Hi to all!
My name is Gloria I. Perez. It's the first time I take part of this forum on PsA.
My struggles started since I was 17 years old. Pain has been my closest friend since then with no definite diagnosis. I read a lot, do a lot of research too.
First told I had Fibromyalgia. Then got epidural shots for my back. Nothing seemed to work.
My skin psoriasis is not so horrible, it is only in one elbow , and both my feet. But my toe nails started changing color and detaching from the bed of the nail. Treated as nail fungus for the past 5 years. Treatments after treatments. Topical medication, laser, even taking out the one of the big toe. Biopsies always came back negative for fungus, but were treated as fungus.
So I decided to be more pro active and it was when I found out about PsA.
I finally started seeing a reumathologist listen to me. He first took some x-rays and run a few lab works , and it was then when he diagnosed me with psoriatic arthritis. All these years without proper treatment. My joints in hands, feet , neck, hip, and lower back are all involved.
Well, he immediately started me on Enbrel last October. After a few months, I was not feeling any better, and had a few infections. He decided to switch me to Humira. For new year insurance issues, I have not started it yet . I am in so much pain lately. Can't wait to give it a try. Please, keep me posted on Humira as PsA treatment, other patient experiences, options, etc.
Thank you for any help you can provide.