Guest guest Posted June 7, 2003 Report Share Posted June 7, 2003 I was diagnosed last November, after a bad relapse (in a matter of two weeks I went from being uncoordinated to not being able to walk. Mega dose of Predisone and two months of physical therapy later I was mostly better. About two months ago I became aware that the MS had progressed to where I was having a difficult time starting when urinating. I think I may have had some MS symptoms for about ten years. I am on my first day after taking LDN before bed last night. Today I noticed it is much easier to get started urinating than it has been for a lone time. About normal in that way. My legs no longer feel like they are knotted up! It had been that way since about January. So I am feeling some major improvements on the first day. Still sleepy a lot today, but I did not take the stimulates I had been taking. It seems pretty wonderful to me so far. It hasn't done a thing for my spelling, but then I never could spell anyway. ----- Original Message ----- From: niksihs low dose naltrexone Sent: Saturday, June 07, 2003 8:58 AM Subject: [low dose naltrexone] LDN/MS Those who have had some changes for the better having MS , how long did it take to see any benifit from LDN ? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2006 Report Share Posted January 3, 2006 ME, TOO. -- Re: [low dose naltrexone] LDN/MS i got my script from my family doc when the speacilistrefused me --- maryrobben <maryrobben@...> wrote:---------------------------------does anyone of a doctor in or near St. Louis, MO whowill prescribeLDN? Thank you. Quote Link to comment Share on other sites More sharing options...
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