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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| 8 | 9 | 10 | 11Los Angeles (Virtual) (6:00 PM PST)Los Angeles (Virtual) (6:00 PM PST)Virtual Support Group Meeting Registration Link: https://hopeforhs.org/regLA Email for More Info: Dermatology@med.usc.edu + Google calendar | 12Wisconsin (Virtual) (5:30 PM Central)Wisconsin (Virtual) (5:30 PM Central)Support Group Meeting Conducted by the Wisconsin Chapter. Registration Link: https://hopeforhs.org/regWisconsin Email for More Info: wisconsin@hopeforhs.org + Google calendar | 13 | 14 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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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.