Has anyone tried low dose naltrexone? It’s an Off label medication that I guess works wonders for MS or any autoimmune disease? It was recommended to me and I was just wondering if anyone has tried it and had any luck?
I know you're looking for personal experience, but I wanted to add our information here as well:
Low Dose Naltrexone
Jess, MS Navigator
I used this for about a year,
My insurance did not cover it so I had to pay out of pocket for it. It was like $40 a month. I found it helped for awhile. I did have some very vivid dreams when taking this and some trouble sleeping. So I stopped.
Your Mileage May Vary.
Did you have any flare ups or new lesions develope while on it?