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NEWS ARCHIVE
Explore our archive of news and updates from the HS Foundation — a curated collection of stories, milestones, and announcements from over the years.
Managing the Psychological Toll of HS
April 24, 2026
Living with hidradenitis suppurativa can take a serious emotional toll—from anxiety and depression to challenges with self-esteem, relationships, and daily life. This article explores why mental health support is a critical part of HS care and offers insight into recognizing, addressing, and treating the psychological burden of the disease. Click to read why caring for your mind matters as much as caring for your skin.
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Understanding Hidradenitis Suppurativa: What You Need to Know
April 24, 2026
Painful lumps, flare-ups in skin folds, delayed diagnosis—hidradenitis suppurativa can be confusing, frustrating, and life-altering. This patient-friendly FAQ explains what HS is (and what it isn’t), who is at risk, why it’s so often misdiagnosed, and what treatment options are available. Click to learn the essential facts every person living with HS should know.
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From Reactive to Proactive: Building Longitudinal Care Plans That Actually Work for Hidradenitis Suppurativa
April 17, 2026
What if dermatologic care didn’t stop at the flare? Discover why shifting from reactive treatment to proactive, longitudinal care plans can lead to better outcomes, stronger patient relationships, and management strategies that truly stand the test of time.
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Beyond the Surface: April 2026
April 10, 2026
Catch the latest from the Hidradenitis Suppurativa Foundation—Board leadership updates, new HS research insights, upcoming clinical guidelines, featured resources, and key events on the horizon.
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Expert Insights on HS: What Every Patient Should Know About Today’s Treatment Landscape
April 1, 2026
In a new episode of the Derms on Drugs podcast, leading dermatology experts discuss the evolving understanding of hidradenitis suppurativa, including treatment strategies, emerging therapies, and what real progress looks like for patients. Tune in to hear practical insights that shed light on where HS care is headed and how it continues to change lives.
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A New Era of Hope for HS: Personalized Treatments Are Changing the Outlook
March 31, 2026
What if HS care could be tailored to you? At the 2026 AAD Annual Meeting, dermatology experts shared how personalized combinations of medical and in‑office surgical treatments are improving outcomes and bringing new hope to people living with moderate to severe hidradenitis suppurativa. Learn how these advances could shape the future of HS care and why they matter now.
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Raising the Bar for HS Outcomes With Barry Resnik, MD
March 15, 2026
Years-long diagnostic delays and incremental treatment approaches have left many patients struggling. Barry Resnik shares how earlier escalation, clearer treatment goals, and a focus on function, not just lesions, could change the trajectory of hidradenitis suppurativa care.
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Standardization of Lesion Classification and Assessment by Investigators in Clinical Trials for Hidradenitis Suppurativa
March 5, 2026
A team of dermatology experts has just agreed on a standardized way to identify and classify HS lesions, potentially transforming how clinical trials measure disease and evaluate treatments. Find out how this new consensus could reshape research and bring us closer to better therapies.
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Understanding Moderate Hidradenitis Suppurativa: Diagnosis, Impact, and Treatment
February 25, 2026
Explore why early recognition and tailored care are vital for patients with moderate hidradenitis suppurativa. This Dermatology Times piece breaks down key challenges in diagnosis, the real impact on quality of life, and evolving treatment strategies, including when to consider systemic and biologic therapies to prevent disease progression.
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“I Lost 15 Years of My Life”: A Man’s Journey With Hidradenitis Suppurativa
February 25, 2026
In a revealing interview conducted by The Educated Patient, Keven Brown opens up about his long, painful battle with hidradenitis suppurativa — from years of misdiagnosis and physical hardship to the emotional toll of living with a chronic condition and the resilience it took to reclaim his life.
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Do GLP-1 medications help signs and symptoms of Hidradenitis Suppurativa?
February 23, 2026
Could a medication commonly used for type 2 diabetes and weight loss also help improve hidradenitis suppurativa? New research explores the potential impact of GLP-1 receptor agonists on HS signs, symptoms, and quality of life. Click to learn what researchers found and what it could mean for people living with HS.
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Hidradenitis Suppurativa in Patients with Skin of Color: Emerging Therapies and Strategies for Effective Management
January 22, 2026
New insights highlight emerging therapies and practical strategies for managing hidradenitis suppurativa in patients with skin of color. Learn how evolving treatments, improved diagnostic approaches, and patient-centered care are reshaping HS management and addressing long-standing gaps in care.
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Timing, Severity, and Therapeutic Choice in Moderate to Severe HS
January 14, 2026
When should HS treatment escalate? This case-based discussion with HS Foundation board member, Dr. Afsaneh Alavi, explores how timing, severity assessment, and therapeutic choice shape outcomes in moderate to severe hidradenitis suppurativa.
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Beyond the Surface: January 2026
January 13, 2026
Catch the latest from the Hidradenitis Suppurativa Foundation — explore new HS insights, updated wound care resources, SHSA 2026 details, and apply for the Mentored Experience Grant by January 31.
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New HS Health Resources Available on Educated Patient
January 5, 2026
A new Hidradenitis Suppurativa Health Resources Hub is now available on the Educated Patient website, offering clear, evidence-based information on HS risk factors, signs and symptoms, diagnosis, treatment options, and more.
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Turning Action Plans Into Power: Personalizing Care for Patients With Hidradenitis Suppurativa
December 16, 2025
Learn how personalized action plans can empower patients with hidradenitis suppurativa by improving communication, clarifying flare management, and supporting more proactive, individualized care.
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Hot Off the Press: SHSA 2025 Abstracts Published in Dermatology & Therapy
December 1, 2025
The full collection of abstracts presented at the 10th Annual Symposium on Hidradenitis Suppurativa Advances (SHSA) has officially been published in the open access journal Dermatology & Therapy. This milestone release makes the latest HS research from international clinicians and scientists widely available to the community.
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Why HS Is So Often Misdiagnosed, With Steven Daveluy, M.D.
November 25, 2025
Many people with Hidradenitis Suppurativa (HS) suffer in silence — not because the disease is rare, but because it’s too often misunderstood. In a revealing interview, Dr. Steven Daveluy uncovers the myths, missed signals and clinical blind spots that delay diagnosis and care.
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Danby Research Grant Supports New Insights into HS
November 18, 2025
Support from the HS Foundation’s Danby Research Grant enabled Dr. Fang’s work examining the cellular mechanisms involved in HS. Her findings are helping to clarify how immune structures form in the skin and may inform future targeted treatment approaches.
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Optimizing HS Visits: A Dermatologist’s Guide to Compassionate, Effective Care
November 16, 2025
Pain, stigma, and delays still too often define the journey for patients with Hidradenitis Suppurativa (HS). This feature HSF leader, Dr. Gretchen Roth, in the Dermatologist offers dermatologists a roadmap to turn HS visits into moments of trust-building, actionable care, and real hope. From empathetic communication to tailored management strategies, learn how one clinic’s compassion driven approach can reshape outcomes for this complex condition.
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