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.

< July 2025 >
SundayMondayTuesdayWednesdayThursdayFridaySaturday
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6 7 8 9Los Angeles (Virtual) ( 6:00 PM PST)Los Angeles (Virtual) ( 6:00 PM PST)Join us for a virtual patient support group meeting hosted by the Los Angeles Chapter.
Topic: HS Washes and Topicals
Registration Link: https://hopeforhs.org/regLA Email for More Info: Dermatology@med.usc.edu + Google calendar
10Wisconsin (Virtual) 5:30 PM CentralWisconsin (Virtual) 5:30 PM CentralSupport Group Meeting Conducted by the Wisconsin Chapter. Email for More Info: wihopeforhs@gmail.com + Google calendar 11 12
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27 28 29HS 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 30New York (In Person) (6:00 PM Eastern)New York (In Person) (6:00 PM Eastern)The NY chapter will be hosting Mark Lazarus, PhD, a clinical psychologist who specializes in CBT (Cognitive Behavioral Therapy) with over 30 years of clinical experience, for a 15-minute presentation, followed by an open Q&A discussion. Dinner will be served. 1991 Marcus Ave, Suite 300
New Hyde Park, NY 11042
Registration Link: https://hopeforhs.org/northwellReg + Google calendar
31Teen Support Group (Virtual) (8:00 PM Eastern)Teen Support Group (Virtual) (8:00 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    
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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.