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 2024 >
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10 11 12 13Los 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 14Birmingham (Virtual) – 5:30 PM CSTBirmingham (Virtual) – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter https://hopeforhs.org/birmingham03 birmingham@hopeforhs.org + Google calendar 15 16
17 18 19Hope for HS New York Chapter (In Person)Hope for HS New York Chapter (In Person)Time: 6:00 pm
Join us in New York as Hope for HS New York hosts their inaugural meeting! 1991 Marcus Ave, Suite 300
New Hyde Park, NY 11042
https://www.hopeforhs.org/NY032024 northwellhopehs@gmail.com + Google calendar
20Minnesota (Virtual) (6:00 PM – 7:30 PM Central)Minnesota (Virtual) (6:00 PM – 7:30 PM Central) https://www.hopeforhs.org/minnesotamtg Minnesota@HopeforHS.org + Google calendar 21 22 23
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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.