Some good news concerning LDN.

Had a neuro appointment two weeks ago and after going through all the usual motions, he asked if I was still taking the LDN. Well....duh......of course. He also asked if I thought it was helping at all.......YES. A couple times the prescription has gotten messed up and after a week without it, my legs were worse, believe it or not, and also my bladder "issues".

He said he feels after having had MS for such a long time (19 years diagnosed, probable 13 before), I should be in worse shape!!! As I've mentioned before, I just wish he would have agreed to let me try it before I became SPMS being none of the injectables were tolerable for me. He also mentioned the clinical trial now being started for LDN and appeared all happy and telling me something new. Why don't they ever listen to us????

If you haven't already, try it, you'll like it!! It's also much cheaper and less painful than those awful injections!!!