howdy folks,
i was diagnosed with rrms just a couple months ago and ive been on the LDN for abot 1 month. i cant say enough good things about the LDN and what its done for me. at the end of july when i left the hospital i was on a walker. yesterday i spent 5 hours at work walking un assisted. (i left my cane in the car and deliberatly, too)my fatigue has gotten so much better. im not 100% yet but im getting better every day.or atleast im getting better at it.
i cant guarentee its the naltrexone thats doing it for me or just the natural cource of the MS, but i wouldnt be able to do that with the copaxone either. i just know that things i had lost, ive gotten back and those things keep improving. i know that the naltrexone isnt a magic cure or a silver bullet and its been suggested that im just feeling plecebo effect of the drug. but if its plecebo i dont care. something is making me feel better and i'll take it.
so far the only side effects ive had was one freaky dream.thats it. just the one. and the best thing is that i can afford this medicine.the rest of the drugs they wanted to put me on would have totaled up to thousands of dollars a month. this one.......25$