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 | 10DC (Virtual) (7:00 PM EDT)DC (Virtual) (7:00 PM EDT)Join us for a virtual patient support group meeting hosted by medical students and physicians at Georgetown University Hospital and Howard University Hospital Registration Link: https://hopeforhs.org/regDC Email for More Info: dc@hopeforhs.org + Google calendar | 11Birmingham (Virtual) (5:30 PM CST)Birmingham (Virtual) (5:30 PM CST)Virtual Support Group Meeting Hosted by the Birmingham, AL Chapter
Registration Link:
https://hopeforhs.org/birminghamReg
Email for More Info:
birmingham@hopeforhs.org
+ Google calendar
New England (Virtual) (6:30 PM EST)New England (Virtual) (6:30 PM EST)Join us for a virtual patient support group meeting hosted by physicians from the New England area. Topic: Traveling with HS Registration Link: https://hopeforhs.org/signupNewEngland Email for More Info: newengland@hopeforhs.org + Google calendar | 12 | 13 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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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.