An online experience focused on people affected by HS
presented by the Hidradenitis Suppurativa Foundation

We are excited to announce the HS Foundation’s second annual virtual patient-focused meeting, April 28-29, 2023! The agenda has been carefully crafted to include participants from across the globe.

Our hope is that the Spotlight HS program will be even larger than last year and make more of an impact for those affected by HS, and we hope you’ll join us as we take our mission to the next level. 

Can't make it on these dates? Don't fret! All sessions will be made available within 24 hours so you can watch them on-demand at your leisure!

Registration is FREE!

For physicians interested in this meeting:

While we appreciate your interest, this is a meeting for patients and caregivers. You may be interested in our meeting for healthcare providers, the SHSA. 


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About Us

The Hidradenitis Suppurativa Foundation is a non-profit organization improving the lives of people affected by HS through advocacy, education and research.

Since our founding in 2005, the Hidradenitis Suppurativa Foundation (HSF) has fostered and encouraged worldwide research by developing and supporting an interdisciplinary family of scientists and physicians and people with HS.

The HS Summit is our newest educational program and will provide educational activities with an integrative and innovative approach for people with HS.