So friends. My husband and I got covid over Christmas (family member brought it with them) and true to form, I have long covid again. Husband is 95% well. My conclusion is that people with lifelong CFS/ME, even though mostly controlled, will be way more susceptible to complications than most. My post covid anxiety is back, and just as before, it peaks right at sundown. I'm able to control it using magnesium and Mexicola if I take them 10 or 15 minutes before the sun sets. If I forget, I go ahead and take them but will have to sit or lie down for a while until they take effect.
We're still using dextrose, but in small amounts. Again, my husband responds to it really well and I make sure his bottle of lemon/glucose water is full when he is in a stressful situation or has to do any public speaking. I feel like it helps me but I wouldn't say it has cured my chonic conditions.