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.

< October 2026 >
SundayMondayTuesdayWednesdayThursdayFridaySaturday
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4 5 6 7 8New England (Virtual) (6:30 PM EST)New England (Virtual) (6:30 PM EST)Join us for a virtual patient support group meeting hosted by physicians from the New England area.
Topic: Open Community Chat
Registration Link: https://hopeforhs.org/signupNewEngland Email for More Info: newengland@hopeforhs.org + Google calendar
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11 12 13 14DC (Virtual) (7:00 PM EDT)DC (Virtual) (7:00 PM EDT)Join us for a virtual patient support group meeting hosted by medical students and physicians at Georgetown University Hospital and Howard University Hospital Registration Link: https://hopeforhs.org/regDC Email for More Info: dc@hopeforhs.org + Google calendar 15Birmingham (Virtual) (5:30 PM CST)Birmingham (Virtual) (5:30 PM CST)Virtual Support Group Meeting Hosted by the Birmingham, AL Chapter Registration Link: https://hopeforhs.org/birminghamReg Email for More Info: birmingham@hopeforhs.org + Google calendar 16 17
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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.