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.

< August 2024 >
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11 12 13 14 15Birmingham (Virtual) – 5:30 PM CSTBirmingham (Virtual) – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter + Google calendar Connecticut (Virtual) 6:30 PM ESTConnecticut (Virtual) 6:30 PM ESTJoin us for a virtual patient support group meeting hosted by physicians at UConn Dermatology + Google calendar 16 17
18Community Meetup Night Owl (Virtual) – 9:00 PM EasternCommunity Meetup Night Owl (Virtual) – 9:00 PM EasternJoin us for a meeting to socialize with other patients and family members. + Google calendar 19 20 21 22 23 24
25 26 27 28Hope for HS Hershey Chapter (Virtual) (5:30 PM EST)Hope for HS Hershey Chapter (Virtual) (5:30 PM EST)Support Group hosted by the Hershey Chapter + Google calendar 29Detroit 6:00 – 8:00 PM Eastern (In Person)Detroit 6:00 – 8:00 PM Eastern (In Person)Join us for free dinner and and in person meeting hosted by our Detroit chapter! Gilmour Auditorium @ 1 Ford Place, Detroit, MI 48202 + Google calendar 30 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.