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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)

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Questions about LDN

 
 
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Old 02-08-2017, 02:31 PM #2
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CRPSbe CRPSbe is offline
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Join Date: Mar 2009
Location: Belgium, Europe
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Originally Posted by Brightcloud View Post
I have several questions about low dose naltroxen. Does it work if one has had CRPS for over 20 years? If it does work well for me, would I most likely need to continue using it for the rest of my life? Or if I got pain relief and felt "stabilized", would I be safe to discontinue using LDN?

Lastly, does anyone mix up their own LDN using 50mg. tablets and distilled water? I have read that some compounding labs have had problems with properly preparing LDN capsules/tablets.

Would appreciate any help on this topic. Thanks!

Brightcloud (trying to stay bright)
You have had CRPS for over 20 years? Me too. I stick to what works for me and I'm not messing with that for something that in my eyes is still experimental (at least in this country it is). No one appears to know anything about this yet.
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All the best, Marleen
=====================
Work related (car) accident September 21, 1995, consequences:
- chondromalacia patellae both knees
- RSD both legs (late diagnosis, almost 3 years into RSD) & spread to arms/hands as of 2008
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