Hurray!
The results of a recent study on treating fibromyalgia with low-does naltrexone (LDN) were just released. Here's a summary of the study from WebMD. A 30% reduction in pain is nothing to sneeze at!
This is great news - finally some hard research! Now they just need to fund studies on CFS and LDN. More information on LDN and my own experiences here. Update: I still take 3 mg of LDN each night. It helped me improve about 10% on the disability scale. That might not seem like a lot, but it meant an increase in my quality of life because I could do more. Maybe with real research, more doctors will be willing to prescribe it.
I have had Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) since March 2002. Both of my sons also got ME/CFS at ages 6 and 10. Our younger son fully recovered after 10 years of mild illness. Our older son still has ME/CFS and also has Lyme disease plus two other tick infections. This blog is about how our family lives with chronic illness, with a focus on improving our conditions and enjoying our lives in spite of these challenges.
1 comment:
Sue... I wonder how soon you saw improvement on LDN? How quickly did you increase your dose? Thanks!
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