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.

< October 2024 >
SundayMondayTuesdayWednesdayThursdayFridaySaturday
    1 2 3 4 5Chair YogaChair YogaTime: 6:00 pm – 7:00 pm
Come do Chair Yoga with us on Facebook Saturday,October 5th at 6pm EST. We will stream the class live to our Hope for HS Community Facebook page. All ages and levels welcome.
In Person:
5421 W. 9 Mile,
Oak Park, MI 48237
Virtually:
https://www.facebook.com/HopeForHS
https://forms.gle/DBtDCtDuk6jrGDN56 + Google calendar
6 7 8 9DC (Virtual) – 7:00 PM ESTDC (Virtual) – 7:00 PM ESTJoin us for a virtual patient support group meeting hosted by medical students and physicians at Georgetown University Hospital and Howard University Hospital https://hopeforhs.org/regDC dc@hopeforhs.org + Google calendar 10 11 12
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20Atlanta (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 21 22 23North Carolina (Virtual) 8:00 PM ESTNorth Carolina (Virtual) 8:00 PM ESTVirtual Support Group Meeting Hosted by the North Carolina Chapter – Dr. Sayed presenting https://hopeforhs.org/nc2024 info@hopeforhs.org + Google calendar 24 25 26
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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.