Notification of MS Societies about LDN

[Guest guest]

To the group from Tom in Edmonton:

What do you think about forwarding opinions, news, etc. about LDN to your applicable MS Societies? From what I have been able to gather, most societies do not seem to even acknowledge its existence, but they publish everything the big drug companies want them to.

Maybe a flood of news about LDN, and feedback from actual patients on the crap drugs the societies seem to be pushing might help raise their level of consciousness.

In Canada, our society won't even let me publish a letter saying that LDN helped me. How about that for censorship!

Also, what do you think about letters to the editor of your local newspapers regarding how some information is being stifled by groups that are supposed to be helping? And maybe the URL of remedyfind.com where of course they will notice that LDN is the No.1 rated treatment for MS sufferers?

We might even be able to coordinate our efforts to get better coverage.

If these suggestions have already been made by others, I apologize, but I have not had access to a computer for some time now and therefore am a little bit out of touch.

Whatever, I would appreciate your comments.

Tom in Edmonton