
SUPPORTING PATIENTS
tremendous isolation and emotional burden that accompanies a life with Hidradenitis Suppurativa.

ADVOCATING FOR CHANGE

RAISING AWARENESS
PEOPLE THOUGHT TO HAVE HIDRADENITIS SUPPURATIVA
AVERAGE TIME UNTIL CORRECT DIAGNOSIS
OF PATIENTS REPORT LOSING A JOB BECAUSE OF HS
MORE LIKELY TO COMPLETE SUICIDE

Walk, Run, or Rest for Hidradenitis Suppurativa Awareness
Hey there! Happy HS Awareness Week! If you've ever longed for a Hidradenitis Suppurativa Awareness race like…
Research Survey – Can you assist?
Could you take a moment to answer a few questions to help researchers? The purpose of this…

We asked Doctors why they are passionate about treating HS
Hope for HS is fortunate to collaborate with a number of dedicated HS specialists. We asked them…

Top tips for people living with HS
For Awareness week Hope for HS asked medical providers, caregivers, and those with HS their top tips…

We asked our volunteers, why Hope for HS?
Hope for HS is a 100% volunteer, grass-roots, patient and caregiver directed non-profit organization, supporting and advocating…

Encouraging Messages!
Sometimes we need some uplifting words to get us through the rough patches. Add your uplifting messages…

Hidradenitis Suppurativa Myth Busters
Written by Helen Bui and medically reviewed by Chris Sayed, MD and Tara Jaleel, MD Hidradenitis Suppurativa…