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.
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
| A website specifically for patientsShine 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.
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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.
