Hello Fibro fam!
I've been reading a lot of great replies to Kt's post on fibro fog...so I wanted to chime in on this in a different way.
Last year I was dx with fibro and lupus and during this time the fog had become relentlis and had made my life come to a stand still. A couple of months ago I added to my list of doctors a lyme literate doctor...not only did she find coinfections of lyme, but candida albicans. I've never known much about candida, except for a yeast infection or two in my life. Long story short, the doc put me on a month of diflucan and next month switch to a different antifungal. After being sick from the die off of this nasty fungus, it is an absolute miracle...I've had 5 good days of no fog. I have not felt this clear headed in years! Am I totally cured? No...but something is definitly changing. Also I have been on a no sugar/gluten diet but recently kocked off fruit except for berrries. I'm telling you about this because there was NO reason for me or the other doctors I'm seeing to suspect candida...but this lyme doc checks everything. If you are on a bunch of medications, like I have been for my lupus and fibro...your gut too could be totally out of whack and be causing candida while adding to your fog. How could it hurt to get it checked?