I know I have HS but an confused by some of the posts
Posted , 6 users are following.
I keep reading on here about people here with HS bursting their boils/abcesses. Or pricking them etc,
I have never been able to do that with any of mine because of the pain and the fact they have no head. Literally the only thing that helps is antibiotics and incision afterwards.
All my abcesses have several big red hot bumps with lesser bumps all around and the rest of the area is red and incredibly painful. The redness and infection spreads all round the area too. How people can bear to prick or even touch them is beyond me as I can't move without pain.
The lesser ones begin to drain a bit but only a bit and pressing on them to drain them further is out of the question because of the pain.
Does everyone have a higher pain threshold than me? x
0 likes, 7 replies
crystal_08850 hypercat
Posted
hypercat crystal_08850
Posted
The only exception to this was a monster one I got a few years ago. It was massively infected and I literally couldn't move without huge pain. The doctor sent to to ER and they said they couldn't do it under a local because it was too big. They did it under a short general and I spent 3 days in hospital and had intravenus ab's coz even then they couldn't get rid of all the infection. Gross. Thankfully I have never had any more as bad as that and hope I never do.
I have been very lucky recently not to have had many (touch wood) but did have a couple of lumps on my leg for ages then they both because infected but ab's sorted them out even if they haven't got rid of all of it. I hope they don't recur.
It's a horrible disease isn't it?
Thanks again for your reply. I hope you are ok at the moment love. x
crystal_08850 hypercat
Posted
My dermatologist said they form because your body is attacking the hole /opening where your hair folical meets your sweat gland. Your body attacks that opening due to your autoimmune system. She has studied it and researched it for a while now.
I'm doing good right now! Cutting nightshades put me in remission but if I slip up and eat just a tad of nightshade I have a cyst flare up within hours! Peanuts also do it to me. Before HS, Peanuts would give me horrible ulcers in my throat and ear canals. When the ulcers stopped, it turned into HS instead of ulcers. I have to stay away from nightshades AND nuts now! It's so hard because I love potatoes but my HS was horrible, I had tried everything and that poison just builds up over time.! It's worth watching ingredients to have my life back!
0124 crystal_08850
Posted
kelly452 hypercat
Posted
I said the exact same in my recent post. Mine seems to get seriously inflamed and excrousiating
I can't seem to sit at times never mind pop them.
You're not alone there. I think maybe it depends in the severity of the outbreak but for ten years I've never been able to touch mine.
mikecrisco hypercat
Posted
This is such a painful process it took months for any surgeon to even do the surgery. They just keep putting me on antibiotics which did nothing and the tracks were getting deeper and spreading. This HS disease is not joke and lots of people don't understand the pain involved in having this..
Good luck to all who have this and let's hope for a cure or even where or what causes it..
Mike C
nikki1734 hypercat
Posted
I've been sent by my dermatologists to hospital for emergency surgery to then have a surgeon put me on IV antibiotics. As I told them, it would only delay the surgery. Antibiotics will only make the problem APPEAR fixed, it will come back. Most of the time it works and they will operate. I think having an exceptional dermatologist helps, and I am blessed to have an outstanding one.