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LAST ACTION SEP 23, 2026  UPDATED SEP 30
S. 5488SENATE BILL · 119TH CONGRESS119TH

Sickle Cell Disease Treatment Centers Act of 2026

Creates grants for networks that coordinate sickle cell disease care and community support.

WHERE IT STANDS

In the Senate Health, Education, Labor, and Pensions Committee since Sept. 23, 2026, 15 days after it was introduced. Most bills never leave committee.

  1. INTRODUCEDINTROSEP 23, 2026
  2. COMMITTEECOMM.IN COMMITTEE
  3. SENATESENATE—
  4. HOUSEHOUSE—
  5. LAWLAW—
Read the text
WHAT IT DOES

What the bill would do, and why it matters

BASED ON THE TEXT AS INTRODUCED
tl;drWRITTEN OCT 4 FROM THE TEXT AS INTRODUCED

Sickle cell disease can require ongoing care from multiple providers and support beyond medical treatment. The bill would fund networks linking medical centers, local providers, and community nonprofits to coordinate care and support. It would also create a national coordinating center and expand data collection on care and health outcomes.

  • INTRODUCED ONLY This bill has been introduced and possibly referred to a committee, but it has not passed any vote. Most introduced bills never become law — they die in committee without a hearing.
  • DATA NOTE No Congressional Research Service summary was available.
WHAT IT WOULD DO · 5 PROVISIONSINTRODUCED IN SENATE
  1. Creates treatment-center grants

    The Secretary of Health and Human Services would award grants to networks that connect a medical hub, at least one spoke, and a community-based nonprofit. The networks would coordinate care for people with sickle cell disease and other heritable hemoglobin disorders.

  2. Supports care and community services

    Grant funds could support coordinated medical and mental health care, provider education, telehealth, and the transition from pediatric to adult care. Funds could also help patients with insurance costs, transportation, social supports, and access to testing and genetic counseling.

  3. Sets up national coordination

    The Secretary would establish a National Sickle Cell Disease Coordinating Center to support grantees, develop a national care strategy, coordinate research and data efforts, and provide technical assistance and public education.

  4. Expands data collection and reporting

    The CDC would coordinate and maintain data on sickle cell disease, related health outcomes, complications, and treatment. The Secretary would report to Congress on the centers’ activities, the patients served, and patient experiences.

  5. Guides where grants go

    The Secretary would focus grant awards, to the extent practicable, on regions with higher per-capita numbers of affected patients and on nationwide access. The Secretary could give priority to eligible networks serving areas with high prevalence or rural areas, or including a qualifying historically Black college or university or minority-serving institution.

THE CONTEXT

The bill’s stated aims include making care more coordinated throughout patients’ lives, improving the transition from pediatric to adult care, and strengthening public awareness and health data. The practical stakes are whether patients can access connected medical care and related community support through a national grant program.

Written from the bill text.

KEY DATES
WITHIN 180 DAYS AFTER ENACTMENT
Secretary publishes a request for stakeholder input
3 YEARS AFTER ENACTMENT
Secretary reports on treatment centers’ impact
EVERY 5 YEARS THEREAFTER
Secretary submits later impact reports
BEFORE EACH NEW GRANT CYCLE
Secretary publishes input request before each new grant cycle
TEXT VERSIONS
  1. ISIntroduced in SenateSEP 23, 20262,759
THE JOURNEY

The path it took, step by step

FROM THE OFFICIAL ACTIONS ON CONGRESS.GOV
  1. IntroducedSEP 23, 2026
    SENATE
    SEP 23, 2026
    By Sen. Hollen with 2 original cosponsors
    Referred to Health, Education, Labor, and Pensions
  2. SAME DAYNOW
    Senate committeeSEP 23, 2026
    HEALTH, EDUCATION, LABOR, & PENSIONS NOW
    SEP 23, 2026
    In committee for 15 days
    No hearing yet
  3. 15 DAYS SO FAR
    Passed the Senate—
    SENATE FLOOR
    —
    Not scheduled
  4. House committee—
    HOUSE
    —
  5. Passed the House—
    HOUSE FLOOR
    —
    Not scheduled
  6. Resolve differencesONLY IF NEEDED
    BOTH CHAMBERS
    ONLY IF NEEDED
    Skipped if the other chamber passes the same text
  7. Signed into law—
    PRESIDENT
    —
    10 days to sign or veto
KEY ACTIONS2 OF 2 · PROCEDURAL STEPS FOLDED
  1. SEP 232026SEP 23, 2026REFERREDRead twice and referred to the Committee on Health, Education, Labor, and Pensions.
  2. SEP 232026SEP 23, 2026INTRODUCEDSENATEIntroduced in Senate
HOW LONG LAWS TAKE119 LAWS THIS CONGRESS

At day 15, this bill is already older than 4% of the laws passed this Congress were when they were signed.

DAYS FROM INTRODUCTION TO SIGNING · ○ CEREMONIAL
YOUR MEMBERS

Where your members stand on it

WHO’S BEHIND IT · 2 COSPONSORS

A coalition from 2 states

PARTY MIX
0 REPUBLICANS2 DEMOCRATS

Plus the sponsor, a Democrat. Every cosponsor is from one party.

COSPONSORS BY STATEEACH BAR IS ONE OF THE STATE’S TWO SENATORS
AK
ME
VT
NH
WA
ID
MT
ND
MN
IL
WI
MI
NY
RI
MA
OR
NV
WY
SD
IA
IN
OH
PA
NJ
CT
CA
UT
CO
NE
MO
KY
WV
VA
MD
DE
AZ
NM
KS
AR
TN
NC
SC
OK
LA
MS
AL
GA
HI
TX
FL
DEMOCRATDEMREPUBLICANREPINDEPENDENTINDSPONSORNOT A COSPONSORNONE
PARTY MIX
0 REPUBLICANS2 DEMOCRATS

Plus the sponsor, a Democrat. Every cosponsor is from one party.

MOMENTUM
SEP 2026 · 2 ORIGINALNOW · 2

Sen. Van Hollen’s record: sponsored 76 bills this Congress. 1 passed the Senate; 0 became law.

EVERY COSPONSOR · IN THE ORDER THEY JOINED2 ACTIVE
READERS · 0 COMMENTS

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READERS’ VIEWS, NOT CHAMBERLIGHT’S

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