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.

< July 2023 >
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9 10New England (Virtual) 7:00 PM ESTNew England (Virtual) 7:00 PM ESTVirtual Support Group Meeting Hosted by the New England Chapter https://hopeforhs.org/NewEng01 + Google calendar 11 12Hershey (Virtual) 5:30 PM ESTHershey (Virtual) 5:30 PM ESTVirtual Support Group Meeting Hosted by the Hershey Chapter https://hopeforhs.org/Hershey01 + Google calendar Los 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://redcap.med.usc.edu/surveys/?s=HR9MPFJTKHRTWWTF + Google calendar 13Birmingham (Virtual) – 5:30 PM CSTBirmingham (Virtual) – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter https://hopeforhs.org/birmreg + Google calendar 14 15
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23 24 25North Carolina (Virtual) 8:00 PM ESTNorth Carolina (Virtual) 8:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter https://www.hopeforhs.org/NC01 + Google calendar 26 27 28 29
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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.