Hello! I'm pretty new to this community, and it seems like a better fit for me than some other online PsA communities have been. My diagnosis of PsA took a long time, probably like most of us. My first diagnosis was fibromyalgia and many years later PsA was added, probably a good 10 years later.. I've been wondering lately do I actually have fibro or was it just the fatigue,brain fog and enthesitis of PsA misdiagnosed as fibro. When my PsA treatment is working, I don't really have the fibro symptoms anymore. Just wondering.