Hi all -

I have been prescribed LDN for my autoimmunity (RA and something else mysterious causing my neuropathy) and I have to say, I feel like it is making my neuropathy worse? I've been on it for almost 3 months and it might be helping my RA, but I ran out of it for a week where I didn't take it and I realize that my neuropathy was better during that week. Is this really a possibility with LDN? Could it really make something worse? I felt like there was no harm in trying it, but maybe I should stop taking it again and see what happens? Thoughts? Any experience with LDN here?

This paper provides evidence that LDN can help with chronic pain though there is nothing specific about neuropathy apart from a couple of animal model studies The use of low-dose naltrexone (LDN) as a novel anti-inflammatory treatment for chronic pain.

Very, very interesting. My rheumatologist scoffed at me when I told her my primary prescribed it. She said it was only successful for people who have fibro.

I experimented with LDN and felt it made my feet feel more numb. My neuropathy is thought to be immune related too.
I don't have pain, or fibro. I even stopped for three weeks and restarted just to be sure it wasn't in my head, but the numbness got worse again.

Wow. Interesting. I really feel like this isn't all in my head, either. And actually, when I went from 1.5mg to 3mg, my legs started burning and tingling and have been ever since. I thought maybe it was just the neuropathy doing its "thing" and it was unrelated, but everything got better when I wasn't taking it. I've stopped again and we'll see. Kind of a bummer because I spent 85 dollars on a 3 month supply. Oh well.

I took 4.5 LDN for close to a month..since all my symptoms started in early October and the symptoms have been changing it's hard for me to say if it was going to work. Also, I have been prescribed so many medications since this started I think I got overwhelmed. So I stopped everything today and I am only going to take gabapentin and nortriptyline fir now. I just saw a neurologist who prescribed melexicane which is supposed to help with pain so I will give it try. I may also revisit the LDN at some point.

Also, if you use Facebook there is a group called Got Endorphins. Everyone in the group uses LDN for a variety of conditions. Its a nice group of supportive people. You may want to join the group and ask them,