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.

< September 2024 >
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8 9 10 11Los 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 NC 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. https://www.hopeforhs.org/espanol info@hopeforhs.org + Google calendar New York (In Person)New York (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
https://www.hopeforhs.org/NY2024 northwellhopehs@gmail.com + Google calendar
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22 23 24 25 26Connecticut (Virtual) 6:30 PM ESTConnecticut (Virtual) 6:30 PM ESTJoin us for a virtual patient support group meeting hosted by physicians at UConn Dermatology https://hopeforhs.org/ct2024 uconn@hopeforhs.org + Google calendar 27 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.