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H.R. 7336
U.S. House•In House Committee
Summary
H.R. 7336, the ALS Better Care Act, was introduced in the House on Feb 3, 2026 by Rep. Janice Schakowsky (D) with 12 co-sponsors. It was referred to Energy And Commerce, and last saw action on Feb 3, 2026: Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
Record
Text
H.R. 7336 has 12 co-sponsors.
hb7336/introduced-in-house.txt119 HR 7336 IH: ALS Better Care ActU.S. House of Representatives2026-02-03text/xmlENPursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.I 119th CONGRESS 2d Session H. R. 7336 IN THE HOUSE OF REPRESENTATIVES February 3, 2026 Ms. Schakowsky (for herself, Mr. Fitzpatrick , Mr. Crow , and Mr. Quigley ) introduced the following bill; which was referred to the Committee on Energy and Commerce , and in addition to the Committee on Ways and Means , for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned A BILLTo amend title XVIII of the Social Security Act to provide coverage of ALS-related services under the Medicare program for individuals diagnosed with amyotrophic lateral sclerosis, and for other purposes.1.Short titleThis Act may be cited as the ALS Better Care Act .2.FindingsCongress makes the following findings:(1)Amyotrophic lateral sclerosis (in this section, referred to as ALS ) is a progressive and debilitating neurodegenerative disease.(2)Key services that include (but are not limited to) providing specialized physician or nurse practitioner support, occupational therapy support, speech pathology support, physical therapy, dietary support, respiratory support, registered nurse support, and coordination of the furnishing of durable medical equipment are crucial for managing the complex medical needs of ALS patients.(3)Studies have shown ALS clinics that provide these key services to ALS patients extend these patients’ lifespans and improve the quality of their lives.(4)These key services are furnished by a range of healthcare professionals.(5)Facilities providing care to ALS patients currently face inadequate Medicare reimbursement for the key services they offer to these patients.(6)Insufficient reimbursement creates significant challenges for facilities specializing in ALS care, resulting in extended wait times for patients in need of crucial services and hampering the ability of these facilities to innovate and improve the quality of care provided to ALS patients.(7)Improved reimbursement rates would encourage facilities to invest in research, innovation, and technology, leading to enhanced treatment options for ALS and improved patient outcomes.(8)Remote medical management options for individuals suffering from ALS must be a crucial part of access to care for such individuals, especially those living in rural areas or care deserts.(9)Telehealth is an essential management option referred to in paragraph (8) and can assist in delivering timely and comprehensive care, as ALS patients living in rural areas or care deserts often face challenges in accessing specialized ALS care and could otherwise be required to travel long distances—often with caregivers or family members.(10)Telehealth is especially important in maintaining access to care for ALS patients as the disease progresses and ALS patients have more limited mobility, which may make it challenging to attend in-person appointments regularly.(11)Low funding and difficulty in staffing for ALS clinical trials delay the development and availability of potential treatments and therapies for individuals living with the disease.(12)Inadequate funding for ALS clinical trials also impedes the ability to attract and retain qualified researchers, clinicians, and support staff, limiting the overall progress and success of these trials.3.Providing for coverage of als-related services under the medicare program for individuals diagnosed with amyotrophic lateral sclerosis(a)In generalSection 1861 of the Social Security Act ( 42 U.S.C. 1395x ) is amended—(1)in subsection (s)(2)—(A)by adding and at the end of subparagraph (JJ); and(B)by adding at the end the following new subparagraph:(KK)ALS-related services (as defined in subsection (nnn)) furnished on or after January 1, 2027;; and(2)by adding at the end the following new subsection:(nnn)ALS-Related Services.—(1)Als-related servicesThe term ALS-related services means the following items and services that are furnished to a covered ALS individual in an outpatient setting by a qualified provider (as defined in section 1834(aa)(6)) (or by another provider of services under an arrangement made by a qualified provider) for the care and treatment of such an individual with respect to the progression of amyotrophic lateral sclerosis:(A)Specialized physician or nurse practitioner support.(B)Occupational therapy support.(C)Speech pathology support.(D)Physical therapy.(E)Dietary support.(F)Respiratory support.(G)Registered nurse support.(H)Coordination of the furnishing of durable medical equipment necessary for the management of the complex medical needs of a covered ALS individual.(2)Covered als individualThe term covered ALS individual means an individual who is medically determined to have amyotrophic lateral sclerosis (as described in section 226(h))..(b)Payment for ALS-Related servicesSection 1834 of the Social Security Act ( 42 U.S.C. 1395m ) is amended by adding at the end the following new subsections:(aa)Payment for ALS-Related Services.—(1)In generalThe Secretary shall implement a payment system under which a single payment determined in accordance with the succeeding paragraphs is made to a qualified provider (as defined in paragraph (6)) for ALS-related services (as defined in paragraph (1) of section 1861(nnn)) furnished to a covered ALS individual (as defined in paragraph (2) of such section) during a visit, in addition to any other payment that may be made for such services under this title.(2)Base payment amount(A)In generalThe amount of the single payment described in paragraph (1) for ALS-related services furnished during a year is equal to—(i)for 2027, $800;(ii)for 2028, $800 (or, if greater, the payment amount recommended by the Comptroller General of the United States in the report described in subparagraph (C)); and(iii)for 2029 and each subsequent year—(I)the amount for the preceding year, increased by the ALS services market basket percentage increase (as defined in clause (i) of subparagraph (B)) for such year; or(II)in the case such year is an applicable year (as defined in clause (ii) of such subparagraph), the payment amount recommended by the Comptroller General in the most recent report submitted under subparagraph (C), if greater than the amount that would be determined for such year under subclause (I).(B)DefinitionsIn this paragraph:(i)ALS services market basket percentage increaseThe term ALS services market basket percentage increase means, for a year, the Secretary’s estimate of the percentage increase in costs of an appropriate mix, as determined by the Secretary, of items and services that are ALS-related services over the preceding year.(ii)Applicable yearThe term applicable year means 2030 and every third year thereafter.(C)Report by the comptroller general(i)In generalNot later than January 1, 2027, and not later than January 1 of every third year thereafter, the Comptroller General of the United States shall, in consultation with qualified providers eligible for payment under this subsection, submit to the Secretary a report that recommends a single payment amount for ALS-related services that takes into account the average amount of payment for each item or service included in ALS-related services that the Comptroller General estimates would have been payable—(I)under this title for such a service based on per patient utilization data from whichever single year during the covered period (as defined in clause (ii)) with respect to such report has the highest per patient utilization of ALS-related services, even if such service is not payable for a particular covered ALS individual because of the application of section 1862(a)(1)(A) with respect to an item or service provided to such individual;(II)in the case an estimate is unable to be determined pursuant to subclause (I), by health insurance issuers and group health plans (as such terms are defined in section 2791 of the Public Health Service Act) and MA plans under part C for such a service, based on such data from whichever single year during the covered period with respect to such report has the highest per patient utilization of ALS-related services; and(III)in the case an estimate is unable to be determined pursuant to subclause (II), based on the recommendation of the Specialty Society Relative Value Scale Update Committee of the American Medical Association or the estimate of the Comptroller General for such a service.(ii)Definition of covered periodIn this subparagraph, the term covered period means—(I)with respect to the first report submitted under this subparagraph, 2022 through 2024;(II)with respect to the second such report, 2026 through 2028; and(III)with respect to the third report and each subsequent report, the period that begins 3 years after the covered period for the preceding report.(3)Payment adjustmentsThe payment system under this subsection shall include a payment adjustment—(A)for each qualified provider that is participating in at least one clinical trial identified on the clinicaltrials.gov database (or any successor database) of the National Institutes of Health to account for the increased cost borne by such a qualified provider during such a clinical trial; and(B)for a medical service or technology which is furnished as a part of ALS-related services for which, as determined by the Secretary—(i)payment under this subsection for such service or technology was not being made in the preceding year; and(ii)the cost of such service or technology is not insignificant in relation to the payment amount (as determined under this subsection) payable for ALS-related services.(4)Mechanism for paymentsFor purposes of making payments for ALS-related services, the Secretary shall establish a mechanism under the payment system under this subsection which makes payment when a qualified provider submits a claim for payment which includes, with respect to a covered ALS individual, an alphanumeric code issued under the International Classification of Diseases, 10th Revision, Clinical Modification ( ICD–10–CM ) and its subsequent revisions that is for the treatment of a diagnosis of amyotrophic lateral sclerosis.(5)No cost sharingPayment under this subsection shall be made only on an assignment-related basis without any cost sharing.(6)Qualified providerIn this section, the term qualified provider means a provider of services that—(A)is capable of furnishing ALS-related services; and(B)meets requirements as the Secretary prescribes by regulation to implement subparagraph (A), in consultation with—(i)covered ALS individuals and their representatives;(ii)physicians who provide ALS-related services and their representatives; and(iii)professional and non-profit organizations with expertise in amyotrophic lateral sclerosis.(7)Implementation(A)In generalExcept as provided under subparagraph (B), the Secretary may implement the provisions of this subsection by program instruction or otherwise.(B)RulemakingThe Secretary shall implement paragraph (6), through notice and comment rulemaking..(c)Conforming amendments(1)Section 1833(t)Section 1833(t) of the Social Security Act ( 42 U.S.C. 1395(t) ) is amended by adding at the end the following new paragraph:(23)Ensuring supplemental payments for als-related servicesAny covered OPD service furnished to a covered ALS individual (as defined in section 1861(nnn)(2)) that is otherwise payable to a qualified provider (as defined in section 1834(aa)(6)) pursuant to paragraph (4) shall be payable under such paragraph notwithstanding any payment made under section 1834(aa)..(2)Definition of arrangementsSection 1861(w)(1) of the Social Security Act ( 42 U.S.C. 1395x(w)(1) ) is amended by inserting qualified provider (as defined in section 1834(aa)(6)) with respect to ALS-related services (as defined in subsection (nnn)), before or hospice program .4.Report on challenges with respect to the administration and staffing of amyotrophic lateral sclerosis clinical trialsNot later than 90 days after the date of the enactment of this Act, the Secretary of Health and Human Services, acting through the Director of the National Institute of Neurological Disorders and Stroke of the National Institutes of Health, shall submit to Congress and publish on the internet website of the agency a report that identifies—(1)any challenges with respect to the administration and staffing of clinical trials for the prevention, diagnosis, mitigation, treatment, or cure of amyotrophic lateral sclerosis;(2)actions that the Director of the National Institute of Neurological Disorders and Stroke can take to address such challenges; and(3)any legislative recommendations (including requests for appropriations) to further improve the administration of such clinical trials.
Tracker
The tracker indicates the progress of this legislation as it moves through the legislative process.
- Introduced2026-02-03
- Passed House
- Passed Senate
- Conference
- To President
- Became Law
To amend title XVIII of the Social Security Act to provide coverage of ALS-related services under the Medicare program for individuals diagnosed with amyotrophic lateral sclerosis, and for other purposes.
Sponsors
Rep. Janice Schakowsky (D) sponsors H.R. 7336, and 12 members have co-sponsored it, 3 of them from the day it was introduced.

Rep. · D–IL-9 · Sponsor
Introduced Feb 3, 2026

Rep. · D–CO-6 · Co-sponsor
Joined Feb 3, 2026 · Original

Rep. · R–PA-1 · Co-sponsor
Joined Feb 3, 2026 · Original

Rep. · D–IL-5 · Co-sponsor
Joined Feb 3, 2026 · Original

Rep. · R–NE-2 · Co-sponsor
Joined Feb 20, 2026

Rep. · D–NY-25 · Co-sponsor
Joined Feb 20, 2026

Rep. · D–IL-13 · Co-sponsor
Joined Apr 9, 2026

Rep. · D–AZ-7 · Co-sponsor
Joined Apr 21, 2026

Rep. · D–OR-5 · Co-sponsor
Joined May 29, 2026

Rep. · D–RI-2 · Co-sponsor
Joined May 29, 2026
Committees
H.R. 7336 went before 2 committees: Ways and Means and Energy and Commerce.
Actions
H.R. 7336 has taken 2 actions since Feb 3, 2026.
| Chamber | Action | |||
|---|---|---|---|---|
Feb 3, 2026 | House | Introduced in House | ||
Feb 3, 2026 | House | Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.Energy and Commerce Committee |
Votes
H.R. 7336 has not gone to a roll call.
Related bills
1 bill is related to H.R. 7336, as Identical bill.
Titles
H.R. 7336 goes by 3 titles, 1 of them short titles.
- ALS Better Care Act — Display Title
- ALS Better Care Act — Short Title(s) as Introduced
- To amend title XVIII of the Social Security Act to provide coverage of ALS-related services under the Medicare program for individuals diagnosed with amyotrophic lateral sclerosis, and for other purposes. — Official Title as Introduced
Lobbying
2 clients hired 2 firms and 3 registered lobbyists who named H.R. 7336 in 4 quarterly filings, 2026. Reported under the Lobbying Disclosure Act; a filing’s income covers everything its registrant worked that quarter, so the amounts below are the filings’, not this bill’s.
Filed under Budget/Appropriations, Health Issues, Veterans, Defense, Medicare/Medicaid, Pharmacy, Taxation/Internal Revenue Code, Welfare.
Clients
Who paid to be heard, by how many filings named the bill.
| Client | Business | State | Firms | Filings | Reported |
|---|---|---|---|---|---|
| I AM ALS | Support the ALS community to raise awareness and advocate for research and treatments. | District of Columbia | 1 | 2 | — |
| THE ALS ASSOCIATION | — | Virginia | 1 | 2 | — |
Firms
Registrants who filed on the bill, by filings.
| Registrant | Clients | Filings | Reported |
|---|---|---|---|
| I AM ALS | 1 | 2 | — |
| THE ALS ASSOCIATION | 1 | 2 | — |
Lobbyists
Named on the filings that cite the bill.
| Lobbyist | Firms | Clients | Filings |
|---|---|---|---|
| DANIEL CRAMER | 1 | 1 | 2 |
| DENISE DEMICHELE-BAILIN | 1 | 1 | 2 |
| DUSTIN WATSON | 1 | 1 | 2 |
Filings
The documents themselves, on the Senate’s Lobbying Disclosure site, largest reported first.
| Client | Registrant | Period | Reported | Document |
|---|---|---|---|---|
| THE ALS ASSOCIATION | THE ALS ASSOCIATION | 2026 second_quarter | $30K | 2nd Quarter - Report |
| I AM ALS | I AM ALS | 2026 second_quarter | $30K | 2nd Quarter - Report |
| I AM ALS | I AM ALS | 2026 first_quarter | $30K | 1st Quarter - Report |
| THE ALS ASSOCIATION | THE ALS ASSOCIATION | 2026 first_quarter | $30K | 1st Quarter - Report |
Classification
The Congressional Research Service files H.R. 7336 under Health, one of its 31 policy areas.
CRS Subjects
CRS assigns every bill one policy area from its 31; H.R. 7336’s is Health.
hr7336/policy-areas.txtConstitutional authority
The clause the sponsor cites as Congress’s power to enact H.R. 7336, as entered in the Congressional Record.
[Congressional Record Volume 172, Number 24 (Tuesday, February 3, 2026)][House]From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]By Ms. SCHAKOWSKY:H.R. 7336.Congress has the power to enact this legislation pursuantto the following:Section 8 of article 1 of the Constitution[Page H1976]
Source: congress.gov · legiscan.com
