I ask because I am a founder member of LDNNow, the UK organisation to get LDN proven and into regular front line use, so I am also a bit of an expert on LDN too, and have very deep understanding of the immunology, biochemistry and other aspects of the use of LDN.
I have SPMS and it has stopped my progression completely, but it cannot stop the neuropathic damage unfortunately, but then that is due to glia response, particularly the dgrowth of astrocytes. I was too far gone before I found LDN for it to completely prevent all problems as it seems to for many.
We are working on =every angle to get the UK government bodies to fund and do the trials and get this drug finalise, so if you or anyone wants informtaon ofr to help us, ** let us know, also sign our petition to the EU please and watch the Dr Chris Steele MBE video.
Cheers