My Story, for my Doctor and me

Hello everyone. I'm going to try to develop a log of events related to my PsA so that I'll have a running report for my doctor when I need help with a flare-up or something. It might be of interest to someone else, so I'll go ahead and publish it here for your reading pleasure.

I hope you all understand that I am NOT a doctor, and anything I say here is only my opinion, or a statement of my personal experience with my disease and should not in any way be taken as advice for someone else to use in their own treatment. That being said, I have found that, for myself, reading other people's experiences sometimes helps me to better understand what I'm going through, so perhaps some of you might see this as helpful, too.

So, good luck to all and here goes: