I went from 7 years of CIDP to being diagnosed with MMN (or so the new neuro’s think). I’d like to hear from others as to your routine and medications to deal with this MMN monster disease. I’d also like to know how you think you got MMN (no other disease please, TY).
I get 240 grams of IgG each month, have been getting this for over 8 years. I have type 1 diabetes that is under control. I take MS Contin, Oxy and OTC pain meds. I drink 10 cups of coffee each day (and night), eat well and live at middle income level. I am a widower at 69 years of age.