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DiscussionSevere brain fog with possible MCTD
Autoimmune Diseases | Last Active: 2 days ago | Replies (21)Comment receiving replies
Replies to "I have MCTD and there are times when I am not all there. Coping skills, like..."
Thank you this is helpful. I also use lists (but then I don't remember where they are) I put alerts in my phone, I write down appointments in a old-timer calender and in my phone but still I get confused. The brain fog is getting worse. I find sleep is important, and make sure to get 7 hours. I do most of what you do, Marye2. But still, it's getting worse now. I had amazing attention and could do many things at once but now I struggle to do one thing without losing my train of thought. Thank you for the idea of EFT tapping. and the book. I also find that having a cup of coffee focuses my mind for a few hours. I am a writer and I drink coffee right when I sit down so that I will be able to work. I am so happy to find this group!!