Re: has LDN helped anyone who has had MS for a long

[Guest guest]

Hello Aamenten, I am in wheelchair since 1988, been diagnosed in 1983, started LDN in September 2004.

I feel better, can do more things, but cannot get out of wheelchair at all.

Tingling in my hands stopped, hear better on my left ear, feeling in my fingers are better, can hold needle. I hope as the time goes I will feel better still.

I am on a lot of natural stuff...

http://www.geocities.com/mumza18/

Zora -Trinidad - West Indies

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Message: 23 Date: Fri, 03 Jun 2005 00:43:49 -0000 From: "aamenten" <aamenten@...>Subject: has LDN helped anyone who has had MS for a long time?I am hoping that users of this group can help me with some information. I have had MS for 43 years. I am somewhere between relapsing/remitting and in more progressive phase of the disease. I take a lot of drugs, including Betaseron, Ivig, Colchicine, and Methotorexate. All these drugs make me sick with side effects, but they do slow the progress of the the disease... I think. What they do not do is give me back what I have lost. I have visual losses, fatigue, weakness that

causes me to use a wheelchair, difficulty speaking for very long, etc. I wish I knew whether LDN has helped anyone who has had MS as long as I have. Has there been any reversal of symptoms--meaning recovery of loss of function? Any information from users who are at a similar stage of the disease will be very helpful. Thank you.__________________________________________________