Re: Be your own advocate for your well-being. Don't be labeled because you have the symptoms called multiple sclerosis.

Hi there Grog,
Of course I remember you. I did look for some of your posts when I checked out the board the other day but didn't see anything in this forum. I am so limited with my time online these days...aarrrgggggghhhh. Good to see you though.
Oh boy...thought I explained the LDN and its purpose but maybe I didn't. It is not meant as any sort of symptom relief per se but many do experience that for sure. Such things as bladder relief and fatigue relief...etc. A general feeling of normalcy is what most people say comes over them. You see, Low Dose Naltrexone is meant to regulate the immune system back to one that is now normal as opposed to one that attacks, so you see, this is the ultimate in identifying the cause and attending to it don't you think? I feel as if I halted the progression of my MS 2 1/2 years ago when I started the LDN therapy. Very thankful, indeed, to have found it I'll tell ya.
At this point in time, the only thing that will prompt me to add another protocol to my regime would be something that would actually reverse the already permanent damage that I had sustained before using the LDN. I am very interested and following up on the stem cell therapy that is actually happening around the world and I hope will one day become commonplace here in the states.
Well Grog, as I said, I am very happy to see you and please don't hesitate to write to me anytime you like, wkendz32@hotmail.com HAPPY HOLIDAYS!! Joyce Tweet