Re: My experience so far with LDN for MS, twomonths, (dont feel anything different)

[Guest guest]

I also have ms and hashimotos with a few other problems. I took copaxone for 6 months after starting ldn. I have been taking ldn since 2008. I did have a boost of energy after first starting. However I found the more processed food I ate the less energy I have. Wheat products are the worst. Wheat causes an opiat response in the brain. Ldn works to block this type of response hence you would get less of an energy boost and less repair to your immune system. Try changes to your diet. It will help. Hope you start feeling better. Mari HailSent from my Verizon Wireless BlackBerryFrom: C <covo@...>Date: Fri, 19 Feb 2010 11:17:13 +1100<low dose naltrexone >Subject: Re: [low dose naltrexone] My experience so far with LDN for MS, twomonths, (dont feel anything different)Are you getting your LDN from a recommended pharmacy?f_a_3d wrote:Hello, I have been taking LDN for two months now. Before taking it I read a lot about LDN and its effects (increased energy, vivid dreaming, etc) but I have not experienced anything of that.I have MS and I am taking copaxone and LDN (4.5 mg) at the same time. I have tried for some days taking just the LDN or some other days taking just the copaxone. In my case, I can't notice any difference. I can't say anything about relapses because I haven't had any relapse but the same I can say when I was taking just the copaxone. So basicaly I cant say for sure if LDN is helping or not. Luckily for me I havent had any relapse since I was diagnosed with MS, but I have been diagnosed only for one year so I guess I am just starting. The thing that really bothers me is that I am tired most of the time. That it one of the reasons I started taking LDN but I can't notice any effect. I am wondering if there are other people like me that dont feel any effect when taking LDN... or am I doing something wrong?