Okay so how does HS work. Does it progressively get into worse stages or can it be prevented or is it stationary in one stage
Omg that’s awesome to know!!! At least he also has experience with HS and the procedure so it gives u so much reassurance. Idk how to even express how thankful I am for answering all my questions
Is or has anyone used the humira treatment and how was the results? Drs wanted me to try it a few years back but it was super expensive even though they had programs that would help the cost and I was worried about the warning about lung issues because my family has lung problems on both sides. I would be interested in anyones results with this treatment and also how hard was it to set up the programs that help pay for it and was it still expensive in the end?? Thanks in advance for any… read more
Baz I’m too young for the shingles vaccine too. I paid out of pocket and made payments to the drs office. Then later it came out that vaccine was not reliable. I took the new vaccine that came out &… read more
Here in the photo is what cream the doctor 👨⚕️ gave me 👇👇👇👍
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 want to switch from using dove products, and I’m also hesitant to use medication.
I would like to know if antibacterial creams can be used on flares and if anyone does use them and if they received any irritation or if it helped.
Well what there giving us most times don't work.... So most of experience on our own. Then we will know SOON that we have made a mistake. That's why I am thankful to have this fourm to let people who… read more
My doctor just prescribed me with spironolactone but my parents are worried about me taking the pill due to the many side effects. Has anyone ever tried this pill to treat HS? Did you experience any side effects? Do you know of any alternative medication?
My first week taking them I had headaches but other than that, I had some minor weightloss (due to it be a diuretic) years later no effects.
I've been on tetracycline antibiotics for around 20 years and find I'm still getting painful outbreaks and appearing in new areas of my body, trying to research alternative meds
It sounds like your doctor needs to try something else. You've become immune to the medicine.
The doctors in my area aren’t well versed with HS so every time I get prescribe a medication it makes no difference, I still ooze and bleed constantly. Now it’s starting to hurt to sit and that’s affecting my work. Are there soaps and lotions I could ask the doctor to prescribe that would help? My HS is pretty severe I’m never without ulcers, I’m just wondering if they’re anything that’ll make them bearable again.
Anyone receiving Remicade infusions? If so, does it heal sores that you already have or just stop new ones