Thanks so much for article recommendation. Interesting. Not that helpful. By this time, now used most of those aids. You are absolutely correct about the funding. Don't think researchers would like it, if they had brain fog. They don't seem to be very aggressive or creative. There has to be link between brain function and brain fog and possibly autoimmune disease. Don't understand why physicians aren't paying attention. Also, there isn't much PR about ME/CFS and its side effects. Just fibromyalgia because drugs which cost patient money and can pay insurance. Still think it would be great to to have ME/CFS
brain fog group. Patients might be brighter than most physicians think not just pests. In passing, I haven't really compensated.
I'm a writer and my career was ruined. Developed ME/CFS while getting MFA and could never really hold job after that. Wish
I could be more positive. If you write, try to keep writing. Also, read as much as possible and have as much social contact as
possible. No meds really worked regardless of what articles said. Some large hospitals have ME/CFS centers and they might
offer help. Again, many thanks for article.