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.

< November 2023 >
SundayMondayTuesdayWednesdayThursdayFridaySaturday
      1 2 3 4
5 6Webinar: Genetic Research Updates (6:00 PM Eastern)Webinar: Genetic Research Updates (6:00 PM Eastern)Dr Sayed presents on research recently published in JAMA on Genetic Variants Associated With Hidradenitis Suppurativa + Google calendar 7 8Los 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 9 10 11
12 13 14 15Minnesota (In Person) (6:00 PM – 7:30 PM Central)Minnesota (In Person) (6:00 PM – 7:30 PM Central)Who: Individuals with HS and Caregivers
Where: M Health Fairview Clinic
14500 99 th Ave N, Maple Grove, MN
Lower Level, Oak Room
Use the West Entrance and check in at Desk B
A brief presentation will be
given by Dr. Noah
Goldfarb, MD, FAAD about
the most recent advances
in the treatment of HS.
14500 99 th Ave N, Maple Grove, MN Map+ Google calendar
Hershey (Virtual) 5:30 PM ESTHershey (Virtual) 5:30 PM ESTVirtual Support Group Meeting Hosted by the Hershey Chapter + Google calendar
16 17 18
19 20 21 22 23 24 25
26 27 28 29 30Detroit 6:00 – 8:00 PM Eastern (In Person)Detroit 6:00 – 8:00 PM Eastern (In Person)Join us for free dinner and and in person meeting hosted by our Detroit chapter! Jillian Ondreyka has agreed to talk about nutrition and HS, and there will be updates from October’s SHSA meeting. Gilmour Auditorium @ 1 Ford Place, Detroit, MI 48202 + Google calendar    
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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.