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.

< September 2023 >
SundayMondayTuesdayWednesdayThursdayFridaySaturday
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10 11 12 13Los 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 14Birmingham (Virtual) – 5:30 PM CSTBirmingham (Virtual) – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter + Google calendar North Carolina (Virtual) 7:00 PM ESTNorth Carolina (Virtual) 7:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter + Google calendar 15 16
17 18 19Holistic Approaches to Treating HS (Virtual) (8:00 pm EST)Holistic Approaches to Treating HS (Virtual) (8:00 pm EST)Join Dr. Steve Daveluy for a Special Presentation:
Holistic Approaches to Treating HS: Exploring the Mind Body Connection and the effects of Battlefield Acupuncture
+ Google calendar
20Hershey (Virtual) 5:30 PM ESTHershey (Virtual) 5:30 PM ESTVirtual Support Group Meeting Hosted by the Hershey Chapter + Google calendar 21 22 23
24 25 26 27 28 29 30
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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.