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LDN newbie/take on the World!!!

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Hi katie,

I'm Jim, rrms. Dx'd in Jan 02, took the interferons until Nov '03, then

started on the LDN Dec11,03 and have been a happy camper ever

since. Just a quick note/story of how it affected me(the ldn)

Day1 Fantastic

Day2 Pretty good

Day3 Ok....could be better

Day4 Oh God, I've got MS, someone please, just shoot me.

Day5 Ok, by afternoon almost pretty good.

Day6 From then, up until now, I've 'leveled off' somewhere in the

range of feeling ok to pretty darned good. And considering that I

was really in the pits, that's quite an accomplishment.

If you haven't been to these web links yet, please investigate them

and it will be not only good reading, but good information for you too.

www.remedyfind.com click on the ms testimonials for a good read.

http://www.low dose naltrexone.org/ldn_and_ms.htm This is like the

introductory page to the next one.

http://www.low dose naltrexone.org/index.htm Everything you wanted to

know about ldn and were afraid to ask. (just joking) Scroll down about

a third of the way, and it will list 'most' of the diseases that ldn is being

used to treat. At about two thirds of the way down is a partial list of

compounding pharmacies that are on the recommended list. I get

mine from Skip's in Florida.

Another good source of information is the Dr. Mercola website.

http://www.mercola.com/2005/apr/27/index.htm

It is common in 'some' to get a 'revisitation' of old symptoms that will?

eventually fade? A lot of us have had that, and then, some haven't.

I've been fortunate in that I've had an almost complete reversal of all

symptoms. Some have come back, but now to such a small degree

they are (most of the time) easily ignored or put up with.

There are a lot of well-informed people here that will be more than

willing to share their experiences and take on the ldn. All you have

to do is ask.

Hope that helps.

Anyway, welcome aboard.

Jim &

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