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.

< April 2023 >
SundayMondayTuesdayWednesdayThursdayFridaySaturday
            1
2 3 4 5 6 7 8
9 10 11 12 13 14 15
16 17 18Miami (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
Dermatology Library
1600 NW 10th Avenue
RMSB 2090
Miami, FL 33136
https://docs.google.com/forms/d/e/1FAIpQLSe7AY8vCvkqqZcUDZ-DFQfmtV6EVn8tZwTBLEpGT1n6NcknBQ/viewform + Google calendar
19 20 21 22
23Atlanta (Virtual) (2:00 PM EST)Atlanta (Virtual) (2:00 PM EST)Virtual Support Group Meeting Hosted by the Atlanta, GA Chapter https://us02web.zoom.us/meeting/register/tZMkceqqrzIvG9X9CRXsrRKs_3oqeEtpKWgH + Google calendar 24 25 26 27 28 29
30            
+ Export Events

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.