That's wonderful, Carol!

I suffered through the DMD's at first....like most everyone does.....with no benefits and only painful and aggravating side effects and site reactions.

I wish everyone who's struggling with their DMD would just give LDN a try. I was skeptical at first, too, but now you couldn't PAY me to go back to an injectible. Especially when I saw no improvement and felt worse than I did before I even knew I had MS.

Most neuro's (mine included) are protecting themselves from liability due to the fact that LDN isn't an approved MS treatment by the FDA. I could care less.....it works for me and that's all I'm going by. I often wonder if it's more $$ driven than anything.