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.

< April 2024 >
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  1 2 3NC 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 4Detroit 6:00 – 8:00 PM Eastern (In Person)Detroit 6:00 – 8:00 PM Eastern (In Person)Join us for free dinner and and in person meeting hosted by our Detroit chapter! Gilmour Auditorium @ 1 Ford Place, Detroit, MI 48202 detroithopeforhs@gmail.com + Google calendar 5 6
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21 22 23 24 25Dallas (Virtual) ( 6:00 PM Central)Dallas (Virtual) ( 6:00 PM Central)Virtual Support Group Meeting Hosted by the Dallas Chapter https://www.hopeforhs.org/dallas01 dallashopeforhs@gmail.com + Google calendar 26 27
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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.