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.

< March 2023 >
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5 6 7 8Los Angeles Virtual Meeting – 6:00 PM PSTLos Angeles Virtual Meeting – 6:00 PM PSTVirtual Support Group Meeting Hosted by the Los Angeles, CA Chapter + Google calendar 9Birmingham Virtual Meeting – 5:30 PM CSTBirmingham Virtual Meeting – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter + Google calendar Birmingham Virtual Meeting – 5:30 PM CSTBirmingham Virtual Meeting – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter + Google calendar 10 11
12 13 14 15Hershey – 5:30 PM ESTHershey – 5:30 PM ESTVirtual Support Group Meeting Hosted by the Hershey Chapter + Google calendar NC Virtual Meeting – 6:30 PM ESTNC Virtual Meeting – 6:30 PM ESTVirtual Support Group Meeting Conducted by the NC Chapter. + Google calendar 16 17 18
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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.