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
Share your experience with COVID-19 + Hidradenitis Suppurativa
A global registry for patients with Hidradenitis Suppurativa that have also had covid-19 has been developed by…
Patient Voice Published by British Journal of Dermatology
Barriers to care and unmet needs are some of the most important topics hidradenitis suppurativa patients discuss…
Livestream Summary of SHSA 2019
At the December 10th, 2019 Hidradenitis Suppurativa support group meeting of the Detroit chapter of Hope for…
Autoimmune Protocol Diet & its Impact on My HS
Hidradenitis suppurativa (HS) is a horrible disease to live with. It is debilitating, stressful, embarrassing, and limits…
Calling for More Hidradenitis Suppurativa Research!
Newsflash? Probably not. Rallying cry? Let's hope so! "Hidradenitis Suppurativa needs more research!" Of course, patients, caregivers,…
Annual HS Benefit That Partners With Local Musicians
Hello, my name is MaKellee Kathryn Doty-Robinson, but to make it way easier, everyone just calls me…