Hello everyone. I am new on here. Obviously very annoyed and discouraged about my HS and would love any tips and recommendations! Ordering the “HS magic ointment” I have seen posted on here. Anyone have good tips or remedies for the scarring?

My husband is in so much pain and has issues sitting/walking. He gets injections from Dermatologist every month to calm it down.

What kind of smell do you have with HS?
Having an issue, but really don't know what's going on. The dr says I have been taking in to much protein, and need a more balanced diet. Been drinking more water and switched up my eating, but the smell seems to keep coming back. Definitely calmed down some, but still smell it from time to time. Please help, never had an issue with it before, after I turned 40 it came out of nowhere.

Has anyone heard about a new treatment for HS being approved by the CDC in a couple of months?

I'm in need of tissue removal and skin grafts. I'm new to the area and in a lot of pain.

Don't know if this is related to HS but when you get a raised bump with no head on it and you squeeze it and a white line comes out - what is that? Does anyone else get them? X

My dermatologist recommended me to use Humira. I have Lupus, but it's remission. Does that affect me to fight infections and lower my immune? I am interested though.

Never really been told what to do or what to use to help during a flare up. I generally squeeze out as much as I can & using shop bought dressings or plasters to cover them before & after rupture but this can cause more skin to be affected & create more lumps. Feels like I can't win so I try my best to make it comfortable enough to get dressed.

Does anyone else have any other skin issues. I’ve noticed my skin has always been sensitive even when I get rashes from allergies. I’m allergic to everything🙃