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

Thank you to everyone who joined us for the HS Foundation’s second annual virtual patient-focused meeting, April 28-29, 2023! 


If you were unable to make it to the live meeting, don't fret! All sessions are available 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. 



Thank you to our sponsors!

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.