Re: LDN and Multiple Sclerosis (MS)

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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