For me it's like a foggy feeling in the head and your not quite all there forgetful do silly things causing accidents get trapped in words your thinking is different not catching all of a conversation and slower picking up simple tasks but since on b12 the fog has lifted for me making me less dangerous around the house only time I feel it again is if mentally fatigued I rest then normally first signs for me is stuttering and saying wrong words and feeling heavy in the head when my mum sees me changing she will say I think you need to have a sleep recharge your talking about toilets again that's my tell tell sign word everything I say when like that has the word toilet in sentence lol can drive you mad as of all words why do I say it for example mum say where's your Hoover oh it's down the toilet mum haha can annoy me when starts my friends and family will say oh she's talking toilets again go rest keza lol .

Brain fog for me it feels like I am there in the moment but, yet not. Hard to explain. I forget things that are said to me, my mind is not clear in its processing at all. Doing things but feeling I am watching someone else do them.

Seems I didnt have it when first diagnosed 10 years ago. The fog brain seems to be correlate with how I'm feeling physically. The worse I feel the worse the fog.

Thank you, when I was being diagnosed they asked me if I had that. I said no. But as I learn more about how FM affects me, I would now say yes. Your comments are helpful.

I've developed an uncontrollable stutter and stammer as well as words coming out jumbled but it's not all the time. Also I am unable to function my main focus is on the pain, spasms, tiredness to be honest, gentle hugs to you all 💕