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Expressing support for the designation of June 1, 2026, through June 7, 2026, as "Hidradenitis Suppurativa Awareness Week".
Expressing support for the designation of June 1, 2026, through June 7, 2026, as ``Hidradenitis Suppurativa Awareness Week''.
Summary
- Expresses support for designating June 1-7, 2026 as "Hidradenitis Suppurativa Awareness Week"
- Recognizes the importance of increasing public awareness and education about Hidradenitis Suppurativa among the public and health professionals
- Recognizes the importance of promoting timely and accurate diagnosis of the disease through improved screening and culturally competent care
- Recognizes the importance of supporting biomedical research to better understand the disease and improve treatment options
- Recognizes the importance of accelerating development of effective treatments and policies that improve access to care for people living with the disease
AI-generated plain-language summary of the bill text — neutral, and may be imperfect. See the full text below for the exact wording.
Sponsor (1)
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Rep. Dingell, Debbie (D-MI) [#6]
1 cosponsor
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Rep. Joyce, John (R-PA) [#13]
Money behind the sponsor
Top reported contributors to Debbie Dingell’s campaign committee (2024 cycle) — who funds the bill’s sponsor, not a claim about this bill. Data from FEC.
- UNIVERSITY OF MICHIGAN $24,944
- THE WONDERFUL COMPANY $13,200
- Employer not reported $9,900
- ANN ARBOR EDUCATIONAL FOUNDATION $6,600
- DAKKOTA INTREGRATED SYSTEMS LLC $6,600
Organizations whose employees gave the most — itemized individual contributions grouped by the donor’s reported employer (FEC Schedule A). Full finance for Debbie Dingell → · Outside spending →
Actions (2)
- Jun 2, 2026 Referred to the House Committee on Energy and Commerce. · house
- Jun 2, 2026 Submitted in House
Similar bills (6)
Bills with similar text or summary — includes reintroductions across Congresses. Ranked by semantic similarity of the bill text (computed locally); a neutral discovery aid, not a claim the bills are duplicates.
Text versions (1)
Bills are re-published as they move (Introduced → Reported → Engrossed → Enrolled …). Each stage below is a separate text; pick two to see what changed. Data from Congress.gov.
Full text
IN THE HOUSE OF REPRESENTATIVES
June 2, 2026
Mrs. Dingell (for herself and Mr. Joyce of Pennsylvania) submitted the following resolution; which was referred to the Committee on Energy and Commerce
RESOLUTION
Expressing support for the designation of June 1, 2026, through June 7, 2026, as “Hidradenitis Suppurativa Awareness Week”.
Whereas Hidradenitis Suppurativa (in this resolution referred to as “HS”) is a chronic, inflammatory skin disease that affects approximately 3,300,000 people in the United States; Whereas HS causes painful, boil-like nodules and abscesses anywhere on the body, and can progress to form tunnels under the skin and cause extensive scarring; Whereas individuals with HS frequently suffer from 5 primary domains of physical and emotional suffering, pain, drainage, odor, itching, and profound psychological distress; Whereas HS is associated with one of the highest completed suicide rates among dermatological diseases, second only to melanoma; Whereas 75 percent of individuals with HS are misdiagnosed or not diagnosed until after age 25, missing critical windows for early intervention and care; Whereas delayed diagnosis contributes to worsening disease progression, higher healthcare costs, avoidable emergency room visits, and unnecessary procedures; Whereas individuals are often diagnosed with HS in the prime of their lives, affecting their ability to work, maintain relationships, and participate fully in society; Whereas there are currently only 3 biologic therapies approved by the Food and Drug Administration for the treatment of HS; Whereas additional research is urgently needed to develop new treatments, understand the pathogenesis of the disease, identify biomarkers of HS, and improve outcomes for HS patients; Whereas Federal policy can play a critical role in improving access to biologic therapies, wound care, and comprehensive care for HS patients; and Whereas designating the first week of June as “Hidradenitis Suppurativa Awareness Week” would increase public awareness, foster understanding, and catalyze progress in diagnosing, treating, and ultimately curing HS: Now, therefore, be it Resolved, That the House of Representatives—
(1) supports the designation of “Hidradenitis Suppurativa Awareness Week”; and
(2) recognizes the importance of—
(A) increasing awareness and education about HS among the public and health professionals;
(B) promoting timely and accurate diagnosis of HS through improved screening and culturally competent care;
(C) supporting biomedical research to better understand HS pathogenesis, treatment efficacy, and long-term outcomes;
(D) accelerating the development of effective treatments and expanding access to existing therapies for HS; and
(E) advancing policies that improve access to care and quality of life for people living with HS and their caregivers. <all>
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