Re: LDN and Multiple Sclerosis (MS) by #28018 ..... Multiple Sclerosis Forum
Date: 11/28/2004 11:17:08 AM ( 20 y ago)
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URL: https://www.curezone.org/forums/fm.asp?i=5122
It's great that LDN is starting to get some recognition. It has given me my life back. A few years back my MS turned Progressive and I had SO many symptoms. Since taking LDN for the last 9 months I have not had ONE new symptom or exacerbation. This comes from someone who has tried everything - believe me. I've had MS for 20 years.
Anyone interested in asking their doctor for LDN should go prepared - remember most doctors haven't even heard of it. I recommend compiling a folder of info.
If you follow the link below it will give you good starting point.
http://brain.hastypastry.net/forums/showthread.php?t=46289
Good luck
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It's great that LDN is starting to get some recognition. It has given me my life back. A few years back my MS turned Progressive and I had SO many symptoms. Since taking LDN for the last 9 months I have not had ONE new symptom or exacerbation. This comes from someone who has tried everything - believe me. I've had MS for 20 years.
Anyone interested in asking their doctor for LDN should go prepared - remember most doctors haven't even heard of it. I recommend compiling a folder of info.
If you follow the link below it will give you good starting point.
http://brain.hastypastry.net/forums/showthread.php?t=46289
Good luck
http://brain.hastypastry.net/forums/showthread.php?t=46289
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