Humira was the first biologic I tried. Tried to convince my doctor that it’s not for me. Insurance protocols interfere. I was on it for a year with on-going chronic flares and no pain relief. Presently; I’m on a DRMD (Otezla), no notable changes in my psoriasis or PsA. Back to Humira; it’s been maybe two years off of it. I’m having health conditions appearing that indicate organ concerns. Again, everyone is different. I hope you get some relief.

Hello 👋🏼! I’m on Humira and I’ve been on it for a while. Like anything else it takes a while. After my second injection I started getting better. Few side effects but they went away as I used it. Everyone is different. I’ve been using it for fifteen years and it’s still working for me. I also used Enbrel but the doctor switched me to the Humira. I take vitamins and supplements to combat the adverse effects. And also exercise I keep myself moving. I also talk to my doctor if any changes. What can I say it’s working for me. Wish you well and hope this helps you. 🤓

I am just going into my 3rd month of using Humira I have been told that it takes up to 3 months to see improvement. So far it is not any worse but not any improvement yet.

I really appreciate Humira.
After all keeping inflammation down it's key to all injuries you know