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This site provides educational information only, not medical advice. Always consult a qualified healthcare provider.
Workplace Resource Center

Hidradenitis Suppurativa
in the Workplace

Practical, honest guidance for navigating work with HS. From requesting accommodations to managing flares during a shift, this resource center covers what you actually need to know.

Important: This resource provides general educational information only. It is not legal advice. Employment law varies significantly by location, employer size, and individual circumstances. For questions about your specific legal rights, consult a qualified employment attorney or disability rights organization.

Why This Resource Exists

HS affects approximately 1% of the population, meaning millions of people are managing it in the workplace every day.

HS is recognized as a qualifying disability under the Americans with Disabilities Act (ADA) in many cases, depending on severity and impact on major life activities.

Fatigue, chronic pain, and unpredictable flares are among the most reported workplace challenges for people with HS.

Studies show HS has the highest Dermatology Life Quality Index (DLQI) score of any skin condition, reflecting its profound impact on daily functioning.

Many HS patients delay disclosing their condition to employers due to stigma and fear of discrimination.

Explore the Resource Center

Each section below is a standalone guide. Start with the topic most relevant to your situation right now.

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