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.

< January 2024 >
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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 https://www.hopeforhs.org/LAReg Dermatology@med.usc.edu + Google calendar 11[CANCELLED] North Carolina (Virtual) 6:00 PM EST[CANCELLED] North Carolina (Virtual) 6:00 PM EST[WILL BE RESCHEDULED]
Virtual Support Group Meeting Hosted by the North Carolina Chapter
info@hopeforhs.org + Google calendar
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14 15 16 17 18Birmingham (Virtual) – 5:30 PM CSTBirmingham (Virtual) – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter https://hopeforhs.org/birmingham03 + Google calendar 19 20
21 22 23 24 25North Carolina (Virtual) 6:00 PM ESTNorth Carolina (Virtual) 6:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter https://hopeforhs.org/nc012024 info@hopeforhs.org + Google calendar 26 27
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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.