Guest guest Posted September 15, 2011 Report Share Posted September 15, 2011 I sent the below message but it failed as I attached a file. I'm re-sending the message and if anyone wants a copy of the file mentioned, please send me your email address. Thanks. Pete, with regards to your comment My partner Margot has advanced secondary progressive MS. She has taken 4.5mg LDN for six months and she has had NO benefit at all from it. When you say 'no benefit', can I ask what it was you were expecting and has Margot got any worse? My partner too has SPMS but it didn't get him out of a wheelchair running marathons and those 'make believe' stories are few and far between. It is annoying when I hear them too. From my experience being on LDN forums for a few years now, it doesn't reverse the disease at all, just stops it from progressing. And if Margot hasn't got any worse in the last six months I would without a shadow of doubt keep her on LDN. Dr Zagon has some excellent studies coming out and I am attaching one which shows how LDN works on autoimmune diseases, cancer and inflammation. I also have Dudley to thank for initially getting me interested in LDN and helping me. For a factual site on LDN, may I recommend you look at www.ldnscience.org? Jayne Crocker LDNNow logo the one to use www.LDNNow.com LDNNow are a political/pressure group of individuals dedicated to getting Low Dose Naltrexone (LDN) accepted into modern medicine and trialled for the myriad of uses it shows benefit for. < Dr Steele MBE, talking about LDN <http://www.ipetitions.com/petition/ldnnow/> Important! Please sign our LDN petition to the European Parliament by clicking here Quote Link to comment Share on other sites More sharing options...
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