Hs has ruined my life and now it is appearing in my armpits. It’s painful and doctors do absolutely nothing. It ruins any idea I have of pursing a relationship and creating a family. I’m just a mess to the point were I just wish I would die. How do you guys manage this disease so gracefully?

Many people suffer from HS (Hidradenitis Suppurativa) and they go years being misdiagnosed and feeling like they are all alone. I know I did. I wanted to create a place where people can share photos, stories, as questions and spread the word so that someone else doesn't have to go through years of pain alone.