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.

< February 2025 >
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9 10 11 12DC (Virtual) – 7:00 PM ESTDC (Virtual) – 7:00 PM ESTJoin us for a virtual patient support group meeting hosted by medical students and physicians at Georgetown University Hospital and Howard University Hospital https://hopeforhs.org/regDC dc@hopeforhs.org + Google calendar 13New England (Virtual) – 6:30 PM ESTNew England (Virtual) – 6:30 PM ESTJoin us for a virtual patient support group meeting hosted by physicians from the New England area.
Topic: Healthy Habits and Nutrition: The HS Connection.
https://hopeforhs.org/signupNewEngland newengland@hopeforhs.org + Google calendar
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23 24 25HS Parent Connection (Virtual) (8:00 PM Eastern)HS Parent Connection (Virtual) (8:00 PM Eastern)Virtual meeting of Hope for HS in partnership with HS Connect. These meetings are intended for parents of teenaged persons living with hidradenitis suppurativa. https://hopeforhs.org/parentmtgsignup teenchapter@hopeforhs.org + Google calendar 26 27Teen Support Group (Virtual) (8:00 PM Eastern)Teen Support Group (Virtual) (8:00 PM Eastern)Virtual meeting of the Hope for HS Teens Chapter in partnership with HS Connect. These meetings are intended for teenaged persons living with hidradenitis suppurativa. https://hopeforhs.org/teenMtgSignup teenchapter@hopeforhs.org + Google calendar 28  
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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.