I’ve only been diagnosed for a few years, but my annual MRI has always had the same “lesion count,” that being “too many to count.” In other words, my MRIs are stable. It is almost time for my annual MRI. Since I have enjoyed such wonderful (though partial) relief from my MS symptoms since I started LDN (September, 2008), I am wondering if there will be any change in my MRI.

Have any of you (us?) had MRIs taken both before and after starting LDN? Was there any change? Better? Worse?