Be seen.
Find your people.
From in-person community events to virtual support groups, HS Connect events are designed to help people living with hidradenitis suppurativa feel informed, supported, and less alone.
Upcoming in-person events
These are the moments our community comes together in person.
Be Seen Brunch
A for-patients, by-patients community gathering with brunch, HS advocate speakers, a photo booth, and an afternoon of meeting your new HS besties.
Empower HS 2026
Our biggest event of the year, bringing together patients, caregivers, advocates, and healthcare professionals for education, connection, and empowerment.
Join a support group
Free, virtual, and built around the community that fits you. Each card links directly to Zoom registration.
More than a traditional support group
HS Connect support groups are intentionally built around shared lived experience, safety, and community care. They are not formal therapy, and no one is expected to share before they feel ready. Each group creates space for honest conversation, practical encouragement, and connection with people who understand the emotional, physical, and day-to-day reality of living with HS or caring for someone who does.
What happens after I register?
We know joining something new can feel intimidating. Here is what you can usually expect when signing up for an HS Connect event or support group.
1. Register
Choose the event or group that feels right for you and complete the GiveButter or Zoom registration form.
2. Check email
You will receive confirmation details, reminders, and links needed to attend.
3. Join when ready
Attend virtually or in person from a space that feels comfortable to you. You can participate in the way that feels right.
4. Connect safely
HS Connect spaces are designed to be supportive, respectful, and centered on lived experience.