This is topic Palmitoylethanolamide, PEA, for nerve pain, neuropathy in forum Medical Questions at LymeNet Flash.
To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/1/137562
Posted by ibrakeforticks (Member # 6785) on :
Reviving this topic as a search shows it hasn't been discussed in a while.
The studies and stories out there suggest this supplement can help with nerve pain.
Anyone take PEA and see benefits for neuropathic pain? Thanks!
http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/133778?#000006
https://www.ncbi.nlm.nih.gov/pubmed/27608657
https://vitalitus.com/pea/
https://www.rs4supplements.com/en/?___from_store=nl
https://www.healthrising.org/blog/2014/09/19/palmitoylethanolamide-pea-medical-food-fibromyalgia-chronic-fatigue-syndrome-mecfs/
https://palmitoylethanolamide4pain.com/
Keywords: Neuropathy, Complex Regional Pain Syndrome, CRPS, Reflex Sympathetic Dystrophy, RSD, Central Pain, hyperaesthesia, allodynia, skin, small fiber, polyneuropathy, Chronic Inflammatory Demyelinating Polyneuropathy, CIDP, autoimmune, ganglionopathy, ganglia, microglia, myelin
Posted by Lymetoo (Member # 743) on :
I take it for MCAS. It helps lessen my reactions. I really like it.
Posted by Rumigirl (Member # 15091) on :
Lymetoo,
What brand/ where do you get it? And how much do you take? (If you don't mind mentioning it).
Posted by Badtick (Member # 9794) on :
PEA did nothing for me. R-ALA worked well. Treating viral infections (HHV-6) got rid of it for good!
Posted by Lymetoo (Member # 743) on :
Ergomax OptiPEA from Amazon.
Posted by Lymetoo (Member # 743) on :
I take one per day.
Posted by ibrakeforticks (Member # 6785) on :
quote:
Originally posted by Badtick:
PEA did nothing for me. R-ALA worked well. Treating viral infections (HHV-6) got rid of it for good!
How did you test for and treat HHV-6? So you think HHV-6 caused neuropathy for you?
Powered by UBB.classic™
6.7.3