Guest guest Posted December 20, 2008 Report Share Posted December 20, 2008 The impact is apparent, Readers Digest has a large circulation and many times you see the magazine in the waiting rooms of doctors and other professional offices and libraries. This can only help and will certainly widen LDN's exposure which is needed. We need this and proper research for it to gain acceptance. I had had MS since 1988 and only first learned about LDN in 2005 and this through the nurse in my neurologists office. She knew I was desperate. LDN was offered by her as as last ditch alternative after I failed and got much worse while using Copaxone, Avonex and Novantrone. The next hope for me was Tysabri, which I was looking forward to using as it was being touted as a wonder drug with a high success rate, but when it started killing people it was pulled from the market and I was told to use Betaseron. I really thought life as I knew it was over for me. I am forever grateful to the nurse who brought me to LDN. I shudder to think we're I'd be now. Art -- > > Do you agree with my assessment of the potential impact? > > Am I deluding myself? > > Please. I need a " reality check. " > > Thanks, > > Joe > Quote Link to comment Share on other sites More sharing options...
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