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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| 7 | 8 | 9 | 10Los 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 | 11North Carolina (Virtual) 5:00 PM ESTNorth Carolina (Virtual) 5:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter – Dr. Jaleel presenting https://hopeforhs.org/nc2024 info@hopeforhs.org + Google calendar | 12 | 13 | ||||||||||||||||||||||||||||||||||||
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| 21Atlanta (Virtual) 2:00 PM ESTAtlanta (Virtual) 2:00 PM ESTVirtual Support Group Meeting Hosted by the Atlanta, GA Chapter https://hopeforhs.org/AtlantaMtg + Google calendar | 22 | 23 | 24 | 25 | 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.