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.

< May 2024 >
SundayMondayTuesdayWednesdayThursdayFridaySaturday
      1 2 3 4
5 6 7 8Los 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 9 10 11
12 13North Carolina (Virtual) 8:00 PM ESTNorth Carolina (Virtual) 8:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter + Google calendar 14 15 16Birmingham (Virtual) – 5:30 PM CSTBirmingham (Virtual) – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter + Google calendar 17 18
19 20 21 22 23 24 25
26 27 28 29 30Dallas (Virtual) ( 6:00 PM Central)Dallas (Virtual) ( 6:00 PM Central)Virtual Support Group Meeting Hosted by the Dallas Chapter + Google calendar 31  
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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.