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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5 6 7 8Los 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 9 10 11
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19 20 21 22 23Webinar: Stress and Health (6:30 PM Eastern)Webinar: Stress and Health (6:30 PM Eastern)Stress and Health: Tips, Tricks, and Methods to Deal With Stress and Emotions Registration Link: https://hopeforhs.org/registerStressWebinar Email for More Info: info@hopeforhs.org + Google calendar 24 25
26 27 28Miami (In Person) (6:00 PM EST)Miami (In Person) (6:00 PM EST)Support Group Meeting Conducted by the Miami Chapter.
To register or for questions, email hopeforhsmiami@gmail.com
Registration Link: https://hopeforhs.org/miamiMtgSignup + Google calendar
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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.