Date:   2/23/2005 6:34:53 AM ( 19 y ago)
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URL:   https://www.curezone.org/forums/fm.asp?i=265267

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Hi there,
I am very sorry to hear about your friend. What I would do if I had a friend with this diagnosis is to tell him about the Low Dose Naltrexone. I currently take it for my MS. There are many diseases that it should work for. If there is an immune system component it should work because the LDN works to regulate the immune system back to one that works. I have been using it for just under 3 years now and am leading a very normal life. I truly feel that my MS progression has been halted. You are so right when you say that western medicine has nothing to offer us. However this is a drug, a drug that is currently out of patent so no pharmaceutical companies will be clamoring to help get some clinical studies done. No reason for them to. There is an LDN conference in New York this June 11th which I certainly plan to attend as I am very passionate about everyone learning of this therapy. I say, do your friend a favor and look into it. You can also see what many are saying about their use with MS over at www.remedyfind.com. The website that was set up for the LDN is www.ldninfo.org. If you have any questions about any of this, I'd be very glad to help. Just write to me anytime. wkendz32@hotmail.com There are several in our LDN yahoo group with ALS that are using it with success. Good luck to your friend....{{{hugs}}}.
 

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