Many in our community have shared experiencing and struggling with the effects of hepatic encephalopathy, also called brain fog. HepatitisC.net advocate Karen described brain fog as "very frightening because we can go in and out of it, depending on how much ammonia is in our blood stream, what we ate, or how well our meds are working. I had HE for many years and didn’t know it."
How does brain fog affect you and your every day life? What coping methods or treatments have helped you reduce your brain fog?