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Bills/119th Congress · House

H.Res. 1331

Introduced

Expressing support for the designation of June 1, 2026, through June 7, 2026, as "Hidradenitis Suppurativa Awareness Week".

Sponsor
DDebbie Dingell· Michigan
Introduced
June 2, 2026
Policy area
Health
Latest action
Referred to the House Committee on Energy and Commerce.June 2, 2026
[Congressional Bills 119th Congress]
[From the U.S. Government Publishing Office]
[H. Res. 1331 Introduced in House (IH)]

<DOC>

119th CONGRESS
2d Session
H. RES. 1331

Expressing support for the designation of June 1, 2026, through June 7, 
2026, as ``Hidradenitis Suppurativa Awareness Week''.

_______________________________________________________________________

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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