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.

< June 2023 >
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4Hope for HS Field Day (In Person)Hope for HS Field Day (In Person)Time: 11:00 am – 2:00 pm
Near Minneapolis? Come join us for in person activities!
Boom Island Park 724 Sibley St NE, Minneapolis, MN 55413 Map https://docs.google.com/document/d/1sz96X1CrrYCYP1xQFYl4UIiJ7qMN5Zz5dXB4k-s_w7s/edit + Google calendar
5 6 7 8 9 10HS Awareness Week Picnic and WalkHS Awareness Week Picnic and WalkTime: 3:00 pm – 5:00 pm
Please join us to spread awareness about HS and connect with the HS community.
This event is FREE and open to the public
Handy Park
26650 Capital Ave
Redford, MI 48239
Map https://runsignup.com/Race/WA%20/Puyallup/HeartsandSolesforHS + Google calendar
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25Atlanta (Virtual) 2:00 PM ESTAtlanta (Virtual) 2:00 PM ESTVirtual Support Group Meeting Hosted by the Atlanta, GA Chapter https://us02web.zoom.us/meeting/register/tZMkceqqrzIvG9X9CRXsrRKs_3oqeEtpKWgH + Google calendar 26 27 28 29 30  
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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.