Here are the latest developments regarding my experiment with low-dose naltrexone (LDN).

I’ve taken my medicine every night for 12 nights now; I have a 30-day supply, so I’m nearing the half-way point of this trial period. I was cautioned to not expect any improvement in my CMP symptoms too quickly, and that certainly seems to be wise advice. There has been no “miracle cure” here, for sure.

I believe I am experiencing small, but perceptible changes, however. The most problematic areas for me have been the tingling & numbness in my left foot and the pain my lower back. Although it’s somewhat difficult to tell (due to the “good-day” / “bad-day” nature of the disease), I’ve been starting to think that there is a little improvement. The primary way I have of gauging this is that, at some points during some days recently, I have realized that I’ve not been thinking about the pain. This is pretty incredible, given that most all of the time (in recent days, weeks, months and even years), awareness of the pain is always with me.

I’m hoping that there is some promise in this treatment, but there’s a long way to go. Especially, since I’ve developed additional pain symptoms recently. Given all the time I’ve spent at the computer in the last two to three weeks to address the problems with my former blog, and then getting this version ready to go online, I’ve developed pain in my right forearm and wrist that is consistent with my 1990 tendonitis diagnosis. Amazingly, though, the Trigger Point Therapy Workbook offers me hope that I can treat this with trigger-point massage therapy (and that this may not, after all, be tendonitis but rather part of my CMP condition).

The bottom line of my thinking for today is that there may be some hope for me and my CMP woes as I combine the self-massage and LDN therapies.