Hidradenitis Suppurativa (HS) is a debilitating, chronic, complex inflammatory illness, also referred to as an immune-mediated inflammatory illness and follicular occlusion.

 

It has a huge impact on the quality of life physically, mentally, and emotionally. HS consists of extremely painful recurring abscesses that can develop anywhere hair follicles are found.  It is possible to experience abscesses or lesions anywhere on our body with the exception of the palms of your hands, soles of your feet, and lips.

 

HS is not contagious. There are three Hurley stages used to determine severity.  There is no cure for HS and the options for treatment are limited.

WHAT IS HIDRADENITIS SUPPURATIVA or HS?​

CONNECT WITH OUR CAUSE

We strive to provide the HS community with knowledge, resources, research, and more, but can't do it without you. Please take the time to read our mission,

share our cause, join us in being heard, and if possible, please donate.

 

You can read about our mission,

goals of our organization and website below

Donate time or money to our mission to further HS awareness and research

*HS Connect is a 501c3; donations are tax deductible

CLINICAL TRIALS | studies | surveys

PARTICIPATE LIKE THE FUTURE OF HS DEPENDS ON IT, BECAUSE IT DOES.

Clinical trials, studies, and surveys are of the utmost importance to further the study of HS.  Please review the open opportunities by clicking below and reaching out to participate.  We cannot do this without YOU!!  

TELL US ABOUT YOU

We want to hear from you! 

Tell us about your experience with HS, how you've overcome or how you deal with having this disease.  We will post your submission on the ' Our Stories' page.

Please allow 5-7 days for your story to be posted. 

If you would like to submit a photo as well, please email to contact@hsconnect.org