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Bill

HR 8620

CARES Hotline Act

119th Congress Introduced by Lou Correa and 6 co-sponsors

The bill would establish a dedicated caregiver hotline to provide information, support, and referrals for those caring for individuals with developmental disabilities.

Introduced in House
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WeVote Research Nonpartisan
Bill Summary · HR 8620

Summary of HR 8620 (118th/119th Session pending action)

Note: This summary reflects the bill as introduced and publicly available information up to the provided action history. It describes the bill’s stated purpose, key provisions, affected stakeholders, and procedural timelines.

Bill at a glance

  • Official title: To amend the Developmental Disabilities Assistance and Bill of Rights Act of 2000 to establish a hotline for caregivers of individuals with developmental disabilities, and for other purposes.
  • Jurisdiction: United States Congress
  • Session: 119
  • Introduced: April 30, 2026
  • Current action: Referred to the House Committee on Energy and Commerce (as of 2026-04-30)
  • Sponsors:
    • Co-sponsors: Eleanor Holmes Norton, Zoe Lofgren, Lou Correa, Rob Menendez, Frederica Wilson, Bennie Thompson

Purpose and intent

  • The bill amends the Developmental Disabilities Assistance and Bill of Rights Act of 2000 to create a dedicated hotline for caregivers of individuals with developmental disabilities.
  • The aim is to provide a direct, accessible channel for support, information, and assistance related to caregiving, access to services, and protections for the rights and well-being of people with developmental disabilities.

Key provisions (as described in summary)

Given the bill text is not provided here, the following provisions are inferred from the title and stated purpose:

  • Establishment of a caregiver hotline: Creation of a centralized telephone and/or digital contact point to assist caregivers of individuals with developmental disabilities.
  • Scope of services: Likely to include guidance on accessing state and federal services, referrals to relevant programs, information about rights and protections, and crisis or problem-resolution assistance.
  • Administration and funding: Provisions would establish which federal agency or office oversees the hotline, budgeting and funding mechanisms, staffing levels, and performance metrics.
  • Coordination with existing programs: Potential alignment or integration with the Developmental Disabilities Assistance and Bill of Rights Act (DD Act) programs, including Protection and Advocacy (P&A) systems, independent living services, and family support initiatives.
  • Data collection and reporting: Provisions may require monitoring, annual reporting on hotline usage and outcomes, and privacy protections for individuals and families.
  • Outreach and accessibility: Requirements to ensure multilingual access, disability accommodations, and broad geographic reach (including rural or underserved areas).

Who would be affected

  • Caregivers of individuals with developmental disabilities: Primary beneficiaries who could access the new hotline for information, referrals, and support.
  • Individuals with developmental disabilities and their families: Indirect beneficiaries through improved support systems and access to services.
  • State and local agencies: Agencies administering DD Act programs may coordinate with the hotline and share information or referrals as appropriate.
  • Advocacy and protection organizations: Organizations involved in DD Act protections (e.g., Protection and Advocacy systems) may interact with or support hotline operations.

Procedural and timeline considerations

  • Introduction and referral: After introduction (April 30, 2026), the bill moves to the House Committee on Energy and Commerce for consideration, which typically involves hearings, markups, and potential amendments.
  • Budget and funding timelines: If enacted, funding would be appropriated according to the bill’s appropriations language and likely aligned with fiscal year budgeting cycles.
  • Implementation timeline (if enacted): The bill would specify a rollout schedule for the hotline, staff hiring, and integration with existing DD Act programs; typical timelines could range from several months to a couple of years depending on funding and administrative processes.

Practical implications

  • A caregiver hotline could provide timely guidance, reduce barriers to services, and improve crisis response for families navigating developmental disability supports.
  • Operational details (hours of operation, languages offered, accessibility features, and privacy protections) will determine the practical usefulness and reach of the hotline.

If you’d like, I can tailor this summary to emphasize specific areas (e.g., funding provisions, anticipated administrative structure, or comparison with existing DD Act programs) or incorporate any official text you provide.

Compiled from official sources — confirm details with the bill’s official record.

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