National Multiple Sclerosis Society Web Artical

[Guest guest]

I would urge all of you that live in America to do what you can to publish your own opinion about LDN. We live in the UK it will in time affect policy here because of your standing in the world in terms of the high regard our authorities have of your medical system.

I find it interesting the web article does not claim to be based on any evidence at all, anecdotal or otherwise. There is no mention of contact with any doctor with experience of LDN or the letters various of you have written saying that it works, unless that is the anecdotal evidence referred to. The theory about MS being an auto immune disease is only one of many and no other theory is mentioned. Indeed the fact that LDN works is potential evidence that the auto immune theory is incorrect.

If you are members of the MS society I would suggest this time you do more than just threaten to withdraw your support. Why not transfer it to the U.K Multiple Sclerosis Resources Centre that is supporting LDN?