I am fairly new to all of this ...I was diagnosed with psoriasis a year ago and PsA since October.
I had to see a new Rheumy yesterday and she thinks my source of pain is Fibro, not PsA. She suggests staying on my methotrexate but also trying neutron for pain. I'm very skeptical about this med also confused and overwhelmed on how to feel about any of this.
Anybody have a similar experience or even encouraging words of wisdom are appreciated ☺
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