Guest guest Posted January 10, 2010 Report Share Posted January 10, 2010 http://www.larrygc.com/mystory is my story so far, since *4/17/2003 ^ > > Hello everyoe, > I'd lke to hear from anyone who is already on LDN for MS. What > improvements have there been and how long is it before you see these > improvements. I start taking LDN next week. > > Roseann > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2010 Report Share Posted January 10, 2010 Art My MS/LDN story/1988 - 2010 http://ldn.proboards.com/index.cgi?board=personal & action=display & thread=867 > > Hello everyoe, > I'd lke to hear from anyone who is already on LDN for MS. What > improvements have there been and how long is it before you see these > improvements. I start taking LDN next week. > > Roseann > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2010 Report Share Posted January 10, 2010 Lyme mimics so many autoimmune system illnesses http://ldn.proboards.com/index.cgi?board=links & action=display & thread=926 LDN's purpose/what MS drugs can be used w/LDN, etc http://ldn.proboards.com/index.cgi?board=links & action=display & thread=772 Why some May have problems with or fail LDN http://ldn.proboards.com/index.cgi?board=links & action=display & thread=779 Dr McCandless, seldom is LDN stand-alone treatment http://ldn.proboards.com/index.cgi?board=links & action=display & thread=1483 > > > > > > Hello everyoe, > > > I'd lke to hear from anyone who is already on LDN for MS. What > > > improvements have there been and how long is it before you see these > > > improvements. I start taking LDN next week. > > > > > > Roseann > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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