Sponsors (26)
Introduced April 1, 2025 by Edward John Markey · Last progress April 1, 2025
The bill directs agencies to reduce paperwork and improve access for family caregivers and beneficiaries, but it provides no new funding or enforcement authority, so real improvements depend on whether and how agencies and states act on the recommendations.
Family caregivers (parents and those caring for people with disabilities) will spend less time re‑submitting the same information because agencies are required to identify and reduce duplicative requests and paperwork.
Family caregivers (parents and people with disabilities) will have improved access to assistance through enhanced outreach, better websites, translation services, ASL‑compatible formats, and shorter call wait times.
Medicaid and Medicare beneficiaries and their caregivers may get faster, more accurate eligibility and appeals decisions because staff must be trained on caregiver‑related program uses and appeals handling.
Parents, families, and state governments may see little or slow change because the bill creates no new funding or enforcement authority, so agencies may lack resources to implement recommended changes fully.
Parents, families, and Medicaid beneficiaries may experience limited short‑term benefit if agencies delay reviews or do not act on recommendations, since improvements depend on agency implementation.
Parents and families may be frustrated if publication of reports and solicitation of input raise expectations but do not lead to meaningful reductions in paperwork or burden.
Based on analysis of 2 sections of legislative text.
Requires CMS and SSA to jointly review and simplify applications, eligibility, forms, and communications across Medicare, Medicaid, CHIP, and Social Security to reduce burdens on family caregivers; no new funding or statutory changes.
Requires the Centers for Medicare & Medicaid Services Administrator and the Social Security Commissioner to jointly review and simplify how people interact with Medicare, Medicaid, CHIP, and Social Security programs so family caregivers can more easily determine eligibility, enroll, keep coverage, and use benefits. Directs agencies to reduce duplicate paperwork, improve communications and access (including translation and accessible formats), train staff, and engage stakeholders, but does not create new funding, authorities, or change underlying law.