Guest guest Posted August 26, 2011 Report Share Posted August 26, 2011 Thanks to everyone who replied to my query about the " Naked MS " website. I appreciate all of your comments and thoughts. Charmoon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2011 Report Share Posted August 26, 2011 IM = intermuscular (an injectin, ususally in the rump) > > > Subject: Re: " Naked MS " > To: mscured > Date: Friday, August 26, 2011, 8:27 AM > > > > > > > > > > > > > > > > > Â > > > > > > > > > > > > > > > > > .....> In my 5 year MS journey I've tried just about everything else----1. pharmaceuticals (Rebif made me worse and Solumedrol didn't help anything at all; Gabapentin for neuropathy was a nightmare to get off of), 2. diet, including supplements and eliminating sensitive foods----(some minor improvements mainly by eliminating gluten and dairy), 3. mercury amalgam replacement and Cutler-style chelation (some improvements in 2.5 years, but I can't be sure it's due to the chelation or diet/ supplements, and I feel I still have a long way to go), 4. LDN (no improvement for well over one year, so I gave up on it), 5. CCSVI treatment (only minor improvements). I still have a hard time walking, which is my main problem. > > > > Similar results as I have had :-( Was diagnosed TWICE w/ MS. Took Rebif (made me worse), Copaxone, LDN (no effect good or bad). Diagnosed w/ Lyme Disease. Recently started IM antibiotics, which REALLY seems to be having positive effect as evidenced by me being able to partly pick up my right leg versus merely dragging it behind me. > > > > I sleep a lot. Feel free to send me a not directly to wake me up :-) > > > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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