Support, Advocacy, and Awareness for Hidradenitis Suppurativa

Supporting Patients. Advocating for Change. Raising Awareness

We offer a private Facebook group, physician attended virtual support group meetings, community meet ups, and an educational webinar series.

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7 8 9 10Los Angeles (Virtual) ( 6:00 PM PST)Los Angeles (Virtual) ( 6:00 PM PST)Virtual Support Group Meeting Hosted by the Los Angeles, CA Chapter + Google calendar 11North Carolina (Virtual) 5:00 PM ESTNorth Carolina (Virtual) 5:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter – Dr. Jaleel presenting + Google calendar 12 13
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21Atlanta (Virtual) 2:00 PM ESTAtlanta (Virtual) 2:00 PM ESTVirtual Support Group Meeting Hosted by the Atlanta, GA Chapter + Google calendar 22 23 24 25 26 27
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 Los Angeles
 New England
 New York
 North Carolina
 Spanish Language
 Washington DC
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Supporting Patients

Our support groups relieve some of the
tremendous isolation and emotional burden that accompanies a life with Hidradenitis Suppurativa.

Advocating for Change

We empower the HS community to interact with payers, researchers, and their government to bring about the change needed to someday find a cure.

Raising Awareness

Raising awareness of Hidradenitis Suppurativa is vital in promoting compassion, understanding, and a correct, timely diagnosis.

We are a 100% volunteer, grass-roots, patient and caregiver directed non-profit organization, supporting and advocating for HS patients since 2013.