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 2026 >
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11 12 13 14Los Angeles (Virtual) ( 6:00 PM PST)Los Angeles (Virtual) ( 6:00 PM PST)Virtual Support Group Meeting Registration Link: https://hopeforhs.org/regLA Email for More Info: Dermatology@med.usc.edu + Google calendar 15Detroit (In-Person) (6:00 PM EST)Detroit (In-Person) (6:00 PM EST)Time: 6:00 pm – 8:00 pm
We are pleased to welcome Jasmine Espy, Founder and CEO of the Association of Hidradenitis Suppurativa and Inflammatory Diseases (AHSID), who will be giving a talk at this meeting followed by a yoga session. Henry Ford Health
1 Ford Place
Detroit, MI 48202
Gilmour Auditorium Map+ Google calendar
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18 19 20 21 22Iowa City (Virtual) (12:30 PM Central)Iowa City (Virtual) (12:30 PM Central)Join us for a virtual patient support group meeting hosted by medical students and physicians at University of Iowa.
Topic: All about HS
Registration Link: https://hopeforhs.org/regIowaCity Email for More Info: iowaCity@hopeforhs.org + Google calendar
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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.