Educational content from HS experts
Those living with hidradenitis suppurativa often have questions about their condition. These resources are here to help patients, their loved ones, and your own practice through education, compassion, and awareness.
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Understanding HS
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Identifying and Diagnosing HS
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Managing and Treating HS
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Support and Resources for HS
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Addressing Health Equity in HS
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Delivering the Diagnosis
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Understanding and Advancements
ACT on HS
EXPLORE HS
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Discussions in HS:
Diagnostic Delays in HS
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Discussions in HS: The Need for Earlier HS Diagnosis and Treatment
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Discussions in HS: HS Treatment Landscape
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Discussions in HS: Considerations for Biologic Therapy in HS
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Discussions in HS: Multidisciplinary Considerations in HS Care
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The Mechanism of Disease
The healthcare providers featured in these videos and podcasts were compensated for their time. These videos and podcasts represent their opinions and do not represent the opinions of Novartis.
Downloadable resources
Spread the word on social
media
Support the early recognition of HS and help shed light on better outcomes. Share these facts on your social media.
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It's time for the
medical community
to rally and
#ShineALightOnHS
A website specifically for patients
Shine a Light on HS is an educational website designed specifically for patients with HS in mind. This site contains information and resources for patients to learn more about their condition.
Visit Patient SiteNational organizations for patient support
The following organizations offer an array of support for those affected by HS. Whether you're diagnosing or referring, you can help patients connect with the care they may need.
HS Connect
HS Connect is a patient-led nonprofit organization committed to connecting the hidradenitis suppurativa community, including patients, family, and clinicians, with resources, support, and solutions. Visit website
HS Foundation
See how healthcare professionals like you can have meaningful and personalized conversations with their patients. Visit website
AAD
The American Academy of Dermatology (AAD) may provide helpful information for patients living with HS and their loved ones. Visit website
Hope for HS
Hope for HS is a 100% volunteer, grass-roots, patient- and caregiver-directed non-profit organization, supporting and advocating for patients with HS. Visit website
The organizations and websites listed above are independently operated and not managed by Novartis Pharmaceuticals Corporation. Novartis assumes no responsibility, nor makes any endorsement, regarding information they may provide.
Understanding the systemic nature
of HS can support earlier diagnosis
Make a referral and find an HS-treating
dermatology provider using the care locator
Reference: 1. Sabat R et al. Nat Rev Dis Primers. 2020;6(1):18.
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