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.

< June 2024 >
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9 10 11 12Hope for HS New York Chapter (In Person)Hope for HS New York Chapter (In Person)Time: 6:00 pm
Join us in New York for an in person meeting. Dinner will be provided. 1991 Marcus Ave, Suite 300
New Hyde Park, NY 11042 + Google calendar
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16 17 18 19NC Spanish Language Meeting (Virtual) (6:30 PM EST)NC Spanish Language Meeting (Virtual) (6:30 PM EST)Virtual Support Group Meeting Conducted by the NC Chapter. This meeting will be in Spanish. Reunión del Grupo de Apoyo Virtual Realizada por el Capítulo NC. Esta reunión será en español. + Google calendar 20 21 22
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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.