Guest guest Posted December 8, 2008 Report Share Posted December 8, 2008 > > My eyes can't see too well today so if this looks too big I am sorry, you know, I went to the neuro on the 29th of November, and he would not even discuss LDN with me, I don't know a damn thing about it, don't understand it, and I had questions about it, kinda pi & & ed me off. If you know what I mean. Anyways, just thought I would put that in here, anyone had that happen to them, of course, I am in the mist of a fibro flare and not MS, but dont see what that has anything to do with the other...lol....not in my mind. > Hugs to all, > Tonya in Texas >============= What part of Texas are you in? Near Dallas or further away? For Fibro...Try Malic Acid, Bromelain 500mg, Niacinamide 500mg, SAMe, and one very important is Allimax allicin powder derived from garlic, see below..... Allimax, 100% Allicin Powder Capsules, 180 mg, 30 Veggie Caps http://www.iherb.com/ProductDetails.aspx?c=1 & pid=3418 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 8, 2008 Report Share Posted December 8, 2008 Tonya in Texas, Forget using a Neurologist, try your PCP. Until recently there was little if anything official about LDN and MS (or any disease). My Neuro wouldn't even talk about it (now I think he has a couple of patients he prescribes it for). I got my PCP to write my first prescription (he said "well, it can't hurt you"). He implied that he was satisfied it wouldn't break me (put me in the poorhouse and gave me credit for some brains and he just assured himself it wouldn't hurt. It is not on a Neurologists paradigm of how to treat MS so I'd skip that route. Larry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2008 Report Share Posted December 9, 2008 I am 100% with Larry on this one. 's Neurologist would not even look at the 60 stories I brought into her. We went elsewhere for his script and did fantastic on LDN. 3 years later I found out 's neurologist had 5 patients on LDN. has now been on LDN for 4 years. I wonder how many patients she has on LDN now? My best Aletha Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2008 Report Share Posted December 9, 2008 I get my LDN prescription through my neurologist. Of course I had to suffer using Avonex, Copaxone and Novantrone for a few years until he prescribed it for me. Art -- > > I am 100% with Larry on this one. 's Neurologist would not even look at the 60 stories I brought into her. We went elsewhere for his script and did fantastic on LDN. 3 years later I found out 's neurologist had 5 patients on LDN. has now been on LDN for 4 years. I wonder how many patients she has on LDN now? > > My best > Aletha > Quote Link to comment Share on other sites More sharing options...
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