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» LymeNet Flash » Questions and Discussion » Medical Questions » Palmitoylethanolamide, PEA, for nerve pain, neuropathy

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Author Topic: Palmitoylethanolamide, PEA, for nerve pain, neuropathy
ibrakeforticks
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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

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Lymetoo
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I take it for MCAS. It helps lessen my reactions. I really like it.

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Rumigirl
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Lymetoo,

What brand/ where do you get it? And how much do you take? (If you don't mind mentioning it).

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Badtick
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PEA did nothing for me. R-ALA worked well. Treating viral infections (HHV-6) got rid of it for good!
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Lymetoo
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Ergomax OptiPEA from Amazon.

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Opinions, not medical advice!

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Lymetoo
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I take one per day.

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Opinions, not medical advice!

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ibrakeforticks
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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?
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