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Yes! Since my diagnosis in 2017, I’ve never had a neurologist prepare me for many of the symptoms, but especially not brain fog. I thought it was just me and that I was losing it until I saw some others talk about it. But, still, I don’t feel like it’s recognized enough or even mentioned much in the medical articles I’ve read.
And the really sad part about that is that it’s had a huge effect on my life and my mental state and my emotions in dealing with brain fog. But yet I don’t feel like it gets the attention it deserves as a symptom of MG