The Hidradenitis Suppurativa Foundation (HSF) and Canadian Hidradenitis Suppurativa Foundation (CHSF) are proud to offer two unique opportunities to engage with the 11th Annual Symposium on Hidradenitis Suppurativa Advances (SHSA), taking place November 6–8, 2026 in Tucson, Arizona.
Whether you're a patient looking to attend or someone passionate about sharing knowledge and experiences, we invite you to apply.
Application Deadline: July 31, 2026
Notification Date: August 17, 2026
📣 Social Media Ambassador Program
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.
Who Should Apply
Members of the HS community, including:
- Patients
- Caregivers
- Clinicians
- Researchers
- Medical students and trainees
- Advocates
What You’ll Do
- Share live updates, takeaways, and reflections from SHSA
- Create engaging content across Instagram, LinkedIn, and/or Facebook
- Amplify voices, research, and community experiences
What You’ll Receive
✅ 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
💜 Patient Scholarship Program
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.
Who Should Apply
Applicants must:
- Be diagnosed with hidradenitis suppurativa (HS). Please have the form completed and ready prior to submitting your application. LINK FORM HERE
- Be able to attend SHSA in person from November 6–8, 2026
- Have an interest in learning more about HS research, care, and community
What to Expect
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.
What You’ll Receive
✅ Complimentary SHSA 2026 registration
✅ Two nights of lodging
✅ Travel reimbursement based on the HS Foundation Travel & Reimbursement Guidelines