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All lobbying filings

I AM ALS

Lobbying for I AM ALS · Support the ALS community to raise awareness and advocate for research and treatments.

 Filing 4th Quarter - Report
4th Quarter (Oct 1 - Dec 31) 2025 · District of Columbia · House · Senate · $30,000.00 expenses · posted Jan 16, 2026

Official filing document

 Bills named in this filing 11
  • S 2587
    Departments of Labor, Health and Human Services, and Education, and Related Agencies Appropriations Act, 2026
  • S 2572
    Department of Defense Appropriations Act, 2026
  • HR 4016
    Department of Defense Appropriations Act, 2026
  • S 2256
    Agriculture, Rural Development, Food and Drug Administration, and Related Agencies Appropriations Act, 2026
  • HR 4121
    Agriculture, Rural Development, Food and Drug Administration, and Related Agencies Appropriations Act, 2026
  • S 925
    Credit for Caring Act of 2025
  • HR 2036
    Credit for Caring Act of 2025
  • S 1261
    CONNECT for Health Act of 2025
  • S 749
    Justice for ALS Veterans Act of 2025
  • HR 1685
    Justice for ALS Veterans Act of 2025
  • HR 6001
    Veterans with ALS Reporting Act
 Lobbying activity 4
Budget/Appropriations

ALS treatment and research funding within FY26 Labor, Health and Human Services, Education and Related Agencies appropriations bill (S.2587) including ACT for ALS and ARPA-H. ALS research funding within the FY26 Defense appropriations bill (S.2572 / H.R.4016)for the Congressional Directed Medical Research Program's ALS Research Program. ALS treatment and research funding for ALS within the FY26 Agriculture, Food and Drug Administration, and Related Agencies appropriations bill (S.2256 / H.R.4121).

Defense

FY26 Defense appropriations bill (S.2572 / H.R.4016) for Congressional Directed Medical Research Program's ALS Research Program.

Health Issues

Reauthorization and fully funding of the ACT for ALS (Public Law 117-79) for continued access to promising treatments and research. (S.925/H.R.2036) Credit for Caring Act to provide relief in the form of a new, non-refundable federal tax credit for eligible working family caregivers. (S.1261) The CONNECT for Health Act to expand coverage of telehealth services through Medicare and make it easier for ALS patients to connect with their doctors. Regulatory flexibility at FDA for expedited pathways to promising treatments for ALS patients because the standard drug approval process (12-14 years) takes too long for people with rapidly progressive terminal conditions with no substantial therapies.

Veterans

(S.749 / H.R.1685) Justice for ALS Veterans Act to extend dependency and indemnity compensation (DIC) benefits to surviving spouses of Veterans who die from ALS, regardless of how long the Veteran lived with the disease. (H.R.6001) Veterans with ALS Reporting Act requiring the Secretary of Veterans Affairs to submit a report on risk reduction strategies to lower the incidence and prevalence of ALS in veterans.

Source: federal Lobbying Disclosure Act filing. Bills are parsed from the activity descriptions.

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