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Hi, when my pain is really bad I use Paracetamols and antihistamines. Also, a large medical dressing if it is rubbing on my clothes.
I didn't have any flares in Mexico, I ate sugar and carbs every day. I got home and tried to look up HS people in some Mexico cities and there don't seem to be any. I have always thought when I go to the Caribbean my HS is good, and I have always thought it was from the salt water? But now I'm wondering if it's the way they cook their food, I find it odd I can't find people from Mexico with HS?????? I got a flare the day after I returned, so back on the diet??? I am puzzled???
Hey Bonbon do you order this Keto from somewhere or you make it yourself?
It helps reduce the swelling upto an extent. But don't expect it to magically cure it.
HS is still a new diagnosis to me and my specialist is not give me many answers to my questions. I typically get the responses “there’s no clinical evidence or studies”, “I don’t know, I just go off of what the patients tell me”.
So I have been on minocycline for 3 months and has not done much for me. I’ve had 1 de roofing and another set for April. I have always lived a healthy lifestyle but am working on making changes. I am using resorcinol cream but have no idea what it’s supposed to do… read more
You will hear this often, but there is no single treatment that works for everyone. Because, it’s true. HS is poorly understood and understudied. I believe the root cause for me is hormonal. My derm… read more
This app has really inspired me and wanting to do more and getting the word out and more people will not have to deal with this disease alone, and more Dr.s. will need / want to learn more about it so they will be forced to help us with a cure or a way to make us more comfortable and for us to deal with this evil disease. Let's discuss. Blessings
Sign me up friend
Please stay encouraged sir. I've had the same surgery on my underarms & it's no joke @ all. Prayers going up
Hi so I’ve just started my journey into finding out if I do indeed suffer from HS. I’ve been suffering for around 20 years but I’ve never looked into an any diagnosis because I thought that was just me. I’ve recently had a pilonidal cyst removed and I’m on a round of antibiotics as my stitches have become infected :(
My doctor has also prescribed me a low dose antibiotic to take for 3 months, a wash and nasal cream to be used for 5 days before they consider referring me to a dermatologist. Did… read more
This is actually what HS will look like in the very beginning 👇👇😁
I was diagnosed with HS over a year ago now and I get abscess in the usually places armpits, etc. But today I woke up with what feels like one on my eye. I had one before that they had to cut open on my eye but I don't know if this is HS related or not.
It is considered atypical for HS to occur in locations without apocrine glands, such as the face and eyelids. It is possible but uncommon to develop HS on the face; facial symptoms may also be caused… read more
I feel like you should reach out to your insurance and see what hospital, doctors, surgeons are in network because that maybe an issue as well
I believe mine is hereditary, I have multiple aunt's & female cousins that have HS. My mom doesn't get them but almost half of the women in my family have it, I'm not sure about the males in my… read more
