Re: MS and LDN

By now many of you have probably been reading lots of posts regarding LDN therapy. Many of the comments seem to zero in on the absence of clinical studies with it and MS and rightfully so. Well now is your chance to do something to try and get this wonderful therapy recognized for what it is. Some very resourceful people in Ireland have decided to gather together 100,000 names via the net on a petition to get a study started on it for all of us. Here is a link to that online petition. http://www.thepetitionsite.com/takeaction/110785607. Time for all of us to ban together and try and get something going with this. I personally don't need a study in order to realize how great this therapy has been for me, but for all those that do, this is your chance to get involved. Please sign and forward this information to anyone you know that might be interested in helping...thanks so much.

http://www.thepetitionsite.com/takeaction/110785607

http://www.ldninfo.org

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