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.
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| Sunday | Monday | Tuesday | Wednesday | Thursday | Friday | Saturday | |||
| 1 | 2 | 3 | 4 | ||||||
| 5 | 6 | 7 | 8Los 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 | 9 | 10 | 11 | |||
| 12 | 13North Carolina (Virtual) 8:00 PM ESTNorth Carolina (Virtual) 8:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter https://hopeforhs.org/nc2024 info@hopeforhs.org + Google calendar | 14 | 15 | 16 | 17 | 18 | |||
| 19 | 20 | 21 | 22 | 23 | 24 | 25 | |||
| 26 | 27 | 28 | 29 | 30 | 31 | ||||
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.