After another flare up of symptom, oddly more severe in different joints this time. I have been referred again. Again taking weeks and weeks to get in. Blood tests normal although was only sent for them 3 weeks after the initial flare up.
I'm gutted as my finger nails are lifting again and sore on a few. This was growing out until this happened again. I'm worried now that PSA is what it is. The joints it's affecting this time are severely affecting my work. As a nail tech it's the finger i grip and twist clients fingers with, ouch!
I also experience a feeling of coming down with something that starts midday to late evening with heat in hands and pain up my arms but feels more like muscle or nerve pain. They seem linked but not. This didn't happen all the time, I've noticed it more when I've been very busy or stressed. When I wake up the next day outs gone again.
Are these symptoms anything to do with PSa?