Guest guest Posted July 14, 2005 Report Share Posted July 14, 2005 HI I'm RRMS Dx'd March 05. I am excited about the prospect of LDN and hope to talk to my neuro next week. I have one nagging question though: Why is there not more info out there (or here) about MRIs showing that LDN is stopping progression? It sounds like LDN is doing wonders for the syptoms of MS, but for someone lucky enough to have minal symptoms, how do I know that symptoms are not just masked? With so many MSers using LDN surely many have annual MRIs that could provide important anecdotal evidence. I posted on this site a few days ago and six people were kind enough to get back to me with their personal successes-THANKS- Anyone got anything that may help me get some answers? Is there any way to email Dr Bihari (myself or my neuro) with such questions? Thanks in advance for any input you may have to offer. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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