Guest guest Posted May 17, 2004 Report Share Posted May 17, 2004 Hi all, I've read all the posts on the MS Soc. and how outraged everyone is so I thought I'd try something else, I'm trying to contact other Ms Foundations not affilated with NMSS I just whipped off an email to the Montel MS foundation (famous talk show host w/MS) to see where they stand on the LDN issue. Of course I just got the usual form letter back saying that the volume of email is too much to answer every one, but please send your check to:... But I got to thinking if alot of emails started to flow into this foundation on this topic maybe they would have to start looking into it. Wishful thinking YES, but not impossible. I'm not even on this drug yet, but all the walls that are put up at even the mention of it has got me pretty fired up about it.(I have noticed any Dr. who has heard of it doesn't say it's bad for you or to not use it just that they won't prescribe it) WHEN I do get it(LDN) , even if it doesn't work for me, it has done alot of good for most of you, so you'll still have me blabbing to anyone who'll listen to get this clinically tested and approved. just another 2 cents. Elaine Quote Link to comment Share on other sites More sharing options...
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