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dudleydelany
Joined: 01 Jan 1970 Posts: 3
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mag3
Joined: 01 Jan 1970 Posts: 4
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Posted: Wed Dec 19, 2007 1:36 am Post subject: LDN (Low-dose Naltrexone)-my experience |
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I have RRMS for about 30+ years. I started LDN 6 months ago. I take 4.5ml each night. I did take Copaxone for 6.5 yrs. Never felt well and in May 07 had a very bad reaction. I started LDN with great results. It is a slow but gradual improvement. I no longer have spasicity. I used to drag my right leg. I no longer drag that leg. I no longer trip over my own feet. My strenght has much improved. I can really sleep for the first time in 20 years. No longer getting up 4-5 times a night to urinate. I have more energy and no longer have to nap everyday. I am more heat tolarent however I do not over expose myself to heat as it will cause my symptoms to flare. I've had no numbness, no tingling. 4.5ml is the appropriete dosage for most everyone but time and time again I find people are prescribed such a low dosage they get no benefits at all. I would suggest anyone who may have tried LDN at less than 4.5ml try it again at the correct dosage to see if they experience benefits. It dosen't happen all at once. Some people don't respond for 2 months maybe 3 months even as long as 6 months. I am very happy with my results even though it's not a cure and will stay on LDN and never again do CRAB drugs. People must also be aware that the immune suppressing drugs (Betaceron, Avonex, Steroids) conflict with LDN and must be stopped in order to benefit from LDN. There is enormouse info on the Internet for anyone who chooses to do their own research.  |
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clubvikram
Joined: 01 Jan 1970 Posts: 1
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Posted: Tue May 27, 2008 6:43 am Post subject: |
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the testimonial is very touching. it is good that you are happy with results, thats true that it's not a cure , and you will have to saty with LDN.
stay away from CRAB drugs, thats all i can say
JWP
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Suffering from an addiction. This website has a lot of great resources and treatment centers. http://www.treatmentcenters.org |
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jdoten
Joined: 01 Jan 1970 Posts: 1
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Posted: Fri Aug 22, 2008 9:42 pm Post subject: Re: LDN (Low-dose Naltrexone)-my experience |
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| mag3 wrote: | I have RRMS for about 30+ years. I started LDN 6 months ago. I take 4.5ml each night. I did take Copaxone for 6.5 yrs. Never felt well and in May 07 had a very bad reaction. I started LDN with great results. It is a slow but gradual improvement. I no longer have spasicity. I used to drag my right leg. I no longer drag that leg. I no longer trip over my own feet. My strenght has much improved. I can really sleep for the first time in 20 years. No longer getting up 4-5 times a night to urinate. I have more energy and no longer have to nap everyday. I am more heat tolarent however I do not over expose myself to heat as it will cause my symptoms to flare. I've had no numbness, no tingling. 4.5ml is the appropriete dosage for most everyone but time and time again I find people are prescribed such a low dosage they get no benefits at all. I would suggest anyone who may have tried LDN at less than 4.5ml try it again at the correct dosage to see if they experience benefits. It dosen't happen all at once. Some people don't respond for 2 months maybe 3 months even as long as 6 months. I am very happy with my results even though it's not a cure and will stay on LDN and never again do CRAB drugs. People must also be aware that the immune suppressing drugs (Betaceron, Avonex, Steroids) conflict with LDN and must be stopped in order to benefit from LDN. There is enormouse info on the Internet for anyone who chooses to do their own research.  |
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doggets
Joined: 01 Jan 1970 Posts: 16
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Posted: Wed Oct 22, 2008 5:39 pm Post subject: LDN |
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This has been the most helpful posting I've read. I had stopped taking Rebif in June, I read this in August and decided to try LDN. The first thing I noticed was the spasicity was all but gone, now after two months my fine motor skills are gradually returning. I can type with both hands, cross my right leg over my left and I feel better then I have in years.
I've been dealing with MS since 1985. Until they find a cure I'll be on LDN
SWD |
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