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.
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| 10 | 11 | 12 | 13Los 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 | 14Birmingham (Virtual) – 5:30 PM CSTBirmingham (Virtual) – 5:30 PM CSTVirtual Support Group Meeting Hosted by the Birmingham, AL Chapter + Google calendar | 15 | 16 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 17 | 18 | 19Hope for HS New York Chapter (In Person)Hope for HS New York Chapter (In Person)Time: 6:00 pm – 12:00 am Join us in New York as Hope for HS New York hosts their inaugural meeting! 1991 Marcus Ave, Suite 300 New Hyde Park, NY 11042 + Google calendar | 20Minnesota (Virtual) (6:00 PM – 7:30 PM Central)Minnesota (Virtual) (6:00 PM – 7:30 PM Central)+ Google calendar | 21 | 22 | 23 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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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.