
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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| 1 | 2 | 3 | 4NC Spanish Language Meeting (6:30 PM Eastern) (Virtual)NC Spanish Language Meeting (6:30 PM Eastern) (Virtual)Virtual Support Group Meeting Conducted by the NC Chapter. This meeting will be in Spanish Registration Link: https://hopeforhs.org/espanol + Google calendar Nevada (Virtual) (7:00 PM PST)Nevada (Virtual) (7:00 PM PST)Virtual Support Group Meeting Hosted by the Nevada Chapter Registration Link: https://hopeforhs.org/regNevada Email for More Info: nevada@hopeforhs.org + Google calendar | 5Chicago (Virtual) (8:00 PM CST)Chicago (Virtual) (8:00 PM CST)Virtual Support Group Meeting Hosted by the Chicago Chapter Topic: HS Advocate Spotlight Registration Link: https://hopeforhs.org/chicagoReg Email for More Info: chicago@hopeforhs.org + Google calendar | 6 | 7 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 8 | 9 | 10 | 11DC (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 | 12New 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: HS Surgery Registration Link: https://hopeforhs.org/signupNewEngland Email for More Info: newengland@hopeforhs.org + Google calendar | 13 | 14 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 15 | 16 | 17 | 18New York (In Person) (6:00 PM Eastern)New York (In Person) (6:00 PM Eastern)Join us for a support group meeting where we will start with a gentle, low-impact yoga flow tutorial focused on improving mobility and range of motion in areas affected by HS, followed by dinner and a group discussion. We encourage you to bring your questions, share your experiences, and engage in what promises to be an informative and uplifting discussion. We look forward to seeing you there!
The meeting is on the 3rd floor in the Dermatology department resident conference room, which is located on the same side as the elevators.
1991 Marcus Ave, Suite 300 New Hyde Park, NY 11042 Registration Link: https://forms.gle/SE5Vmc1CDypiMYfY6%20 + Google calendar | 19 | 20 | 21 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 22 | 23Teen Support Group (Virtual) (8:30 PM Eastern)Teen Support Group (Virtual) (8:30 PM Eastern)Virtual meeting of the Hope for HS Teens Chapter in partnership with HS Connect. These meetings are intended for teenaged persons living with hidradenitis suppurativa. Registration Link: https://hopeforhs.org/teenMtgSignup Email for More Info: teenchapter@hopeforhs.org + Google calendar | 24HS Parent Connection (Virtual) (8:00 PM Eastern)HS Parent Connection (Virtual) (8:00 PM Eastern)Virtual meeting of Hope for HS in partnership with HS Connect. These meetings are intended for parents of teenaged persons living with hidradenitis suppurativa. Registration Link: https://hopeforhs.org/parentmtgsignup Email for More Info: teenchapter@hopeforhs.org + Google calendar | 25Virginia (Virtual) (5:30 PM Eastern)Virginia (Virtual) (5:30 PM Eastern)Virtual support group meeting hosted by the Virginia Chapter If you have any topics that you would like to see covered in a future meeting, please drop us a line at virginia@hopeforhs.org Registration Link: https://hopeforhs.org/regVirginia Email for More Info: virginia@hopeforhs.org + Google calendar | 26Birmingham (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 | 27 | 28 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Our support groups relieve some of the
tremendous isolation and emotional burden that accompanies a life with Hidradenitis Suppurativa.

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 of Hidradenitis Suppurativa is vital in promoting compassion, understanding, and a correct, timely diagnosis.