Re: Re: Protocol for LDN - have MS

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The normal protocol for LDN is 1.5mg for 30 days, 3mg, for 30 days then the max dosage 4.5mg there after if you can handle it. If not people usually back down to 3mg and stay there.

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From: NANCY <nancyrekowski@...>low dose naltrexone Sent: Thursday, January 15, 2009 11:25:54 AMSubject: [low dose naltrexone] Re: new to group - have MS

I have PPMS and went from Rebif to LDN but you can not take the two together. It seems as though your Doc knows that the Rebif isn't working but afraid to commit totally to LDN. The script for 2.5 also seems out of whack as you should start at 1.5 for a few weeks, then begin 3.0. Most people with MS do not use a higher dose than 3.0.I also did IV Solumedrol (aka, draino) & Decadron monthly. I was fortunate that after I began LDN, I had no need for the IV steroids. One of the reasons I began LDN was so that I could finally get off the steroids. You can't do IV steroids and LDN so you must make a choice. For me...LDN was the right choice.>> Hi all,> I have

recently become a member of this group and this is my first > post. After looking through many of the various topics being discussed > about naltrexone, dosages, side effects etc., I would like to ask about > taking Rebif and naltrexone at the same time. (again) I saw my > neurologist on Monday of this week and asked about discontinuing the > rebif and trying naltrexone. I was told that I could try the naltrexone > if I wanted to, was warned about having very bad dreams, was told that > another patient had done this and had serious set backs, and...was told > to keep taking the rebif and start the naltrexone at 2.5mg.> I feel very conflicted at this point. My dr. does stay very current on > ms issues, but I am not sure about this latest suggestion. I am also > supposed to go next Friday for an IV infusion of decadron. Solumedrol > did

not help the numbness in my hands (which is getting worse) and I > had a bad reaction after the second IVIG treatment I tried. Also, I > asked if my records showed if I had been tested for Lyme's (no) so I > have had the blood work done and will wait for the results. > Thanks,> a>