Humeria is working for me. I took it for 8 weeks and the boils did dry up I decided to stop because self injections are difficult for me. After 2 months I had a flare up lesions increased pain increased severely. I started the injections again in January thing are normal now. People do react differently to medications hopefully there will be more treatments options in the near future. As I mentioned before 52 years suffering with this disease severe pain, bedridden weeks at a time, missing work 4 surgeries, pain meds, antibiotics in my experience Humeria is a blessing for me.

I agree with Kelly. I realize not everyone will get all or any of the side effects, but the side effects are awful, and some of them would be worse than HS! Very scary drug!

Humira has become the "go to" drug for HS. I have never personally taken it, but it does seem to help most people. There is no "one size fits all" treatment for HS. What works for some will not necessarily work for everyone. Doctors need to acknowledge this and patients have to advocate for themselves. They were using Botox for a while and for some reason they stopped. That is another treatment that I have not used. But, there's always going to be some sort of consequence/side effect to every treatment. It's choosing the lesser of two evils and deciding what you can or can not live with. 🤗

Im going to say YES. Humera makes you feel a hole lot better

Cynthia, I am on the keto diet and have no active hs.......basically no sugar and no carbs...(no potatoes, pasta, breads and rices)....just meat and veggies.