This Group is to help people who suffer with HS and their families. No one should ever feel alone with this disease! Please feel Free to invite whoever you would like, post anything relating to HS. Ask questions. Make people aware of this horrible disease!Facebook Facebook Support Group
Facebook Group: Hidradenitis Suppurativa Support Group for patients,friends & family
Hidradenitis suppurativa (HS) Non-Profit (501c3) 2017 Registration
We are currently fundraising for the Non-Profit (501c3) registration of HSAWARENESS.ORG and our growing organization NGO at large. We cannot realize this next and essential step for our critical work without you.
“I WILL NOT HIDE” Hidradenitis suppurativa (HS) Patient Stories Book Series
The “I WILL NOT HIDE” Hidradenitis Suppurativa book series is now available. These patient story volumes tell the stories of Hidradenitis Suppurativa (HS) patients in vivid and personal narrative. Told by HS patients themselves.
HSAWARENESS EMAIL UPDATES
Join our mailing list to learn more about the measurable results being made for the patients of rare and orphan disease communities.