Life Update - PsA update and some whingeing.
Hey guys. Todays post is going to be a bit less cheerful, because to be honest, I'm just not feeling it. I've been asked alot lately if I have PsA. The simple answer is yes. I've said many times that for me, my skin is a back seat issue, which I know is the case for many of us. My joints are my top concern, and the cause of most of my pain. Before I started Humira, I was diagnosed with PsA - I was about 19 at official diagnosis, but had the symptoms from about 15/16. It started in my lower back and particularly in my Sacroiliac joint. I tried massage, and physio, I was given a support belt, and told to wear it as often as possible. It was one that was designed to pull my pelvis back in, as the joints were being pushed apart. Then my hip joints started to go. I was regularly only able to walk with crutches, after a while I was told that I had recurring bursitis, and best course of action was to do cortisone shots into the joints as needed. Centerlink sent me for a ...