Guest guest Posted November 21, 2008 Report Share Posted November 21, 2008 I started using Naltrexone over 6 of 7 or more years ago for my R/R MS. Now doctor thinks I am SP and anyone on this forum know how much importance and usefulness I put in those labels. I think my stress level is reduced by not worrying about what "type" of MS I have. There is another subject in which I don't follow the majority which is when I take my LDN (4.5 mg). I have been fortunate that I have had no ill side-effects and take it at Bedtime (i.e., when I go to sleep). This just makes the most since to me as the drug works with my body's rhythms. I don't believe my location on the planet makes a difference while I do feel that my body's natural rhythms are relevant. That is why I believe if I worked a factory graveyard shift I would take LDN later than I do now or if I lived in the Antarctic I would still take it at bedtime no matter the clock time. I have been exacerbation free since I started LDN (which I use in addition to Copaxone which is supplied to me by the "Chronic Disease Fund"). I am open to hearing any arguments to the contrary. Larry Quote Link to comment Share on other sites More sharing options...
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