The House of Representatives has introduced HR562, a non-binding resolution titled Supporting the goals and ideals of Alzheimer’s and Brain Awareness Month. The bill gathers a long list of “whereas” findings about the scope of Alzheimer’s and related dementias—prevalence, cost, caregiver burden, disparities, and stigma—and then resolves that the House supports the goals of Alzheimer’s and Brain Awareness Month and encourages Americans to educate themselves, advocate for research, care, and support services, and offer support to those living with the disease and their families.
The resolution is a symbolic expression rather than a directive with enforceable obligations. It was introduced by Representative Barragán and referred to the Committee on Energy and Commerce; there is no funding or regulatory mandate attached to the measure.
At a Glance
What It Does
Establishes a non-binding resolution that expresses support for Alzheimer’s and Brain Awareness Month and calls on the public to educate themselves, advocate for research, and support affected individuals and families.
Who It Affects
Affects the general public, caregivers, patients, families, advocacy groups, and healthcare providers who interact with Alzheimer’s and dementia communities; it signals congressional attention to these issues without creating new duties on individuals or entities.
Why It Matters
Sets a formal congressional stance to elevate public awareness, reduce stigma, and potentially shape future advocacy and policy discussions around research, care, and support services.
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What This Bill Actually Does
This bill is a non-binding resolution, not a new law. It starts with a series of findings describing the scale and impact of Alzheimer’s disease and other dementias: millions live with the condition, caregiving is widespread and burdensome, and disparities exist across Black, Latino, and Asian communities.
It also notes the substantial economic costs and the lack of a preventive cure. The body of the resolution then states that the House supports the goals and ideals of Alzheimer’s and Brain Awareness Month and encourages Americans to learn about the disease, advocate for research and care, and offer support to those affected and their families.
Importantly, the measure does not appropriate funds or impose new regulatory requirements; it is a show of support and a call to action in the form of education and advocacy. The resolution was introduced by Representative Barragán and sent to the Committee on Energy and Commerce for consideration, consistent with its status as a non-binding House resolution.
The Five Things You Need to Know
The bill is a non-binding House resolution with no enforceable duties.
It recognizes June as Alzheimer’s and Brain Awareness Month and calls for awareness activities.
It urges education about Alzheimer’s and dementia and advocacy for research, care, and support services.
It acknowledges caregiver burdens and racial/ethnic disparities in Alzheimer’s outcomes.
It was introduced by Rep. Barragán on June 30, 2025 and referred to the Committee on Energy and Commerce.
Section-by-Section Breakdown
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Findings and purpose
This section compiles the “whereas” findings detailing the scope of Alzheimer’s disease and dementias, the mortality ranking, the lifetime risk, the cost to society, and the burden on caregivers. It also highlights demographic disparities and stigma that hinder diagnosis and access to care. The purpose is to establish a factual backdrop that motivates Congress to acknowledge the issue publicly.
Resolution and aims
The core of the bill declares that the House supports the goals and ideals of Alzheimer’s and Brain Awareness Month and expresses a desire for national engagement in education, advocacy for research, and support for patients and caregivers. This portion translates the findings into a formal, non-binding stance and a set of suggested public-facing actions.
Public engagement and non-binding actions
This section specifies the non-binding expectations for the public—educating themselves, advocating for research and care, and offering support to those affected. It clarifies that the resolution creates no new mandates or funding streams; any actions would depend on existing programs and future appropriations.
Procedural note
The bill’s text concludes with the standard “Now, therefore, be it Resolved” language and confirms referral to the Committee on Energy and Commerce. This preserves the typical legislative path for resolutions and signals the bill’s role as an expression of sentiment rather than a regulatory instrument.
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Explore Healthcare in Codify Search →Who Benefits and Who Bears the Cost
Every bill creates winners and losers. Here's who stands to gain and who bears the cost.
Who Benefits
- People living with Alzheimer’s disease or other dementias gain from heightened awareness and visibility of resources.
- Family members and informal caregivers benefit from recognition of their burdens and potential access to supportive communities.
- Alzheimer’s associations and dementia advocacy groups gain a national-facing platform to advance education and fundraising efforts.
- Health care providers and care teams receive clearer public emphasis on care and support needs.
- Researchers and advocacy funders may see increased public and political attention that can bolster support for studies and programs.
Who Bears the Cost
- No direct funding obligation is created by the resolution; costs would be limited to ongoing public awareness activities undertaken within existing budgets.
- Federal agencies and the Committee on Energy and Commerce would bear minor administrative costs if they engage in public outreach within current capabilities.
- Nonprofit organizations and private-sector partners may incur costs if they launch or expand awareness campaigns in response to the resolution, though such actions are voluntary and not mandated.
Key Issues
The Core Tension
Symbolic support versus material action: the bill calls for education and advocacy without directing funding or policy changes, raising questions about how much momentum a non-binding resolution can generate in the absence of budgetary commitments.
The resolution is symbolic and designed to raise awareness rather than to fund or regulate. Its effectiveness depends on whether public interest translates into measurable advocacy and support for dementia care, research, and services.
A key tension is that the measure presumes interest and action from the public without committing additional resources, which can limit its practical impact to visibility and a signaling effect. The absence of explicit funding directions means any subsequent improvements in care or research would rely on separate appropriations and policy initiatives.
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