My vision worsens with my pain levels. I finally got glasses and they help, but not when my pain increases drastically. I was wondering if anyone else experiences vision changes, and how they deal with it?
Yes I had vision changes over the years with my fibro.
Blurry vision and dry eyes are a pain to live with but it's not deadly.
Good reading.
HA! Ha
I don't know if it's related to fibro or not, but my vision changes constantly. Sometimes I'm fine with my glasses, and other times I have trouble seeing anything. I also get double vision occasionally. Had my eyes checked and it's not a physical problem with them, and neurologist couldn't find anything specific wrong either. So I just live with it.