*Open to US and Canadian residents only.
Help bring SHSA to life by sharing the experience in real time.
For the first time, SHSA will include a group of official Social Media Ambassadors—individuals from across the HS community who will highlight key moments, insights, and conversations throughout the conference.
Members of the HS community, including:
✅ Complimentary SHSA 2026 registration
✅ Two nights of lodging
✅ Behind-the-scenes access to leading HS discussions
✅ Opportunities to connect and grow your voice within the community
The Hidradenitis Suppurativa Foundation (HSF) and Canadian Hidradenitis Suppurativa Foundation (CHSF) are pleased to offer the SHSA 2026 Patient Scholarship Program, designed to make the Symposium on Hidradenitis Suppurativa Advances (SHSA) more accessible to individuals living with HS.
While SHSA is a scientifically focused meeting for clinicians and researchers, we recognize how valuable this experience is for patients. Many attendees living with HS find the opportunity to hear directly from experts, learn about emerging research, and connect with others in the community both empowering and meaningful.
This program aims to reduce financial barriers and support patients who are interested in attending SHSA in person.
Applicants must:
As a Patient Scholar, you will have the opportunity to:
✅ Attend educational and scientific sessions
✅ Gain insight into current and emerging HS research
✅ Hear directly from leading clinicians and experts
✅ Connect with others in the HS community including providers, patients, and industry representatives
✅ Experience a conference environment dedicated to improving HS care
Please note: While some sessions are highly scientific, many patients find value in exposure to the latest developments and perspectives in the field.
✅ Complimentary SHSA 2026 registration
✅ Two nights of lodging
✅ Travel reimbursement based on the HS Foundation Travel & Reimbursement Guidelines