What does my PsA feel like?
Friday, February 12th, 2010Even without the writings of Kelly Young, before my diagnosis I had a bit of an idea, from a few diagnosed RA friends, what their days were like. The research they do on treatments, the ways they get through the day.
But reading isn’t feeling. Though the entry linked above made me glad I did finally listen to my body shouting at me that something was wrong. Maybe I’ve “caught” the PsA diagnosis early enough (and the treatment methods now let doctors treat before joint damage sets in) that I can put off the degenerative part of this disease as long as possible.