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
7YEARS
AVERAGE TIME UNTIL CORRECT DIAGNOSIS
10%
OF PATIENTS REPORT LOSING A JOB BECAUSE OF HS
2x
MORE LIKELY TO COMPLETE SUICIDE
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…
Hidradenitis Suppurativa Awareness Week State Proclamations 2019
For the third year running, Hope for HS is organizing a campaign to get Hidradenitis Suppurativa Awareness…
The Skin We’re In: Part 3: How Can I Balance My Microbiome?
A change in diet might be the first order of business. It stands to reason that what…
Documentary Filmmakers at April 23rd Meeting
Hope for HS is pleased to share exciting news! A documentary team from PBS will be doing…