Re: Been on LDN since July 2004

[Guest guest]

Keep on with the LDN. It may take more time but you may eventually get some releif. When I got on the LDN almost three years ago, I was a little disappointed because everyone was saying that since being on the LDN, they didn't have to get up every two hours to releive their bladder. I was still having that problem. Every two hours without fail, I was waking to go to the bathroom. Now in the last month, I am noticing that I go every four hours instead of two hours. So I guess that it is just taking a little longer with me but things are improving in that area.

Good Luck

Marie

[low dose naltrexone] Been on LDN since July 2004

Been reading everybodies posts since July 2004. I thought it was time to share a little about me. I was Dx'd with probable MS June of 2004. I have been on LDN since July 2004 after reading about it on this site. This of course was against the advice of my Nuero. I am doing really good since taking LDN. No more fatigue, no more skin sensitivities, less brain fog and no progression. Still get tingling/buzzing in my hands and feet when under stress plus at times they can get very hot. The tingling/buzzing/hot were some of the very first symptoms that I had. Apparently they are here to stay. Anybody have any ideas on how to solve or lessen that problem aside from avoiding stress? Thank you all for the information you provide on this site.You guys are all AWESOME!!!!Keep up the good work!!!!