Re: MS and LDN

Hi there Arfie,
I'd be happy to share my experience with the LDN. I will try to make a long story short and say that I had few bouts of Optic Neuritis which is what led to me discovering that I had MS. I went about my life after my eyesight came back and did remarkably well, not knowing that the endorphin producing exercise that I was doing was what no doubt saved me all those years. I only started to go downhill a few years ago when I slacked off of the exercise. Luckily I found the LDN before there was too much damage. Now, I have some balance issues and cannot walk for any long lengths before I must sit but other then that am doing quite well now. Am on the LDN for about 22 months now and quite convinced it is halting any further progression of the MS. If you want to know more, please do not hesitate to write...wkendz32@hotmail.com I am quite enthused to help anyone find this therapy as I think of it as a Godsend. Hope you find it too. Tweet