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.

< May 2023 >
  1 2 3 4 5 6NC Spanish Language Meeting (Virtual) (2:00 PM EST)NC Spanish Language Meeting (Virtual) (2:00 PM EST)Virtual Support Group Meeting Conducted by the NC Chapter. This meeting will be in Spanish + Google calendar
7 8 9 10Los Angeles (Virtual) ( 6:00 PM PST)Los Angeles (Virtual) ( 6:00 PM PST)Virtual Support Group Meeting Hosted by the Los Angeles, CA Chapter + Google calendar 11 12 13
14 15 16 17Hershey (Virtual) 5:30 PM ESTHershey (Virtual) 5:30 PM ESTVirtual Support Group Meeting Hosted by the Hershey Chapter + Google calendar 18 19 20
21 22 23 24 25Webinar on Biologics (8pm EST)Webinar on Biologics (8pm EST)Join Dr. Martin Okun for an informative session on Biologics. What are they? How do they work? What about side effects? + Google calendar 26 27
28 29 30 31      

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.