SUPPORTING PATIENTS
Our support groups relieve some of the
tremendous isolation and emotional burden that accompanies a life with Hidradenitis Suppurativa.
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.
1 IN 100
PEOPLE THOUGHT TO HAVE HIDRADENITIS SUPPURATIVA
7 YEARS
AVERAGE TIME UNTIL CORRECT DIAGNOSIS
10%
OF PATIENTS REPORT LOSING A JOB BECAUSE OF HS
2x
MORE LIKELY TO COMPLETE SUICIDE
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…