search history will be tracked or your data weaponized (SEC. 2).

The Practical Impact

This legislation essentially formalizes the federal government’s role in providing a clear, unbiased source of reproductive health information, countering the patchwork of state laws and the flood of online misinformation. While the bill is very specific about what must be included, the Secretary of HHS still has significant discretion in designing the campaign to be “culturally competent” and “effective.” That means the quality of the rollout will depend heavily on HHS’s execution. However, by requiring consultation with licensed healthcare professionals and reproductive rights organizations, the bill ensures the campaign is grounded in medical reality and the practical needs of people seeking care. The bottom line: if this rolls out as intended, finding out where, when, and how to access reproductive healthcare should get a whole lot simpler and safer.